Found 363 hits Enz. Inhib. hit(s) with Target = 'Ubiquitin carboxyl-terminal hydrolase isozyme L1' 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 |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Mus musculus (Mouse)) | BDBM53441
(MLS001000876 | N-(1H-benzimidazol-2-yl)-3-chlorany...)Show InChI InChI=1S/C14H10ClN3O/c15-10-5-3-4-9(8-10)13(19)18-14-16-11-6-1-2-7-12(11)17-14/h1-8H,(H2,16,17,18,19) | PDB MMDB
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| 400 | -36.5 | 880 | n/a | n/a | n/a | n/a | 7.6 | 25 |
Brigham and Women's Hospital
| Assay Description Inhibition activity and selectivity for UCH-L1 and UCH-L3. |
Chem Biol 10: 837-46 (2003)
Article DOI: 10.1016/j.chembiol.2003.08.010 BindingDB Entry DOI: 10.7270/Q20Z71P9 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50514120
(CHEMBL3407553)Show SMILES CC(=O)O\N=C1/C(=O)N(Cc2cc(Cl)ccc2Cl)c2ccc(Cl)cc12 Show InChI InChI=1S/C17H11Cl3N2O3/c1-9(23)25-21-16-13-7-12(19)3-5-15(13)22(17(16)24)8-10-6-11(18)2-4-14(10)20/h2-7H,8H2,1H3/b21-16- | PDB MMDB
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| 400 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Dana-Farber Cancer Institute
Curated by ChEMBL
| Assay Description Competitive inhibition of UCHL1 in human H1299 cells using Ub-AMC substrate |
J Med Chem 63: 2731-2750 (2020)
Article DOI: 10.1021/acs.jmedchem.9b01138 BindingDB Entry DOI: 10.7270/Q2GF0XTC |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411563
(CHEMBL540117)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccc2ccccc2c1 Show InChI InChI=1S/C19H12N2O4S/c20-14-12-8-13(19(24)25)17(23)21-18(12)26-16(14)15(22)11-6-5-9-3-1-2-4-10(9)7-11/h1-8H,20H2,(H,21,23)(H,24,25) | PDB MMDB
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| Article PubMed
| 740 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411574
(CHEMBL553923)Show SMILES Cc1ccc(cc1)C(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O Show InChI InChI=1S/C16H12N2O4S/c1-7-2-4-8(5-3-7)12(19)13-11(17)9-6-10(16(21)22)14(20)18-15(9)23-13/h2-6H,17H2,1H3,(H,18,20)(H,21,22) | PDB MMDB
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| Article PubMed
| 910 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411577
(CHEMBL536998)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C15H9ClN2O4S/c16-7-3-1-6(2-4-7)11(19)12-10(17)8-5-9(15(21)22)13(20)18-14(8)23-12/h1-5H,17H2,(H,18,20)(H,21,22) | PDB MMDB
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| 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411568
(CHEMBL536764)Show SMILES CC(C)(C)c1ccc(cc1)C(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O Show InChI InChI=1S/C19H18N2O4S/c1-19(2,3)10-6-4-9(5-7-10)14(22)15-13(20)11-8-12(18(24)25)16(23)21-17(11)26-15/h4-8H,20H2,1-3H3,(H,21,23)(H,24,25) | PDB MMDB
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| Article PubMed
| 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411581
(CHEMBL537224)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1cccc2ccccc12 Show InChI InChI=1S/C19H12N2O4S/c20-14-12-8-13(19(24)25)17(23)21-18(12)26-16(14)15(22)11-7-3-5-9-4-1-2-6-10(9)11/h1-8H,20H2,(H,21,23)(H,24,25) | PDB MMDB
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| Article PubMed
| 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411570
(CHEMBL537225)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)C1CCCCC1 Show InChI InChI=1S/C15H16N2O4S/c16-10-8-6-9(15(20)21)13(19)17-14(8)22-12(10)11(18)7-4-2-1-3-5-7/h6-7H,1-5,16H2,(H,17,19)(H,20,21) | PDB MMDB
