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Details

Stereochemistry RACEMIC
Molecular Formula C26H30Cl2F3NO.ClH
Molecular Weight 536.885
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOFANTRINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=WANGFTDWOFGECH-UHFFFAOYSA-N
InChI=1S/C26H30Cl2F3NO.ClH/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;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
H77DL0Y630
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOFANTRINE HYDROCHLORIDE
EP   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN  
Official Name English
9-(3-(DIBUTYLAMINO)-1-HYDROXYPROPYL)-1,3-DICHLORO-6-(TRIFLUOROMETHYL)PHENANTHRENE HYDROCHLORIDE
Systematic Name English
HALOFANTRINE HYDROCHLORIDE [MART.]
Common Name English
HALOFANTRINE HYDROCHLORIDE [USAN]
Common Name English
(±)-HALOFANTRINE HYDROCHLORIDE
Common Name English
9-PHENANTHRENEMETHANOL, 1,3-DICHLORO-.ALPHA.-(2-(DIBUTYLAMINO)ETHYL)-6-(TRIFLUOROMETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
1,3-Dichloro-α-[2-(dibutylamino)ethyl]-6-(trifluoromethyl)-9-phenanthrenemethanol hydrochloride
Systematic Name English
HALOFANTRINE HYDROCHLORIDE [VANDF]
Common Name English
HALOFANTRINE HYDROCHLORIDE [EP IMPURITY]
Common Name English
HALOFANTRINE HCL
Common Name English
HALOFANTRINE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
HALOFANTRINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
9-PHENANTHRENEMETHANOL, 1,3-DICHLORO-.ALPHA.-(2-(DIBUTYLAMINO)ETHYL)-6-(TRIFLUOROMETHYL)-, HYDROCHLORIDE
Systematic Name English
Halofantrine hydrochloride [WHO-DD]
Common Name English
WR-171669
Code English
HALOFANTRINE HYDROCHLORIDE [MI]
Common Name English
SKF-102886
Code English
HALFAN
Brand Name English
Code System Code Type Description
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
DRUG BANK
DBSALT001186
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
EVMPD
SUB02451MIG
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
58130
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
SMS_ID
100000088512
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
PUBCHEM
37392
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
C65839
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
ECHA (EC/EINECS)
252-895-4
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
H77DL0Y630
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
DTXSID0045464
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
106927-11-1
Created by admin on Fri Dec 15 15:43:15 UTC 2023 , Edited by admin on Fri Dec 15 15:43:15 UTC 2023
SUPERSEDED
CAS
36167-63-2
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
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PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY