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Details

Stereochemistry ABSOLUTE
Molecular Formula C33H38N2O6
Molecular Weight 558.6646
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of A-192621

SMILES

CCCOC1=CC=C(C=C1)[C@H]2[C@@H]([C@H](CN2CC(=O)NC3=C(CC)C=CC=C3CC)C4=CC=C5OCOC5=C4)C(O)=O

InChI

InChIKey=LQEHCKYYIXQEBM-FUKIBTTHSA-N
InChI=1S/C33H38N2O6/c1-4-16-39-25-13-10-23(11-14-25)32-30(33(37)38)26(24-12-15-27-28(17-24)41-20-40-27)18-35(32)19-29(36)34-31-21(5-2)8-7-9-22(31)6-3/h7-15,17,26,30,32H,4-6,16,18-20H2,1-3H3,(H,34,36)(H,37,38)/t26-,30-,32+/m1/s1

HIDE SMILES / InChI

Molecular Formula C33H38N2O6
Molecular Weight 558.6646
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Endothelin receptor B antagonists decrease glioma cell viability independently of their cognate receptor.
2008-11-28
Differential roles of peripheral and spinal endothelin receptors in the micturition reflex in rats.
2004-10
Endothelin B receptor blockade inhibits dynamics of cell interactions and communications in melanoma cell progression.
2004-02-15
Endothelins regulate mediator production of rat tissue-cultured mucosal mast cells. Up-regulation of Th1 and inhibition of Th2 cytokines.
2002-05
Endothelin and blood pressure regulation in the female rat: studies in normal pregnancy and with nitric oxide synthase inhibition-induced hypertension.
2000
Pyrrolidine-3-carboxylic acids as endothelin antagonists. 4. Side chain conformational restriction leads to ET(B) selectivity.
1999-09-09
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:14:41 GMT 2025
Edited
by admin
on Mon Mar 31 22:14:41 GMT 2025
Record UNII
5XE882529E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
A-192621
Common Name English
A-192621-1
Preferred Name English
3-Pyrrolidinecarboxylic acid, 4-(1,3-benzodioxol-5-yl)-1-[2-[(2,6-diethylphenyl)amino]-2-oxoethyl]-2-(4-propoxyphenyl)-, (2R,3R,4S)-
Systematic Name English
A-192621.1
Code English
(2R,3R,4S)-4-(1,3-Benzodioxol-5-yl)-1-[2-[(2,6-diethylphenyl)amino]-2-oxoethyl]-2-(4-propoxyphenyl)-3-pyrrolidinecarboxylic acid
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID701102953
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
PRIMARY
PUBCHEM
5310991
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
PRIMARY
CAS
195529-26-1
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
CAS
195529-54-5
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
PRIMARY
CAS
600732-05-6
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
5XE882529E
Created by admin on Mon Mar 31 22:14:41 GMT 2025 , Edited by admin on Mon Mar 31 22:14:41 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
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ACTIVE MOIETY