CHEBI:156550 - pyrrolomycin A

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name pyrrolomycin A
ChEBI ID CHEBI:156550
Definition A member of the class of pyrroles that is 1H-pyrrole which is substituted by chloro groups at positions 2 and 3 and by a nitro group position 4. It is the simplest member of the pyrrolomycins, a family of natural products found in several species of the Streptomyces genus. The compound is active against Gram-positive and Gram-negative bacteria and some genera of fungi.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Martin Larralde
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C4H2Cl2N2O2
Net Charge 0
Average Mass 180.970
Monoisotopic Mass 179.94933
InChI InChI=1S/C4H2Cl2N2O2/c5-3-2(8(9)10)1-7-4(3)6/h1,7H
InChIKey CDHAYBUDIPNGGJ-UHFFFAOYSA-N
SMILES [O-][N+](=O)C1=CNC(Cl)=C1Cl
Metabolite of Species Details
Streptomyces vitaminophilus (NCBI:txid76728) of strain ATCC 31673 See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
(via antibiotic antifungal agent )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing pyrrolomycin A (CHEBI:156550) has role antibacterial agent (CHEBI:33282)
pyrrolomycin A (CHEBI:156550) has role bacterial metabolite (CHEBI:76969)
pyrrolomycin A (CHEBI:156550) is a C-nitro compound (CHEBI:35716)
pyrrolomycin A (CHEBI:156550) is a antibiotic antifungal agent (CHEBI:86478)
pyrrolomycin A (CHEBI:156550) is a organochlorine compound (CHEBI:36683)
pyrrolomycin A (CHEBI:156550) is a pyrroles (CHEBI:26455)
IUPAC Name
2,3-dichloro-4-nitro-1H-pyrrole
Synonyms Sources
2,3-dichloro-4-nitropyrrole ChemIDplus
antibiotic SF 2080A KNApSAcK
SF-2080 A ChEBI
SF-2080A ChemIDplus
Manual Xrefs Databases
117581 ChemSpider
C00018376 KNApSAcK
View more database links
Registry Numbers Types Sources
6195547 Reaxys Registry Number Reaxys
79763-01-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17158935 PubMed citation SUBMITTER
26798098 PubMed citation Europe PMC
7309630 PubMed citation Europe PMC
7333969 PubMed citation Europe PMC
Last Modified
25 January 2021