| Reaction Details |
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 | Report a problem with these data |
| Target | Transcriptional activator Myb |
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| Ligand | BDBM50595895 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_2218219 (CHEMBL5131351) |
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| IC50 | 8.7±n/a nM |
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| Citation |  Köhler, LHF; Reich, S; Yusenko, M; Klempnauer, KH; Shaikh, AH; Ahmed, K; Begemann, G; Schobert, R; Biersack, B A New Naphthopyran Derivative Combines ACS Med Chem Lett13:1783-1790 (2022) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Transcriptional activator Myb |
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| Name: | Transcriptional activator Myb |
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| Synonyms: | MYB | MYB_HUMAN | Proto-oncogene c-Myb |
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| Type: | PROTEIN |
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| Mol. Mass.: | 72345.36 |
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| Organism: | Homo sapiens |
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| Description: | ChEMBL_120654 |
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| Residue: | 640 |
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| Sequence: | MARRPRHSIYSSDEDDEDFEMCDHDYDGLLPKSGKRHLGKTRWTREEDEKLKKLVEQNGT
DDWKVIANYLPNRTDVQCQHRWQKVLNPELIKGPWTKEEDQRVIELVQKYGPKRWSVIAK
HLKGRIGKQCRERWHNHLNPEVKKTSWTEEEDRIIYQAHKRLGNRWAEIAKLLPGRTDNA
IKNHWNSTMRRKVEQEGYLQESSKASQPAVATSFQKNSHLMGFAQAPPTAQLPATGQPTV
NNDYSYYHISEAQNVSSHVPYPVALHVNIVNVPQPAAAAIQRHYNDEDPEKEKRIKELEL
LLMSTENELKGQQVLPTQNHTCSYPGWHSTTIADHTRPHGDSAPVSCLGEHHSTPSLPAD
PGSLPEESASPARCMIVHQGTILDNVKNLLEFAETLQFIDSFLNTSSNHENSDLEMPSLT
STPLIGHKLTVTTPFHRDQTVKTQKENTVFRTPAIKRSILESSPRTPTPFKHALAAQEIK
YGPLKMLPQTPSHLVEDLQDVIKQESDESGIVAEFQENGPPLLKKIKQEVESPTDKSGNF
FCSHHWEGDSLNTQLFTQTSPVADAPNILTSSVLMAPASEDEDNVLKAFTVPKNRSLASP
LQPCSSTWEPASCGKMEEQMTSSSQARKYVNAFSARTLVM
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| BDBM50595895 |
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| n/a |
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| Name | BDBM50595895 |
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| Synonyms: | CHEMBL321336 |
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| Type | Small organic molecule |
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| Emp. Form. | C20H13N3O3 |
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| Mol. Mass. | 343.3355 |
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| SMILES | NC1=C(C#N)C(c2cccc(c2)[N+]([O-])=O)c2ccc3ccccc3c2O1 |c:1| |
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| Structure | 
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