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

Details

Stereochemistry RACEMIC
Molecular Formula C18H26ClN3.2ClH
Molecular Weight 392.794
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLOROQUINE HYDROCHLORIDE

SMILES

Cl.Cl.CCN(CC)CCCC(C)NC1=CC=NC2=C1C=CC(Cl)=C2

InChI

InChIKey=PCFGECQRSMVKCC-UHFFFAOYSA-N
InChI=1S/C18H26ClN3.2ClH/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18;;/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21);2*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 C18H26ClN3
Molecular Weight 319.872
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 16:28:01 UTC 2023
Edited
by admin
on Fri Dec 15 16:28:01 UTC 2023
Record UNII
NT0J0815S5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLOROQUINE HYDROCHLORIDE
MART.   ORANGE BOOK   USP   VANDF   WHO-DD  
Common Name English
1,4-PENTANEDIAMINE, N(SUP 4)-(7-CHLORO-4-QUINOLINYL)-N(SUP 1),N (SUP 1)-DIETHYL-, DIHYDROCHLORIDE
Common Name English
CHLOROQUINE HYDROCHLORIDE [USP IMPURITY]
Common Name English
CHLOROQUINE HCL
Common Name English
Chloroquine hydrochloride [WHO-DD]
Common Name English
7-(Chloro-4-[[4-diethylamino)-1-methylbutyl]amino]quinoline dihydrochloride
Common Name English
CHLOROQUINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
CHLOROQUINE HYDROCHLORIDE [MART.]
Common Name English
CHLOROQUINE HYDROCHLORIDE [VANDF]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C271
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C65318
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
CAS
3545-67-3
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
DRUG BANK
DBSALT001317
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
ECHA (EC/EINECS)
222-592-1
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
FDA UNII
NT0J0815S5
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
SMS_ID
100000084735
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
ChEMBL
CHEMBL76
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
EVMPD
SUB01237MIG
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
EPA CompTox
DTXSID501026664
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
RXCUI
451796
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY RxNorm
PUBCHEM
83820
Created by admin on Fri Dec 15 16:28:02 UTC 2023 , Edited by admin on Fri Dec 15 16:28:02 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY