Found 52 hits of Enzyme Inhibition Constant Data Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272468
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCC(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:20,t:16| Show InChI InChI=1S/C27H38FNO6/c1-6-16(3)29-23(34)35-27(22(33)14-30)15(2)11-20-19-8-7-17-12-18(31)9-10-24(17,4)26(19,28)21(32)13-25(20,27)5/h9-10,12,15-16,19-21,30,32H,6-8,11,13-14H2,1-5H3,(H,29,34)/t15-,16?,19-,20-,21-,24-,25-,26-,27-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272523
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19-,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272400
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-5-6-7-12-30-24(35)36-28(23(34)16-31)17(2)13-21-20-9-8-18-14-19(32)10-11-25(18,3)27(20,29)22(33)15-26(21,28)4/h10-11,14,17,20-22,31,33H,5-9,12-13,15-16H2,1-4H3,(H,30,35)/t17-,20-,21-,22-,25-,26-,27-,28-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272434
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C27H38FNO6/c1-15-11-19-18-8-7-16-12-17(31)9-10-24(16,5)26(18,28)20(32)13-25(19,6)27(15,21(33)14-30)35-22(34)29-23(2,3)4/h9-10,12,15,18-20,30,32H,7-8,11,13-14H2,1-6H3,(H,29,34)/t15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272399
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:20,t:16| Show InChI InChI=1S/C27H38FNO6/c1-5-6-11-29-23(34)35-27(22(33)15-30)16(2)12-20-19-8-7-17-13-18(31)9-10-24(17,3)26(19,28)21(32)14-25(20,27)4/h9-10,13,16,19-21,30,32H,5-8,11-12,14-15H2,1-4H3,(H,29,34)/t16-,19-,20-,21-,24-,25-,26-,27-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272520
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H40FNO6/c1-17-13-22-21-10-9-18-14-20(33)11-12-26(18,2)28(21,30)23(34)15-27(22,3)29(17,24(35)16-32)37-25(36)31-19-7-5-4-6-8-19/h11-12,14,17,19,21-23,32,34H,4-10,13,15-16H2,1-3H3,(H,31,36)/t17-,21-,22-,23-,26-,27-,28-,29-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272398
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:19,t:15| Show InChI InChI=1S/C26H36FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h8-9,12,15,18-20,29,31H,5-7,10-11,13-14H2,1-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272494
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C28H38FNO6/c1-16-12-21-20-9-8-17-13-19(32)10-11-25(17,2)27(20,29)22(33)14-26(21,3)28(16,23(34)15-31)36-24(35)30-18-6-4-5-7-18/h10-11,13,16,18,20-22,31,33H,4-9,12,14-15H2,1-3H3,(H,30,35)/t16-,20-,21-,22-,25-,26-,27-,28-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272397
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:18,t:14| Show InChI InChI=1S/C25H34FNO6/c1-5-27-21(32)33-25(20(31)13-28)14(2)10-18-17-7-6-15-11-16(29)8-9-22(15,3)24(17,26)19(30)12-23(18,25)4/h8-9,11,14,17-19,28,30H,5-7,10,12-13H2,1-4H3,(H,27,32)/t14-,17-,18-,19-,22-,23-,24-,25-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 5.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272522
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19+,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 5.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272493
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)CC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C31H46FNO6/c1-18-13-22-21-10-9-19-14-20(35)11-12-28(19,7)30(21,32)23(36)15-29(22,8)31(18,24(37)16-34)39-25(38)33-27(5,6)17-26(2,3)4/h11-12,14,18,21-23,34,36H,9-10,13,15-17H2,1-8H3,(H,33,38)/t18-,21-,22-,23-,28-,29-,30-,31-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.70 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272521
(Adamantan-1-yl-carbamic acid (8S,9R,10S,11S,13S,14...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC12CC3CC(CC(C3)C1)C2)C(=O)CO |r,c:11,t:7,TLB:26:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,26:27:30:34.33.32| Show InChI InChI=1S/C33H44FNO6/c1-18-8-25-24-5-4-22-12-23(37)6-7-29(22,2)32(24,34)26(38)16-30(25,3)33(18,27(39)17-36)41-28(40)35-31-13-19-9-20(14-31)11-21(10-19)15-31/h6-7,12,18-21,24-26,36,38H,4-5,8-11,13-17H2,1-3H3,(H,35,40)/t18-,19?,20?,21?,24-,25-,26-,29-,30-,31?,32-,33-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272492
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H42FNO6/c1-17-13-21-20-8-7-18-14-19(33)9-10-26(18,5)28(20,30)22(34)15-27(21,6)29(17,23(35)16-32)37-24(36)31-12-11-25(2,3)4/h9-10,14,17,20-22,32,34H,7-8,11-13,15-16H2,1-6H3,(H,31,36)/t17-,20-,21-,22-,26-,27-,28-,29-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 12.3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272433
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCC=C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C26H34FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h5,8-9,12,15,18-20,29,31H,1,6-7,10-11,13-14H2,2-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 17.4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272432
