Page last updated: 2024-11-13

ascorbate-2-phosphate

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

Description

ascorbate-2-phosphate: inhibitor of ascorbate-2-sulfate sulfohydrolase from bovine liver [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

L-ascorbic acid 2-phosphate : An aldonolactone phosphate that is the 2-phosphate ester of L-ascorbic acid. It can stimulate collagen formation. [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 CID54679073
CHEMBL ID1161237
CHEMBL ID1963242
CHEBI ID167162
SCHEMBL ID34770
MeSH IDM0058155

Synonyms (33)

Synonym
l-ascorbic acid 2-(dihydrogen phosphate)
23313-12-4
CHEBI:167162
(5r)-5-[(1s)-1,2-dihydroxyethyl]-4-hydroxy-2-oxo-2,5-dihydrofuran-3-yl dihydrogen phosphate
l-ascorbyl-2-phosphate
l-ascorbyl-2-monophosphate
2-o-phosphono-l-ascorbic acid
l-ascorbic acid, 2-(dihydrogen phosphate)
ascorbyl-2-monophosphate
l-ascorbic acid 2-phosphate
ascorbyl monophosphate
ascorbate-2-phosphate
ascorbyl-2-phosphate
CHEMBL1161237
unii-vkx4pm7299
vkx4pm7299 ,
AKOS015918227
AKOS015893085
SCHEMBL34770
CHEMBL1963242
109620-90-8
l-ascorbic acid-2-phosphate sodium
l-ascorbate-2-phosphate
MIJPAVRNWPDMOR-ZAFYKAAXSA-N
ascorbic acid 2-monophosphate
HY-103701
CS-0033168
[(2r)-2-[(1s)-1,2-dihydroxyethyl]-3-hydroxy-5-oxo-2h-furan-4-yl] dihydrogen phosphate
2-o-phosphonohex-1-enofuranos-3-ulose
DTXSID00945987
l-ascorbyl-2-phosphate [who-dd]
l-ascorbic acid 2-phosphoric acid ester
vitamincphosphate

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Hand-foot skin reaction is recognized as one of the most common adverse events related to multiple tyrosine kinase inhibitors, but an effective prevention method has not been identified."( Effects of Ascorbyl-2-phosphate Magnesium on Human Keratinocyte Toxicity and Pathological Changes by Sorafenib.
Bito, T; Hirai, M; Hirano, T; Ishida, T; Kaku, K; Kume, M; Makimoto, H; Nakagawa, T; Nishigori, C; Nishioka, T; Shichiri, H; Yamamoto, K; Yano, I, 2017
)
0.46

Compound-Compound Interactions

ExcerptReferenceRelevance
"The aim of this study was to evaluate inhibitory effects of L-ascorbic acid-2-O-phosphate-Na(2) (APS), a pro-vitamin C, combined with hyperthermia on adipogenic differentiation of mouse stromal cells, OP9."( Repressive effects of a capacitive-resistive electric transfer (CRet) hyperthermic apparatus combined with provitamin C on intracellular lipid-droplets formation in adipocytes.
Kato, S; Miwa, N; Saitoh, Y, 2013
)
0.39
"OP9 preadipocytes were differentiated with serum replacement, administered with APS, and simultaneously treated with hyperthermia using a capacitive-resistive electric transfer (CRet) apparatus, which was conducted repeatedly twice a day."( Repressive effects of a capacitive-resistive electric transfer (CRet) hyperthermic apparatus combined with provitamin C on intracellular lipid-droplets formation in adipocytes.
Kato, S; Miwa, N; Saitoh, Y, 2013
)
0.39

Bioavailability

ExcerptReferenceRelevance
" The bioavailability of APP relative to AsA, as estimated by the change in plasma AsA concentration, was evaluated during 24-h periods of supplementation."( Relative bioavailability of L-ascorbyl-2-polyphosphate in broiler chickens.
Brake, J; Pardue, SL; Seib, PA; Wang, XY, 1993
)
0.29
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aldonolactone phosphate
[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]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID232873Free radical scavenging assessed as color reduction of DPPH2002Journal of medicinal chemistry, Jan-17, Volume: 45, Issue:2
Synthesis and characterization of a series of novel monoacylated ascorbic acid derivatives, 6-O-acyl-2-O-alpha-D-glucopyranosyl-L-ascorbic acids, as skin antioxidants.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (205)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (2.93)18.7374
1990's51 (24.88)18.2507
2000's51 (24.88)29.6817
2010's72 (35.12)24.3611
2020's25 (12.20)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 40.71

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index40.71 (24.57)
Research Supply Index5.46 (2.92)
Research Growth Index5.42 (4.65)
Search Engine Demand Index61.94 (26.88)
Search Engine Supply Index2.10 (0.95)

This Compound (40.71)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials11 (4.93%)5.53%
Reviews2 (0.90%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other210 (94.17%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Clinical Study of an Ascorbic Acid Derivative Dentifrice in Patients With Gingivitis [NCT02102295]Phase 3300 participants (Actual)Interventional2006-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]