About: catechol

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About: catechol Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

any compound containing an o-diphenol component

Attributes	Values
rdf:type	Item
description	any compound containing an o-diphenol component (en) każdy związek chemiczny zawierający pierścień benzenowy z dwiema grupami hydroksylowymi w układzie orto (pl)
rdfs:label	catechol (en) catéchol (fr) katechol (pl)
skos:prefLabel	catechol (en) catéchol (fr) katechol (pl)
name	catechol (en) catéchol (fr) katechol (pl)
instance of	wds:Q71956349-fc3a9573-4633-d7fa-b1a0-22e824bb1cef
part of	wds:Q71956349-6009B775-F935-4640-A759-A1EA6AC2E852 wds:Q71956349-ABBB09D9-C31C-4379-B1ED-D366493F7968 wds:Q71956349-B60EBE6D-36A6-40A4-9BC3-6FD9519941C2
instance of	structural class of chemical entities
part of	catechol-containing compound catabolic process catechol-containing compound biosynthetic process catechol-containing compound metabolic process
subclass of	wds:Q71956349-4a486a45-4116-efdc-933d-b2549e1e2472
subclass of	dihydroxybenzene
canonical SMILES	wds:Q71956349-0BC514B6-4F1C-4F25-8574-479C1FA68893
ChEBI ID	wds:Q71956349-348c5542-484f-7820-d616-e1fb6e7f9ecd
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_33566
canonical SMILES	OC1=C(O)C()=C()C()=C1
ChEBI ID	33566
Commons category	wds:Q71956349-9603c209-46fb-1134-657b-c7a6f6cda998
Commons category	Catechols
skos:altLabel	catechols (en) katechole (pl)
UMLS CUI	wds:Q71956349-486B048A-0DDA-4753-B7FF-0AAC3D8EC371
JSTOR topic ID	wds:Q71956349-AFAF76CF-3F0D-4FDE-8AD3-44130CB67D4A
MeSH descriptor ID	wds:Q71956349-86F152D0-B93F-4769-9DBC-D00B30EB3F14
MeSH tree code	wds:Q71956349-4c5a106e-4ae7-b1b2-c1da-341d6f96d34d
topic's main category	wds:Q71956349-94EB8EDC-62DF-42BF-959F-7D8E654D46CC
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D002396
MeSH tree code	http://id.nlm.nih.gov/mesh/D02.455.426.559.389.657.166
UMLS CUI	C0007413
JSTOR topic ID	catechols
MeSH descriptor ID	D002396
MeSH tree code	D02.455.426.559.389.657.166
topic's main category	Category:Catechols
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71956349
is subclass of of	urushiol alkyl caffeate ester 3-(all-trans-octaprenyl)benzene-1,2-diol oleuropein aglycone 11-hydroxysugiol 3-methyl-4-nitrocatechol 11-hydroxyferruginol 11,20-dihydroxyferruginol 11,20-dihydroxysugiol 5-methyl-3-nitrocatechol
is subclass of of	wds:Q19944476-d0fbd175-427b-2dc7-54f3-b2bf13a96c34 wds:Q74417704-A27C589F-0CDC-414D-AE1C-5A6148FA1340 wds:Q74411127-2104B016-AC1E-4A99-93B9-549E0AD844D7 wds:Q75035808-35152473-8C65-42B0-AC73-4B9488CFF8CA wds:Q74411620-8BA71199-442D-49E7-820F-AEF945AC889F wds:Q74418189-4825DF37-0CBB-47A5-9F8D-8E80FDC7B333 wds:Q74410660-9366E2E9-EBB7-44D0-8212-F104031F8356 wds:Q74417558-53460EFE-2AB1-49D6-A011-6325D0B12673 wds:Q74411133-23A9E151-97AA-41AD-99E1-7189C6EA82D2 wds:Q74417754-FB6DE646-7861-4698-98F8-7FDE4826E5AC
is has part(s) of	catechol-containing compound catabolic process catechol-containing compound biosynthetic process catechol-containing compound metabolic process
is main subject of	Electronic and resonance Raman spectra of iron(III) complexes of enterobactin, catechol, and N-methyl-2,3-dihydroxybenzamide Distribution of catechol compounds in human brain ACTIVATION OF HAGEMAN FACTOR BY SOLUTIONS OF ELLAGIC ACID THE EFFECTS OF ANAESTHESIA INDUCED BY URETHANE OR PHENOBARBITONE UPON THE DISTRIBUTION OF PERIPHERAL CATECHOL AMINES IN THE RAT CONTACT SENSITIVITY AND IMMUNOLOGIC UNRESPONSIVENESS IN ADULT GUINEA PIGS TO A COMPONENT OF POISON IVY EXTRACT, 3-N-PENTADECYLCATECHOL ENZYMATIC FORMATION OF CATECHOL FROM ANTHRANILIC ACID Effect of metal binding on the conformation of enterobactin. Proton and carbon-13 nuclear magnetic resonance study On the interaction of some catechol derivatives with the iron atom of soybean lipoxygenase SALICYLATE HYDROXYLASE, A MONOOXYGENASE REQUIRING FLAVIN ADENINE DINUCLEOTIDE. II. THE MECHANISM OF SALICYLATE HYDROXYLATION TO CATECHOL INDUCTION AND MULTI-SENSITIVE END-PRODUCT REPRESSION IN THE ENZYMIC PATHWAY DEGRADING MANDELATE IN PSEUDOMONAS FLUORESCENS Immunologic Competence of Patients With Psoriasis Receiving Cytotoxic Drug Therapy Morphological and pharmacological effects of reserpine, given alone or after iproniazid, on the catechol amines of the adrenal glands of the rat POTENTIATION OF SOME CATECHOL AMINES BY PHENOXYBENZAMINE, GUANETHIDINE AND COCAINE THE METABOLISM OF HALOGEN-SUBSTITUTED BENZOIC ACIDS BY PSEUDOMONAS FLUORESCENS THE EFFECT OF FASTING ON THE HYPERGLYCAEMIC RESPONSES TO CATECHOL AMINES IN RATS Synthesis of 3,4-dihydroxyphenyl-l-alanine from l-tyrosine and pyrocatechol by crystalline β-tyrosinase Kinetics and mechanism of the metal chelate catalyzed oxidation of pyrocatechols Mechanism of β-Ketoadipate Formation by Bacteria NMR spectra of estrogen catechols Copper(II) chelation by Dopa, epinephrine, and other catechols Appearance of catechol amines during development of Rana pipiens A SENSITIVE METHOD FOR THE ASSAY OF CATECHOL AMINES A Brief Review of Sympathomimetic Bronchodilators and a Description of a New Selective Agent, Rimiterol Hydrobromide Catechol amine levels during light and deep anesthesia Effect of Endotoxin on Plasma Catechol Amines and Serum Serotonin Catechol oxygenases of Pseudomonas putida mutant strains THE EFFECT OF PRENYLAMINE ON THE METABOLISM OF CATECHOL AMINES AND 5-HYDROXYTRYPTAMINE IN BRAIN AND ADRENAL MEDULLA URINARY EXCRETION OF CATECHOL AMINES IN THE RAT AFTER THEIR LIBERATION BY RESERPINE OR DEXAMPHETAMINE Kinetics and complex formation of molybdate with catechol Delayed contact sensitivity to catechols. IV. Stereochemical conformation of the antigenic determinant Melanoproteins I. reactions between enzyme-generated quinones and amino acids STUDIES ON SILKWORM TYROSINASE The affinity and efficacy of the selective β1-adrenoceptor stimulant RO363 at β1- and β2-adrenoceptor sites

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