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GLASS

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Go to the GPCR, ligand, or experimental data tables.
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GPCR

Name	Neurotensin receptor type 1
Species	Homo sapiens (Human)
Gene	NTSR1
Synonym	NTSR1 NTS1 receptor NTRH NTR1 NTR NT-R-1 NT-1R neurotensin receptor type 1 neurotensin receptor 1 (high affinity) Levocabastin-insensitive neurotensin receptor High-affinity levocabastine-insensitive neurotensin receptor [ Show all ]
Disease	Acute or chronic pain Alcohol use disorders Pain Inflammatory bowel disease Neurological disease
Length	418
Amino acid sequence	MRLNSSAPGTPGTPAADPFQRAQAGLEEALLAPGFGNASGNASERVLAAPSSELDVNTDIYSKVLVTAVYLALFVVGTVGNTVTAFTLARKKSLQSLQSTVHYHLGSLALSDLLTLLLAMPVELYNFIWVHHPWAFGDAGCRGYYFLRDACTYATALNVASLSVERYLAICHPFKAKTLMSRSRTKKFISAIWLASALLAVPMLFTMGEQNRSADGQHAGGLVCTPTIHTATVKVVIQVNTFMSFIFPMVVISVLNTIIANKLTVMVRQAAEQGQVCTVGGEHSTFSMAIEPGRVQALRHGVRVLRAVVIAFVVCWLPYHVRRLMFCYISDEQWTPFLYDFYHYFYMVTNALFYVSSTINPILYNLVSANFRHIFLATLACLCPVWRRRRKRPAFSRKADSVSSNHTLSSNATRETLY
UniProt	P30989
Protein Data Bank	N/A
GPCR-HGmod model	P30989
3D structure model	This predicted structure model is from GPCR-EXP P30989.
BioLiP	N/A
Therapeutic Target Database	T02728
ChEMBL	CHEMBL4123
IUPHAR	309
DrugBank	N/A

Ligand

Name	MLS000390145
Molecular formula	C22H15ClN2O
IUPAC name	(E)-2-(1H-benzimidazol-2-yl)-3-(3-chlorophenyl)-1-phenylprop-2-en-1-one
Molecular weight	358.825
Hydrogen bond acceptor	2
Hydrogen bond donor	1
XlogP	5.6
Synonyms	AC1O1IPK SMR000259409 (E)-2-(1H-benzimidazol-2-yl)-3-(3-chlorophenyl)-1-phenylprop-2-en-1-one HMS2549K04 AKOS008003677 ZINC4864419 (E)-2-(1H-benzimidazol-2-yl)-3-(3-chlorophenyl)-1-phenyl-2-propen-1-one CHEMBL1550862 BDBM54254 (E)-2-(1H-benzimidazol-2-yl)-3-(3-chlorophenyl)-1-phenyl-prop-2-en-1-one cid_6122140 [ Show all ]
Inchi Key	DFXBECUFRBOWLA-JXAWBTAJSA-N
Inchi ID	InChI=1S/C22H15ClN2O/c23-17-10-6-7-15(13-17)14-18(21(26)16-8-2-1-3-9-16)22-24-19-11-4-5-12-20(19)25-22/h1-14H,(H,24,25)/b18-14-
PubChem CID	6122140
ChEMBL	CHEMBL1550862
IUPHAR	N/A
BindingDB	54254
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
EC50	8480.0 nM	, PubChem BioAssay data set	BindingDB,ChEMBL

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