Reaction Details |
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Target | Cytochrome P450 1B1 |
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Ligand | BDBM50045924 |
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Substrate/Competitor | n/a |
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Meas. Tech. | EROD Assay |
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pH | 8±0 |
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Temperature | 310.15±0 K |
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Ki | 74.3±n/a nM |
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Km | 158±0 nM |
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Citation | Katsuyama, Y; Funa, N; Miyahisa, I; Horinouchi, S Synthesis of unnatural flavonoids and stilbenes by exploiting the plant biosynthetic pathway in Escherichia coli. Chem Biol14:613-21 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Cytochrome P450 1B1 |
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Name: | Cytochrome P450 1B1 |
Synonyms: | CP1B1_HUMAN | CYP1B1 | CYPIB1 | Cytochrome P450 1B1 (CYP1B1) |
Type: | PROTEIN |
Mol. Mass.: | 60861.81 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1474523 |
Residue: | 543 |
Sequence: | MGTSLSPNDPWPLNPLSIQQTTLLLLLSVLATVHVGQRLLRQRRRQLRSAPPGPFAWPLI
GNAAAVGQAAHLSFARLARRYGDVFQIRLGSCPIVVLNGERAIHQALVQQGSAFADRPAF
ASFRVVSGGRSMAFGHYSEHWKVQRRAAHSMMRNFFTRQPRSRQVLEGHVLSEARELVAL
LVRGSADGAFLDPRPLTVVAVANVMSAVCFGCRYSHDDPEFRELLSHNEEFGRTVGAGSL
VDVMPWLQYFPNPVRTVFREFEQLNRNFSNFILDKFLRHCESLRPGAAPRDMMDAFILSA
EKKAAGDSHGGGARLDLENVPATITDIFGASQDTLSTALQWLLLLFTRYPDVQTRVQAEL
DQVVGRDRLPCMGDQPNLPYVLAFLYEAMRFSSFVPVTIPHATTANTSVLGYHIPKDTVV
FVNQWSVNHDPLKWPNPENFDPARFLDKDGLINKDLTSRVMIFSVGKRRCIGEELSKMQL
FLFISILAHQCDFRANPNEPAKMNFSYGLTIKPKSFKVNVTLRESMELLDSAVQNLQAKE
TCQ
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BDBM50045924 |
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n/a |
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Name | BDBM50045924 |
Synonyms: | (E)-3,5-stilbenediol | (E)-5-(2-phenylethenyl)-1,3-benzenediol | 5-[(1E)-2-phenylethenyl]benzene-1,3-diol | 5-[(E)-2-phenylvinyl]benzene-1,3-diol | CHEMBL101506 | Stilbene, 1f | pinosylvine | trans-3,5-dihydroxystilbene | trans-pinosylvin |
Type | Small organic molecule |
Emp. Form. | C14H12O2 |
Mol. Mass. | 212.2439 |
SMILES | Oc1cc(O)cc(\C=C\c2ccccc2)c1 |
Structure |
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