InChI=1S/C21H31NO7S/c22-16(21(28)29)15-30-18(17(23)11-10-14-20(26)27)12-8-6-4-2-1-3-5-7-9-13-19(24)25/h1-2,4-8,12,16-18,23H,3,9-11,13-15,22H2,(H,24,25)(H,26,27)(H,28,29)/b2-1-,6-4+,7-5-,12-8+/t16-,17-,18+/m0/s1 |
OXCSBZDIZXLXRX-AVYHYKEVSA-N |
[H][C@](N)(CS[C@H](\C=C\C=C\C=C/C\C=C/CCC(O)=O)[C@@H](O)CCCC(O)=O)C(O)=O |
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Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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View more via ChEBI Ontology
(4Z,7Z,9E,11E,13R,14S)-13-(L-cystein-S-yl)-14-hydroxyoctadeca-4,7,9,11-tetraenedioic acid
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(4Z,7Z,9E,11E,13R,14S)-13-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}-14-hydroxyoctadeca-4,7,9,11-tetraenedioic acid
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18-carboxy-19,20-dinor-LTE4
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ChEBI
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18-carboxy-19,20-dinor-LTE4
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ChEBI
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18-carboxy-dinor-leukotriene E4
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ChEBI
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18-carboxy-dinor-LTE4
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ChEBI
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18-carboxy-dinor-LTE4
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HMDB
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4588801
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Reaxys Registry Number
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Reaxys
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2174886
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PubMed citation
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Europe PMC
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7663693
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PubMed citation
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Europe PMC
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8484009
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PubMed citation
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Europe PMC
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