Page last updated: 2024-11-12

resolvin d2

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

resolvin D2: structure in first source; a potent endogenous regulator of excessive inflammatory responses that acts via multiple cellular targets to stimulate resolution and preserve immune vigilance [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

resolvin D2 : A member of the class of resolvins that is (4Z,8E,10Z,12E,14E,19Z)-docosahexaenoic acid carrying three hydroxy substituents at positions 7, 16 and 17 (the 7S,16R,17S-stereoisomer). [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID11383310
CHEBI ID81565
SCHEMBL ID3407534
MeSH IDM0541537

Synonyms (19)

Synonym
(4z,7s,8e,10z,12e,14e,16r,17s,19z)-7,16,17-trihydroxydocosa-4,8,10,12,14,19-hexaenoic acid
C18179
resolvin d2
SCHEMBL3407534
810668-37-2
7s,16r,17s-trihydroxy-4z,8e,10z,12e,14e,19z-docosahexaenoic acid
CHEBI:81565
(4z,7r,8e,10z,12e,14e,16r,17s,19z)-7,16,17-trihydroxydocosa-4,8,10,12,14,19-hexaenoic acid
rvd2
IKFAUGXNBOBQDM-XFMPMKITSA-N
LMFA04030001
AKOS027307761
Q60998704
HY-121636
CS-0082932
resolvin d2-[d5]
STARBLD0018119
DTXSID801347465
(4z,7s,8e,10z,12e,14e,16r,17s,19z)-7,16,17-trihydroxy-4,8,10,12,14,19-docosahexaenoic acid

Research Excerpts

Overview

Resolvin D2 (RvD2) is a proresolving ligand that acts through the G-protein-coupled receptor called GPR18. It is a very potent TRPV1 and TRPA1 inhibitor in DRG neurons.

ExcerptReferenceRelevance
"Resolvin D2 (RvD2) is a proresolving ligand that acts through the G-protein-coupled receptor called GPR18."( Resolvin D2-G-Protein Coupled Receptor 18 Enhances Bone Marrow Function and Limits Steatosis and Hepatic Collagen Accumulation in Aging.
Adam, AP; Aydin, HB; Biswas, N; Bonin, JL; Chen, A; Decker, C; DiPersio, CM; Duarte, GA; Eid, M; Fitzgerald, H; Fredman, G; Gilliard, K; Khan, S; Lipscomb, M; MacNamara, KC; Marinello, M; Mena, HA; Nabage, M; Rahtes, A; Ramos, RB; Sadhu, S; Spite, M, 2023
)
3.07
"Resolvin D2 (RvD2) is a very potent TRPV1 and TRPA1 inhibitor in DRG neurons, and decreases inflammatory pain in mice acting on the GPR18 receptor, via TRPV1/TRPA1-independent mechanisms."( Resolvin D1 and D2 Inhibit Transient Receptor Potential Vanilloid 1 and Ankyrin 1 Ion Channel Activation on Sensory Neurons via Lipid Raft Modification.
Biró-Sütő, T; Erostyák, J; Helyes, Z; Horváth, Á; Kecskés, A; Kecskés, M; Makkai, G; Payrits, M; Pohóczky, K; Sághy, É; Szőke, É; Szolcsányi, J, 2020
)
1.28
"Resolvin D2 (RvD2) is a potent anti-inflammatory lipid mediator."( Resolvin D2 supports MCF-7 cell proliferation via activation of estrogen receptor.
Al-Zaubai, N; Johnstone, CN; Leong, MM; Li, J; Rizzacasa, M; Stewart, AG, 2014
)
2.57

Treatment

ExcerptReferenceRelevance
"Treatment with resolvin D2 reduced skin inflammation in Alox15 KO mice."( Anti-inflammatory role of 15-lipoxygenase contributes to the maintenance of skin integrity in mice.
Akindehin, S; Jung, YS; Kim, SN; Kwon, HJ; Lee, YH; Lim, KM; Maddipati, KR; Saha, A; Seong, JK; Son, YH; Sung, JH, 2018
)
0.82
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (5)

RoleDescription
human xenobiotic metaboliteAny human metabolite produced by metabolism of a xenobiotic compound in humans.
anti-inflammatory agentAny compound that has anti-inflammatory effects.
estrogen receptor agonistAn agonist at the estrogen receptor.
anti-obesity agentAny substance which is used to reduce or control weight.
rat metaboliteAny mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (4)

ClassDescription
resolvinHydroxy fatty acids that are di- or trihydroxy metabolites of the polyunsaturated omega-3 fatty acids, particularly icosapentaenoic acid, docosahexaenoic acid and docosapentaenoic acid.
triolA chemical compound containing three hydroxy groups.
secondary allylic alcoholAn allylic alcohol in which the carbon atom that links the double bond to the hydroxy group is also attached to one other carbon and one hydrogen.
hydroxy polyunsaturated fatty acidAny polyunsaturated fatty acid carrying one or more hydroxy substituents.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (81)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (1.23)29.6817
2010's54 (66.67)24.3611
2020's26 (32.10)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.24

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index28.24 (24.57)
Research Supply Index4.45 (2.92)
Research Growth Index6.91 (4.65)
Search Engine Demand Index31.58 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (28.24)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (3.66%)5.53%
Reviews3 (3.66%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other76 (92.68%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]