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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5NO
Molecular Weight 107.11
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NICOTINALDEHYDE

SMILES

O=CC1=CN=CC=C1

InChI

InChIKey=QJZUKDFHGGYHMC-UHFFFAOYSA-N
InChI=1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of nicotinamidases: steady state kinetic parameters, classwide inhibition by nicotinaldehydes, and catalytic mechanism.
2010-12-14
4-Methyl-1-(3-pyridyl-methyl-idene)thio-semicarbazide.
2010-11-27
Kinetics and inhibition of nicotinamidase from Mycobacterium tuberculosis.
2010-11-09
6-Hy-droxy-4-(pyridin-3-yl)-5-(2-thienyl-carbon-yl)-6-trifluoro-meth-yl-3,4,5,6-tetra-hydro-pyrimidin-2(1H)-one.
2010-10-20
High-resolution crystal structures of Streptococcus pneumoniae nicotinamidase with trapped intermediates provide insights into the catalytic mechanism and inhibition by aldehydes .
2010-10-12
4-Dimethyl-amino-N'-(3-pyridyl-methyl-idene)benzohydrazide.
2010-09-25
Pharmacological evaluation and characterizations of newly synthesized 1,2,4-triazoles.
2010-09
Ortho-rhom-bic modification of bis-[4-(3-pyridyl-methyl-idene-amino)-phen-yl]methane.
2010-08-18
Nicotinaldehyde [2,8-bis-(trifluoro-meth-yl)quinolin-4-yl]hydrazone monohydrate.
2010-08-11
Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus.
2010-07-15
catena-Poly[[(nitrato-κO,O')silver(I)]-μ-N,N'-bis-(3-pyridyl-methyl-idene)benzene-1,4-diamine].
2010-07-07
Novel and convenient synthesis of 1-(pyridinylmethyl)-2-naphthols and 1-(pyridinylmethylene)-2-tetralones from 2-tetralones.
2010-05
4-Nitro-N'-[(E)-3-pyridylmethyl-idene]benzohydrazide.
2010-03-31
Aroylguanidine-based factor Xa inhibitors: the discovery of BMS-344577.
2009-12-15
Synthesis and pharmacological evaluation of novel N-alkyl/aryl substituted thiazolidinone arecoline analogues as muscarinic receptor 1 agonist in Alzheimer's dementia models.
2009-12
Methyl 3-(3-pyridylmethyl-ene)carbazate.
2009-10-31
N'-[(E)-3-Pyridylmethyl-idene]benzo-hydrazide.
2009-10-03
Bis(ethanol-κO)bis-(pyridine-3-carb-aldehyde-κN thio-semicarbazone)bis-(thio-cyanato-κN)iron(II)-pyridine-3-carbaldehyde thio-semicarbazone (1/2).
2009-07-01
Hydrogensquarates of 3-nicotinoyl and 3-isonicotinoyl coumarin--crystal structures and spectroscopic elucidation.
2009-07
Micellar complexes of all-trans retinoic acid with polyvinylalcohol-nicotinoyl esters as new parenteral formulations in neuroblastoma.
2009-05
1,4-Bis(3-pyridylmethyl-eneamino-meth-yl)benzene.
2009-01-10
Density functional theory calculations of the internal rotations and vibrational spectra of 2-, 3- and 4-formyl pyridine.
2009-01
Emission of volatile chemicals from flowering dogwood (cornus Florida L.) flowers.
2008-10-22
The utility of oligopeptidase in brain-targeting delivery of an enkephalin analogue by prodrug design.
2008-10-20
Chemical derivatization of peptides containing phosphorylated serine/threonine for efficient ionization and quantification in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2008-04
1,3-Di-3-pyridyl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine.
2008-02-13
Synthesis and in vitro evaluation of N-nicotinoylglycyl-2-(5-fluorouracil-1-yl)-D,L-glycine as a colon-specific prodrug of 5-fluorouracil.
2007-04
Synthesis of pyridine-carboxylate derivatives of hydroxysteroids for liquid chromatography-electrospray ionization-mass spectrometry.
2007-01
Synthesis and evaluation of the antiinflammatory activity of N-[2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-oxo-thiazolidin-3-yl]-nicotinamide.
2007
Ozone's impact on public health: contributions from indoor exposures to ozone and products of ozone-initiated chemistry.
2006-10
Synthesis of multisubstituted quinolines from Baylis-Hillman adducts obtained from substituted 2-chloronicotinaldehydes and their antimicrobial activity.
2006-07-01
Molecular cloning and characterization of a novel lactate dehydrogenase gene from Clonorchis sinensis.
2006-06
FT-IR and FT-RAMAN investigations of nicotinaldehyde.
2006-05-01
Synthesis and characterization of a new family of spin bearing TTF ligands.
2006-03-31
Effect of ozone on nicotine desorption from model surfaces: evidence for heterogeneous chemistry.
2006-03-15
Anti-malarial activity of Baylis-Hillman adducts from substituted 2-chloronicotinaldehydes.
2005-12-15
Protein stoichiometry of a multiprotein complex, the human spliceosomal U1 small nuclear ribonucleoprotein: absolute quantification using isotope-coded tags and mass spectrometry.
2005-01-28
Apoptosis induced by picolinic acid-related compounds in HL-60 cells.
2001-10
Efficient enantiomeric synthesis of pyrrolidine and piperidine alkaloids from tobacco.
2001-09-21
Patents
Name Type Language
NSC-8952
Preferred Name English
NICOTINALDEHYDE
INCI   WHO-DD  
INCI  
Official Name English
PYRIDINE-3-ALDEHYDE
Common Name English
NICOTINIC ALDEHYDE
Common Name English
3-PYRIDINALDEHYDE
Systematic Name English
3-FORMYLPYRIDINE
Systematic Name English
3-PYRIDINECARBOXALDEHYDE
Systematic Name English
Nicotinaldehyde [WHO-DD]
Common Name English
Code System Code Type Description
MESH
C014785
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID2022044
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
PRIMARY
NSC
8952
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
PRIMARY
CHEBI
28345
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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EVMPD
SUB14644MIG
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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CAS
500-22-1
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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WIKIPEDIA
Pyridine-3-carboxaldehyde
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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ECHA (EC/EINECS)
207-900-4
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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SMS_ID
100000079971
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
PRIMARY
FDA UNII
840R4IDQ1T
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
PRIMARY
PUBCHEM
10371
Created by admin on Mon Mar 31 18:42:18 GMT 2025 , Edited by admin on Mon Mar 31 18:42:18 GMT 2025
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