About: hydroxyeicosatetraenoic acid

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eicosatetraenoic acids substituted in any position by one or more hydroxy groups, intermediates in biosynthetic processes leading from arachidonic acid

Attributes	Values
rdf:type	Item
description	eicosatetraenoic acids substituted in any position by one or more hydroxy groups, intermediates in biosynthetic processes leading from arachidonic acid (en)
rdfs:label	hydroxyeicosatetraenoic acid (en) ヒドロキシエイコサテトラエン酸 (ja)
skos:prefLabel	hydroxyeicosatetraenoic acid (en) ヒドロキシエイコサテトラエン酸 (ja)
name	hydroxyeicosatetraenoic acid (en) ヒドロキシエイコサテトラエン酸 (ja)
instance of	wds:Q65658502-60cdc5b2-46b4-0020-5880-140c32178360
instance of	Wikimedia set index article
subclass of	wds:Q65658502-0e945d79-4f3a-e5fb-a96e-a1b345905b08
subclass of	organic compound
skos:altLabel	hydroxyeicosatetraenoic acids (en)
OpenAlex ID	wds:Q65658502-82BB050B-3D87-4378-8830-B27B9DCD87C5
UMLS CUI	wds:Q65658502-40284D04-6591-43A4-9C67-D2C30C449632
MeSH descriptor ID	wds:Q65658502-464355cc-43a4-697b-2cb4-29a6d8ad4a37
Microsoft Academic ID	wds:Q65658502-373AA974-10EE-4034-9B9E-8F37529B7963
MeSH tree code	wds:Q65658502-1b2f1767-427c-ec2c-2fd9-d826c9ac77b3 wds:Q65658502-6d77307b-4277-4651-2eae-9d9592bd7f1f
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D006893
Microsoft Academic ID	https://makg.org/entity/2779630222
MeSH tree code	http://id.nlm.nih.gov/mesh/D10.251.355.255.100.300 http://id.nlm.nih.gov/mesh/D10.251.355.310.166.550
OpenAlex ID	C2779630222
UMLS CUI	C0020349
MeSH descriptor ID	D006893
Microsoft Academic ID	2779630222
MeSH tree code	D10.251.355.255.100.300 D10.251.355.310.166.550
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q65658502 Hydroxyeicosatetraenoic acid https://ja.wikipedia.org/wiki/%E3%83%92%E3%83%89%E3%83%AD%E3%82%AD%E3%82%B7%E3%82%A8%E3%82%A4%E3%82%B3%E3%82%B5%E3%83%86%E3%83%88%E3%83%A9%E3%82%A8%E3%83%B3%E9%85%B8
is main subject of	Heterogeneity of human polymorphonuclear leukocyte receptors for leukotriene B4. Identification of a subset of high affinity receptors that transduce the chemotactic response Potentiating actions of hydroxyeicosatetraenoates on human neutrophil degranulation responses to leukotriene B4 and phorbol myristate acetate Neutrophil degranulation responses to combinations of arachidonate metabolites and platelet-activating factor Augmentation of IgE-mediated release of histamine by 5-hydroxyeicosatetraenoic acid and 12-hydroxyeicosatetraenoic acid Lipoxygenation of arachidonic acid as a source of polymorphonuclear leukocyte chemotactic factors in synovial fluid and tissue in rheumatoid arthritis and spondyloarthritis Lipoxins: novel series of biologically active compounds formed from arachidonic acid in human leukocytes Characterization of leukotriene A4 and B4 bioysnthesis Inhibition of leukotriene biosynthesis by the leukocyte product 15-hydroxy-5,8,11,13-eicosatetraenoic acid A novel dioxygenation product of arachidonic acid possesses potent chemotactic activity for human polymorphonuclear leukocytes Complement receptor enhancement and chemotaxis of human neutrophils and eosinophils by leukotrienes and other lipoxygenase products The separation of leukotrienes and hydroxyeicosatetraenoic acid metabolites of arachidonic acid by high performance liquid chromatography (HPLC) Vitamin E modulates the lipoxygenation of arachidonic acid in leukocytes Stimulus specificity of the generation of leukotrienes by dog mastocytoma cells The combined use of isolated strips of guinea-pig lung parenchyma and ileum as a sensitive and selective bioassay for leukotriene B4 Arachidonic acid metabolism of the murine eosinophil. II. Involvement of the lipoxygenase pathway in the response to the lymphokine eosinophil stimulation promoter Arachidonic acid metabolism in purified human lung mast cells Chemotactic leukotrienes in psoriasis Studies on the mechanism of formation of the 5S,12S-dihydroxy-6,8,10,14(E,Z,E,Z)-icosatetraenoic acid in leukocytes Stimulation of Hexose Uptake by Human Eosinophils with Chemotactic Factors Comparative activity of natural mono-, di- and tri-hydroxy derivatives of arachidonic acid on guinea-pig lungs: Myotropic effect and stimulation of cyclooxygenase activity Fatty acid structural requirements for leukotriene biosynthesis Separation of major prostaglandins, leukotrienes, and monoHETEs by high performance liquid chromatography The production of 5-HETE and leukotriene B in rat neutrophils from carrageenan pleural exudates Arachidonate metabolism in the mouse thyroid implication of the lipoxygenase pathway in thyrotropin action Stable isotope labelled 5-lipoxygenase metabolites of arachidoic acid: Analysis by negative ion chemical ionization mass spectrometry Enhancement of neutrophil- and eosinophil-mediated complement-dependent killing of schistosomula of Schistosoma mansoni in vitro by leukotriene B4 Characteristics of leukotriene (LT) and hydroxy eicosatetraenoic acid (HETE) synthesis in human leukocytes : Effect of arachidonic acid concentration Stereospecificity of leukotriene B4 and structure-function relationships for chemotaxis of human neutrophils Mediation of leukocyte components of inflammatory reactions by lipoxygenase products of arachidonic acid Esterification of 12-hydroxy-5,8,10,14-eicosatetraenoate into mouse thyroid lipids: possible physiological significance In vivo Evidence for the Chemotactic Activity of Cyclooxygenase- and Lipoxygenase-Dependent Compounds Using a Corneal Implantation Technique An analysis of the relationship between 5-lipoxygenase product generation and the secretion of preformed mediators from mouse bone marrow-derived mast cells Conformational analysis of lipoxin A, lipoxin B and their trans-isomers Effects of 12-hydroxy- and 12-hydroperoxy-5,8,10,14-eicosatetraenoic acids on the synthesis of 5-hydroxy-6,8,11,14-eicosatetraenoic acid and leukotriene B4 in human blood leukocytes Double dioxygenation of arachidonic acid in leukocytes by lipoxygenases Pharmacologic mediators of bronchoconstriction Effects of leukotrienes on in vitro neutrophil functions 15-hydroxy-5, 8, 11, 13-eicosatetraenoic acid (15-HETE) formation by rabbit peritoneal tissue Pinpointing the cause of mucus production
is main subject of	wds:Q28366047-5CECE69C-51C6-4418-9F94-97AC258E927C wds:Q42244795-8F0F89FB-E5A3-4817-9348-257540F66258 wds:Q46683173-F8F2AD24-1A7E-40CA-B9A6-5217B631736A wds:Q72431057-697A457A-2264-43E7-A3BE-BAF1FDD121B6 wds:Q72725472-6C7A021D-D2E2-452D-BD25-18CA7DD2BCD6 wds:Q70193833-41DF9F74-A02B-4EBC-8B5D-092DE59BF685 wds:Q70199158-CA281088-4026-4C5D-9EB2-B88BC2C9FF72 wds:Q24681163-6F469720-25AE-4F7B-BAB3-98271161F4B9 wds:Q42246045-1417A683-CF48-429A-9234-50E70AF20C7D wds:Q41553821-DC2C9F95-3D0E-434E-86B8-76D8E67EBC89 wds:Q70166572-E9475AE1-804D-487C-8B5A-47A0FC827EEA wds:Q70192040-F452D037-2809-45A5-954A-00EC962C4D18 wds:Q70193899-82B2D08C-DD10-47FC-B387-7AF2EB3747E0 wds:Q70152804-23A7F286-4C51-4710-B06F-C09DC10FD335 wds:Q36348087-D1D778C9-F57C-4E50-B2B7-26D96700ABDE wds:Q72934712-74107FA8-4D5E-4632-BFBA-03F83CBD97D8 wds:Q70166472-5352241B-8B33-4FB7-AB1B-29246D9DA740 wds:Q70180600-90D5B275-F60C-49FF-AF03-E0B5CE340A22 wds:Q72783989-B0B5E301-32AD-4B26-BAD6-DB4C50A2222D wds:Q72954187-79373611-940E-4FB4-8125-35DC8259A67F wds:Q72884823-6E53AC8D-F795-4D92-A831-785AF4561545 wds:Q68343152-B86CDAB3-6D86-4021-AAB6-37359774FCED wds:Q72919113-395E3841-49DC-4A2D-991D-86B536E9228C wds:Q70799199-65DF45F3-285A-4005-8B3C-2EB545D97306 wds:Q72783741-15CD0808-1BAF-432E-91A3-18A542D982BD wds:Q72934726-0AADC0CF-647A-4003-A268-5A1BBB953D02 wds:Q28622785-9E722EAD-352C-4B0E-B85D-B4D27003AA09 wds:Q72386261-45EEB478-8A77-4B34-B158-22CA52089FDD wds:Q53967522-46D870FB-4A7B-4425-8CAE-1EF9894EF7B0

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