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

Details

Stereochemistry ACHIRAL
Molecular Formula C2H6N2.ClH
Molecular Weight 94.543
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETAMIDINE HYDROCHLORIDE

SMILES

Cl.CC(N)=N

InChI

InChIKey=WCQOBLXWLRDEQA-UHFFFAOYSA-N
InChI=1S/C2H6N2.ClH/c1-2(3)4;/h1H3,(H3,3,4);1H

HIDE SMILES / InChI

Molecular Formula C2H6N2
Molecular Weight 58.0824
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Diacetamidinium sulfate.
2010-11-27
Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance.
2010-11-25
Characterization and inactivation of an agmatine deiminase from Helicobacter pylori.
2010-04
N-(4-Chloro-phen-yl)ethanimidamide.
2010-03-27
Nickel(II) and iron(III) selective off-on-type fluorescence probes based on perylene tetracarboxylic diimide.
2010-03-07
Tholinomics--chemical analysis of nitrogen-rich polymers.
2010-02-15
Haloacetamidine-based inactivators of protein arginine deiminase 4 (PAD4): evidence that general acid catalysis promotes efficient inactivation.
2010-01-25
Four-component synthesis of fully substituted 1,2,4-triazoles.
2010
Reactions of Pd(II) with chelate-tethered 2,6-diaminopurine derivatives: N3-coordination and reaction of the purine system.
2009-12-07
4-Bromo-N,N'-bis-(4-methoxy-phen-yl)benzamidine.
2009-10-17
Pain modulation by nitric oxide in the spinal cord.
2009-09
Amidinoanthracyclines - a new group of potential anti-hepatitis C virus compounds.
2009-04
Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives.
2008-12-21
Di-μ-chlorido-bis-[dichlorido(N,N-diethyl-acetamidinato)(N,N-diethyl-acetamidine)titanium(IV)] acetonitrile disolvate.
2007-12-06
Synthesis and antibacterial activity of 5-adamantan-1-yl-methyl analogues of trimethoprim.
2007-03-16
Glutamate-stimulated peroxynitrite production in a brain-derived endothelial cell line is dependent on N-methyl-D-aspartate (NMDA) receptor activation.
2007-01-15
Mimicking biological cation-transport based on sphere-surface supramolecular chemistry: simultaneous interaction of porous capsules with molecular plugs and passing cations.
2007
Synthesis, characterization and thermolysis of 1,1-diamino-2,2-dinitroethylene (FOX-7) and its salts.
2006-09-21
Differential effects of selective and non-selective inhibition of nitric oxide synthase on the expression and activity of cyclooxygenase-2 during gastric ulcer healing.
2006-05-01
Inhibition or knock out of inducible nitric oxide synthase result in resistance to bleomycin-induced lung injury.
2005-06-14
Kinetic analysis of zymogen autoactivation in the presence of a reversible inhibitor.
2004-12
Novel adamantylated pyrimidines and their preliminary biological evaluations.
2004-12
Probing the effect of the amidinium group and the phenyl ring on the thermodynamics of binding of benzamidinium chloride to trypsin.
2004-11-07
N1-(2,6-Dimethylphenyl)-N2-hydroxy-alpha-oxo-alpha-phenylacetamidine.
2004-02
Electrosurface phenomena at polymer films for biosensor applications.
2003-04-14
Synthesis of anellated carbasugars from (--)-quinic acid.
2003-01-31
NMR and ab initio studies of amination of ketenimine: direct evidence for a mechanism involving a vinylidenediamine as an intermediate.
2002-06-14
[Effect of linker length on the photomodification process of tyrosine residues in N-(tyrosyl)-N'-(5-azido-2-nitrobenzoyl)diaminoalkanes].
2002-01-29
Inhibition of human parainfluenza virus type 1 sialidase by analogs of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid.
2001-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:09:15 GMT 2025
Edited
by admin
on Mon Mar 31 19:09:15 GMT 2025
Record UNII
M2026K4JCF
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-7595
Preferred Name English
ACETAMIDINE HYDROCHLORIDE
MI  
Systematic Name English
ACETAMIDINIUM CHLORIDE
Systematic Name English
ACETAMIDINE HYDROCHLORIDE [MI]
Common Name English
ACETAMIDINE, MONOHYDROCHLORIDE
Common Name English
ETHANAMIDINE HYDROCHLORIDE
Systematic Name English
METHYLAMIDINE HYDROCHLORIDE
Common Name English
ACETIMIDINIUM CHLORIDE
Common Name English
SN-4455
Code English
ETHANIMIDAMIDE, HYDROCHLORIDE (1:1)
Systematic Name English
ACEDIAMINE HYDROCHLORIDE
Common Name English
ACETAMIDINE, HYDROCHLORIDE
Systematic Name English
.ALPHA.-AMINO-.ALPHA.-IMINOETHANE HYDROCHLORIDE
Systematic Name English
ETHANIMIDAMIDE, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-700-9
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
PUBCHEM
67170
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID2059564
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
CAS
124-42-5
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
MESH
C023731
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
FDA UNII
M2026K4JCF
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
MERCK INDEX
m1315
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY Merck Index
NSC
7595
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE