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Details

Stereochemistry RACEMIC
Molecular Formula C20H24O5
Molecular Weight 344.4016
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TERBUFIBROL

SMILES

CC(C)(C)C1=CC=C(OCC(O)COC2=CC=C(C=C2)C(O)=O)C=C1

InChI

InChIKey=PXODZCMXOZRVEN-UHFFFAOYSA-N
InChI=1S/C20H24O5/c1-20(2,3)15-6-10-18(11-7-15)25-13-16(21)12-24-17-8-4-14(5-9-17)19(22)23/h4-11,16,21H,12-13H2,1-3H3,(H,22,23)

HIDE SMILES / InChI

Molecular Formula C20H24O5
Molecular Weight 344.4016
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Terbufibrol, an antihyperlipoproteinemic agent that blocks the hepatic cholesterol synthesis in a step between acetate and HMG-CoA (3-hydroxy-3-methylglutaryl-CoA). Information about the current use of this compound is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Mode of action of terbufibrol (INN) a hypolipidemic agent on rat liver sterol synthesis.
1982
The hypocholesterolemic effect of terbufibrol and other drugs in normal and hypercholesterolemic baboons.
1979-04
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:01:40 GMT 2025
Edited
by admin
on Mon Mar 31 18:01:40 GMT 2025
Record UNII
W41Z308IA3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TERBUFIBROL
INN  
INN  
Official Name English
(±)-P-(3-(P-TERT-BUTYLPHENOXY)-2-HYDROXYPROPOXY)BENZOIC ACID
Preferred Name English
P-(3-(P-TERT-BUTYLPHENOXY)-2-HYDROXYPROPOXY)BENZOIC ACID
Common Name English
terbufibrol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
Code System Code Type Description
PUBCHEM
41907
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
NCI_THESAURUS
C91031
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
MESH
C020508
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
SMS_ID
100000082704
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID60866568
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
ChEMBL
CHEMBL2107542
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
FDA UNII
W41Z308IA3
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
CAS
56488-59-6
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
EVMPD
SUB10912MIG
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
INN
3961
Created by admin on Mon Mar 31 18:01:40 GMT 2025 , Edited by admin on Mon Mar 31 18:01:40 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY