Reaction Details |
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Target | Mitogen-activated protein kinase 10 |
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Ligand | BDBM50169974 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_304976 (CHEMBL829309) |
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IC50 | 9400±n/a nM |
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Citation | Gaillard, P; Jeanclaude-Etter, I; Ardissone, V; Arkinstall, S; Cambet, Y; Camps, M; Chabert, C; Church, D; Cirillo, R; Gretener, D; Halazy, S; Nichols, A; Szyndralewiez, C; Vitte, PA; Gotteland, JP Design and synthesis of the first generation of novel potent, selective, and in vivo active (benzothiazol-2-yl)acetonitrile inhibitors of the c-Jun N-terminal kinase. J Med Chem48:4596-607 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Mitogen-activated protein kinase 10 |
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Name: | Mitogen-activated protein kinase 10 |
Synonyms: | Jnk3 | MK10_RAT | Mapk10 | Prkm10 | c-Jun N-terminal kinase 3 |
Type: | PROTEIN |
Mol. Mass.: | 52534.34 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_1460661 |
Residue: | 464 |
Sequence: | MSLHFLYYCSEPTLDVKIAFCQGFDKHVDVSSVVKHYNMSKSKVDNQFYSVEVGDSTFTV
LKRYQNLKPIGSGAQGIVCAAYDAVLDRNVAIKKLSRPFQNQTHAKRAYRELVLMKCVNH
KNIISLLNVFTPQKTLEEFQDVYLVMELMDANLCQVIQMELDHERMSYLLYQMLCGIKHL
HSAGIIHRDLKPSNIVVKSDCTLKILDFGLARTAGTSFMMTPYVVTRYYRAPEVILGMGY
KENVDIWSVGCIMGEMVRHKILFPGRDYIDQWNKVIEQLGTPCPEFMKKLQPTVRNYVEN
RPKYAGLTFPKLFPDSLFPADSEHNKLKASQARDLLSKMLVIDPAKRISVDDALQHPYIN
VWYDPAEVEAPPPQIYDKQLDEREHTIEEWKELIYKEVMNSEEKTKNGVVKGQPSPSGAA
VNSSESLPPSSSVNDISSMSTDQTLASDTDSSLEASAGPLGCCR
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BDBM50169974 |
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n/a |
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Name | BDBM50169974 |
Synonyms: | (2Z)-1,3-benzothiazol-2(3H)-ylidene[2-(dimethylamino)pyrimidin-4-yl]acetonitrile | CHEMBL190380 |
Type | Small organic molecule |
Emp. Form. | C15H13N5S |
Mol. Mass. | 295.362 |
SMILES | CN(C)c1nccc(n1)C(C#N)c1nc2ccccc2s1 |
Structure |
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