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| CHEMBL PC cid PC sid UniChem
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| Article PubMed
| 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50326016
(3-amino-2-benzoyl-6-oxo-6,7-dihydrothieno[2,3-b]py...)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1 Show InChI InChI=1S/C15H10N2O4S/c16-10-8-6-9(15(20)21)13(19)17-14(8)22-12(10)11(18)7-4-2-1-3-5-7/h1-6H,16H2,(H,17,19)(H,20,21) | PDB MMDB
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| 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Nat Chem Biol 3: 697-705 (2007)
Article DOI: 10.1038/nchembio.2007.43 BindingDB Entry DOI: 10.7270/Q2KW5G7P |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50326016
(3-amino-2-benzoyl-6-oxo-6,7-dihydrothieno[2,3-b]py...)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1 Show InChI InChI=1S/C15H10N2O4S/c16-10-8-6-9(15(20)21)13(19)17-14(8)22-12(10)11(18)7-4-2-1-3-5-7/h1-6H,16H2,(H,17,19)(H,20,21) | PDB MMDB
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| 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411572
(CHEMBL539345)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C16H9F3N2O4S/c17-16(18,19)7-3-1-6(2-4-7)11(22)12-10(20)8-5-9(15(24)25)13(23)21-14(8)26-12/h1-5H,20H2,(H,21,23)(H,24,25) | PDB MMDB
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| Article PubMed
| 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411573
(CHEMBL557989)Show SMILES COc1ccccc1C(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O Show InChI InChI=1S/C16H12N2O5S/c1-23-10-5-3-2-4-7(10)12(19)13-11(17)8-6-9(16(21)22)14(20)18-15(8)24-13/h2-6H,17H2,1H3,(H,18,20)(H,21,22) | PDB MMDB
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| Article PubMed
| 5.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411575
(CHEMBL536763)Show SMILES Cc1ccccc1C(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O Show InChI InChI=1S/C16H12N2O4S/c1-7-4-2-3-5-8(7)12(19)13-11(17)9-6-10(16(21)22)14(20)18-15(9)23-13/h2-6H,17H2,1H3,(H,18,20)(H,21,22) | PDB MMDB
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| Article PubMed
| 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411579
(CHEMBL539346)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1Cl Show InChI InChI=1S/C15H9ClN2O4S/c16-9-4-2-1-3-6(9)11(19)12-10(17)7-5-8(15(21)22)13(20)18-14(7)23-12/h1-5H,17H2,(H,18,20)(H,21,22) | PDB MMDB
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| Article PubMed
| 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411566
(CHEMBL536995)Show InChI InChI=1S/C13H14N2O4S/c1-13(2,3)9(16)8-7(14)5-4-6(12(18)19)10(17)15-11(5)20-8/h4H,14H2,1-3H3,(H,15,17)(H,18,19) | PDB MMDB
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| Article PubMed
| 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411567
(CHEMBL537227)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1cccs1 Show InChI InChI=1S/C13H8N2O4S2/c14-8-5-4-6(13(18)19)11(17)15-12(5)21-10(8)9(16)7-2-1-3-20-7/h1-4H,14H2,(H,15,17)(H,18,19) | PDB MMDB
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| Article PubMed
| 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411578
(CHEMBL539094)Show SMILES COc1ccc(cc1)C(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O Show InChI InChI=1S/C16H12N2O5S/c1-23-8-4-2-7(3-5-8)12(19)13-11(17)9-6-10(16(21)22)14(20)18-15(9)24-13/h2-6H,17H2,1H3,(H,18,20)(H,21,22) | PDB MMDB
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| Article PubMed
| 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411580
(CHEMBL557988)Show SMILES COC(=O)c1cc2c(N)c(sc2[nH]c1=O)C(=O)c1ccc(C)cc1 Show InChI InChI=1S/C17H14N2O4S/c1-8-3-5-9(6-4-8)13(20)14-12(18)10-7-11(17(22)23-2)15(21)19-16(10)24-14/h3-7H,18H2,1-2H3,(H,19,21) | PDB MMDB
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| >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411562
(CHEMBL540118)Show InChI InChI=1S/C10H8N2O4S/c1-3(13)7-6(11)4-2-5(10(15)16)8(14)12-9(4)17-7/h2H,11H2,1H3,(H,12,14)(H,15,16) | PDB MMDB
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| >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411571
(CHEMBL537226)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccncc1 Show InChI InChI=1S/C14H9N3O4S/c15-9-7-5-8(14(20)21)12(19)17-13(7)22-11(9)10(18)6-1-3-16-4-2-6/h1-5H,15H2,(H,17,19)(H,20,21) | PDB MMDB
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| Article PubMed
| 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411576
(CHEMBL556784)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)N1CCCCC1 Show InChI InChI=1S/C14H15N3O4S/c15-9-7-6-8(14(20)21)11(18)16-12(7)22-10(9)13(19)17-4-2-1-3-5-17/h6H,1-5,15H2,(H,16,18)(H,20,21) | PDB MMDB
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| Article PubMed
| >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411569
(CHEMBL538583)Show InChI InChI=1S/C9H7N3O4S/c10-4-2-1-3(9(15)16)7(14)12-8(2)17-5(4)6(11)13/h1H,10H2,(H2,11,13)(H,12,14)(H,15,16) | PDB MMDB
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| >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50411564
(CHEMBL536997)Show SMILES Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1C(F)(F)F Show InChI InChI=1S/C16H9F3N2O4S/c17-16(18,19)9-4-2-1-3-6(9)11(22)12-10(20)7-5-8(15(24)25)13(23)21-14(7)26-12/h1-5H,20H2,(H,21,23)(H,24,25) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Harvard Medical School
Curated by ChEMBL
| Assay Description Inhibition of UCHL1 |
Bioorg Med Chem Lett 17: 3729-32 (2007)
Article DOI: 10.1016/j.bmcl.2007.04.027 BindingDB Entry DOI: 10.7270/Q2HT2QJ5 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445149
((2S,4S)-4-Fluoro-2-(4-(5-methyl-1H-pyrazol-4-yl)in...)Show SMILES Cc1[nH]ncc1-c1cccc2N(CCc12)C(=O)[C@@H]1C[C@H](F)CN1C#N |r| | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM552974
((2S,4S)-4-fluoro-2-(4-(5- | US11319287, Example 29)Show SMILES FC1C[C@H](N(C1)C#N)C(=O)N1CCc2c1cccc2-c1c[nH]nc1C(F)(F)F | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445160
((S)-2-(4-(1H-pyrrolo[2,3-b]- pyridin-4-yl)indoline...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1ccnc2[nH]ccc12 Show InChI InChI=1S/C21H19N5O/c22-13-25-11-2-5-19(25)21(27)26-12-8-16-14(3-1-4-18(16)26)15-6-9-23-20-17(15)7-10-24-20/h1,3-4,6-7,9-10,19H,2,5,8,11-12H2,(H,23,24)/t19-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445158
((S)-2-(5-(3-(trifluoro- methyl)-1H-pyrazol-4- yl)i...)Show SMILES FC(F)(F)c1n[nH]cc1-c1ccc2CN(Cc2c1)C(=O)[C@@H]1CCCN1C#N Show InChI InChI=1S/C18H16F3N5O/c19-18(20,21)16-14(7-23-24-16)11-3-4-12-8-26(9-13(12)6-11)17(27)15-2-1-5-25(15)10-22/h3-4,6-7,15H,1-2,5,8-9H2,(H,23,24)/t15-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445088
((S)-2-(4-(1H-pyrrolo [2,3-b]pyridin-3- yl)indoline...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1c[nH]c2ncccc12 Show InChI InChI=1S/C21H19N5O/c22-13-25-10-3-7-19(25)21(27)26-11-8-15-14(4-1-6-18(15)26)17-12-24-20-16(17)5-2-9-23-20/h1-2,4-6,9,12,19H,3,7-8,10-11H2,(H,23,24)/t19-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445080
((S)-2-(4-(5-(Trifluoromethyl)-1H-pyrazol-4-yl)indo...)Show SMILES FC(F)(F)c1[nH]ncc1-c1cccc2N(CCc12)C(=O)[C@@H]1CCCN1C#N |r| | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445149
((2S,4S)-4-Fluoro-2-(4-(5-methyl-1H-pyrazol-4-yl)in...)Show SMILES Cc1[nH]ncc1-c1cccc2N(CCc12)C(=O)[C@@H]1C[C@H](F)CN1C#N |r| | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445080
((S)-2-(4-(5-(Trifluoromethyl)-1H-pyrazol-4-yl)indo...)Show SMILES FC(F)(F)c1[nH]ncc1-c1cccc2N(CCc12)C(=O)[C@@H]1CCCN1C#N |r| | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445088
((S)-2-(4-(1H-pyrrolo [2,3-b]pyridin-3- yl)indoline...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1c[nH]c2ncccc12 Show InChI InChI=1S/C21H19N5O/c22-13-25-10-3-7-19(25)21(27)26-11-8-15-14(4-1-6-18(15)26)17-12-24-20-16(17)5-2-9-23-20/h1-2,4-6,9,12,19H,3,7-8,10-11H2,(H,23,24)/t19-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445090
((2S,4S)-4-fluoro-2-(4-(5-(trifluoromethyl)-1H-pyra...)Show SMILES F[C@H]1C[C@H](N(C1)C#N)C(=O)N1CCc2c1cccc2-c1cn[nH]c1C(F)(F)F Show InChI InChI=1S/C18H15F4N5O/c19-10-6-15(26(8-10)9-23)17(28)27-5-4-12-11(2-1-3-14(12)27)13-7-24-25-16(13)18(20,21)22/h1-3,7,10,15H,4-6,8H2,(H,24,25)/t10-,15-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445158
((S)-2-(5-(3-(trifluoro- methyl)-1H-pyrazol-4- yl)i...)Show SMILES FC(F)(F)c1n[nH]cc1-c1ccc2CN(Cc2c1)C(=O)[C@@H]1CCCN1C#N Show InChI InChI=1S/C18H16F3N5O/c19-18(20,21)16-14(7-23-24-16)11-3-4-12-8-26(9-13(12)6-11)17(27)15-2-1-5-25(15)10-22/h3-4,6-7,15H,1-2,5,8-9H2,(H,23,24)/t15-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445160
((S)-2-(4-(1H-pyrrolo[2,3-b]- pyridin-4-yl)indoline...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1ccnc2[nH]ccc12 Show InChI InChI=1S/C21H19N5O/c22-13-25-11-2-5-19(25)21(27)26-12-8-16-14(3-1-4-18(16)26)15-6-9-23-20-17(15)7-10-24-20/h1,3-4,6-7,9-10,19H,2,5,8,11-12H2,(H,23,24)/t19-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | <100 | n/a | n/a | n/a | n/a | n/a | n/a |
MISSION THERAPEUTICS LIMITED
US Patent
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 (μM) in 50% DMSO in a 96-well p... |
US Patent US10669234 (2020)
BindingDB Entry DOI: 10.7270/Q22N559S |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50594734
(CHEMBL5191704) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113970 BindingDB Entry DOI: 10.7270/Q2BV7MNZ |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50589875
(8RK64)Show SMILES [N-]=[N+]=NCC(=O)N1CCc2nc(NC(=O)[C@H]3CCN(C3)C#N)sc2C1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.2c01113 BindingDB Entry DOI: 10.7270/Q21C21TN |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM50589875
(8RK64)Show SMILES [N-]=[N+]=NCC(=O)N1CCc2nc(NC(=O)[C@H]3CCN(C3)C#N)sc2C1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.2c01113 BindingDB Entry DOI: 10.7270/Q21C21TN |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445098
((S)-2-(4-(3-cyclopropyl-1H- pyrazol-4-yl)indoline-...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1c[nH]nc1C1CC1 Show InChI InChI=1S/C20H21N5O/c21-12-24-9-2-5-18(24)20(26)25-10-8-15-14(3-1-4-17(15)25)16-11-22-23-19(16)13-6-7-13/h1,3-4,11,13,18H,2,5-10H2,(H,22,23)/t18-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445099
((S)-2-(4-(2-aminopyrimidin- 4-yl)indoline-1- carbo...)Show SMILES Nc1nccc(n1)-c1cccc2N(CCc12)C(=O)[C@@H]1CCCN1C#N Show InChI InChI=1S/C18H18N6O/c19-11-23-9-2-5-16(23)17(25)24-10-7-13-12(3-1-4-15(13)24)14-6-8-21-18(20)22-14/h1,3-4,6,8,16H,2,5,7,9-10H2,(H2,20,21,22)/t16-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445100
((S)-2-(4-(Pyridin-4-yl)indoline-1-carbonyl)pyrroli...)Show SMILES O=C([C@@H]1CCCN1C#N)N1CCc2c1cccc2-c1ccncc1 |r| Show InChI InChI=1S/C19H18N4O/c20-13-22-11-2-5-18(22)19(24)23-12-8-16-15(3-1-4-17(16)23)14-6-9-21-10-7-14/h1,3-4,6-7,9-10,18H,2,5,8,11-12H2/t18-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445107
((S)-1-Cyano-N-(4-(2-methoxyphenyl)thiazol-2-yl)-N-...)Show SMILES COc1ccccc1-c1csc(n1)N(C)C(=O)[C@@H]1CCCN1C#N |r| Show InChI InChI=1S/C17H18N4O2S/c1-20(16(22)14-7-5-9-21(14)11-18)17-19-13(10-24-17)12-6-3-4-8-15(12)23-2/h3-4,6,8,10,14H,5,7,9H2,1-2H3/t14-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445108
((S)-1-cyano-N-(4-(3- methoxyphenyl)thiazol-2- yl)-...)Show SMILES COc1cccc(c1)-c1csc(n1)N(C)C(=O)[C@@H]1CCCN1C#N Show InChI InChI=1S/C17H18N4O2S/c1-20(16(22)15-7-4-8-21(15)11-18)17-19-14(10-24-17)12-5-3-6-13(9-12)23-2/h3,5-6,9-10,15H,4,7-8H2,1-2H3/t15-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445113
((S)-N-(4-(3-chlorophenyl)- thiazol-2-yl)-1-cyano-N...)Show SMILES CN(C(=O)[C@@H]1CCCN1C#N)c1nc(cs1)-c1cccc(Cl)c1 Show InChI InChI=1S/C16H15ClN4OS/c1-20(15(22)14-6-3-7-21(14)10-18)16-19-13(9-23-16)11-4-2-5-12(17)8-11/h2,4-5,8-9,14H,3,6-7H2,1H3/t14-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445114
((S)-N-(4-(2-chlorophenyl)- thiazol-2-yl)-1-cyano-N...)Show SMILES CN(C(=O)[C@@H]1CCCN1C#N)c1nc(cs1)-c1ccccc1Cl Show InChI InChI=1S/C16H15ClN4OS/c1-20(15(22)14-7-4-8-21(14)10-18)16-19-13(9-23-16)11-5-2-3-6-12(11)17/h2-3,5-6,9,14H,4,7-8H2,1H3/t14-/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445115
((S)-1-cyano-N-methyl-N-(4-phenylthiazol-2-yl)pyrro...)Show SMILES CN(C(=O)[C@@H]1CCCN1C#N)c1nc(cs1)-c1ccccc1 |r| Show InChI InChI=1S/C16H16N4OS/c1-19(15(21)14-8-5-9-20(14)11-17)16-18-13(10-22-16)12-6-3-2-4-7-12/h2-4,6-7,10,14H,5,8-9H2,1H3/t14-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445132
((2S,4S)-1-Cyano-4-methoxy-N-methyl-N-(4-phenylthia...)Show SMILES CO[C@H]1C[C@H](N(C1)C(=O)OC(C)(C)C)C(=O)N(C)c1nc(cs1)-c1ccccc1 |r| Show InChI InChI=1S/C21H27N3O4S/c1-21(2,3)28-20(26)24-12-15(27-5)11-17(24)18(25)23(4)19-22-16(13-29-19)14-9-7-6-8-10-14/h6-10,13,15,17H,11-12H2,1-5H3/t15-,17-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445135
(4-(1-(Cyano-L-prolyl)indolin-4-yl)-1H-pyrazole-5-c...)Show SMILES CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCc2c1cccc2-c1cn[nH]c1C#N |r| | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445137
((S)-2-(4-(2-Aminopyridin-4-yl)indoline-1-carbonyl)...)Show SMILES CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCc2c1cccc2-c1ccnc(N)c1 |r| Show InChI InChI=1S/C23H28N4O3/c1-23(2,3)30-22(29)27-12-5-8-19(27)21(28)26-13-10-17-16(6-4-7-18(17)26)15-9-11-25-20(24)14-15/h4,6-7,9,11,14,19H,5,8,10,12-13H2,1-3H3,(H2,24,25)/t19-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L1
(Homo sapiens (Human)) | BDBM445140
((S)-1-cyano-N-(4- (6-methoxypyridin- 2-yl)thiazol-...)Show SMILES COc1cccc(n1)-c1csc(n1)N(C)C(=O)[C@@H]1CCCN1C#N Show InChI InChI=1S/C16H17N5O2S/c1-20(15(22)13-6-4-8-21(13)10-17)16-19-12(9-24-16)11-5-3-7-14(18-11)23-2/h3,5,7,9,13H,4,6,8H2,1-2H3/t13-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well po... |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2CN774X |
More data for this Ligand-Target Pair | |