Reaction Details |
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Target | Target of rapamycin complex 2 subunit MAPKAP1 |
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Ligand | BDBM50535043 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1929668 (CHEMBL4432844) |
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IC50 | 15±n/a nM |
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Citation | Cansfield, AD; Ladduwahetty, T; Sunose, M; Ellard, K; Lynch, R; Newton, AL; Lewis, A; Bennett, G; Zinn, N; Thomson, DW; Rüger, AJ; Feutrill, JT; Rausch, O; Watt, AP; Bergamini, G CZ415, a Highly Selective mTOR Inhibitor Showing in Vivo Efficacy in a Collagen Induced Arthritis Model. ACS Med Chem Lett7:768-73 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Target of rapamycin complex 2 subunit MAPKAP1 |
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Name: | Target of rapamycin complex 2 subunit MAPKAP1 |
Synonyms: | MAPKAP1 | MIP1 | Mitogen-activated protein kinase 2-associated protein 1 | SAPK-interacting protein 1 | SIN1 | SIN1_HUMAN | Stress-activated map kinase-interacting protein 1 | TORC2 subunit MAPKAP1 | Target of rapamycin complex 2 subunit MAPKAP1 | mSIN1 |
Type: | PROTEIN |
Mol. Mass.: | 59129.70 |
Organism: | Homo sapiens |
Description: | ChEMBL_119716 |
Residue: | 522 |
Sequence: | MAFLDNPTIILAHIRQSHVTSDDTGMCEMVLIDHDVDLEKIHPPSMPGDSGSEIQGSNGE
TQGYVYAQSVDITSSWDFGIRRRSNTAQRLERLRKERQNQIKCKNIQWKERNSKQSAQEL
KSLFEKKSLKEKPPISGKQSILSVRLEQCPLQLNNPFNEYSKFDGKGHVGTTATKKIDVY
LPLHSSQDRLLPMTVVTMASARVQDLIGLICWQYTSEGREPKLNDNVSAYCLHIAEDDGE
VDTDFPPLDSNEPIHKFGFSTLALVEKYSSPGLTSKESLFVRINAAHGFSLIQVDNTKVT
MKEILLKAVKRRKGSQKVSGPQYRLEKQSEPNVAVDLDSTLESQSAWEFCLVRENSSRAD
GVFEEDSQIDIATVQDMLSSHHYKSFKVSMIHRLRFTTDVQLGISGDKVEIDPVTNQKAS
TKFWIKQKPISIDSDLLCACDLAEEKSPSHAIFKLTYLSNHDYKHLYFESDAATVNEIVL
KVNYILESRASTARADYFAQKQRKLNRRTSFSFQKEKKSGQQ
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BDBM50535043 |
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n/a |
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Name | BDBM50535043 |
Synonyms: | CHEMBL4577549 |
Type | Small organic molecule |
Emp. Form. | C22H29N5O4S |
Mol. Mass. | 459.562 |
SMILES | CCNC(=O)Nc1ccc(cc1)-c1nc2c(CS(=O)(=O)C2(C)C)c(n1)N1CCOC[C@@H]1C |r| |
Structure |
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