Reaction Details |
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Target | Polyphenol oxidase 2 |
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Ligand | BDBM50324035 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_647410 (CHEMBL1217571) |
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Ki | 9850±n/a nM |
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Citation | Bandgar, BP; Totre, JV; Gawande, SS; Khobragade, CN; Warangkar, SC; Kadam, PD Synthesis of novel 3,5-diaryl pyrazole derivatives using combinatorial chemistry as inhibitors of tyrosinase as well as potent anticancer, anti-inflammatory agents. Bioorg Med Chem18:6149-55 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Polyphenol oxidase 2 |
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Name: | Polyphenol oxidase 2 |
Synonyms: | Monophenol monooxygenase | Monophenol oxidase | PPO2 | PPO2_AGABI | Tyrosinase |
Type: | Protein |
Mol. Mass.: | 63923.66 |
Organism: | Agaricus bisporus (Common mushroom) |
Description: | O42713 |
Residue: | 556 |
Sequence: | MSLIATVGPTGGVKNRLNIVDFVKNEKFFTLYVRSLELLQAKEQHDYSSFFQLAGIHGLP
FTEWAKERPSMNLYKAGYCTHGQVLFPTWHRTYLSVLEQILQGAAIEVAKKFTSNQTDWV
QAAQDLRQPYWDWGFELMPPDEVIKNEEVNITNYDGKKISVKNPILRYHFHPIDPSFKPY
GDFATWRTTVRNPDRNRREDIPGLIKKMRLEEGQIREKTYNMLKFNDAWERFSNHGISDD
QHANSLESVHDDIHVMVGYGKIEGHMDHPFFAAFDPIFWLHHTNVDRLLSLWKAINPDVW
VTSGRNRDGTMGIAPNAQINSETPLEPFYQSGDKVWTSASLADTARLGYSYPDFDKLVGG
TKELIRDAIDDLIDERYGSKPSSGARNTAFDLLADFKGITKEHKEDLKMYDWTIHVAFKK
FELKESFSLLFYFASDGGDYDQENCFVGSINAFRGTAPETCANCQDNENLIQEGFIHLNH
YLARDLESFEPQDVHKFLKEKGLSYKLYSRGDKPLTSLSVKIEGRPLHLPPGEHRPKYDH
TQARVVFDDVAVHVIN
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BDBM50324035 |
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n/a |
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Name | BDBM50324035 |
Synonyms: | 2-[5-(2-Chloro-4-nitro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydroxymethyl-1-methyl-pyrrolidin-3-yl)-3,5-dimethoxyphenol | CHEMBL1214239 |
Type | Small organic molecule |
Emp. Form. | C23H25ClN4O6 |
Mol. Mass. | 488.921 |
SMILES | COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(cc2Cl)[N+]([O-])=O)c(O)c1C1CCN(C)C1CO |
Structure |
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