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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H23NO5S
Molecular Weight 449.519
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LY-510929

SMILES

CC1=C(CCOC2=CC=C(C[C@H](OC3=CC=CC=C3)C(O)=O)C=C2)N=C(O1)C4=CC=CS4

InChI

InChIKey=ACJLLRYCNQTXAG-QFIPXVFZSA-N
InChI=1S/C25H23NO5S/c1-17-21(26-24(30-17)23-8-5-15-32-23)13-14-29-19-11-9-18(10-12-19)16-22(25(27)28)31-20-6-3-2-4-7-20/h2-12,15,22H,13-14,16H2,1H3,(H,27,28)/t22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H23NO5S
Molecular Weight 449.519
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Detection of left ventricular hypertrophy in rats administered a peroxisome proliferator-activated receptor alpha/gamma dual agonist using natriuretic peptides and imaging.
2010-04
Design and synthesis of alpha-aryloxy-alpha-methylhydrocinnamic acids: a novel class of dual peroxisome proliferator-activated receptor alpha/gamma agonists.
2004-05-06
Bombesin-like peptides in health and disease. Proceedings of an international symposium. October 13-16, 1987, Rome, Italy. A tribute to Vittorio Erspamer, M.D.
1988
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:14:55 GMT 2025
Edited
by admin
on Mon Mar 31 22:14:55 GMT 2025
Record UNII
0YSL9C6AHT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LY-510929
Code English
BENZENEPROPANOIC ACID, 4-(2-(5-METHYL-2-(2-THIENYL)-4-OXAZOLYL)ETHOXY)-.ALPHA.-PHENOXY-, (.ALPHA.S)-
Preferred Name English
LY510929
Code English
Code System Code Type Description
PUBCHEM
146675094
Created by admin on Mon Mar 31 22:14:55 GMT 2025 , Edited by admin on Mon Mar 31 22:14:55 GMT 2025
PRIMARY
FDA UNII
0YSL9C6AHT
Created by admin on Mon Mar 31 22:14:55 GMT 2025 , Edited by admin on Mon Mar 31 22:14:55 GMT 2025
PRIMARY
CAS
471854-50-9
Created by admin on Mon Mar 31 22:14:55 GMT 2025 , Edited by admin on Mon Mar 31 22:14:55 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY