CHEBI:138645 - resolvin D5

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ChEBI Name resolvin D5
ChEBI ID CHEBI:138645
Definition A member of the class of resolvins that is (4Z,8E,10Z,13Z,15E,19Z)-docosahexaenoic acid carrying two hydroxy substituents at positions 7 and 17 (the 7S,17S-stereoisomer).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Bijay
Supplier Information No supplier information found for this compound.
Download Molfile XML SDF
Formula C22H32O4
Net Charge 0
Average Mass 360.494
Monoisotopic Mass 360.23006
InChI InChI=1S/C22H32O4/c1-2-3-10-15-20(23)16-11-7-5-4-6-8-12-17-21(24)18-13-9-14-19-22(25)26/h3,5-13,16-17,20-21,23-24H,2,4,14-15,18-19H2,1H3,(H,25,26)/b7-5-,8-6-,10-3-,13-9-,16-11+,17-12+/t20-,21+/m0/s1
InChIKey CFOFZYMMJZILHE-XGTWDWJNSA-N
SMILES CC\C=C/C[C@H](O)\C=C\C=C/C\C=C/C=C/[C@@H](O)C\C=C/CCC(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: PubMed
Trypanosoma cruzi (NCBI:txid5693) See: PubMed
Oncorhynchus mykiss (NCBI:txid8022) See: PubMed
Homo sapiens (NCBI:txid9606) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): human xenobiotic metabolite
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
marine xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound in marine macro- and microorganisms.
animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
specialised pro-resolving mediator
A class of cell signaling molecules enzymatically derived from n-3 long chain polyunsaturated fatty acids that have important roles in orchestrating the resolution of tissue inflammation.
(via resolvin )
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
specialised pro-resolving mediator
A class of cell signaling molecules enzymatically derived from n-3 long chain polyunsaturated fatty acids that have important roles in orchestrating the resolution of tissue inflammation.
(via resolvin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing resolvin D5 (CHEBI:138645) has role animal metabolite (CHEBI:75767)
resolvin D5 (CHEBI:138645) has role anti-inflammatory agent (CHEBI:67079)
resolvin D5 (CHEBI:138645) has role human metabolite (CHEBI:77746)
resolvin D5 (CHEBI:138645) has role human xenobiotic metabolite (CHEBI:76967)
resolvin D5 (CHEBI:138645) has role marine xenobiotic metabolite (CHEBI:83399)
resolvin D5 (CHEBI:138645) has role mouse metabolite (CHEBI:75771)
resolvin D5 (CHEBI:138645) has role platelet aggregation inhibitor (CHEBI:50427)
resolvin D5 (CHEBI:138645) is a diol (CHEBI:23824)
resolvin D5 (CHEBI:138645) is a hydroxy polyunsaturated fatty acid (CHEBI:140345)
resolvin D5 (CHEBI:138645) is a resolvin (CHEBI:132120)
resolvin D5 (CHEBI:138645) is a secondary allylic alcohol (CHEBI:134396)
resolvin D5 (CHEBI:138645) is conjugate acid of resolvin D5(1−) (CHEBI:140352)
Incoming resolvin D5(1−) (CHEBI:140352) is conjugate base of resolvin D5 (CHEBI:138645)
IUPAC Name
(4Z,7S,8E,10Z,13Z,15E,17S,19Z)-7,17-dihydroxydocosa-4,8,10,13,15,19-hexaenoic acid
Synonyms Sources
(4Z,7S,8E,10Z,13Z,15E,17S,19Z)-7,17-dihydroxydocosahexaenoic acid ChEBI
7(S),17(S)-diHDHA ChEBI
7(S),17(S)-resolvin D5 ChEBI
7S,17S-diHDHA ChEBI
7S,17S-dihydroxy-4Z,8E,10Z,13Z,15E,19Z-docosahexaenoic acid ChEBI
resolvin-D5 ChEBI
RvD5 ChEBI
Manual Xrefs Databases
45743318 ChemSpider
FDB023286 FooDB
HMDB0004038 HMDB
LMFA04030003 LIPID MAPS
View more database links
Registry Number Type Source
578008-43-2 CAS Registry Number ChEBI
Citations
Last Modified
25 May 2021