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Details

Stereochemistry ACHIRAL
Molecular Formula C23H38NO2.Na
Molecular Weight 383.5431
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETABEN SODIUM

SMILES

[Na+].CCCCCCCCCCCCCCCCNC1=CC=C(C=C1)C([O-])=O

InChI

InChIKey=RIEGDRWQKNITRV-UHFFFAOYSA-M
InChI=1S/C23H39NO2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20-24-22-18-16-21(17-19-22)23(25)26;/h16-19,24H,2-15,20H2,1H3,(H,25,26);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C23H38NO2
Molecular Weight 360.5533
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cetaben has been identified as an anti-atherosclerotic hypolipidaemic substance. Cetaben is a unique, PPARα-independent peroxisome proliferator with hypolipidemic activity that inhibits cholesterol synthesis in the human hepatoma Hep-G2 cells resulting in reversible changes in Golgi morphology. Cetaben represents an exceptional type of peroxisome proliferator, specifically affecting peroxisomes, without having a negative influence on the processes of peroxisome biogenesis. Cetaben raised only the peroxisomal enzymes, acyl-CoA oxidase, glycerone-phosphate acyltransferase, D-amino-acid oxidase, catalase, and urate oxidase. Cetaben sodium has being shown to be an antiatherosclerotic agent.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Guinea pigs: cetaben (90 mg/kg/day, p.o.) inhibited the development of atherosclerotic lesions in guinea pigs fed a cholesterol and vitamin D2-rich diet. https://www.ncbi.nlm.nih.gov/pubmed/6604004
The effects of cetaben and clofibric acid were compared on the activities of peroxisomal enzymes in the liver and kidney of male Wistar rats. Cetaben at 200 mg/kg body wt increased the activities of all of the enzymes in the liver. The data obtained in the dose-response study of cetaben revealed a significant rise in the activities of peroxisomal enzymes in both the liver and kidney at doses of 50-100 mg/kg body wt administered over 10 days, but the maximal effect was observed at 250 mg/kg.
Route of Administration: Oral
In Vitro Use Guide
The activity of the peroxisomal bifunctional enzyme was not affected in HepG2 cells by clofibric acid and cetaben, whereas the mRNA level was elevated to 2.3 fold by 10 umol/l cetaben. At high concentrations of cetaben all enzyme activities were decreased in both cell lines due to its high cytotoxicity.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:52 GMT 2023
Edited
by admin
on Fri Dec 15 15:23:52 GMT 2023
Record UNII
433YPU24B8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CETABEN SODIUM
USAN  
USAN  
Official Name English
CL-203821
Code English
SODIUM P-(HEXADECYLAMINO)BENZOATE
Common Name English
BENZOIC ACID, 4-(HEXADECYLAMINO)-, SODIUM SALT
Common Name English
CETABEN SODIUM [USAN]
Common Name English
CL 203,821
Code English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C72984
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID30214254
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
ChEMBL
CHEMBL31907
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
PUBCHEM
23703815
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
FDA UNII
433YPU24B8
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
CAS
64059-66-1
Created by admin on Fri Dec 15 15:23:52 GMT 2023 , Edited by admin on Fri Dec 15 15:23:52 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY