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Details

Stereochemistry RACEMIC
Molecular Formula C26H30Cl2F3NO
Molecular Weight 500.424
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOFANTRINE

SMILES

CCCCN(CCCC)CCC(O)C1=C2C=CC(=CC2=C3C=C(Cl)C=C(Cl)C3=C1)C(F)(F)F

InChI

InChIKey=FOHHNHSLJDZUGQ-UHFFFAOYSA-N
InChI=1S/C26H30Cl2F3NO/c1-3-5-10-32(11-6-4-2)12-9-25(33)23-16-22-21(14-18(27)15-24(22)28)20-13-17(26(29,30)31)7-8-19(20)23/h7-8,13-16,25,33H,3-6,9-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C26H30Cl2F3NO
Molecular Weight 500.424
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:15 UTC 2023
Edited
by admin
on Fri Dec 15 15:43:15 UTC 2023
Record UNII
Q2OS4303HZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOFANTRINE
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
9-PHENANTHRENEMETHANOL, 1,3-DICHLORO-.ALPHA.-(2-(DIBUTYLAMINO)ETHYL)-6-(TRIFLUOROMETHYL)-
Systematic Name English
(±)-HALOFANTRINE
Common Name English
HALOFANTRINE [VANDF]
Common Name English
Halofantrine [WHO-DD]
Common Name English
DL-WR-171669
Code English
HALOFANTRINE [MI]
Common Name English
1,3-DICHLORO-.ALPHA.-(2-(DIBUTYLAMINO)ETHYL)-6-(TRIFLUOROMETHYL)-9-PHENANTHRENEMETHANOL
Systematic Name English
halofantrine [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC P01BX01
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
NCI_THESAURUS C271
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
FDA ORPHAN DRUG 61791
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
NDF-RT N0000175482
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
Code System Code Type Description
WIKIPEDIA
HALOFANTRINE
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID0023119
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
SMS_ID
100000083941
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
MESH
C023768
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
MERCK INDEX
m5900
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY Merck Index
CAS
66051-63-6
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
SUPERSEDED
ECHA (EC/EINECS)
274-104-1
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
DRUG BANK
DB01218
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL1107
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
CAS
69756-53-2
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
RXCUI
50749
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY RxNorm
EVMPD
SUB07998MIG
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
FDA UNII
Q2OS4303HZ
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
DRUG CENTRAL
1350
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
PUBCHEM
37393
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
NCI_THESAURUS
C65838
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
INN
4749
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
LACTMED
Halofantrine
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE ACTIVE -> PARENT
Related Record Type Details
ACTIVE MOIETY