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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H26FNO5
Molecular Weight 451.4867
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of KRP-101

SMILES

CC[C@@H](CC1=CC=C(OC)C(=C1)C(=O)NCC2=CC=C(OC3=CC=C(F)C=C3)C=C2)C(O)=O

InChI

InChIKey=VRHOBXXCNBZJRX-IBGZPJMESA-N
InChI=1S/C26H26FNO5/c1-3-19(26(30)31)14-18-6-13-24(32-2)23(15-18)25(29)28-16-17-4-9-21(10-5-17)33-22-11-7-20(27)8-12-22/h4-13,15,19H,3,14,16H2,1-2H3,(H,28,29)(H,30,31)/t19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C26H26FNO5
Molecular Weight 451.4867
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 12:12:51 GMT 2023
Edited
by admin
on Sat Dec 16 12:12:51 GMT 2023
Record UNII
V123C0BB32
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
KRP-101
Common Name English
BENZENEPROPANOIC ACID, .ALPHA.-ETHYL-3-((((4-(4-FLUOROPHENOXY)PHENYL)METHYL)AMINO)CARBONYL)-4-METHOXY-, (.ALPHA.S)-
Systematic Name English
KRP 101
Code English
(2S)-2-((3-((4-(4-FLUOROPHENOXY)PHENYL)METHYLCARBAMOYL)-4-METHOXY-PHENYL)METHYL)BUTANOIC ACID
Systematic Name English
Code System Code Type Description
CAS
311770-26-0
Created by admin on Sat Dec 16 12:12:51 GMT 2023 , Edited by admin on Sat Dec 16 12:12:51 GMT 2023
PRIMARY
PUBCHEM
9825046
Created by admin on Sat Dec 16 12:12:51 GMT 2023 , Edited by admin on Sat Dec 16 12:12:51 GMT 2023
PRIMARY
FDA UNII
V123C0BB32
Created by admin on Sat Dec 16 12:12:51 GMT 2023 , Edited by admin on Sat Dec 16 12:12:51 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
Kyorin Pharmaceutical Co. Ltd.'s PPAR.ALPHA. agonist, KRP-101, has completed Phase IIa testing to treat dyslipidemia.
ACTIVE MOIETY
The present study investigated the effects of a potent and subtype-selective PPARalpha agonist, KRP-101, in a nonrodent insulin-resistant animal model under pair-fed conditions. KRP-101 administration resulted in a significantly lower weight of overall visceral fat, which is associated with increased adiponectin and decreased leptin in serum. KRP-101 administration improved hyperglycemia and hyperinsulinemia as well as dyslipidemia in dogs fed a high-fat diet. Oral glucose tolerance test showed that KRP-101 administration improved glucose intolerance. The KRP-101 group showed a markedly lower hepatic triglyceride concentration.