Reaction Details |
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Target | Beta-glucuronidase |
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Ligand | BDBM50284055 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1726779 (CHEMBL4142057) |
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IC50 | 200±n/a nM |
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Citation | Taha, M; Ullah, H; Al Muqarrabun, LMR; Khan, MN; Rahim, F; Ahmat, N; Ali, M; Perveen, S Synthesis of bis-indolylmethanes as new potential inhibitors of ?-glucuronidase and their molecular docking studies. Eur J Med Chem143:1757-1767 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-glucuronidase |
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Name: | Beta-glucuronidase |
Synonyms: | β-Glucuronidase | BGLR_HUMAN | Beta-G1 | Beta-glucuronidase | GUSB | beta-Glucuronidase (β-glucuronidase) |
Type: | Protein |
Mol. Mass.: | 74736.05 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 651 |
Sequence: | MARGSAVAWAALGPLLWGCALGLQGGMLYPQESPSRECKELDGLWSFRADFSDNRRRGFE
EQWYRRPLWESGPTVDMPVPSSFNDISQDWRLRHFVGWVWYEREVILPERWTQDLRTRVV
LRIGSAHSYAIVWVNGVDTLEHEGGYLPFEADISNLVQVGPLPSRLRITIAINNTLTPTT
LPPGTIQYLTDTSKYPKGYFVQNTYFDFFNYAGLQRSVLLYTTPTTYIDDITVTTSVEQD
SGLVNYQISVKGSNLFKLEVRLLDAENKVVANGTGTQGQLKVPGVSLWWPYLMHERPAYL
YSLEVQLTAQTSLGPVSDFYTLPVGIRTVAVTKSQFLINGKPFYFHGVNKHEDADIRGKG
FDWPLLVKDFNLLRWLGANAFRTSHYPYAEEVMQMCDRYGIVVIDECPGVGLALPQFFNN
VSLHHHMQVMEEVVRRDKNHPAVVMWSVANEPASHLESAGYYLKMVIAHTKSLDPSRPVT
FVSNSNYAADKGAPYVDVICLNSYYSWYHDYGHLELIQLQLATQFENWYKKYQKPIIQSE
YGAETIAGFHQDPPLMFTEEYQKSLLEQYHLGLDQKRRKYVVGELIWNFADFMTEQSPTR
VLGNKKGIFTRQRQPKSAAFLLRERYWKIANETRYPHSVAKSQCLENSLFT
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BDBM50284055 |
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n/a |
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Name | BDBM50284055 |
Synonyms: | CHEMBL4177204 |
Type | Small organic molecule |
Emp. Form. | C40H32N6O8 |
Mol. Mass. | 724.7175 |
SMILES | Cc1ccc(cc1)C(c1c[nH]c2ccc(cc12)C(=O)N\N=C\c1c(O)cc(O)cc1O)c1c[nH]c2ccc(cc12)C(=O)N\N=C\c1c(O)cc(O)cc1O |
Structure |
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