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CC(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:19,t:15| Show InChI InChI=1S/C26H36FNO6/c1-14(2)28-22(33)34-26(21(32)13-29)15(3)10-19-18-7-6-16-11-17(30)8-9-23(16,4)25(18,27)20(31)12-24(19,26)5/h8-9,11,14-15,18-20,29,31H,6-7,10,12-13H2,1-5H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 21.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272435
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES COC(=O)[C@H](C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:22,t:18| Show InChI InChI=1S/C27H36FNO8/c1-14-10-19-18-7-6-16-11-17(31)8-9-24(16,3)26(18,28)20(32)12-25(19,4)27(14,21(33)13-30)37-23(35)29-15(2)22(34)36-5/h8-9,11,14-15,18-20,30,32H,6-7,10,12-13H2,1-5H3,(H,29,35)/t14-,15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 28.6 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272469
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCC(C)(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-7-24(3,4)30-23(35)36-28(22(34)15-31)16(2)12-20-19-9-8-17-13-18(32)10-11-25(17,5)27(19,29)21(33)14-26(20,28)6/h10-11,13,16,19-21,31,33H,7-9,12,14-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 55.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272520
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H40FNO6/c1-17-13-22-21-10-9-18-14-20(33)11-12-26(18,2)28(21,30)23(34)15-27(22,3)29(17,24(35)16-32)37-25(36)31-19-7-5-4-6-8-19/h11-12,14,17,19,21-23,32,34H,4-10,13,15-16H2,1-3H3,(H,31,36)/t17-,21-,22-,23-,26-,27-,28-,29-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272523
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19-,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 176 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Glucocorticoid receptor
(Homo sapiens (Human)) | BDBM50272470
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C28H40FNO6/c1-16-11-20-19-8-7-17-12-18(32)9-10-25(17,5)27(19,29)21(33)13-26(20,6)28(16,22(34)14-31)36-23(35)30-15-24(2,3)4/h9-10,12,16,19-21,31,33H,7-8,11,13-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 352 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human glucocorticoid receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272398
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:19,t:15| Show InChI InChI=1S/C26H36FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h8-9,12,15,18-20,29,31H,5-7,10-11,13-14H2,1-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 394 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272433
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCC=C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C26H34FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h5,8-9,12,15,18-20,29,31H,1,6-7,10-11,13-14H2,2-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272397
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:18,t:14| Show InChI InChI=1S/C25H34FNO6/c1-5-27-21(32)33-25(20(31)13-28)14(2)10-18-17-7-6-15-11-16(29)8-9-22(15,3)24(17,26)19(30)12-23(18,25)4/h8-9,11,14,17-19,28,30H,5-7,10,12-13H2,1-4H3,(H,27,32)/t14-,17-,18-,19-,22-,23-,24-,25-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Progesterone receptor
(Homo sapiens (Human)) | BDBM50272493
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)CC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C31H46FNO6/c1-18-13-22-21-10-9-19-14-20(35)11-12-28(19,7)30(21,32)23(36)15-29(22,8)31(18,24(37)16-34)39-25(38)33-27(5,6)17-26(2,3)4/h11-12,14,18,21-23,34,36H,9-10,13,15-17H2,1-8H3,(H,33,38)/t18-,21-,22-,23-,28-,29-,30-,31-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human progesterone receptor |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272493
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)CC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C31H46FNO6/c1-18-13-22-21-10-9-19-14-20(35)11-12-28(19,7)30(21,32)23(36)15-29(22,8)31(18,24(37)16-34)39-25(38)33-27(5,6)17-26(2,3)4/h11-12,14,18,21-23,34,36H,9-10,13,15-17H2,1-8H3,(H,33,38)/t18-,21-,22-,23-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 23.2 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272398
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:19,t:15| Show InChI InChI=1S/C26H36FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h8-9,12,15,18-20,29,31H,5-7,10-11,13-14H2,1-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 18.7 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272435
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES COC(=O)[C@H](C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:22,t:18| Show InChI InChI=1S/C27H36FNO8/c1-14-10-19-18-7-6-16-11-17(31)8-9-24(16,3)26(18,28)20(32)12-25(19,4)27(14,21(33)13-30)37-23(35)29-15(2)22(34)36-5/h8-9,11,14-15,18-20,30,32H,6-7,10,12-13H2,1-5H3,(H,29,35)/t14-,15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 211 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272397
