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

Details

Stereochemistry ACHIRAL
Molecular Formula C23H26Cl2O6
Molecular Weight 469.355
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SIMFIBRATE

SMILES

CC(C)(OC1=CC=C(Cl)C=C1)C(=O)OCCCOC(=O)C(C)(C)OC2=CC=C(Cl)C=C2

InChI

InChIKey=JLRNKCZRCMIVKA-UHFFFAOYSA-N
InChI=1S/C23H26Cl2O6/c1-22(2,30-18-10-6-16(24)7-11-18)20(26)28-14-5-15-29-21(27)23(3,4)31-19-12-8-17(25)9-13-19/h6-13H,5,14-15H2,1-4H3

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://link.springer.com.sci-hub.cc/article/10.1007/BF03286654

Simfibrate, a derivative of clofibrate, is a hypolipidemic drug, that lowers serum chlolesterol and triglycerids. Under the brand name Cholesolvin it is indicated for hyperlipidaemia associated with arteriosclerosis, cerebral atherosclerosis, coronary arteriosclerosis, hypertension, diabetes.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Cholesolvin

Approved Use

Indications: hyperlipidaemia associated with arteriosclerosis, cerebral atherosclerosis, coronary arteriosclerosis, hypertension, diabetes.
PubMed

PubMed

TitleDatePubMed
Response to: Laparoscopic cholecystectomy is safe and effective for the treatment of biliary dyskinesia in the pediatric population.
2010 Dec
Patents

Sample Use Guides

In Vivo Use Guide
1.5 g/day P.O
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
SIMFIBRATE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
SIMFIBRATE [MI]
Common Name English
CLY-503
Code English
Simfibrate [WHO-DD]
Common Name English
simfibrate [INN]
Common Name English
SIMFIBRATE [JAN]
Common Name English
CHOLESOLVIN
Brand Name English
SIMFIBRATE [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC C10AB06
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
NCI_THESAURUS C98150
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
WHO-VATC QC10AB06
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
Code System Code Type Description
EVMPD
SUB10527MIG
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
DRUG CENTRAL
2444
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
PUBCHEM
5217
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
SMS_ID
100000083535
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
CAS
14929-11-4
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
WIKIPEDIA
SIMFIBRATE
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
MERCK INDEX
m9945
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C72998
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
DRUG BANK
DB13433
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
INN
2732
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
238-998-7
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID8057647
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105435
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY
FDA UNII
L2R75RQX26
Created by admin on Fri Dec 15 16:18:45 GMT 2023 , Edited by admin on Fri Dec 15 16:18:45 GMT 2023
PRIMARY