About: pyrrole

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any chemical compound having a five-membered, aromatic ring with one nitrogen heteroatom

Attributes	Values
rdf:type	Item
owl:sameAs	pyrrole
description	any chemical compound having a five-membered, aromatic ring with one nitrogen heteroatom (en) każdy związek chemiczny zawierający pięcioczłonowy, aromatyczny pierścień z jednym heteroatomem azotu (pl)
rdfs:label	pirol (pl) pirol (sl) pyrrole (en) 吡咯 (zh) piroloj (eo) pirroli (it) pyrol (cs)
skos:prefLabel	pirol (pl) pirol (sl) pyrrole (en) 吡咯 (zh) piroloj (eo) pirroli (it) pyrol (cs)
name	pirol (pl) pirol (sl) pyrrole (en) 吡咯 (zh) piroloj (eo) pirroli (it) pyrol (cs)
image	wds:Q67954132-da8c4779-4d7c-01f5-8d11-ad9da7269a1d
instance of	wds:Q67954132-4b86455c-4821-2428-0127-17c4faf6438c
NL CR AUT ID	wds:Q67954132-FDC86E93-FC26-4AB2-8568-DF104E6741F2
image
instance of	structural class of chemical entities
NL CR AUT ID	ph124840
subclass of	wds:Q67954132-6f79e6e6-4327-de6f-9290-6a842aa4d072
subclass of	azole
Encyclopædia Britannica Online ID	wds:Q67954132-B1A9512C-4A3D-4275-8774-D4DAA26741A3
Encyclopædia Britannica Online ID	science/pyrrole
ChEBI ID	wds:Q67954132-2301c907-42b5-4893-ebd3-79eb552e855b
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_26455
ChEBI ID	26455
Commons category	wds:Q67954132-084b7a97-46fc-3d2a-9869-39cd968766f8
Commons category	Pyrroles
skos:altLabel	pirole (pl) pyroly (cs) pyrroles (en)
NALT ID	wds:Q67954132-DCBA5E9F-B56D-4F55-B6D1-5DA263DBEC49
UMLS CUI	wds:Q67954132-B45BAE31-028A-40A0-816D-0E8DF824E5BE
JSTOR topic ID	wds:Q67954132-4AEB865D-2FA9-4DA9-AA86-D08DFD606233
MeSH descriptor ID	wds:Q67954132-ea31574d-4e0b-c4fa-80ce-c9fa91e8595c
BNCF Thesaurus ID	wds:Q67954132-34C5574F-4480-4FA5-9626-ADA261E7AB2D
MeSH tree code	wds:Q67954132-920c75ea-4436-9eb2-34b0-bce603eb877d
topic's main category	wds:Q67954132-d0a1b031-4d21-2f69-c106-dbaa8f530e98
NALT ID	https://lod.nal.usda.gov/nalt/45391
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D011758
BNCF Thesaurus ID	http://purl.org/bncf/tid/32992
MeSH tree code	http://id.nlm.nih.gov/mesh/D03.383.129.578
NALT ID	45391
UMLS CUI	C0034325
JSTOR topic ID	pyrroles
MeSH descriptor ID	D011758
BNCF Thesaurus ID	32992
MeSH tree code	D03.383.129.578
topic's main category	Category:Pyrroles
is about of	pyrrole https://www.wikidata.org/wiki/Special:EntityData/Q67954132
is subclass of of	pyrrole prodigiosin pyrrole alkaloid maleimides 7-{4-[anilino(oxo)methyl]-2-(4-fluorophenyl)-3-phenyl-5-propan-2-yl-1-pyrrolyl}-3,5-dihydroxyheptanoic acid dipyrrins dibenzopyrrole
is subclass of of	wds:Q242627-9A59121F-2185-43EA-8C48-CEFCE5B2F89E wds:Q27166314-02210e79-4d80-50e4-e0ab-4b8813c981d9 wds:Q74805037-cfffaa85-43f6-9e8b-e9b4-1af29a54f4d5 wds:Q109378676-92CBD2DD-F614-4CD1-8871-6C2255C8B25E wds:Q415663-B3712C25-8EC7-4A33-8F62-69D08BCCCAF7 wds:Q74569152-43079A53-12BD-4CB4-930D-58744D368DDC wds:Q67954676-2d309c78-4e1b-0c39-2dcf-cdf84f96ce4d
is main subject of	THE RELATION BETWEEN STRUCTURE AND FUNCTION IN HEMOGLOBINS Tuberculosis and other opportunistic infections in tofacitinib-treated patients with rheumatoid arthritis A novel proteasome inhibitor NPI-0052 as an anticancer therapy METABOLISM AND FUNCTION OF BACTERIAL LIPIDS. II. BIOSYNTHESIS OF PHOSPHOLIPIDS IN ESCHERICHIA COLI Distamycin and Penta-N-Methylpyrrolecarboxamide Binding Sites on Native DNA A Comparison of Methidiumproyl-EDTA-Fe(II) Footprinting and DNA Affinity Cleaving Efficacy of conventional synthetic disease-modifying antirheumatic drugs, glucocorticoids and tofacitinib: a systematic literature review informing the 2013 update of the EULAR recommendations for management of rheumatoid arthritis The preventive effect of atorvastatin on atrial fibrillation: a meta-analysis of randomized controlled trials The Synthesis of Tenuazonic and Congeneric Tetramic Acids Novobiocin and coumermycin inhibit DNA supercoiling catalyzed by DNA gyrase Structure of the complexes of distamycin type antibiotics and actinomycin D with DNA: new data on the localization of these antibiotics within the DNA narrow groove Conformational features of distamycin-DNA and netropsin-DNA complexes by Raman spectroscopy The interconversion of glutamic acid and proline. V. The reduction of delta 1-pyrroline-5-carboxylic acid to proline Determination of D-amino acid oxidase activity in insect tissues using D-allohydroxyproline as substrate Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides Inhibition by temperature of the terminal step in biosynthesis of prodigiosin Studies on pyrrolnitrin, a new antibiotic. 3. Structure of pyrrolnitrin Antiviral Activity of Tenuazonic Acid Map of distamycin, netropsin, and actinomycin binding sites on heterogeneous DNA: DNA cleavage-inhibition patterns with methidiumpropyl-EDTA.Fe(II) JAK inhibitors: treatment efficacy and safety profile in patients with psoriasis Structure and Activity of the Prosthetic Group of Methanol Dehydrogenase Effects of the Antibiotics Netropsin and Distamycin A on the Structure and Function of Nucleic Acids Systematic review of escalated imatinib doses compared with sunitinib or best supportive care, for the treatment of people with unresectable/metastatic gastrointestinal stromal tumours whose disease has progressed on the standard imatinib dose Activity and potential role of licofelone in the management of osteoarthritis

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