Reaction Details |
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Target | Muscarinic acetylcholine receptor M2 |
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Ligand | BDBM50165023 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_302412 (CHEMBL875203) |
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Ki | 3582±n/a nM |
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Citation | Kaur, K; Aeron, S; Bruhaspathy, M; Shetty, SJ; Gupta, S; Hegde, LH; Silamkoti, AD; Mehta, A; Chugh, A; Gupta, JB; Sarma, PK; Kumar, N Design, synthesis and activity of novel derivatives of oxybutynin and tolterodine. Bioorg Med Chem Lett15:2093-6 (2005) [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_RAT | Cholinergic, muscarinic M2 | Chrm-2 | Chrm2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 51555.53 |
Organism: | RAT |
Description: | P10980 |
Residue: | 466 |
Sequence: | MNNSTNSSNNGLAITSPYKTFEVVFIVLVAGSLSLVTIIGNILVMVSIKVNRHLQTVNNY
FLFSLACADLIIGVFSMNLYTLYTVIGYWPLGPVVCDLWLALDYVVSNASVMNLLIISFD
RYFCVTKPLTYPVKRTTKMAGMMIAAAWVLSFILWAPAILFWQFIVGVRTVEDGECYIQF
FSNAAVTFGTAIAAFYLPVIIMTVLYWHISRASKSRIKKEKKEPVANQDPVSPSLVQGRI
VKPNNNNMPGGDGGLEHNKIQNGKAPRDGVTENCVQGEEKESSNDSTSVSAVASNMRDDE
ITQDENTVSTSLGHSRDDNSKQTCIKIVTKAQKGDVCTPTSTTVELVGSSGQNGDEKQNI
VARKIVKMTKQPAKKKPPPSREKKVTRTILAILLAFIITWAPYNVMVLINTFCAPCIPNT
VWTIGYWLCYINSTINPACYALCNATFKKTFKHLLMCHYKNIGATR
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BDBM50165023 |
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n/a |
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Name | BDBM50165023 |
Synonyms: | CHEMBL424832 | N-[4-(3-Aza-bicyclo[3.1.0]hex-3-yl)-but-2-ynyl]-2-cyclohexyl-2-hydroxy-2-phenyl-acetamide |
Type | Small organic molecule |
Emp. Form. | C23H30N2O2 |
Mol. Mass. | 366.4965 |
SMILES | OC(C1CCCCC1)(C(=O)NCC#CCN1CC2CC2C1)c1ccccc1 |
Structure |
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