Page last updated: 2024-12-04

2,3-dinor-thromboxane b2

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

Cross-References

ID SourceID
PubMed CID5283138
CHEBI ID89991
SCHEMBL ID3344355
MeSH IDM0092756

Synonyms (15)

Synonym
2,3-dinor-thromboxane b2
LMFA03030003
2,3-dinor-txb2
9s,11,15s-trihydroxy-2,3-dinor-thromboxa-5z,13e-dien-1-oic acid
NCGC00161340-01
BML2-G02
(z)-5-[(2r,3s,4s)-4,6-dihydroxy-2-[(e,3s)-3-hydroxyoct-1-enyl]oxan-3-yl]pent-3-enoic acid
63250-09-9
SCHEMBL3344355
CHEBI:89991
2,3-dinorthromboxane
2,3-dinor-thromboxane
Q27162208
2,3-dinor thromboxane b2 lipid maps(r) ms standard
PD020567

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" During long-term dosing with the synthetic inhibitor, inhibition of thromboxane biosynthesis was incomplete, which would permit continued thromboxane-dependent platelet aggregation to occur."( Increased thromboxane biosynthesis in a human preparation of platelet activation: biochemical and functional consequences of selective inhibition of thromboxane synthase.
Doran, JB; FitzGerald, GA; Reilly, IA; Smith, B, 1986
)
0.27
" To address this hypothesis, we used dosing with nimesulide, which inhibited COX-2 ex vivo, depressed urinary 2,3 dinor 6-keto PGF(1alpha) by approximately 60% but had no effect on thromboxane formation by platelets, which only express COX-1."( Acceleration of atherogenesis by COX-1-dependent prostanoid formation in low density lipoprotein receptor knockout mice.
FitzGerald, GA; Li, H; Praticò, D; Tillmann, C; Zhang, ZB, 2001
)
0.31
" Administration of aspirin at a dosage of 1 mg/kg, PO, every 24 hours for 7 days did not significantly decrease urinary 11-dehydroTXB(2) concentration, but administration of the single aspirin dose of 10 mg/kg did significantly decrease 11-dehydroTXB(2) concentration by a median of 45."( Evaluation of effects of low-dose aspirin administration on urinary thromboxane metabolites in healthy dogs.
Byron, JK; Hoh, CM; McMichael, MA; Smith, SA, 2011
)
0.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
thromboxaneA class of oxygenated oxane derivatives, originally derived from prostaglandin precursors in platelets, that stimulate aggregation of platelets and constriction of blood vessels.
[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]

Pathways (1)

PathwayProteinsCompounds
Arachidonic acid (AA, ARA) oxylipin metabolism076

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (152)

TimeframeStudies, This Drug (%)All Drugs %
pre-199058 (38.16)18.7374
1990's77 (50.66)18.2507
2000's15 (9.87)29.6817
2010's1 (0.66)24.3611
2020's1 (0.66)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials20 (12.99%)5.53%
Reviews1 (0.65%)6.00%
Case Studies1 (0.65%)4.05%
Observational0 (0.00%)0.25%
Other132 (85.71%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]