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:18,t:14| Show InChI InChI=1S/C25H34FNO6/c1-5-27-21(32)33-25(20(31)13-28)14(2)10-18-17-7-6-15-11-16(29)8-9-22(15,3)24(17,26)19(30)12-23(18,25)4/h8-9,11,14,17-19,28,30H,5-7,10,12-13H2,1-4H3,(H,27,32)/t14-,17-,18-,19-,22-,23-,24-,25-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 15.9 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272433
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCC=C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C26H34FNO6/c1-5-10-28-22(33)34-26(21(32)14-29)15(2)11-19-18-7-6-16-12-17(30)8-9-23(16,3)25(18,27)20(31)13-24(19,26)4/h5,8-9,12,15,18-20,29,31H,1,6-7,10-11,13-14H2,2-4H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 39 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272434
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C27H38FNO6/c1-15-11-19-18-8-7-16-12-17(31)9-10-24(16,5)26(18,28)20(32)13-25(19,6)27(15,21(33)14-30)35-22(34)29-23(2,3)4/h9-10,12,15,18-20,30,32H,7-8,11,13-14H2,1-6H3,(H,29,34)/t15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.60 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272468
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCC(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:20,t:16| Show InChI InChI=1S/C27H38FNO6/c1-6-16(3)29-23(34)35-27(22(33)14-30)15(2)11-20-19-8-7-17-12-18(31)9-10-24(17,4)26(19,28)21(32)13-25(20,27)5/h9-10,12,15-16,19-21,30,32H,6-8,11,13-14H2,1-5H3,(H,29,34)/t15-,16?,19-,20-,21-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 0.800 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272470
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C28H40FNO6/c1-16-11-20-19-8-7-17-12-18(32)9-10-25(17,5)27(19,29)21(33)13-26(20,6)28(16,22(34)14-31)36-23(35)30-15-24(2,3)4/h9-10,12,16,19-21,31,33H,7-8,11,13-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 0.100 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272492
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H42FNO6/c1-17-13-21-20-8-7-18-14-19(33)9-10-26(18,5)28(20,30)22(34)15-27(21,6)29(17,23(35)16-32)37-24(36)31-12-11-25(2,3)4/h9-10,14,17,20-22,32,34H,7-8,11-13,15-16H2,1-6H3,(H,31,36)/t17-,20-,21-,22-,26-,27-,28-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 21 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272492
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H42FNO6/c1-17-13-21-20-8-7-18-14-19(33)9-10-26(18,5)28(20,30)22(34)15-27(21,6)29(17,23(35)16-32)37-24(36)31-12-11-25(2,3)4/h9-10,14,17,20-22,32,34H,7-8,11-13,15-16H2,1-6H3,(H,31,36)/t17-,20-,21-,22-,26-,27-,28-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 646 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272523
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19-,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 4.90 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272494
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C28H38FNO6/c1-16-12-21-20-9-8-17-13-19(32)10-11-25(17,2)27(20,29)22(33)14-26(21,3)28(16,23(34)15-31)36-24(35)30-18-6-4-5-7-18/h10-11,13,16,18,20-22,31,33H,4-9,12,14-15H2,1-3H3,(H,30,35)/t16-,20-,21-,22-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.80 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272434
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C27H38FNO6/c1-15-11-19-18-8-7-16-12-17(31)9-10-24(16,5)26(18,28)20(32)13-25(19,6)27(15,21(33)14-30)35-22(34)29-23(2,3)4/h9-10,12,15,18-20,30,32H,7-8,11,13-14H2,1-6H3,(H,29,34)/t15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5.30 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272400
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-5-6-7-12-30-24(35)36-28(23(34)16-31)17(2)13-21-20-9-8-18-14-19(32)10-11-25(18,3)27(20,29)22(33)15-26(21,28)4/h10-11,14,17,20-22,31,33H,5-9,12-13,15-16H2,1-4H3,(H,30,35)/t17-,20-,21-,22-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 117 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272399
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:20,t:16| Show InChI InChI=1S/C27H38FNO6/c1-5-6-11-29-23(34)35-27(22(33)15-30)16(2)12-20-19-8-7-17-13-18(31)9-10-24(17,3)26(19,28)21(32)14-25(20,27)4/h9-10,13,16,19-21,30,32H,5-8,11-12,14-15H2,1-4H3,(H,29,34)/t16-,19-,20-,21-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 22 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272432
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES CC(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:19,t:15| Show InChI InChI=1S/C26H36FNO6/c1-14(2)28-22(33)34-26(21(32)13-29)15(3)10-19-18-7-6-16-11-17(30)8-9-23(16,4)25(18,27)20(31)12-24(19,26)5/h8-9,11,14-15,18-20,29,31H,6-7,10,12-13H2,1-5H3,(H,28,33)/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272493
