Page last updated: 2024-11-13

ascorbic acid 2-o-glucoside

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

Description

ascorbic acid 2-O-glucoside: has same vitamin C activity as L-ascorbic acid [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID54693473
CHEMBL ID2011961
CHEBI ID81685
SCHEMBL ID37903
SCHEMBL ID2388533
MeSH IDM0179812

Synonyms (42)

Synonym
ascorbic acid 2-o-glucoside
2-o-alpha-d-glucopyranosyl-l-ascorbic acid
l-ascorbic acid-2-glucoside
C18339
129499-78-1
aa-2g
pyrido(1,2-a)indol-6(7h)-one, 8,9-dihydro-7-(hydroxy(5-methyl-1h-imidazol-4-yl)methyl)-10-propyl-, (r*,s*)-
l-ascorbic acid 2-o-alpha-glucoside
unii-2v52r0nhxw
2v52r0nhxw ,
S3215
AKOS015999708
l-ascorbic acid 2-glucoside
l-ascorbic acid, 2-o-,.alpha.-d-glucopyranosyl-
aa2g
ascorbyl glucoside
ascorbic acid 2-o-glucoside [who-dd]
ascorbyl glucoside [inci]
CHEMBL2011961
chebi:81685 ,
SCHEMBL37903
MLSJBGYKDYSOAE-DCWMUDTNSA-N
SCHEMBL2388533
2-o-a-d-glucopyranosyl-l-ascorbic acid, >=98% (hplc)
ascorbyl glucoside, pharmaceutical secondary standard; certified reference material
1,4-bis(2,2,2-trifluoroethoxy)-2-(trichloroacetyl)benzene
DTXSID50926423
l-ascorbicacid2-glucoside
Q27155554
F20404
DB11335
DS-17832
EX-A2888
(r)-5-((s)-1,2-dihydroxyethyl)-4-hydroxy-3-(((2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl)oxy)furan-2(5h)-one
2-o-a-d-glucopyranosyl-l-ascorbic acid?
HY-N6821
CS-0100234
2-o-|a-d-glucopyranosyl-l-ascorbic acid
(2r)-2-[(1s)-1,2-dihydroxyethyl]-3-hydroxy-4-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2h-furan-5-one
l-ascorbic acid 2-o-|a-glucoside
2-o--d-glucopyranosyl-l-ascorbic acid
sandawha vitamin c brightening essence

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
"The bioavailability of a series of novel acylated ascorbic acid derivatives, 6-O-acyl-2-O-alpha-D-glucopyranosyl-L-ascorbic acids (6-Acyl-AA-2G), as an ascorbic acid (AA) supplement was investigated in rats and guinea pigs."( Bioavailability of a series of novel acylated ascorbic acid derivatives, 6-O-acyl-2-O-alpha-D-glucopyranosyl-L-ascorbic acids, as an ascorbic acid supplement in rats and guinea pigs.
Fujinami, Y; Kawasaki, D; Matsumoto, K; Tai, A; Yamamoto, I, 2002
)
0.31
"Ascorbic acid 2-glucoside (AA2G), glucosylated ascorbic acid (AA), has superior properties for bioavailability and stability compared to AA."( Ascorbic Acid 2-Glucoside Pretreatment Protects Cells from Ionizing Radiation, UVC, and Short Wavelength of UVB.
Allum, AJ; Buckner, MA; Froning, CE; Haskins, AH; Kato, TA; Maeda, J; Miller, CD; Mussallem, JT, 2020
)
0.56
" However, these have disadvantages, including chemical instability, photodegradation, poor bioavailability or biological activity."( Ascorbic acid 2-glucoside: An ascorbic acid pro-drug with longer-term antioxidant efficacy in skin.
Bacqueville, D; Bessou-Touya, S; Borotra, N; Chaves, F; Duplan, H; Gaudry, AL; Genies, C; Jacques, C; Sanches, F; Tourette, A, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
glycosideA glycosyl compound resulting from the attachment of a glycosyl group to a non-acyl group RO-, RS-, RSe-, etc. The bond between the glycosyl group and the non-acyl group is called a glycosidic bond. By extension, the terms N-glycosides and C-glycosides are used as class names for glycosylamines and for compounds having a glycosyl group attached to a hydrocarbyl group respectively. These terms are misnomers and should not be used. The preferred terms are glycosylamines and C-glycosyl compounds, respectively.
[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 (35)

Assay IDTitleYearJournalArticle
AID652725Cytotoxicity against human RD cells assessed maximun non-toxic concentration2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652746Antioxidant activity using deaerated 0.1 M alpha-glycerophosphate as substrate assessed as hydroxy radical level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462745Antioxidant activity assessed as DPPH free radical scavenging activity by measuring radical-scavenging activity factor (moles of radicals scavenged by each mol of antioxidant) at 20 uM measured at 10 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652726Antiviral activity against Herpes simplex virus type 1 infected in human RD cells assessed as inhibition of virus-induced cytopathic effect2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652727Selectivity ratio of MNTD for human RD cells to EC50 for HSV12012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652736Antioxidant activity using deaerated ethanol as substrate assessed as 2,3-butanediol level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 2.05 +/- 0.09 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462744Antioxidant activity assessed as time duration for DPPH free radical scavenging activity at 20 uM by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652730Antioxidant activity using ethanol as substrate assessed as H2O2 level at 1 mmol/L after gamma-irradiation by spectrophotometry (Rvb = 7.54 +/- 0.27 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652735Antioxidant activity using deaerated ethanol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 1.94 +/- 0.17 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462741Antioxidant activity assessed as DPPH free radical scavenging activity by measuring AA-2G-DPPH adducts formation at 200 uM measured within 10 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652905Antioxidant activity using deaerated 0.1 M alpha-glucosophosphate as substrate assessed as inorganic phosphate level at 1 mmol/L after gamma-irradiation (Rvb = 2.63 +/- 0.05 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652739Antioxidant activity using deaerated 1 M ethanol as substrate assessed as 2,3-butanediol level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 1.93 +/- 0.15 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652743Antioxidant activity using deaerated 1 M ethylene glycol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 3.24 +/- 0.19 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652734Antioxidant activity using 1M ethanol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652906Antioxidant activity using deaerated 0.1 M alpha-glucosophosphate as substrate assessed as hydroxy radical level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462738Antioxidant activity assessed as DPPH free radical scavenging activity by measuring retention time of AA-2G-DPPH product at 20 uM incubated for 30 mins by HPLC method2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652742Antioxidant activity using deaerated 3 M ethylene glycol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462739Antioxidant activity assessed as DPPH free radical scavenging activity by measuring AA-2G-DPPH product formation at 0.25 to 0.75 mM incubated for 30 mins by HPLC method2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652744Antioxidant activity using deaerated 1 M ethylene glycol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462740Antioxidant activity assessed as DPPH free radical scavenging activity by measuring AA-2G-DPPH adducts formation at 5 mM incubated for 10 to 30 mins by 1H NMR spectroscopy2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652741Antioxidant activity using deaerated 3 M ethylene glycol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 9.05 +/- 1.03 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462748Antioxidant activity assessed as DPPH free radical scavenging activity by measuring radical-scavenging activity factor (moles of radicals scavenged by each mol of antioxidant) at 20 uM measured at 120 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID1462742Antioxidant activity assessed as DPPH free radical scavenging activity by measuring AA-2G-DPPH adducts level at 200 uM measured at 10 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652729Antioxidant activity using ethanol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 7.06 +/- 0.28 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462746Antioxidant activity assessed as DPPH free radical scavenging activity by measuring radical-scavenging activity factor (moles of radicals scavenged by each mol of antioxidant) at 20 uM measured at 15 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652738Antioxidant activity using deaerated 1 M ethanol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 0.18 +/- 0.04 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID1462743Antioxidant activity assessed as DPPH free radical scavenging activity by measuring amount of compound consumed at 200 uM measured at 10 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID1462747Antioxidant activity assessed as DPPH free radical scavenging activity by measuring radical-scavenging activity factor (moles of radicals scavenged by each mol of antioxidant) at 20 uM measured at 30 mins by HPLC2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Structural evidence for the DPPH radical-scavenging mechanism of 2-O-α-d-glucopyranosyl-l-ascorbic acid.
AID652732Antioxidant activity using 1M ethanol as substrate assessed as acetaldehyde level at 1 mmol/L after gamma-irradiation by gas chromatography (Rvb = 4.31 +/- 0.23 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652731Antioxidant activity using ethanol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652740Antioxidant activity using deaerated 1 M ethanol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652733Antioxidant activity using 1M ethanol as substrate assessed as H2O2 level at 1 mmol/L after gamma-irradiation by spectrophotometry (Rvb = 2.73 +/- 0.18 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652745Antioxidant activity using deaerated 0.1 M alpha-glycerophosphate as substrate assessed as inorganic phosphate level at 1 mmol/L after gamma-irradiation (Rvb = 3.44 +/- 0.12 10'7 mol/J)2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652728Selectivity ratio of MNTD for human RD cells to EC90 for HSV12012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
AID652737Antioxidant activity using deaerated ethanol as substrate assessed as hydroxy radical additive level at 1 mmol/L after gamma-irradiation2012Bioorganic & medicinal chemistry letters, Apr-01, Volume: 22, Issue:7
Radical-regulating and antiviral properties of ascorbic acid and its derivatives.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (109)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's21 (19.27)18.2507
2000's23 (21.10)29.6817
2010's45 (41.28)24.3611
2020's20 (18.35)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.06

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

MetricThis Compound (vs All)
Research Demand Index10.06 (24.57)
Research Supply Index4.74 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.06)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (2.73%)5.53%
Reviews4 (3.64%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other103 (93.64%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]