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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H15Cl2N
Molecular Weight 268.182
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORNAPHAZINE

SMILES

ClCCN(CCCl)C1=CC=C2C=CC=CC2=C1

InChI

InChIKey=XCDXSSFOJZZGQC-UHFFFAOYSA-N
InChI=1S/C14H15Cl2N/c15-7-9-17(10-8-16)14-6-5-12-3-1-2-4-13(12)11-14/h1-6,11H,7-10H2

HIDE SMILES / InChI

Molecular Formula C14H15Cl2N
Molecular Weight 268.182
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chlornaphazine was developed as a drug to treat Hodgkin's disease. However this compound caused bladder tumors, it was manifested human carcinogen, that is why its use was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Epidemiology of urinary bladder cancer: from tumor development to patient's death.
2007-06
Chlornaphazine and chlorambucil induce dominant lethal mutations in male mice.
2003-03
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:30:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:30:59 GMT 2025
Record UNII
U46E473275
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CB 1048
Preferred Name English
CHLORNAPHAZINE
HSDB   INN   MI  
INN  
Official Name English
CHLORNAPHAZINE [IARC]
Common Name English
R 48
Code English
CHLORNAPHAZINE [MI]
Common Name English
CB-1048
Code English
CHLORNAPHAZINE [HSDB]
Common Name English
chlornaphazine [INN]
Common Name English
NSC-62209
Code English
N,N-BIS(2-CHLOROETHYL)-2-NAPHTHYLAMINE
Systematic Name English
R-48
Code English
Classification Tree Code System Code
NCI_THESAURUS C697
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2107519
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-785-0
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
NSC
62209
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
DRUG CENTRAL
604
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
MERCK INDEX
m3378
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID3060087
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
FDA UNII
U46E473275
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
SMS_ID
100000081846
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
WIKIPEDIA
CHLORNAPHAZINE
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
INN
1314
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
EVMPD
SUB06189MIG
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
NCI_THESAURUS
C1047
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
PUBCHEM
10307
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
CAS
494-03-1
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
HSDB
2745
Created by admin on Mon Mar 31 18:30:59 GMT 2025 , Edited by admin on Mon Mar 31 18:30:59 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY