U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H27N3O4S
Molecular Weight 393.5
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GR-113808

SMILES

CN1C=C(C(=O)OCC2CCN(CCNS(C)(=O)=O)CC2)C3=C1C=CC=C3

InChI

InChIKey=MOZPSIXKYJUTKI-UHFFFAOYSA-N
InChI=1S/C19H27N3O4S/c1-21-13-17(16-5-3-4-6-18(16)21)19(23)26-14-15-7-10-22(11-8-15)12-9-20-27(2,24)25/h3-6,13,15,20H,7-12,14H2,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of 5-HT in globus pallidus on haloperidol-induced catalepsy in rats.
2009-04-17
Metoclopramide stimulates catecholamine- and granin-derived peptide secretion from pheochromocytoma cells through activation of serotonin type 4 (5-HT4) receptors.
2009-03
New insights into the human 5-HT4 receptor binding site: exploration of a hydrophobic pocket.
2004-10
Regulation of ion transport by 5-hydroxytryptamine in rat colon.
2004-07
Mechanism of action of the cisapride-induced vasodilatation in renal vasculature of rat.
2004-03
BIMU 1 and RS 67333, two 5-HT4 receptor agonists, modulate spontaneous alternation deficits induced by scopolamine in the mouse.
2003-06
5-HT decreases contractile and electrical activities in lymphatic vessels of the guinea-pig mesentery: role of 5-HT 7-receptors.
2003-05
5-HT7 receptor-mediated relaxation of the oviduct in nonpregnant proestrus pigs.
2003-02-14
New benzo[h][1,6]naphthyridine and azepino[3,2-c]quinoline derivatives as selective antagonists of 5-HT4 receptors: binding profile and pharmacological characterization.
2003-01-02
Central 5-HT(4) receptors and dopamine-dependent motor behaviors: searching for a functional role.
2002-04
5HT4(a) and 5-HT4(b) receptors have nearly identical pharmacology and are both expressed in human atrium and ventricle.
2001-02
New arylpiperazine derivatives as antagonists of the human cloned 5-HT(4) receptor isoforms.
2000-10-05
Pharmacological characterization of the human 5-HT(4(d)) receptor splice variant stably expressed in Chinese hamster ovary cells.
2000-10
Structure of the human serotonin 5-HT4 receptor gene and cloning of a novel 5-HT4 splice variant.
2000-02
Cloning, expression, and pharmacology of four human 5-hydroxytryptamine 4 receptor isoforms produced by alternative splicing in the carboxyl terminus.
1998-06
Cloning and expression of a human serotonin 5-HT4 receptor cDNA.
1997-11
Cloning and expression of human 5-HT4S receptors. Effect of receptor density on their coupling to adenylyl cyclase.
1997-10-20
[3H]RS 57639, a high affinity, selective 5-HT4 receptor partial agonist, specifically labels guinea-pig striatal and rat cloned (5-HT4S and 5-HT4L) receptors.
1997-04-01
Cloning, expression and pharmacology of the mouse 5-HT(4L) receptor.
1996-11-25
Name Type Language
1H-INDOLE-3-CARBOXYLIC ACID, 1-METHYL-, (1-(2-((METHYLSULFONYL)AMINO)ETHYL)-4-PIPERIDINYL)METHYL ESTER
Preferred Name English
GR-113808
Common Name English
Code System Code Type Description
FDA UNII
ZT350OYT3I
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY
PUBCHEM
119376
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY
CHEBI
73380
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY
WIKIPEDIA
GR-113808
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY
CAS
144625-51-4
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID40162772
Created by admin on Mon Mar 31 22:36:11 GMT 2025 , Edited by admin on Mon Mar 31 22:36:11 GMT 2025
PRIMARY