Reaction Details |
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Target | Aromatase |
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Ligand | BDBM8938 |
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Substrate/Competitor | BDBM8592 |
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Meas. Tech. | CYP17 Assay |
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Citation | Hutschenreuter, TU; Ehmer, PB; Hartmann, RW Synthesis of hydroxy derivatives of highly potent non-steroidal CYP 17 inhibitors as potential metabolites and evaluation of their activity by a non cellular assay using recombinant human enzyme. J Enzyme Inhib Med Chem19:17-32 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Aromatase |
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Name: | Aromatase |
Synonyms: | ARO1 | Aromatase | CP19A_HUMAN | CYAR | CYP19 | CYP19A1 | CYPXIX | Cytochrome P-450AROM | Cytochrome P450 19A1 | Cytochrome P450 2C19 | Cytochrome P450-C19 (CYP19) | Estrogen synthetase | FL cytokine receptor precursor | P-450AROM |
Type: | Enzyme |
Mol. Mass.: | 57888.92 |
Organism: | Homo sapiens (Human) |
Description: | P11511 |
Residue: | 503 |
Sequence: | MVLEMLNPIHYNITSIVPEAMPAATMPVLLLTGLFLLVWNYEGTSSIPGPGYCMGIGPLI
SHGRFLWMGIGSACNYYNRVYGEFMRVWISGEETLIISKSSSMFHIMKHNHYSSRFGSKL
GLQCIGMHEKGIIFNNNPELWKTTRPFFMKALSGPGLVRMVTVCAESLKTHLDRLEEVTN
ESGYVDVLTLLRRVMLDTSNTLFLRIPLDESAIVVKIQGYFDAWQALLIKPDIFFKISWL
YKKYEKSVKDLKDAIEVLIAEKRRRISTEEKLEECMDFATELILAEKRGDLTRENVNQCI
LEMLIAAPDTMSVSLFFMLFLIAKHPNVEEAIIKEIQTVIGERDIKIDDIQKLKVMENFI
YESMRYQPVVDLVMRKALEDDVIDGYPVKKGTNIILNIGRMHRLEFFPKPNEFTLENFAK
NVPYRYFQPFGFGPRGCAGKYIAMVMMKAILVTLLRRFHVKTLQGQCVESIQKIHDLSLH
PDETKNMLEMIFTPRNSDRCLEH
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BDBM8938 |
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BDBM8592 |
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Name | BDBM8938 |
Synonyms: | 7-(1H-Imidazol-5-ylmethyl)-8-methyl-5,6-dihydro-naphthalen-2,3-diol | 7-(1H-imidazol-5-ylmethyl)-8-methyl-5,6-dihydronaphthalene-2,3-diol | BW19 analog 3 | dihydronaphthalene derivative |
Type | Small organic molecule |
Emp. Form. | C15H16N2O2 |
Mol. Mass. | 256.2997 |
SMILES | CC1=C(Cc2cnc[nH]2)CCc2cc(O)c(O)cc12 |c:1| |
Structure |
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