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)CC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C31H46FNO6/c1-18-13-22-21-10-9-19-14-20(35)11-12-28(19,7)30(21,32)23(36)15-29(22,8)31(18,24(37)16-34)39-25(38)33-27(5,6)17-26(2,3)4/h11-12,14,18,21-23,34,36H,9-10,13,15-17H2,1-8H3,(H,33,38)/t18-,21-,22-,23-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 156 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272520
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H40FNO6/c1-17-13-22-21-10-9-18-14-20(33)11-12-26(18,2)28(21,30)23(34)15-27(22,3)29(17,24(35)16-32)37-25(36)31-19-7-5-4-6-8-19/h11-12,14,17,19,21-23,32,34H,4-10,13,15-16H2,1-3H3,(H,31,36)/t17-,21-,22-,23-,26-,27-,28-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.30 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272521
(Adamantan-1-yl-carbamic acid (8S,9R,10S,11S,13S,14...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC12CC3CC(CC(C3)C1)C2)C(=O)CO |r,c:11,t:7,TLB:26:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,26:27:30:34.33.32| Show InChI InChI=1S/C33H44FNO6/c1-18-8-25-24-5-4-22-12-23(37)6-7-29(22,2)32(24,34)26(38)16-30(25,3)33(18,27(39)17-36)41-28(40)35-31-13-19-9-20(14-31)11-21(10-19)15-31/h6-7,12,18-21,24-26,36,38H,4-5,8-11,13-17H2,1-3H3,(H,35,40)/t18-,19?,20?,21?,24-,25-,26-,29-,30-,31?,32-,33-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 3.40 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272522
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19+,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 21.5 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272521
(Adamantan-1-yl-carbamic acid (8S,9R,10S,11S,13S,14...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC12CC3CC(CC(C3)C1)C2)C(=O)CO |r,c:11,t:7,TLB:26:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,26:27:30:34.33.32| Show InChI InChI=1S/C33H44FNO6/c1-18-8-25-24-5-4-22-12-23(37)6-7-29(22,2)32(24,34)26(38)16-30(25,3)33(18,27(39)17-36)41-28(40)35-31-13-19-9-20(14-31)11-21(10-19)15-31/h6-7,12,18-21,24-26,36,38H,4-5,8-11,13-17H2,1-3H3,(H,35,40)/t18-,19?,20?,21?,24-,25-,26-,29-,30-,31?,32-,33-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 9.80 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272435
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES COC(=O)[C@H](C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:22,t:18| Show InChI InChI=1S/C27H36FNO8/c1-14-10-19-18-7-6-16-11-17(31)8-9-24(16,3)26(18,28)20(32)12-25(19,4)27(14,21(33)13-30)37-23(35)29-15(2)22(34)36-5/h8-9,11,14-15,18-20,30,32H,6-7,10,12-13H2,1-5H3,(H,29,35)/t14-,15-,18-,19-,20-,24-,25-,26-,27-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 83 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272469
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCC(C)(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-7-24(3,4)30-23(35)36-28(22(34)15-31)16(2)12-20-19-9-8-17-13-18(32)10-11-25(17,5)27(19,29)21(33)14-26(20,28)6/h10-11,13,16,19-21,31,33H,7-9,12,14-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 53.3 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272522
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19+,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 70.3 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272520
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H40FNO6/c1-17-13-22-21-10-9-18-14-20(33)11-12-26(18,2)28(21,30)23(34)15-27(22,3)29(17,24(35)16-32)37-25(36)31-19-7-5-4-6-8-19/h11-12,14,17,19,21-23,32,34H,4-10,13,15-16H2,1-3H3,(H,31,36)/t17-,21-,22-,23-,26-,27-,28-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272523
((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...)Show SMILES C[C@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19-,23-,24-,25-,28-,29-,30-,31-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 37.3 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Tyrosine aminotransferase
(Rattus norvegicus) | BDBM50272469
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCC(C)(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-7-24(3,4)30-23(35)36-28(22(34)15-31)16(2)12-20-19-9-8-17-13-18(32)10-11-25(17,5)27(19,29)21(33)14-26(20,28)6/h10-11,13,16,19-21,31,33H,7-9,12,14-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 705 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |
Interstitial collagenase
(Homo sapiens (Human)) | BDBM50272400
((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...)Show SMILES CCCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-5-6-7-12-30-24(35)36-28(23(34)16-31)17(2)13-21-20-9-8-18-14-19(32)10-11-25(18,3)27(20,29)22(33)15-26(21,28)4/h10-11,14,17,20-22,31,33H,5-9,12-13,15-16H2,1-4H3,(H,30,35)/t17-,20-,21-,22-,25-,26-,27-,28-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 18 | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of glucocorticoid-mediated human MMP1 expression in PMA stimulated A549 cells assessed as MMP1 protein level by ELISA |
Bioorg Med Chem 16: 7535-42 (2008)
Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX |
More data for this Ligand-Target Pair | |