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Details

Stereochemistry ACHIRAL
Molecular Formula C5H10ClN3O3
Molecular Weight 195.604
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELMUSTINE

SMILES

OCCNC(=O)N(CCCl)N=O

InChI

InChIKey=YJZJEQBSODVMTH-UHFFFAOYSA-N
InChI=1S/C5H10ClN3O3/c6-1-3-9(8-12)5(11)7-2-4-10/h10H,1-4H2,(H,7,11)

HIDE SMILES / InChI

Molecular Formula C5H10ClN3O3
Molecular Weight 195.604
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Elmustine (1-(2-hydroxyethyl)3-(2-chloroethyl)-3-nitrosourea or HECNU) is an alkylating agent with antineoplastic properties. Elmustine is monofunctional and bifunctional alkylating agent that form, in a quantitatively minor reaction, DNA-DNA crosslinks. In vitro, by far the most abundant alkylation products of DNA are those resulting from 2-hydroxyethylation. Elmustine is especially highly active against intracerebrally implanted tumors. It was in Phase II clinical trials for the treatment of glioma. Elmustine development has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Interdependent regulation of insulin receptor kinase activity by ADP and hydrogen peroxide.
2005-02-04

Sample Use Guides

Phase II study: forty adults with recurring brain gliomas were treated with elmustine 130 mg/m2, given i.v. every 5 to 6 weeks (mean 5.4) and corticosteroids
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:02:06 GMT 2025
Edited
by admin
on Mon Mar 31 18:02:06 GMT 2025
Record UNII
NAT2FD82D7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ELMUSTINE
INN   MART.  
INN  
Official Name English
NSC-294895
Preferred Name English
ELMUSTINE [MART.]
Common Name English
elmustine [INN]
Common Name English
1-(2-CHLOROETHYL)-3-(2-HYDROXYETHYL)-1-NITROSOUREA
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C699
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
Code System Code Type Description
MESH
C013876
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
ECHA (EC/EINECS)
262-429-1
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
ChEMBL
CHEMBL284907
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
SMS_ID
100000080748
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
PUBCHEM
68804
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
NCI_THESAURUS
C73262
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
INN
5300
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
NSC
294895
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
CAS
60784-46-5
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID80209610
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
EVMPD
SUB06490MIG
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
FDA UNII
NAT2FD82D7
Created by admin on Mon Mar 31 18:02:06 GMT 2025 , Edited by admin on Mon Mar 31 18:02:06 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY