Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H6ClN |
| Molecular Weight | 79.529 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCCl
InChI
InChIKey=VKPPFDPXZWFDFA-UHFFFAOYSA-N
InChI=1S/C2H6ClN/c3-1-2-4/h1-2,4H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Basic stages of organizing antineoplastic chemotherapy in Russia. Role of the Russian Oncological Scientific Center named for N. N. Blokhina, Russian Academy of Medical Sciences]. | 2001 |
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| A new inhibitor design strategy for carboxypeptidase A as exemplified by N-(2-chloroethyl)-N-methylphenylalanine. | 2001 Feb |
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| Identification of new aqueous chemical degradation products of isophosphoramide mustard. | 2001 Jun |
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| Phenotypes of Drosophila homologs of human XPF and XPG to chemically-induced DNA modifications. | 2001 May 9 |
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| Structure--activity relationships among novel phenoxybenzamine-related beta-chloroethylamines. | 2002 May |
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| Thiosugar nucleosides. Synthesis and biological activity of 1,3,4-thiadiazole, thiazoline and thiourea derivatives of 5-thio-D-glucose. | 2004 |
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| Conjugates of phthalocyanines with oligonucleotides as reagents for sensitized or catalytic DNA modification. | 2006 |
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| Kinetic study of DNA modification by phthalocyanine derivative of the oligonucleotide. | 2006 |
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| Synthesis and in vitro antileukemic activity of some new 1,3-(oxytetraethylenoxy)cyclotriphosphazene derivatives. | 2006 Jan 26 |
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| Regioselective synthesis of N-beta-hydroxyethylaziridines by the ring-opening reaction of epoxides with aziridine generated in situ. | 2006 Mar 16 |
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| Genotoxicants target distinct molecular networks in neonatal neurons. | 2006 Nov |
|
| Synthesis of DNA-directed pyrrolidinyl and piperidinyl confined alkylating chloroalkylaminoanthraquinones: potential for development of tumor-selective N-oxides. | 2006 Nov 30 |
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| Antihypertensive activity of chitin derivatives. | 2006 Oct 15 |
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| Superparamagnetic poly(methyl methacrylate) beads for nattokinase purification from fermentation broth. | 2006 Sep |
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| Alkylation potency and protein specificity of aromatic urea derivatives and bioisosteres as potential irreversible antagonists of the colchicine-binding site. | 2007 Jul 1 |
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| Synthesis and in vitro antiproliferative activity of new 1,3-(oxytetraethylenoxy)-cyclotriphosphazene derivatives. | 2007 May-Jun |
|
| High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease. | 2007 Oct |
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| Selective alkylation of beta(II)-tubulin and thioredoxin-1 by structurally related subsets of aryl chloroethylureas leading to either anti-microtubules or redox modulating agents. | 2008 Aug 1 |
|
| The new analogues of nitrogen mustard with one, two or three 2-chloroethylamino fragments. Reactions with nucleophiles. | 2008 Nov-Dec |
|
| DNA repair modulates the vulnerability of the developing brain to alkylating agents. | 2009 Mar 1 |
|
| Determination of silver(I) by differential pulse voltammetry using a glassy carbon electrode modified with synthesized N-(2-aminoethyl)-4,4'-bipyridine. | 2010 |
|
| 1-Methyl-4H-3,1-benzoxazine-2,4(1H)dione. | 2010 Feb 20 |
|
| Angiotensin-I-converting enzyme (ACE) inhibitors from marine resources: prospects in the pharmaceutical industry. | 2010 Mar 31 |
|
| (E)-2,4-Dichloro-6-{1-[(2-chloro-eth-yl)imino]-eth-yl}phenol. | 2010 Nov 10 |
|
| Complexation properties and synthesis of a novel Schiff base with triphenylene nucleus. | 2010 Nov 15 |
|
| Methylene blue: revisited. | 2010 Oct |
Patents
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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689-98-5
Created by
admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
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10871
Created by
admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
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13369
Created by
admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
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DTXSID10218977
Created by
admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
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P7YLY3O329
Created by
admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
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PRIMARY |
PARENT (METABOLITE)
SUBSTANCE RECORD
