Found 150 hits with Last Name = 'sukenick' and Initial = 'g' 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 |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554392
(CHEMBL4751044)Show SMILES COC[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554394
(CHEMBL4784875)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554397
(CHEMBL4741140)Show SMILES COC[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 0.800 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554389
(CHEMBL4796570)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554385
(CHEMBL4764897)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554386
(CHEMBL4758484)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.60 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554384
(CHEMBL4784015)Show SMILES COC[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554395
(CHEMBL4763116)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516225
(CHEMBL4521524)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1cc(ccc1F)-c1ccccc1F |r| Show InChI InChI=1S/C30H34F2N4O5S/c1-19-9-12-21(13-10-19)42(40,41)36-26(18-27(37)35-30(2,3)4)29(39)34-16-15-33-28(38)23-17-20(11-14-25(23)32)22-7-5-6-8-24(22)31/h5-14,17,26,36H,15-16,18H2,1-4H3,(H,33,38)(H,34,39)(H,35,37)/t26-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554358
(CHEMBL4754892)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554357
(CHEMBL4516988)Show SMILES CC(C)(C)ONC(=O)C[C@H](NC(=O)CCc1ccccc1)C(=O)N[C@@H](Cc1ccc(F)cc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554388
(CHEMBL4759896)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)C(=O)c1c[nH]c2ccccc12)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554359
(CHEMBL4758527)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 5.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554383
(CHEMBL4782251)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 7.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554393
(CHEMBL4764263)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554391
(CHEMBL4776824)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554365
(CHEMBL4764833)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc(OC)c1 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554388
(CHEMBL4759896)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)C(=O)c1c[nH]c2ccccc12)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity in human KARPAS-1106P cells incubated for 2 hrs by proteasome-Glo assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554396
(CHEMBL4764229)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554390
(CHEMBL4784421)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554373
(CHEMBL4764343)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554367
(CHEMBL4762452)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554376
(CHEMBL4746069)Show SMILES CC(C)(C)CNC(=O)C[C@H](NC(=O)CCc1ccccc1)C(=O)N[C@@H](Cc1ccc(F)cc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516218
(CHEMBL4458871)Show SMILES Cc1cc(no1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1cc(ccc1F)-c1ccccc1F |r| Show InChI InChI=1S/C27H31F2N5O6S/c1-16-13-24(33-40-16)41(38,39)34-22(15-23(35)32-27(2,3)4)26(37)31-12-11-30-25(36)19-14-17(9-10-21(19)29)18-7-5-6-8-20(18)28/h5-10,13-14,22,34H,11-12,15H2,1-4H3,(H,30,36)(H,31,37)(H,32,35)/t22-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554395
(CHEMBL4763116)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity in human KARPAS-1106P cells incubated for 2 hrs by proteasome-Glo assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516228
(CHEMBL4538027)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1ccccc1O |r| Show InChI InChI=1S/C24H32N4O6S/c1-16-9-11-17(12-10-16)35(33,34)28-19(15-21(30)27-24(2,3)4)23(32)26-14-13-25-22(31)18-7-5-6-8-20(18)29/h5-12,19,28-29H,13-15H2,1-4H3,(H,25,31)(H,26,32)(H,27,30)/t19-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554368
(CHEMBL4795707)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)Cc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554362
(CHEMBL4747215)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2[nH]ccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554397
(CHEMBL4741140)Show SMILES COC[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity in human KARPAS-1106P cells incubated for 2 hrs by proteasome-Glo assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516233
(CHEMBL4584213)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1ccc(Cl)cc1 |r| Show InChI InChI=1S/C24H31ClN4O5S/c1-16-5-11-19(12-6-16)35(33,34)29-20(15-21(30)28-24(2,3)4)23(32)27-14-13-26-22(31)17-7-9-18(25)10-8-17/h5-12,20,29H,13-15H2,1-4H3,(H,26,31)(H,27,32)(H,28,30)/t20-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 38 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516219
(CHEMBL4461840)Show SMILES COc1cccc(c1)C(=O)NCCNC(=O)[C@H](CC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1 |r| Show InChI InChI=1S/C25H34N4O6S/c1-17-9-11-20(12-10-17)36(33,34)29-21(16-22(30)28-25(2,3)4)24(32)27-14-13-26-23(31)18-7-6-8-19(15-18)35-5/h6-12,15,21,29H,13-14,16H2,1-5H3,(H,26,31)(H,27,32)(H,28,30)/t21-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 38 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554386
(CHEMBL4758484)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 39 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity in human KARPAS-1106P cells incubated for 2 hrs by proteasome-Glo assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554382
(CHEMBL4779742)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)N1CCCCC1)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid PDB UniChem
| Article PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554387
(CHEMBL4782050)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 51 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554389
(CHEMBL4796570)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)c1cc(C)on1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity in human KARPAS-1106P cells incubated for 2 hrs by proteasome-Glo assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50554384
(CHEMBL4784015)Show SMILES COC[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 55 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human constitutive 20S proteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554398
(CHEMBL4799140)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NS(=O)(=O)c1ccc(C)cc1)C(=O)NCc1ccc(F)c2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 56 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50554388
(CHEMBL4759896)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NC(C)(C)C)NC(=O)C(=O)c1c[nH]c2ccccc12)C(=O)NCc1cccc2ccccc12 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 59 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human constitutive 20S proteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516210
(CHEMBL4567620)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1c(O)cccc1F |r| Show InChI InChI=1S/C24H31FN4O6S/c1-15-8-10-16(11-9-15)36(34,35)29-18(14-20(31)28-24(2,3)4)22(32)26-12-13-27-23(33)21-17(25)6-5-7-19(21)30/h5-11,18,29-30H,12-14H2,1-4H3,(H,26,32)(H,27,33)(H,28,31)/t18-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 73 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554363
(CHEMBL4763630)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2cccnc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 84 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50554369
(CHEMBL4745016)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)C(F)(F)F)C(=O)NCc1cccc2ccccc12 |r| | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 99 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human 20S immunoproteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516220
(CHEMBL4445784)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1ccccc1 |r| Show InChI InChI=1S/C24H32N4O5S/c1-17-10-12-19(13-11-17)34(32,33)28-20(16-21(29)27-24(2,3)4)23(31)26-15-14-25-22(30)18-8-6-5-7-9-18/h5-13,20,28H,14-16H2,1-4H3,(H,25,30)(H,26,31)(H,27,29)/t20-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50554365
(CHEMBL4764833)Show SMILES COC[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc(OC)c1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 101 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human constitutive 20S proteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50516225
(CHEMBL4521524)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1cc(ccc1F)-c1ccccc1F |r| Show InChI InChI=1S/C30H34F2N4O5S/c1-19-9-12-21(13-10-19)42(40,41)36-26(18-27(37)35-30(2,3)4)29(39)34-16-15-33-28(38)23-17-20(11-14-25(23)32)22-7-5-6-8-24(22)31/h5-14,17,26,36H,15-16,18H2,1-4H3,(H,33,38)(H,34,39)(H,35,37)/t26-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S constitutive proteasome using suc-LLVY-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516213
(CHEMBL4444494)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1cccc(c1)C#C |r| Show InChI InChI=1S/C26H32N4O5S/c1-6-19-8-7-9-20(16-19)24(32)27-14-15-28-25(33)22(17-23(31)29-26(3,4)5)30-36(34,35)21-12-10-18(2)11-13-21/h1,7-13,16,22,30H,14-15,17H2,2-5H3,(H,27,32)(H,28,33)(H,29,31)/t22-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 112 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50554385
(CHEMBL4764897)Show SMILES C[C@H](NC(=O)[C@H](CCC(=O)NC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2ccccc12 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| KEGG PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human constitutive 20S proteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516221
(CHEMBL4521059)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1cccc(F)c1 |r| Show InChI InChI=1S/C24H31FN4O5S/c1-16-8-10-19(11-9-16)35(33,34)29-20(15-21(30)28-24(2,3)4)23(32)27-13-12-26-22(31)17-6-5-7-18(25)14-17/h5-11,14,20,29H,12-13,15H2,1-4H3,(H,26,31)(H,27,32)(H,28,30)/t20-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 128 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516232
(CHEMBL4515222)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1ccccc1F |r| Show InChI InChI=1S/C24H31FN4O5S/c1-16-9-11-17(12-10-16)35(33,34)29-20(15-21(30)28-24(2,3)4)23(32)27-14-13-26-22(31)18-7-5-6-8-19(18)25/h5-12,20,29H,13-15H2,1-4H3,(H,26,31)(H,27,32)(H,28,30)/t20-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 169 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-5
(Homo sapiens (Human)) | BDBM50554362
(CHEMBL4747215)Show SMILES C[C@H](NC(=O)[C@H](CC(=O)NOC(C)(C)C)NC(=O)CCc1ccccc1)C(=O)NCc1cccc2[nH]ccc12 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of human constitutive 20S proteasome beta 5 chymotrypsin-like activity |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01520 BindingDB Entry DOI: 10.7270/Q22R3WB6 |
More data for this Ligand-Target Pair | |
Proteasome subunit beta type-8
(Homo sapiens (Human)) | BDBM50516227
(CHEMBL4448635)Show SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CC(=O)NC(C)(C)C)C(=O)NCCNC(=O)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H31FN4O5S/c1-16-5-11-19(12-6-16)35(33,34)29-20(15-21(30)28-24(2,3)4)23(32)27-14-13-26-22(31)17-7-9-18(25)10-8-17/h5-12,20,29H,13-15H2,1-4H3,(H,26,31)(H,27,32)(H,28,30)/t20-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 179 | n/a | n/a | n/a | n/a | n/a | n/a |
Weill Cornell Medicine
Curated by ChEMBL
| Assay Description Inhibition of human beta5 20S immunoproteasome using Ac-ANW-AMC as substrate |
J Med Chem 62: 6137-6145 (2019)
Article DOI: 10.1021/acs.jmedchem.9b00363 BindingDB Entry DOI: 10.7270/Q2862KTQ |
More data for this Ligand-Target Pair | |