Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H15Cl2NO2 |
Molecular Weight | 276.159 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC1=CC=C(C=C1)N(CCCl)CCCl
InChI
InChIKey=RQAFMLCWWGDNLI-UHFFFAOYSA-N
InChI=1S/C12H15Cl2NO2/c13-5-7-15(8-6-14)11-3-1-10(2-4-11)9-12(16)17/h1-4H,5-9H2,(H,16,17)
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Cytotoxic steroids with antiestrogenic activity of the 11alpha-acyloxyestra-1,3,5(10)-triene series]. | 2006 Mar-Apr |
|
Aneugenic potential of the nitrogen mustard analogues melphalan, chlorambucil and p-N,N-bis(2-chloroethyl)aminophenylacetic acid in cell cultures in vitro. | 2007 Apr 1 |
|
Cytogenetic and antineoplastic effects of modified steroidal alkylators. | 2010 Feb |
|
Fluorescence in situ hybridization in combination with the comet assay and micronucleus test in genetic toxicology. | 2010 Sep 15 |
Patents
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID40146714
Created by
admin on Fri Dec 15 17:09:02 GMT 2023 , Edited by admin on Fri Dec 15 17:09:02 GMT 2023
|
PRIMARY | |||
|
10477-72-2
Created by
admin on Fri Dec 15 17:09:02 GMT 2023 , Edited by admin on Fri Dec 15 17:09:02 GMT 2023
|
PRIMARY | |||
|
32842A3UZP
Created by
admin on Fri Dec 15 17:09:02 GMT 2023 , Edited by admin on Fri Dec 15 17:09:02 GMT 2023
|
PRIMARY | |||
|
71964
Created by
admin on Fri Dec 15 17:09:02 GMT 2023 , Edited by admin on Fri Dec 15 17:09:02 GMT 2023
|
PRIMARY | |||
|
25306
Created by
admin on Fri Dec 15 17:09:02 GMT 2023 , Edited by admin on Fri Dec 15 17:09:02 GMT 2023
|
PRIMARY |
PARENT (METABOLITE ACTIVE)
SUBSTANCE RECORD