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

Details

Stereochemistry ACHIRAL
Molecular Formula 2C19H29N5O2.C4H6O4
Molecular Weight 837.0198
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAVOLTIDINE SUCCINATE

SMILES

OC(=O)CCC(O)=O.CN1N=C(CO)N=C1NCCCOC2=CC=CC(CN3CCCCC3)=C2.CN4N=C(CO)N=C4NCCCOC5=CC=CC(CN6CCCCC6)=C5

InChI

InChIKey=IRLVOMNMSKSKMH-UHFFFAOYSA-N
InChI=1S/2C19H29N5O2.C4H6O4/c2*1-23-19(21-18(15-25)22-23)20-9-6-12-26-17-8-5-7-16(13-17)14-24-10-3-2-4-11-24;5-3(6)1-2-4(7)8/h2*5,7-8,13,25H,2-4,6,9-12,14-15H2,1H3,(H,20,21,22);1-2H2,(H,5,6)(H,7,8)

HIDE SMILES / InChI
LAVOLTIDINE, also known as loxtidine, is a highly potent and selective histamine H2-receptor antagonist. It is a member of triazoles. It produces gastric carcinoid tumors in rodents that is why its clinical development was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
The CCK(2) receptor antagonist, YF476, inhibits Mastomys ECL cell hyperplasia and gastric carcinoid tumor development.
2010 Jun 8
Name Type Language
LAVOLTIDINE SUCCINATE
USAN  
USAN  
Official Name English
LAVOLTIDINE SUCCINATE [USAN]
Common Name English
AH 23844 HEMISUCCINATE
Code English
AH-23844 HEMISUCCINATE
Code English
1-METHYL-5-((3-((.ALPHA.-PIPERIDINO-M-TOLYL)OXY)PROPYL)AMINO)-1H-1,2,4-TRIAZOLE-3-METHANOL SUCCINATE (2:1) (SALT)
Systematic Name English
LOXOTIDINE SUCCINATE
Common Name English
AH-23844A
Code English
1-METHYL-5-((3-(3-(1-PIPERIDINYLMETHYL)PHENOXY)PROPYL)AMINO)-1H-1,2,4-TRIAZOLE-3-METHANOL
Systematic Name English
AH 23844A
Code English
1H-1,2,4-TRIAZOLE-3-METHANOL, 1-METHYL-5-((3-(3-(1-PIPERIDINYLMETHYL)PHENOXY)PROPYL)AMINO)-, BUTANEDIOATE (2:1) (SALT)
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C170099
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
USAN
BB-34
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
FDA UNII
YSJ55YKG2J
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110857
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
PUBCHEM
55472
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID50235426
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY
CAS
86160-82-9
Created by admin on Fri Dec 15 15:35:40 GMT 2023 , Edited by admin on Fri Dec 15 15:35:40 GMT 2023
PRIMARY