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Details

Stereochemistry ACHIRAL
Molecular Formula C5H5NO
Molecular Weight 95.0993
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYRROLE-2-CARBOXALDEHYDE

SMILES

O=CC1=CC=CN1

InChI

InChIKey=ZSKGQVFRTSEPJT-UHFFFAOYSA-N
InChI=1S/C5H5NO/c7-4-5-2-1-3-6-5/h1-4,6H

HIDE SMILES / InChI

Molecular Formula C5H5NO
Molecular Weight 95.0993
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Culture of explants from the sponge Mycale cecilia to obtain bioactive mycalazal-type metabolites.
2010-10
Domino approach for the synthesis of pyrrolo[1,2-alpha]pyrazine from vinyl azides.
2010-09-03
Study of conformations and hydrogen bonds in the configurational isomers of pyrrole-2-carbaldehyde oxime by 1H, 13C and 15N NMR spectroscopy combined with MP2 and DFT calculations and NBO analysis.
2010-09
Spectroscopic characterization and biological activity of Zn(II), Cd(II), Sn(II) and Pb(II) complexes with Schiff base derived from pyrrole-2-carboxaldehyde and 2-amino phenol.
2010-08
Site-specific fluorescent probing of RNA molecules by unnatural base-pair transcription for local structural conformation analysis.
2010-07
Metal based biologically active compounds: design, synthesis, and antibacterial/antifungal/cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes.
2010-07
1-[2-(4-Chloro-benz-yloxy)-2-phenyl-ethyl]-1H-benzotriazole.
2010-05-08
A unique fluorescent base analogue for the expansion of the genetic alphabet.
2010-04-14
Infrared spectra and photochemistry of matrix-isolated pyrrole-2-carbaldehyde.
2010-02-25
Bench-to-bedside review: therapeutic management of invasive candidiasis in the intensive care unit.
2010
Site-specific incorporation of extra components into RNA by transcription using unnatural base pair systems.
2010
2-[(E)-(1H-Pyrrol-2-ylmethyl-idene)hydrazinyl]pyridine monohydrate.
2009-11-28
Computational study on the conformation and vibration frequencies of β-sheet of ε-polylysine in vacuum.
2009-07-29
1,2-Bis(1H-pyrrol-2-ylmethyl-ene)diazane monohydrate.
2009-07-08
6-Phenyl-5a,6,6a,7,12,13a-hexa-hydro-5H-benzo[6,7]indolizino[3,2-a]pyrrolizine.
2009-06-06
Gastrointestinal opportunistic infections in human immunodeficiency virus disease.
2009-04
Fungal nail infections: diagnosis and management.
2009-02
Site-specific incorporation of functional components into RNA by transcription using unnatural base pair systems.
2009
N-[(Z)-(1-Methyl-1H-pyrrol-2-yl)methyl-idene]-1H-1,2,4-triazol-5-amine.
2008-12-10
(Z)-5-Fluoro-3-[(1H-pyrrol-2-yl)methyl-ene]indolin-2-one.
2008-12-03
Monomeric, dimeric and 1D chain polymeric copper(ii) complexes of a pyrrole-containing tridentate Schiff-base ligand and its 4-brominated analogue.
2008-11-21
A new synthesis of symmetric boraindacene (BODIPY) dyes.
2008-10-28
Removal of phytotoxic compounds from torrefied grass fibres by plant-beneficial microorganisms.
2008-10
Amino(oligo)thiophene-based environmentally sensitive biomembrane chromophores.
2008-09-05
Safety assessment of dairy microorganisms: Geotrichum candidum.
2008-09-01
Phosphoserine aminoacylation of tRNA bearing an unnatural base anticodon.
2008-08-01
Synthesis, biological evaluation and molecular modelling of N-heterocyclic dipeptide aldehydes as selective calpain inhibitors.
2008-07-15
Synthesis of amidolanthanides with new chiral biaryl-based NNO ligands and their use as catalysts for enantioselective hydroamination/cyclization.
2008-05-19
Tris[2-(pyrrol-2-ylmethyl-eneamino)eth-yl]amine.
2008-02-27
Bis[N,N'-bis-[(1H-pyrrol-2-yl)methyl-ene]cyclo-hexane-1,2-diamine]titanium(IV) tetra-hydro-furan solvate.
2008-01-30
Suppression of blood lipid concentrations by volatile Maillard reaction products.
2008-01-24
