InChI=1S/C19H29NO7S/c20-14(19(26)27)13-28-16(15(21)9-8-12-18(24)25)10-6-4-2-1-3-5-7-11-17(22)23/h1-4,6,10,14-16,21H,5,7-9,11-13,20H2,(H,22,23)(H,24,25)(H,26,27)/b3-1-,4-2+,10-6+/t14-,15-,16+/m0/s1 |
LDJCPGIDJQSRGG-XFJBKEMKSA-N |
N[C@@H](CS[C@H](\C=C\C=C\C=C/CCCC(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
Outgoing
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16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
has functional parent
leukotriene E4
(CHEBI:15650)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
has role
metabolite
(CHEBI:25212)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
is a
L-cysteine thioether
(CHEBI:27532)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
is a
icosanoid
(CHEBI:23899)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
is a
non-proteinogenic L-α-amino acid
(CHEBI:83822)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
is a
secondary alcohol
(CHEBI:35681)
16-carboxy-17,18,19,20-tetranor-leukotriene E3
(CHEBI:74014)
is a
tricarboxylic acid
(CHEBI:27093)
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(5Z,7E,9E,11R,12S)-11-(L-cystein-S-yl)-12-hydroxyhexadeca-5,7,9-trienedioic acid
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(5Z,7E,9E,11R,12S)-11-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}-12-hydroxyhexadeca-5,7,9-trienedioic acid
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15-carboxy-14,15-dihydro-16,17,18,19,20-pentanor-leukotriene E4
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ChEBI
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16-carboxy-14,15-dihydro-17,18,19,20-tetranor-leukotriene E4
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ChEBI
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16-carboxy-14,15-dihydro-17,18,19,20-tetranor-LTE4
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ChEBI
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16-carboxy-14,15-dihydro-17,18,19,20-tetranor-LTE4
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ChEBI
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16-carboxy-17,18,19,20-tetranor-LTE3
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ChEBI
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16-carboxy-17,18,19,20-tetranor-LTE3
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ChEBI
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16-carboxy-tetranor-leukotriene E3
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ChEBI
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16-carboxy-tetranor-LTE3
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ChEBI
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16-carboxy-tetranor-LTE3
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ChEBI
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122069-63-0
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CAS Registry Number
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Reaxys
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4577467
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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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2558763
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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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