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

Details

Stereochemistry RACEMIC
Molecular Formula C20H13ClF3NO3
Molecular Weight 407.77
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLOXACRINE

SMILES

ON1C2=C(C(=O)CC(C2)C3=CC=C(C=C3)C(F)(F)F)C(=O)C4=C1C=CC(Cl)=C4

InChI

InChIKey=AWHZKKVSUJJVNL-UHFFFAOYSA-N
InChI=1S/C20H13ClF3NO3/c21-13-5-6-15-14(9-13)19(27)18-16(25(15)28)7-11(8-17(18)26)10-1-3-12(4-2-10)20(22,23)24/h1-6,9,11,28H,7-8H2

HIDE SMILES / InChI

Molecular Formula C20H13ClF3NO3
Molecular Weight 407.77
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

FLOXACRINE, a dihydroacridinedione derivative, is an antimalarial agent. It showed high potency against blood-induced infection of drug-sensitive and drug-resistant lines of Plasmodium berghei in animal models.

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of new drugs for chemoprophylaxis of malaria.
2001-07
Short report: floxacrine analog WR 243251 inhibits hematin polymerization.
2001-07
Development of new drugs for chemoprophylaxis of malaria.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:09:01 GMT 2025
Edited
by admin
on Mon Mar 31 18:09:01 GMT 2025
Record UNII
V09GC6329G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-CHLORO-3,4-DIHYDRO-10-HYDROXY-3-(.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-P-TOLYL)-1,9(2H)ACRIDANDIONE
Preferred Name English
FLOXACRINE
INN  
INN  
Official Name English
floxacrine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C271
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
NCI_THESAURUS C250
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
Code System Code Type Description
INN
3849
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
PUBCHEM
68708
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
SMS_ID
100000081021
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
ChEMBL
CHEMBL333634
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
EVMPD
SUB07658MIG
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
CAS
53966-34-0
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
FDA UNII
V09GC6329G
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
NCI_THESAURUS
C65701
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
MESH
C022008
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID30866373
Created by admin on Mon Mar 31 18:09:01 GMT 2025 , Edited by admin on Mon Mar 31 18:09:01 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY