Found 37 hits of ic50 for UniProtKB: P15374 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50590284
(CHEMBL5192316)Show SMILES O=C(Nc1ncc(s1)-c1ccc(cc1)C#C)[C@H]1CCN(C1)C#N |r| | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1039/d1md00218j BindingDB Entry DOI: 10.7270/Q27S7SQ9 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50590283
(CHEMBL5169766 | US20230303547, Reference Example D)Show SMILES O=C(Nc1ncc(s1)-c1ccccc1)[C@H]1CCN(C1)C#N |r| | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1039/d1md00218j BindingDB Entry DOI: 10.7270/Q27S7SQ9 |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50431630
(KRX-0401 | PERIFOSINE)Show SMILES CCCCCCCCCCCCCCCCCCOP([O-])(=O)OC1CC[N+](C)(C)CC1 Show InChI InChI=1S/C25H52NO4P/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-24-29-31(27,28)30-25-20-22-26(2,3)23-21-25/h25H,4-24H2,1-3H3 | PDB MMDB
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UniProtKB/SwissProt
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MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 50 | 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 L3
(Homo sapiens (Human)) | BDBM53421
(4-Cyclohexyl-2-phenyl-quinazoline | 4-cyclohexyl-2...)Show InChI InChI=1S/C20H20N2/c1-3-9-15(10-4-1)19-17-13-7-8-14-18(17)21-20(22-19)16-11-5-2-6-12-16/h2,5-8,11-15H,1,3-4,9-10H2 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM50594731
(CHEMBL1241028) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 600 | 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 L3
(Homo sapiens (Human)) | BDBM50069764
(CHEMBL3407501)Show InChI InChI=1S/C17H8FNO3/c18-10-7-5-9(6-8-10)17-19-13-14(20)11-3-1-2-4-12(11)15(21)16(13)22-17/h1-8H | PDB MMDB
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Similars
| Article PubMed
| n/a | n/a | 2.16E+3 | 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 L3
(Homo sapiens (Human)) | BDBM50594730
(CHEMBL5193983)Show SMILES COC(=O)c1cc(c(N)c(n1)-c1ccc2C(=O)C(OC)=C(N)C(=O)c2n1)-c1ccc(OC)c(OC)c1O |t:20| | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 5.00E+3 | 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 L3
(Homo sapiens (Human)) | BDBM50594729
(CHEBI:27485 | CHEMBL1397260)Show SMILES CCCCC[C@H](O)\C=C\[C@@H]1[C@@H](C\C=C/CCCC(O)=O)C=CC1=O |c:20| | PDB MMDB
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MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.00E+4 | 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 L3
(Homo sapiens (Human)) | BDBM50538571
(CHEMBL4635160)Show SMILES C[C@H]1CNCC[C@H]1Oc1c(C)cc(Cl)cc1-c1ccnc2cc(CN3C(=O)C4C(C3=O)C4(C)C)sc12 |r| Show InChI InChI=1S/C28H30ClN3O3S/c1-14-9-16(29)10-19(24(14)35-21-6-7-30-12-15(21)2)18-5-8-31-20-11-17(36-25(18)20)13-32-26(33)22-23(27(32)34)28(22,3)4/h5,8-11,15,21-23,30H,6-7,12-13H2,1-4H3/t15-,21+,22?,23?/m0/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
RAPT Therapeutics, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human GST-tagged UCHL3 expressed in Escherichia coli assessed as cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine1... |
J Med Chem 63: 5398-5420 (2020)
Article DOI: 10.1021/acs.jmedchem.0c00245 BindingDB Entry DOI: 10.7270/Q2XK8K2T |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM65518
(5-Chloro-1-[(2,5-dichlorophenyl)methyl]-1H-indole-...)Show SMILES CC(=O)ON=C1C(=O)N(Cc2cc(Cl)ccc2Cl)c2ccc(Cl)cc12 |w:4.3| 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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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.41E+4 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50442907
