Page last updated: 2024-12-07

galactosyl-(1-3)galactose

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

Description

galactosyl-(1-3)galactose: RN given refers to (alpha-D)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID123781
CHEBI ID183881
SCHEMBL ID6810449
MeSH IDM0155242

Synonyms (30)

Synonym
CHEBI:183881
13168-24-6
(2r,3s,4s,5r)-2,4,5,6-tetrahydroxy-3-[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal
3alpha-galactobiose
3-o-alpha-d-galactosylgalactose
galactose alpha 1-3 galactose
galactosyl-alpha-(1-3)galactose
gal-alpha-1-3-gal
galalpha(1,3)gal
unii-xw90kq841p
gal alpha(1,3)gal
d-galactose, 3-o-alpha-d-galactopyranosyl-
galactosyl-(1-3)galactose
xw90kq841p ,
3-o-(|a-d-galactopyranosyl)-d-galactose
SCHEMBL6810449
galactobiose, 3.alpha.-
d-galactose, 3-o-.alpha.-d-galactopyranosyl-
3.alpha.-d-galp-(1-3)-d-gal
d-galactopyranose, 3-o-.alpha.-d-galactopyranosyl-
galactose, 3-o-.alpha.-d-galactopyranosyl
alpha-gal free epitope
3-.alpha.-galactobiose
3-o-.alpha.-d-galactopyranosyl-d-galactopyranose
galactopyranoside, d-galactopyranosyl, .alpha.-d-
galactose-.alpha.-1,3-galactose
galactopyranose, 3-o-.alpha.-d-galactopyranosyl-
DTXSID30927317
3-o-(-d-galactopyranosyl)-d-galactose
Q27294027

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" Herein we report on the stability of UP 920 in biological media and its pharmacokinetic profile."( Biostability and pharmacokinetics of LJP 920, an octameric Gal (alpha1-3) Gal conjugate for the inhibition of xenotransplantation rejection.
Jack, RM; Jia, L; Linnik, MD; Yu, L, 2001
)
0.31

Dosage Studied

ExcerptRelevanceReference
" Since one can not simply increase the dosage of the drugs used, immunomodulation or tolerance induction of the recipient would be the most desirable approach."( Induction of long-term peripheral microchimerism in non-human primates in a model of xenogeneic peripheral tolerance induction.
Chikobava, M; Haverich, A; Laaf, G; Lapin, B; Martin, U; Schröder, C; Simon, AR; Steinhoff, G; Templin, C; Tessmann, R; Wiebe, K, 2002
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
O-acyl carbohydrateA carbohydrate derivative in which the hydrogen atom of at least one alcoholic hydroxy group of a carbohydrate has been replaced by an acyl substituent.
[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 (449)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (0.89)18.7374
1990's115 (25.61)18.2507
2000's224 (49.89)29.6817
2010's83 (18.49)24.3611
2020's23 (5.12)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.36

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 Index10.36 (24.57)
Research Supply Index6.21 (2.92)
Research Growth Index6.57 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.36)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (0.61%)5.53%
Reviews33 (6.69%)6.00%
Case Studies28 (5.68%)4.05%
Observational0 (0.00%)0.25%
Other429 (87.02%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]