Reaction Details |
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Target | Muscarinic acetylcholine receptor M2 |
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Ligand | BDBM50228363 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_495765 (CHEMBL1007884) |
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IC50 | 6280±n/a nM |
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Citation | Vu, CB; Bemis, JE; Disch, JS; Ng, PY; Nunes, JJ; Milne, JC; Carney, DP; Lynch, AV; Smith, JJ; Lavu, S; Lambert, PD; Gagne, DJ; Jirousek, MR; Schenk, S; Olefsky, JM; Perni, RB Discovery of imidazo[1,2-b]thiazole derivatives as novel SIRT1 activators. J Med Chem52:1275-83 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Muscarinic acetylcholine receptor M2 |
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Name: | Muscarinic acetylcholine receptor M2 |
Synonyms: | ACM2_HUMAN | CHRM2 | Cholinergic, muscarinic M2 | Muscarinic acetylcholine receptor M2 and M4 | Muscarinic acetylcholine receptor M2 and M5 | RecName: Full=Muscarinic acetylcholine receptor M2 |
Type: | GPCR |
Mol. Mass.: | 51730.61 |
Organism: | Homo sapiens (Human) |
Description: | P08172 |
Residue: | 466 |
Sequence: | MNNSTNSSNNSLALTSPYKTFEVVFIVLVAGSLSLVTIIGNILVMVSIKVNRHLQTVNNY
FLFSLACADLIIGVFSMNLYTLYTVIGYWPLGPVVCDLWLALDYVVSNASVMNLLIISFD
RYFCVTKPLTYPVKRTTKMAGMMIAAAWVLSFILWAPAILFWQFIVGVRTVEDGECYIQF
FSNAAVTFGTAIAAFYLPVIIMTVLYWHISRASKSRIKKDKKEPVANQDPVSPSLVQGRI
VKPNNNNMPSSDDGLEHNKIQNGKAPRDPVTENCVQGEEKESSNDSTSVSAVASNMRDDE
ITQDENTVSTSLGHSKDENSKQTCIRIGTKTPKSDSCTPTNTTVEVVGSSGQNGDEKQNI
VARKIVKMTKQPAKKKPPPSREKKVTRTILAILLAFIITWAPYNVMVLINTFCAPCIPNT
VWTIGYWLCYINSTINPACYALCNATFKKTFKHLLMCHYKNIGATR
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BDBM50228363 |
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n/a |
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Name | BDBM50228363 |
Synonyms: | CHEMBL257991 | N-(2-(3-(piperazin-1-ylmethyl)imidazo[2,1-b]thiazol-6-yl)phenyl)quinoxaline-2-carboxamide | SRT-1720 |
Type | Small organic molecule |
Emp. Form. | C25H23N7OS |
Mol. Mass. | 469.561 |
SMILES | O=C(Nc1ccccc1-c1cn2c(CN3CCNCC3)csc2n1)c1cnc2ccccc2n1 |
Structure |
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