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Details

Stereochemistry ACHIRAL
Molecular Formula C18H25Cl3O2
Molecular Weight 379.749
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of K-111

SMILES

OC(=O)C(Cl)(Cl)CCCCCCCCCCC1=CC=C(Cl)C=C1

InChI

InChIKey=GPCJDSXBRMKASP-UHFFFAOYSA-N
InChI=1S/C18H25Cl3O2/c19-16-12-10-15(11-13-16)9-7-5-3-1-2-4-6-8-14-18(20,21)17(22)23/h10-13H,1-9,14H2,(H,22,23)

HIDE SMILES / InChI

Molecular Formula C18H25Cl3O2
Molecular Weight 379.749
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of PPARalpha activation of macrophages on the secretion of inflammatory cytokines in cultured adipocytes.
2007-04-30
Drug evaluation: K-111, an insulin-sensitizing peroxisome proliferator-activated receptor alpha agonist.
2007-04
Reduced coronary reserve in response to short-term ischaemia and vasoactive drugs in ex vivo hearts from diabetic mice.
2006-03
Skeletal muscle glycogen synthase subcellular localization: effects of insulin and PPAR-alpha agonist (K-111) administration in rhesus monkeys.
2005-06
Effect of BM 17.0744, a PPARalpha ligand, on the metabolism of perfused hearts from control and diabetic mice.
2005-02
Human adipocyte fatty acid-binding protein (aP2) gene promoter-driven reporter assay discriminates nonlipogenic peroxisome proliferator-activated receptor gamma ligands.
2004-11
Biochemical and morphological effects of K-111, a peroxisome proliferator-activated receptor (PPAR)alpha activator, in non-human primates.
2004-07-15
The effects of K-111, a new insulin-sensitizer, on metabolic syndrome in obese prediabetic rhesus monkeys.
2003-10
Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-alpha activator.
2002-09
Peroxisome proliferator-activated receptor-alpha ligands inhibit cardiac lipoprotein lipase activity.
2001-08
BM 17.0744: a structurally new antidiabetic compound with insulin-sensitizing and lipid-lowering activity.
1999-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:59:12 GMT 2025
Edited
by admin
on Wed Apr 02 09:59:12 GMT 2025
Record UNII
TM9XQR923G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
K-111
Code English
2,2-DICHLORO-12-(4-CHLOROPHENYL)DODECANOIC ACID
Preferred Name English
K111
Code English
K111 (PHARMACEUTICAL)
Code English
.ALPHA.,.ALPHA.,4-TRICHLOROBENZENEDODECANOIC ACID
Common Name English
BM-17.0744
Code English
BM170744
Code English
BM-170744
Code English
BENZENEDODECANOIC ACID, .ALPHA.,.ALPHA.,4-TRICHLORO-
Systematic Name English
Code System Code Type Description
CAS
221564-97-2
Created by admin on Wed Apr 02 09:59:12 GMT 2025 , Edited by admin on Wed Apr 02 09:59:12 GMT 2025
PRIMARY
FDA UNII
TM9XQR923G
Created by admin on Wed Apr 02 09:59:12 GMT 2025 , Edited by admin on Wed Apr 02 09:59:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID901286589
Created by admin on Wed Apr 02 09:59:12 GMT 2025 , Edited by admin on Wed Apr 02 09:59:12 GMT 2025
PRIMARY
PUBCHEM
9929731
Created by admin on Wed Apr 02 09:59:12 GMT 2025 , Edited by admin on Wed Apr 02 09:59:12 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> ACTIVATOR
Related Record Type Details
ACTIVE MOIETY