Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H21Cl2N3O |
| Molecular Weight | 378.296 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C2N=C3C=C(Cl)C=CC3=C(NCCCNCCCl)C2=C1
InChI
InChIKey=OAPNFEMIOBGOHM-UHFFFAOYSA-N
InChI=1S/C19H21Cl2N3O/c1-25-14-4-6-17-16(12-14)19(23-9-2-8-22-10-7-20)15-5-3-13(21)11-18(15)24-17/h3-6,11-12,22H,2,7-10H2,1H3,(H,23,24)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Frameshift mutations induced by the acridine mustard ICR-191 in embryos and in the adult gill and hepatopancreas of rpsL transgenic zebrafish. | 2005-10-15 |
|
| Alleviation of mutagenic effects of polycyclic aromatic agents (quinacrine mustard, ICR-191 and ICR-170) by caffeine and pentoxifylline. | 2003-09-29 |
|
| Ethanol-enhanced cytotoxicity of alkylating agents. | 2002-03 |
|
| Induction of light emission by luminescent bacteria treated with UV light and chemical mutagens. | 2002 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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17070-44-9
Created by
admin on Mon Mar 31 19:52:21 GMT 2025 , Edited by admin on Mon Mar 31 19:52:21 GMT 2025
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C004294
Created by
admin on Mon Mar 31 19:52:21 GMT 2025 , Edited by admin on Mon Mar 31 19:52:21 GMT 2025
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28241
Created by
admin on Mon Mar 31 19:52:21 GMT 2025 , Edited by admin on Mon Mar 31 19:52:21 GMT 2025
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96O8D10RM2
Created by
admin on Mon Mar 31 19:52:21 GMT 2025 , Edited by admin on Mon Mar 31 19:52:21 GMT 2025
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PRIMARY |
SALT/SOLVATE (PARENT)
SUBSTANCE RECORD
