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Details

Stereochemistry ACHIRAL
Molecular Formula C3H7N
Molecular Weight 57.0944
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALLYLAMINE

SMILES

NCC=C

InChI

InChIKey=VVJKKWFAADXIJK-UHFFFAOYSA-N
InChI=1S/C3H7N/c1-2-3-4/h2H,1,3-4H2

HIDE SMILES / InChI

Molecular Formula C3H7N
Molecular Weight 57.0944
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Co-culture of hepatocytes and fibroblasts by micropatterned immobilization of beta-galactose derivatives.
2004-08
Regulation of alpha7-integrin expression in vascular smooth muscle by injury-induced atherosclerosis.
2004-07
Biomimetic glucose recognition using molecularly imprinted polymer hydrogels.
2004-05
Modulation of cyclin dependent kinase inhibitor proteins and ERK1/2 activity in allylamine-injured vascular smooth muscle cells.
2004-04-15
Fabrication of polyelectrolyte multilayer films comprising nanoblended layers.
2004-03-03
Hypolipidemic therapy and cholesterol absorption.
2004-03
Polyelectrolyte-modified short microchannel for cation separation.
2004-03
Studies of interaction between poly(allylamine hydrochloride) and double helix DNA by spectral methods.
2004-02-15
Biocompatible fluorescent nanocrystals for immunolabeling of membrane proteins and cells.
2004-01-01
Selective inhibitors of membrane-bound semicarbazide-sensitive amine oxidase (SSAO) activity in mammalian tissues.
2004-01
Quantitative study of HIV-1 Tat peptide and TAR RNA interaction inhibited by poly(allylamine hydrochloride).
2003-12-12
Enantioselective alpha-silyl amino acid synthesis by reverse-aza-Brook rearrangement.
2003-11-27
Organomercury bioconjugate synthesis and characterization by matrix-assisted laser desorption ionization mass spectrometry.
2003-11-20
Overview of pharmacologic therapy for the treatment of dyslipidemia.
2003-11-14
The efficacy and safety of terbinafine in children.
2003-11
3-D surface charges modulate protrusive and contractile contacts of chondrosarcoma cells.
2003-11
Inhibition of bovine plasma amine oxidase by 1,4-diamino-2-butenes and -2-butynes.
2003-10-15
Construction of a molecular imprinting catalyst using target analogue template and its application for an amperometric fructosylamine sensor.
2003-10-15
Surface properties of and cell adhesion onto allylamine-plasma-coated polyethylenterephtalat membranes.
2003-10
[Treatment of interdigital tinea pedis].
2003-09-05
Synthesis and structure-activity studies of novel orally active non-terpenoic 2,3-oxidosqualene cyclase inhibitors.
2003-07-17
Effect of the polycation nature on the structure of layer-by-layer electrostatically self-assembled multilayers of polyphenol oxidase.
2003-07-15
The use of oral antifungal agents to treat onychomycosis.
2003-07
Acute generalized exanthematous pustulosis induced by terbinafine.
2003-06-14
Asymmetric synthesis of alpha-amino allyl, benzyl, and propargyl silanes by metalation and rearrangement.
2003-05-29
Reduction of a 1-aza-1,3-diene to a 1-azabut-2-ene-1,4-diyl dianion: an unusual reaction course.
2003-05-25
Fabrication and photoelectric response of poly(allylamine hydrochloride)/PM thin films by layer-by-layer deposition technique.
2003-05-23
Highly potent propargylamine and allylamine inhibitors of bovine plasma amine oxidase.
2003-05-16
Colesevelam HCl: a non-systemic lipid-altering drug.
2003-05
Iodine atom transfer [3 + 2] cycloaddition reaction with electron-rich alkenes using N-tosyliodoaziridine derivatives as novel azahomoallyl radical precursors.
2003-04-18
N-silyl-tethered radical cyclizations: a new synthesis of gamma-amino alcohols.
2003-04-17
alpha-Keto amides as precursors to heterocycles--generation and cycloaddition reactions of piperazin-5-one nitrones.
2003-04-07
In vitro antifungal activity of new series of homoallylamines and related compounds with inhibitory properties of the synthesis of fungal cell wall polymers.
2003-04-03
Identifying effective and/or safe doses by stepwise confidence intervals for ratios.
2003-03-30
Beyond statins. New drugs can work with, or in place of, cholesterol-lowering statins.
2003-02
Fullerene-coated beads as reusable catalysts.
2003-01-24
Rational design of cytophilic and cytophobic polyelectrolyte multilayer thin films.
2003-01-14
Persistent and recurrent tinea corporis in children treated with combination antifungal/ corticosteroid agents.
2003-01
Simple preparation of biotinylated RNA by transcription via an unnatural base pair.
2003
Ultrasensitive probing of the protein resistance of PEG surfaces by secondary ion mass spectrometry.
2002-12
Development of a new Lewis acid-catalyzed [3,3]-sigmatropic rearrangement: the allenoate-Claisen rearrangement.
2002-11-20
Nanoencapsulated microcrystalline particles for superamplified biochemical assays.
2002-11-01
Rifampicin and treatment of cholestatic pruritus.
2002-11
Rapid access to tetracyclic ring system of lennoxamine type natural product by combined use of a novel three-component reaction and Pummerer cyclization.
2002-10-21
Ring-closing metathesis of chiral allylamines. Enantioselective synthesis of (2S,3R,4S)-3,4-dihydroxyproline.
2002-10-04
Promising therapies for cholesterol reduction.
2002-09
Semicarbazide-sensitive amine oxidase and extracellular matrix deposition by smooth-muscle cells.
2002
A novel strategy for the synthesis of neoglycoconjugates from deacylated deep rough lipopolysaccharides.
2002
p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride).
2001-11-07
Colesevelam.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:09 GMT 2025
Record UNII
48G762T011
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-7600
Preferred Name English
ALLYLAMINE
HSDB   MI  
Systematic Name English
ALLYLAMINE [HSDB]
Common Name English
ALLYLAMINE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
7853
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-463-9
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
MESH
D000499
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
MERCK INDEX
m1548
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID8024440
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
HSDB
2065
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
WIKIPEDIA
ALLYLAMINE
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
CAS
107-11-9
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
NSC
7600
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY
FDA UNII
48G762T011
Created by admin on Mon Mar 31 18:35:09 GMT 2025 , Edited by admin on Mon Mar 31 18:35:09 GMT 2025
PRIMARY