(Acetyl Isogambogic Acid | CHEMBL3039433)Show SMILES [H]C12[#6]-[#6@H]-3-[#6]=[#6]4-[#6](=O)-c5c(-[#8]-[#6](-[#6])=O)c6-[#6]=[#6]C([#6])([#6]-[#6]\[#6]=[#6](\[#6])-[#6])[#8]-c6c(-[#6]\[#6]=[#6](\[#6])-[#6])c5-[#8][C@@]14C([#6]\[#6]=[#6](/[#6])-[#6](-[#8])=O)([#8]C2([#6])[#6])[#6]-3=O |r,c:15,t:4,TLB:34:35:44.45:48.3.2,4:3:35:44.45,THB:5:35:44.45:48.3.2,49:48:35:44.45,45:1:5.4:36.48| Show InChI InChI=1S/C40H46O9/c1-21(2)11-10-16-38(9)17-15-27-32(47-38)26(13-12-22(3)4)34-30(33(27)46-24(6)41)31(42)28-19-25-20-29-37(7,8)49-39(35(25)43,40(28,29)48-34)18-14-23(5)36(44)45/h11-12,14-15,17,19,25,29H,10,13,16,18,20H2,1-9H3,(H,44,45)/b23-14+/t25-,29?,38?,39?,40-/m1/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.54E+4 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50326012
(3-(acetoxyimino)-5-bromo-1-(3,4-dichlorobenzyl)ind...)Show SMILES CC(=O)ON=C1C(=O)N(Cc2ccc(Cl)c(Cl)c2)c2ccc(Br)cc12 |w:4.3| Show InChI InChI=1S/C17H11BrCl2N2O3/c1-9(23)25-21-16-12-7-11(18)3-5-15(12)22(17(16)24)8-10-2-4-13(19)14(20)6-10/h2-7H,8H2,1H3 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM50326014
(3-(acetoxyimino)-1-(3,4-dichlorobenzyl)-5-iodoindo...)Show SMILES CC(=O)ON=C1C(=O)N(Cc2ccc(Cl)c(Cl)c2)c2ccc(I)cc12 |w:4.3| Show InChI InChI=1S/C17H11Cl2IN2O3/c1-9(23)25-21-16-12-7-11(20)3-5-15(12)22(17(16)24)8-10-2-4-13(18)14(19)6-10/h2-7H,8H2,1H3 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM200235
(Rifampicin | cid_5381226)Show SMILES CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C2=O)c2C(=O)\C(=C\NN4CCN(C)CC4)C(NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)=C(O)c2c(O)c3C |wU:45.47,41.43,37.39,43.45,35.37,6.6,wD:2.1,39.41,50.53,c:33,t:3,35,54,(15.1,-5.61,;13.64,-5.11,;13.35,-3.6,;14.73,-2.92,;16.01,-3.78,;17.39,-3.1,;17.5,-1.56,;18.99,-1.94,;18.12,-.17,;16.98,.86,;15.65,.09,;15.97,-1.41,;16.45,-2.87,;14.32,.86,;12.94,.04,;14.28,-.72,;11.54,.83,;10.21,.05,;9.44,1.38,;9.43,2.92,;8.1,3.69,;8.09,5.23,;9.42,6,;9.42,7.54,;10.76,5.24,;10.76,3.7,;11.54,2.43,;10.16,1.76,;9.14,.62,;9.33,-.91,;7.86,1.48,;7.43,2.96,;6.47,.8,;6.37,-.73,;4.99,-1.41,;4.49,-2.87,;3.08,-2.24,;5.5,-4.03,;4.48,-5.18,;7.04,-4.13,;6.8,-5.65,;7.9,-2.85,;7.67,-1.33,;9.41,-2.56,;10.9,-2.2,;10.69,-3.42,;10.98,-4.93,;10.48,-6.38,;11.5,-7.54,;8.97,-6.68,;12.07,-2.74,;13.58,-2.44,;12.94,3.22,;12.96,4.76,;14.32,2.4,;15.65,3.17,;15.65,4.71,;16.98,2.4,;18.32,3.17,)| Show InChI InChI=1S/C43H58N4O12/c1-21-12-11-13-22(2)42(55)45-33-28(20-44-47-17-15-46(9)16-18-47)37(52)30-31(38(33)53)36(51)26(6)40-32(30)41(54)43(8,59-40)57-19-14-29(56-10)23(3)39(58-27(7)48)25(5)35(50)24(4)34(21)49/h11-14,19-21,23-25,29,34-35,39,44,49-51,53H,15-18H2,1-10H3,(H,45,55)/b12-11+,19-14+,22-13-,28-20+/t21-,23+,24+,25+,29-,34-,35+,39+,43-/m0/s1 | PDB MMDB
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B.MOAD antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.48E+4 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50594733
(CHEMBL4303698)Show SMILES CC(=O)O\N=C1\C(=O)N(Cc2cc(Cl)ccc2Cl)c2ccc(Cl)cc12 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.50E+4 | 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 L3
(Homo sapiens (Human)) | BDBM50326013
(3-(acetoxyimino)-5-bromo-1-(2,5-dichlorobenzyl)ind...)Show SMILES CC(=O)ON=C1C(=O)N(Cc2cc(Cl)ccc2Cl)c2ccc(Br)cc12 |w:4.3| Show InChI InChI=1S/C17H11BrCl2N2O3/c1-9(23)25-21-16-13-7-11(18)2-5-15(13)22(17(16)24)8-10-6-12(19)3-4-14(10)20/h2-7H,8H2,1H3 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM205457
