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GPCR

Name	Muscarinic acetylcholine receptor M1
Species	Homo sapiens (Human)
Gene	CHRM1
Synonym	cholinergic receptor cholinergic receptor, muscarinic 1 cholinergic receptor, muscarinic 1, CNS Chrm-1 M1 receptor M1R M1 muscarinic acetylcholine receptor [ Show all ]
Disease	Functional bowel syndrome; Irritable bowel syndrome Glaucoma Peptic ulcer Parkinsonism; Extrapyramidal disorders secondary to neuroleptic drug therapy Visceral spasms Parkinson's disease; Dystonia Parkinson's disease Neurological disease Neuropathic pain Overactive bladder disorder Excessive sweating; Stomach ulcer Cognitive disorders Chronic obstructive pulmonary disease Schizophrenia Schizophrenia; Dementia Schizophrenia; Schizoaffective disorders Unspecified Urinary incontinence Anesthesia Alzheimer disease Abdominal stomach pain; Irritable bowel syndrome [ Show all ]
Length	460
Amino acid sequence	MNTSAPPAVSPNITVLAPGKGPWQVAFIGITTGLLSLATVTGNLLVLISFKVNTELKTVNNYFLLSLACADLIIGTFSMNLYTTYLLMGHWALGTLACDLWLALDYVASNASVMNLLLISFDRYFSVTRPLSYRAKRTPRRAALMIGLAWLVSFVLWAPAILFWQYLVGERTVLAGQCYIQFLSQPIITFGTAMAAFYLPVTVMCTLYWRIYRETENRARELAALQGSETPGKGGGSSSSSERSQPGAEGSPETPPGRCCRCCRAPRLLQAYSWKEEEEEDEGSMESLTSSEGEEPGSEVVIKMPMVDPEAQAPTKQPPRSSPNTVKRPTKKGRDRAGKGQKPRGKEQLAKRKTFSLVKEKKAARTLSAILLAFILTWTPYNIMVLVSTFCKDCVPETLWELGYWLCYVNSTINPMCYALCNKAFRDTFRLLLLCRWDKRRWRKIPKRPGSVHRTPSRQC
UniProt	P11229
Protein Data Bank	5cxv
GPCR-HGmod model	P11229
3D structure model	This structure is from PDB ID 5cxv.
BioLiP	BL0339262, BL0339261, BL0339263
Therapeutic Target Database	T28893
ChEMBL	CHEMBL216
IUPHAR	13
DrugBank	BE0000092

Ligand

Name	CHEMBL73661
Molecular formula	C28H40N2O2S
IUPAC name	1-[1-[4-(4-tert-butylphenyl)sulfonylphenyl]ethyl]-4-cyclohexylpiperazine
Molecular weight	468.7
Hydrogen bond acceptor	4
Hydrogen bond donor	0
XlogP	6.2
Synonyms	1-[alpha-Methyl-4-(4-tert-butylphenylsulfonyl)benzyl]-4-cyclohexylpiperazine BDBM50092987 1-{1-[4-(4-tert-Butyl-benzenesulfonyl)-phenyl]-ethyl}-4-cyclohexyl-piperazine
Inchi Key	AHUKWGFWYLCACE-UHFFFAOYSA-N
Inchi ID	InChI=1S/C28H40N2O2S/c1-22(29-18-20-30(21-19-29)25-8-6-5-7-9-25)23-10-14-26(15-11-23)33(31,32)27-16-12-24(13-17-27)28(2,3)4/h10-17,22,25H,5-9,18-21H2,1-4H3
PubChem CID	44312464
ChEMBL	CHEMBL73661
IUPHAR	N/A
BindingDB	50092987
DrugBank	N/A
Structure SDF download
Lipinski's druglikeness	This ligand has a partition coefficient log P greater than 5.

Experimental Data

Parameter	Value	Reference	Database source
Ki	85.0 nM	PMID11055332	BindingDB,ChEMBL

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