Synthesis, characterization and DNA-binding properties of four Zn(II) complexes with bis(pyrrol-2-yl-methyleneamine) ligands.
2008-01-01
An efficient unnatural base pair for PCR amplification.
2007-12-19
The multiple Maillard reactions of ribose and deoxyribose sugars and sugar phosphates.
2007-12-10
Spectral, IR and magnetic studies of Mn(II), Co(II), Ni(II) and Cu(II) complexes with pyrrole-2-carboxyaldehyde thiosemicarbazone (L).
2007-11
Cytostatic evaluations of nucleoside analogs related to unnatural base pairs for a genetic expansion system.
2007-10-15
A concise synthesis of butylcycloheptylprodigiosin.
2007-05-10
Distinct M and P helical complexes of H2O and metal ions NiII, CuII, and ZnII with enantiomerically pure chiral bis(pyrrol-2-ylmethyleneamine)cyclohexane ligands: crystal structures and circular dichroism properties.
2007-04-30
Infrared spectroscopy of pyrrole-2-carboxaldehyde and its dimer: a planar beta-sheet peptide model?
2007-04-07
Regiocontrolled synthesis of pyrrole-2-carboxaldehydes and 3-pyrrolin-2-ones from pyrrole Weinreb amides.
2006-08-18
An unnatural base pair system for in vitro replication and transcription.
2006
Copper complexes of imidazole-2-, pyrrole-2- and indol-3-carbaldehyde thiosemicarbazones: inhibitory activity against fungi and bacteria.
2005-11
In vivo anticancer, anti-inflammatory, and toxicity studies of mixed-ligand Cu(II) complexes of dien and its Schiff dibases with heterocyclic aldehydes and 2-amino-2-thiazoline. Crystal structure of [Cu(dien)(Br)(2a-2tzn)](Br)(H(2)O).
2005-11
Biochemical and structural characterization of a novel class of inhibitors of the type 1 insulin-like growth factor and insulin receptor kinases.
2005-07-12
Chemistry and biological effects of melanoidins and glyceraldehyde-derived pyridinium as advanced glycation end products.
2005-06
Synthesis of mono- and disubstituted porphyrins: A- and 5,10-A2-type systems.
2005-05-20
Non-hydrogen-bonded base pairs for specific transcription.
2005
A reinvestigation of 4-hydroxyindole-6-carboxylate synthesis from pyrrole-2-carboxaldehyde: a facile synthesis of indoles and indolizines.
2004-10-01
Antibacterial Role of SO(4), NO(3), C(2)O(4) and CH(3)CO(2) Anions on Cu(II) and Zn(II) Complexes of a Thiadiazole-derived Pyrrolyl Schiff Base.
2002
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.
1989-03-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:53:46 GMT 2025
Edited
by admin
on Mon Mar 31 19:53:46 GMT 2025
Record UNII
068TSM6S6P
Record Status Validated (UNII)
Record Version
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Name Type Language
PYRROLE-2-CARBOXALDEHYDE
Systematic Name English
NSC-112885
Preferred Name English
2-PYRROLYLCARBOXALDEHYDE
Common Name English
2-FORMYLPYRROLE
Systematic Name English
PYRROLE-2-ALDEHYDE
Systematic Name English
2-PYRROLALDEHYDE
Systematic Name English
2-PYRROLECARBOXALDEHYDE
Systematic Name English
1H-PYRROLE-2-CARBOXALDEHYDE
Systematic Name English
NSC-66394
Code English
2-PYRROLECARBALDEHYDE
Systematic Name English
PYRROLE-2-FORMALDEHYDE
Systematic Name English
Code System Code Type Description
CHEBI
59978
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
FDA UNII
068TSM6S6P
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
CAS
1003-29-8
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID3061392
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
NSC
66394
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
NSC
112885
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
PUBCHEM
13854
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY
ECHA (EC/EINECS)
213-705-5
Created by admin on Mon Mar 31 19:53:46 GMT 2025 , Edited by admin on Mon Mar 31 19:53:46 GMT 2025
PRIMARY