((2R,4aS,6aR,6aS,14aS,14bR)-10-hydroxy-2,4a,6a,6a,9...)Show SMILES CC1=C(O)C(=O)C=C2C1=CC=C1[C@@]2(C)CC[C@@]2(C)[C@@H]3C[C@@](C)(CC[C@]3(C)CC[C@]12C)C(O)=O |r,c:1,6,11,t:9| Show InChI InChI=1S/C29H38O4/c1-17-18-7-8-21-27(4,19(18)15-20(30)23(17)31)12-14-29(6)22-16-26(3,24(32)33)10-9-25(22,2)11-13-28(21,29)5/h7-8,15,22,31H,9-14,16H2,1-6H3,(H,32,33)/t22-,25-,26-,27+,28-,29+/m1/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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MCE PC cid PC sid PDB UniChem
| Article PubMed
| n/a | n/a | 3.21E+4 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50326015
(5-(4-butylphenyl)-4-(4-isopropylphenyl)-4H-1,2,4-t...)Show SMILES CCCCc1ccc(cc1)-c1n[nH]c(=S)n1-c1ccc(cc1)C(C)C Show InChI InChI=1S/C21H25N3S/c1-4-5-6-16-7-9-18(10-8-16)20-22-23-21(25)24(20)19-13-11-17(12-14-19)15(2)3/h7-15H,4-6H2,1-3H3,(H,23,25) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM50594732
(CHEMBL5195092) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4.70E+4 | 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 L3
(Homo sapiens (Human)) | BDBM50242207
(CHEMBL455364 | Mangiferin)Show SMILES OC[C@H]1O[C@@H](Oc2c(O)cc3oc4cc(O)c(O)cc4c(=O)c3c2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C19H18O12/c20-4-11-14(25)16(27)17(28)19(30-11)31-18-8(23)3-10-12(15(18)26)13(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,14,16-17,19-23,25-28H,4H2/t11-,14-,16+,17-,19+/m1/s1 | PDB MMDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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CHEMBL KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 5.26E+4 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM24778
(2-methyl-1,4-dihydronaphthalene-1,4-dione | 2-meth...)Show InChI InChI=1S/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H3 | PDB MMDB
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| n/a | n/a | 7.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of UCHL3 in human H1299 cells |
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 L3
(Homo sapiens (Human)) | BDBM24778
(2-methyl-1,4-dihydronaphthalene-1,4-dione | 2-meth...)Show InChI InChI=1S/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H3 | PDB MMDB
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| Article PubMed
| n/a | n/a | 7.10E+4 | 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 L3
(Homo sapiens (Human)) | BDBM50552483
(CHEMBL4763594)Show SMILES Nc1ccc(cc1)-c1cn(Cc2cc(cc(c2)-c2cccc(c2)C(O)=O)C(O)=O)nn1 | PDB MMDB
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| n/a | n/a | 7.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of recombinant human UCHL3 assessed as reduction in cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine110-glycine using... |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115931 BindingDB Entry DOI: 10.7270/Q2R49VFD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50538549
(CHEMBL4641424)Show SMILES Nc1cc(ccn1)-c1cc(Cl)cc2CC(Oc12)C(=O)N1CCNCC1 Show InChI InChI=1S/C18H19ClN4O2/c19-13-7-12-8-15(18(24)23-5-3-21-4-6-23)25-17(12)14(10-13)11-1-2-22-16(20)9-11/h1-2,7,9-10,15,21H,3-6,8H2,(H2,20,22) | PDB MMDB
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| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
RAPT Therapeutics, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human GST-tagged UCHL3 expressed in Escherichia coli assessed as cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine1... |
J Med Chem 63: 5398-5420 (2020)
Article DOI: 10.1021/acs.jmedchem.0c00245 BindingDB Entry DOI: 10.7270/Q2XK8K2T |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50270667
(CHEMBL4130194)Show SMILES CC(Cc1ccccc1)C(=O)N1CCC(O)(Cn2cnc3ccccc3c2=O)CC1 Show InChI InChI=1S/C24H27N3O3/c1-18(15-19-7-3-2-4-8-19)22(28)26-13-11-24(30,12-14-26)16-27-17-25-21-10-6-5-9-20(21)23(27)29/h2-10,17-18,30H,11-16H2,1H3 | PDB MMDB
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| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
RAPT Therapeutics, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human GST-tagged UCHL3 expressed in Escherichia coli assessed as cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine1... |
J Med Chem 63: 5398-5420 (2020)
Article DOI: 10.1021/acs.jmedchem.0c00245 BindingDB Entry DOI: 10.7270/Q2XK8K2T |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23421
(1-benzyl-3-hydroxy-4-[(5-methylfuran-2-yl)carbonyl...)Show SMILES Cc1ccc(o1)C(=O)C1C(N(Cc2ccccc2)C(=O)C1=O)c1cccnc1 Show InChI InChI=1S/C22H18N2O4/c1-14-9-10-17(28-14)20(25)18-19(16-8-5-11-23-12-16)24(22(27)21(18)26)13-15-6-3-2-4-7-15/h2-12,18-19H,13H2,1H3 | PDB MMDB
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| n/a | n/a | 1.03E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50069762
(CHEMBL3182437 | ML323 | US9802904, 87)Show SMILES CC(C)c1ccccc1-c1ncc(C)c(NCc2ccc(cc2)-n2ccnn2)n1 Show InChI InChI=1S/C23H24N6/c1-16(2)20-6-4-5-7-21(20)23-24-14-17(3)22(27-23)25-15-18-8-10-19(11-9-18)29-13-12-26-28-29/h4-14,16H,15H2,1-3H3,(H,24,25,27) | PDB MMDB
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| n/a | n/a | >1.14E+5 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM65524
((-)-Aricine | Heterophylline (VAN) | Quinovatine)Show SMILES COC(=O)C1=CO[C@@H](C)[C@@H]2CN3CCc4c([nH]c5cc(OC)ccc45)[C@@H]3C[C@H]12 |t:4| Show InChI InChI=1S/C22H26N2O4/c1-12-17-10-24-7-6-15-14-5-4-13(26-2)8-19(14)23-21(15)20(24)9-16(17)18(11-28-12)22(25)27-3/h4-5,8,11-12,16-17,20,23H,6-7,9-10H2,1-3H3/t12-,16-,17-,20-/m0/s1 | PDB MMDB
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| n/a | n/a | >1.14E+5 | n/a | n/a | n/a | n/a | 7.5 | 25 |
University of Delaware
| Assay Description Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff... |
ACS Chem Biol 12: 2399-2407 (2017)
Article DOI: 10.1021/acschembio.7b00543 BindingDB Entry DOI: 10.7270/Q21J97WD |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23427
(5-(4-fluorophenyl)-3-hydroxy-4-[(5-methylfuran-2-y...)Show SMILES Cc1ccc(o1)C(=O)C1C(N(Cc2cccnc2)C(=O)C1=O)c1ccc(F)cc1 Show InChI InChI=1S/C22H17FN2O4/c1-13-4-9-17(29-13)20(26)18-19(15-5-7-16(23)8-6-15)25(22(28)21(18)27)12-14-3-2-10-24-11-14/h2-11,18-19H,12H2,1H3 | PDB MMDB
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| n/a | n/a | 1.23E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23426
(3-hydroxy-5-(4-methoxyphenyl)-1-(1,3,4-thiadiazol-...)Show SMILES COc1ccc(cc1)C1C(C(=O)c2cccs2)C(=O)C(=O)N1c1nncs1 Show InChI InChI=1S/C18H13N3O4S2/c1-25-11-6-4-10(5-7-11)14-13(15(22)12-3-2-8-26-12)16(23)17(24)21(14)18-20-19-9-27-18/h2-9,13-14H,1H3 | PDB MMDB
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| n/a | n/a | 1.54E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50271098
(CHEMBL4129140)Show SMILES CC(=O)C1=C(O)C(=O)N(CCc2ccc(Cl)c(Cl)c2)C1c1ccc(Br)cc1 |c:3| Show InChI InChI=1S/C20H16BrCl2NO3/c1-11(25)17-18(13-3-5-14(21)6-4-13)24(20(27)19(17)26)9-8-12-2-7-15(22)16(23)10-12/h2-7,10,18,26H,8-9H2,1H3 | PDB MMDB
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| n/a | n/a | >2.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Progenra, Inc.
Curated by ChEMBL
| Assay Description Inhibition of UCH-L3 (unknown origin) using Ub-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by flu... |
J Med Chem 61: 422-443 (2018)
Article DOI: 10.1021/acs.jmedchem.7b00498 BindingDB Entry DOI: 10.7270/Q2CR5WVG |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM50608424
(CHEMBL5267683) | PDB MMDB
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TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23425
(ChemBridge CNS-Set 7909542, 5 | N-{3-[1-acetyl-5-(...)Show SMILES CCS(=O)(=O)Nc1cccc(c1)C1=NN(C(C1)c1cccs1)C(C)=O |t:13| Show InChI InChI=1S/C17H19N3O3S2/c1-3-25(22,23)19-14-7-4-6-13(10-14)15-11-16(17-8-5-9-24-17)20(18-15)12(2)21/h4-10,16,19H,3,11H2,1-2H3 | PDB MMDB
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| n/a | n/a | >3.31E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23424
(ChemBridge CNS-Set 6382507, 4 | N-cyclopropyl-2-[(...)Show SMILES COc1ccc(cc1)N(CC(=O)NC1CC1)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C19H22N2O4S/c1-14-3-11-18(12-4-14)26(23,24)21(13-19(22)20-15-5-6-15)16-7-9-17(25-2)10-8-16/h3-4,7-12,15H,5-6,13H2,1-2H3,(H,20,22) | PDB MMDB
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| n/a | n/a | >3.34E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23429
(2-[benzene(3-methoxyphenyl)sulfonamido]-N-cyclopen...)Show SMILES COc1cccc(c1)N(CC(=O)NC1CCCC1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C20H24N2O4S/c1-26-18-11-7-10-17(14-18)22(15-20(23)21-16-8-5-6-9-16)27(24,25)19-12-3-2-4-13-19/h2-4,7,10-14,16H,5-6,8-9,15H2,1H3,(H,21,23) | PDB MMDB
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| n/a | n/a | >3.86E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23430
(4-({[5-(furan-2-yl)-4-phenyl-4H-1,2,4-triazol-3-yl...)Show InChI InChI=1S/C16H13N5OS2/c17-15-18-11(9-23-15)10-24-16-20-19-14(13-7-4-8-22-13)21(16)12-5-2-1-3-6-12/h1-9H,10H2,(H2,17,18) | PDB MMDB
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| n/a | n/a | >3.87E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |
Ubiquitin carboxyl-terminal hydrolase isozyme L3
(Homo sapiens (Human)) | BDBM23428
(ChemBridge CNS-Set 6699002, 8 | N-cyclopropyl-2-[(...)Show SMILES COc1ccc(cc1)S(=O)(=O)N(CC(=O)NC1CC1)c1ccc(C)cc1 Show InChI InChI=1S/C19H22N2O4S/c1-14-3-7-16(8-4-14)21(13-19(22)20-15-5-6-15)26(23,24)18-11-9-17(25-2)10-12-18/h3-4,7-12,15H,5-6,13H2,1-2H3,(H,20,22) | PDB MMDB
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| n/a | n/a | >4.01E+5 | n/a | n/a | n/a | n/a | 7.8 | 22 |
Waseda University
| Assay Description Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission... |
Bioorg Med Chem 15: 6810-8 (2007)
Article DOI: 10.1016/j.bmc.2007.07.016 BindingDB Entry DOI: 10.7270/Q2ZK5DZK |
More data for this Ligand-Target Pair | |