Reaction Details |
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Target | Tyrosine-protein kinase Fyn |
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Ligand | BDBM13268 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_304745 (CHEMBL829344) |
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IC50 | 1±n/a nM |
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Citation | Chen, P; Norris, D; Das, J; Spergel, SH; Wityak, J; Leith, L; Zhao, R; Chen, BC; Pitt, S; Pang, S; Shen, DR; Zhang, R; De Fex, HF; Doweyko, AM; McIntyre, KW; Shuster, DJ; Behnia, K; Schieven, GL; Barrish, JC Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitors. Bioorg Med Chem Lett14:6061-6 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase Fyn |
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Name: | Tyrosine-protein kinase Fyn |
Synonyms: | FYN | FYN_HUMAN | Proto-oncogene Syn | Proto-oncogene c-Fyn | SLK | SRC | Src-like kinase | p59-Fyn |
Type: | Enzyme |
Mol. Mass.: | 60762.21 |
Organism: | Homo sapiens (Human) |
Description: | P06241 |
Residue: | 537 |
Sequence: | MGCVQCKDKEATKLTEERDGSLNQSSGYRYGTDPTPQHYPSFGVTSIPNYNNFHAAGGQG
LTVFGGVNSSSHTGTLRTRGGTGVTLFVALYDYEARTEDDLSFHKGEKFQILNSSEGDWW
EARSLTTGETGYIPSNYVAPVDSIQAEEWYFGKLGRKDAERQLLSFGNPRGTFLIRESET
TKGAYSLSIRDWDDMKGDHVKHYKIRKLDNGGYYITTRAQFETLQQLVQHYSERAAGLCC
RLVVPCHKGMPRLTDLSVKTKDVWEIPRESLQLIKRLGNGQFGEVWMGTWNGNTKVAIKT
LKPGTMSPESFLEEAQIMKKLKHDKLVQLYAVVSEEPIYIVTEYMNKGSLLDFLKDGEGR
ALKLPNLVDMAAQVAAGMAYIERMNYIHRDLRSANILVGNGLICKIADFGLARLIEDNEY
TARQGAKFPIKWTAPEAALYGRFTIKSDVWSFGILLTELVTKGRVPYPGMNNREVLEQVE
RGYRMPCPQDCPISLHELMIHCWKKDPEERPTFEYLQSFLEDYFTATEPQYQPGENL
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BDBM13268 |
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n/a |
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Name | BDBM13268 |
Synonyms: | BMS-354825 2-Heteroarylamino-thiazole Analog 12m | CHEMBL364623 | N-(2-Chloro-6-methylphenyl)-2-[(2,6-dimethyl-4-pyrimidinyl)-amino]-1,3-thiazole-5-carboxamide | N-(2-chloro-6-methylphenyl)-2-[(2,6-dimethylpyrimidin-4-yl)amino]-1,3-thiazole-5-carboxamide |
Type | Small organic molecule |
Emp. Form. | C17H16ClN5OS |
Mol. Mass. | 373.86 |
SMILES | Cc1cc(Nc2ncc(s2)C(=O)Nc2c(C)cccc2Cl)nc(C)n1 |
Structure |
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