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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N
Molecular Weight 107.1531
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYLAMINE

SMILES

NCC1=CC=CC=C1

InChI

InChIKey=WGQKYBSKWIADBV-UHFFFAOYSA-N
InChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2

HIDE SMILES / InChI

Molecular Formula C7H9N
Molecular Weight 107.1531
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bivalent inhibition of human beta-tryptase.
2001 Apr
Characterization of a model compound for the lysine tyrosylquinone cofactor of lysyl oxidase.
2001 Feb 16
Selective inhibition of amine oxidases differently potentiate the hypophagic effect of benzylamine in mice.
2001 Feb 9
Neuroprotective and cognition-enhancing properties of MK-801 flexible analogs. Structure-activity relationships.
2001 Jun
Formation of unusual glutamate conjugates of 1-[3-(aminomethyl)phenyl]-N-[3-fluoro-2'-(methylsulfonyl)-[1,1'-biphenyl]-4-yl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC 423) and its analogs: the role of gamma-glutamyltranspeptidase in the biotransformation of benzylamines.
2001 Oct
Catalytic turnover of benzylamine by a model for the lysine tyrosylquinone (LTQ) cofactor of lysyl oxidase.
2001 Oct 3
Fine structural recognition specificities of IgE antibodies distinguishing amoxicilloyl and amoxicillanyl determinants in allergic subjects.
2001 Sep-Oct
Activity staining of plasma amine oxidase after polyacrylamide gel electrophoresis and its application to natural inhibitor screening.
2002 Aug
Octahedral-tetrahedral equilibrium and solvent exchange of cobalt(II) ions in primary alkylamines.
2002 Aug 26
High-performance liquid chromatographic determination of biogenic amines in poultry carcasses.
2002 Aug 28
Effects of high temperature and disinfectants on the viability of Sarcocystis neurona sporocysts.
2002 Dec
DPC-423 Bristol-Myers Squibb.
2002 Feb
In vitro metabolism of tresperimus by human vascular semicarbazide-sensitive amine oxidase.
2002 Jun
Determination of the dissociation constants (pKa) of basic acetylcholinesterase inhibitors by reversed-phase liquid chromatography.
2002 Jun 7
beta-Lactam allergenic determinants: fine structural recognition of a cross-reacting determinant on benzylpenicillin and cephalothin.
2002 Nov
Photosynthetic electron transport inhibition by 2-substituted 4-alkyl-6-benzylamino-1,3,5-triazines with thylakoids from wild-type and atrazine-resistant Chenopodium album.
2002 Nov-Dec
Histamine antilipolytic action in rat adipocytes: comparison with the effect of tyramine.
2003 Apr
Semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 activity exerts an antidiabetic action in Goto-Kakizaki rats.
2003 Apr
The inhibition of semicarbazide-sensitive amine oxidase by aminohexoses.
2003 Apr 11
Semicarbazide-sensitive amine oxidases in pig dental pulp.
2003 Apr 11
Inhibition of six copper-containing amine oxidases by the antidepressant drug tranylcypromine.
2003 Apr 11
Induction and characterization of a novel amine oxidase from the yeast Kluyveromyces marxianus.
2003 Apr 15
Inhibition of rat fat cell lipolysis by monoamine oxidase and semicarbazide-sensitive amine oxidase substrates.
2003 Apr 18
A short diastereoselective synthesis of the putative alkaloid jamtine, using a tandem pummerer/mannich cyclization sequence.
2003 Feb 7
New findings in the study on the intercalation of bisdaunorubicin and its monomeric analogues with naked and nucleus DNA.
2003 Jun 15
The first highly enantioselective homogeneously catalyzed asymmetric reductive amination: synthesis of alpha-N-benzylamino acids.
2003 May 16
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:10:46 GMT 2023
Edited
by admin
on Fri Dec 15 17:10:46 GMT 2023
Record UNII
A1O31ROR09
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZYLAMINE
HSDB   MI  
Systematic Name English
NSC-8046
Code English
BENZYLAMINE [HSDB]
Common Name English
BENZYLAMINE [MI]
Common Name English
PHENYLMETHANAMINE
Common Name English
LACOSAMIDE IMPURITY J [EP IMPURITY]
Common Name English
Code System Code Type Description
PUBCHEM
7504
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
NSC
8046
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
SMS_ID
100000181074
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-854-1
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
MERCK INDEX
m2398
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY Merck Index
CHEBI
225238
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
DRUG BANK
DB02464
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
FDA UNII
A1O31ROR09
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
CHEBI
40538
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
CAS
100-46-9
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID5021839
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
RXCUI
2374339
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
HSDB
2795
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
MESH
C030796
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
WIKIPEDIA
BENZYLAMINE
Created by admin on Fri Dec 15 17:10:46 GMT 2023 , Edited by admin on Fri Dec 15 17:10:46 GMT 2023
PRIMARY
Related Record Type Details
DERIVATIVE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP