Target
Muscarinic acetylcholine receptor M3
Ligand
BDBM200746
Substrate
n/a
Meas. Tech.
Muscarinic Receptor Binding Assay
IC50
2.2±n/a nM
Citation
 Aiguade Bosch, JGual Roig, SPrat Quinones, MPuig Duran, C Cyclohexylamine derivatives having β2 adrenergic agonist and M3 muscarinic antagonist activities US Patent  US9233108 Publication Date 1/12/2016 
Target
Name:
Muscarinic acetylcholine receptor M3
Synonyms:
ACM3_HUMAN | CHRM3 | Cholinergic, muscarinic M3 | Muscarinic Receptors M3 | Muscarinic receptor M3 | RecName: Full=Muscarinic acetylcholine receptor M3
Type:
Enzyme
Mol. Mass.:
66151.03
Organism:
Homo sapiens (Human)
Description:
P20309
Residue:
590
Sequence:
MTLHNNSTTSPLFPNISSSWIHSPSDAGLPPGTVTHFGSYNVSRAAGNFSSPDGTTDDPLGGHTVWQVVFIAFLTGILALVTIIGNILVIVSFKVNKQLKTVNNYFLLSLACADLIIGVISMNLFTTYIIMNRWALGNLACDLWLAIDYVASNASVMNLLVISFDRYFSITRPLTYRAKRTTKRAGVMIGLAWVISFVLWAPAILFWQYFVGKRTVPPGECFIQFLSEPTITFGTAIAAFYMPVTIMTILYWRIYKETEKRTKELAGLQASGTEAETENFVHPTGSSRSCSSYELQQQSMKRSNRRKYGRCHFWFTTKSWKPSSEQMDQDHSSSDSWNNNDAAASLENSASSDEEDIGSETRAIYSIVLKLPGHSTILNSTKLPSSDNLQVPEEELGMVDLERKADKLQAQKSVDDGGSFPKSFSKLPIQLESAVDTAKTSDVNSSVGKSTATLPLSFKEATLAKRFALKTRSQITKRKRMSLVKEKKAAQTLSAILLAFIITWTPYNIMVLVNTFCDSCIPKTFWNLGYWLCYINSTVNPVCYALCNKTFRTTFKMLLLCQCDKKKRRKQQYQQRQSVIFHKRAPEQAL
  
Inhibitor
Name:
BDBM200746
Synonyms:
US9233108, 8 | US9757383, Example 8
Type:
Small organic molecule
Emp. Form.:
C39H44N4O8S2
Mol. Mass.:
760.919
SMILES:
CN(CCNC(=O)COc1ccc(CNC[C@H](O)c2ccc(O)c3[nH]c(=O)ccc23)cc1)[C@H]1CC[C@@H](CC1)OC(=O)C(O)(c1cccs1)c1cccs1 |wU:35.41,wD:16.16,32.34,(5.24,5.56,;5.24,4.02,;6.58,3.25,;7.91,4.02,;9.25,3.25,;10.58,4.02,;10.58,5.56,;11.91,3.25,;13.25,4.02,;14.58,3.25,;15.91,4.02,;17.25,3.25,;17.25,1.71,;18.58,.94,;19.91,1.71,;21.25,.94,;22.58,1.71,;22.58,3.25,;23.92,.94,;23.92,-.6,;25.25,-1.37,;26.58,-.6,;27.92,-1.37,;26.58,.94,;27.92,1.71,;27.92,3.25,;29.25,4.02,;26.58,4.02,;25.25,3.25,;25.25,1.71,;15.91,.94,;14.58,1.71,;3.91,3.25,;2.58,4.02,;1.24,3.25,;1.24,1.71,;2.58,.94,;3.91,1.71,;-.09,.94,;-.09,-.6,;1.24,-1.37,;-1.42,-1.37,;-2.19,-.03,;-2.76,-2.14,;-2.92,-3.67,;-4.43,-3.99,;-5.2,-2.66,;-4.16,-1.51,;-.65,-2.7,;.88,-2.86,;1.2,-4.37,;-.14,-5.14,;-1.28,-4.11,)|
Structure:
Search PDB for entries with ligand similarity: