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Details

Stereochemistry ACHIRAL
Molecular Formula C3H7N3.ClH
Molecular Weight 121.569
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINOIMIDAZOLINE HYDROCHLORIDE

SMILES

Cl.NC1=NCCN1

InChI

InChIKey=RZISTNHSOMNHDE-UHFFFAOYSA-N
InChI=1S/C3H7N3.ClH/c4-3-5-1-2-6-3;/h1-2H2,(H3,4,5,6);1H

HIDE SMILES / InChI

Molecular Formula C3H7N3
Molecular Weight 85.1078
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
Asymmetrical diaromatic guanidinium/2-aminoimidazolinium derivatives: synthesis and DNA affinity.
2009-11-26
Aplysinopsins--marine indole alkaloids: chemistry, bioactivity and ecological significance.
2009-05-19
Guanidine and 2-aminoimidazoline aromatic derivatives as alpha2-adrenoceptor ligands: searching for structure-activity relationships.
2009-02-12
1-(3-Chloro-phen-yl)-3-(1-p-tolyl-imidazolidin-2-yl-idene)urea.
2008-12-06
Trachycladindoles A-G: cytotoxic heterocycles from an Australian marine sponge, Trachycladus laevispirulifer.
2008-08-07
Guanidine and 2-aminoimidazoline aromatic derivatives as alpha2-adrenoceptor antagonists. 2. Exploring alkyl linkers for new antidepressants.
2008-06-12
New bis(2-aminoimidazoline) and bisguanidine DNA minor groove binders with potent in vivo antitrypanosomal and antiplasmodial activity.
2008-02-28
Optical resolution of (+/-)-1,2-Bis(2-methylphenyl)ethylene-1,2-diamine as a chiral framework for 2-iminoimidazolidine with 2-methylphenyl pendant and the guanidine-catalyzed asymmetric michael reaction of tert-butyl diphenyliminoacetate and ethyl acrylate.
2008-01-04
Guanidine and 2-aminoimidazoline aromatic derivatives as alpha(2)-adrenoceptor antagonists, 1: toward new antidepressants with heteroatomic linkers.
2007-09-06
DFT study and Monte Carlo simulation on proton transfers of 2-amino-2-oxazoline, 2-amino-2-thiazoline, and 2-amino-2-imidazoline in the gas phase and in water.
2005-07-30
Titanium complexes with imidazolin-2-iminato ligands.
2004-04-07
Synthesis and group 4 complexes of tris(pyrrolyl-alpha-methyl)amine.
2004-01-12
2,6-di(pyrimidin-4-yl)pyridine ligands with nitrogen-containing auxiliaries: the formation of functionalized molecular clefts upon metal coordination.
2003-12-29
Discovery of a series of (4,5-dihydroimidazol-2-yl)-biphenylamine 5-HT7 agonists.
2003-01-20
I(2)-imidazoline binding site affinity of a structurally different type of ligands.
2002-05
Guanidinium and aminoimidazolinium derivatives of N-(4-piperidyl)propanamides as potential ligands for mu opioid and I2-imidazoline receptors: synthesis and pharmacological screening.
2002-04
An ab initio investigation of 2-amino-2-imidazoline: a key moiety in chemical and biochemical processes.
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:01:02 GMT 2025
Edited
by admin
on Mon Mar 31 22:01:02 GMT 2025
Record UNII
OOW43632VL
Record Status Validated (UNII)
Record Version
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Name Type Language
2-AMINOIMIDAZOLINE HYDROCHLORIDE
Systematic Name English
NSC-8153
Preferred Name English
2-IMIDAZOLINE, 2-AMINO-, HYDROCHLORIDE
Systematic Name English
2-AMINO-2-IMIDAZOLINE, MONOHYDROCHLORIDE
Common Name English
1H-IMIDAZOL-2-AMINE, 4,5-DIHYDRO-, MONOHYDROCHLORIDE
Systematic Name English
1H-IMIDAZOL-2-AMINE, 4,5-DIHYDRO-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID60181400
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
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PUBCHEM
12797539
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
NSC
8153
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
FDA UNII
OOW43632VL
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
CAS
26893-38-9
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY