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Details

Stereochemistry ACHIRAL
Molecular Formula C20H22N2O5
Molecular Weight 370.3991
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of APABETALONE

SMILES

COC1=CC2=C(C(=O)NC(=N2)C3=CC(C)=C(OCCO)C(C)=C3)C(OC)=C1

InChI

InChIKey=NETXMUIMUZJUTB-UHFFFAOYSA-N
InChI=1S/C20H22N2O5/c1-11-7-13(8-12(2)18(11)27-6-5-23)19-21-15-9-14(25-3)10-16(26-4)17(15)20(24)22-19/h7-10,23H,5-6H2,1-4H3,(H,21,22,24)

HIDE SMILES / InChI

Molecular Formula C20H22N2O5
Molecular Weight 370.3991
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 04:36:35 UTC 2023
Edited
by admin
on Sat Dec 16 04:36:35 UTC 2023
Record UNII
8R4A7GDZ1D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
APABETALONE
INN   USAN   WHO-DD  
USAN   INN  
Official Name English
RVX-000222
Code English
APABETALONE [USAN]
Common Name English
2-[4-(2-Hydroxyethoxy)-3,5-dimethylphenyl]-5,7-dimethoxyquinazolin-4(3H)-one
Systematic Name English
RVX000222
Code English
apabetalone [INN]
Common Name English
Apabetalone [WHO-DD]
Common Name English
RVX-208
Code English
Code System Code Type Description
PUBCHEM
135564749
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
DRUG BANK
DB12000
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
FDA UNII
8R4A7GDZ1D
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
WIKIPEDIA
Apabetalone
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
CAS
1044870-39-4
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
EPA CompTox
DTXSID90146502
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
INN
9884
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
NCI_THESAURUS
C171748
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
USAN
DE-35
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
SMS_ID
100000169103
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
EVMPD
SUB182763
Created by admin on Sat Dec 16 04:36:35 UTC 2023 , Edited by admin on Sat Dec 16 04:36:35 UTC 2023
PRIMARY
Related Record Type Details
TARGET->ACTIVATOR OF EXPRESSION
TARGET -> INHIBITOR
Suppressed gene expression of VI mediators in monocytes and endothelial cells by inhibiting BET-dependent transcription induced by multiple inflammatory stimuli. In CVD patients, apabetalone treatment reduced circulating levels of VI mediators, an outcome conducive with atherosclerotic plaque stabilization and MACE reduction.
IC50
Related Record Type Details
ACTIVE MOIETY