Page last updated: 2024-12-08

gulose

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

Description

gulose: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

gulopyranose : The pyranose form of gulose. [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]

gulose : An aldohexose that is the C-3 epimer of galactose. [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 CID441033
CHEMBL ID2093058
CHEBI ID4191
CHEBI ID37691
CHEBI ID27611
SCHEMBL ID77612
MeSH IDM0160670

Synonyms (23)

Synonym
GUL ,
CHEBI:4191 ,
d-gulopyranose ,
d-gulose ,
d-gulo-hexose
C06465
gulose
d-gulopyranoside
CHEMBL2093058
SCHEMBL77612
gulopyranose
d-gul
gulopyranoside
WQZGKKKJIJFFOK-CBPJZXOFSA-N
W-202726
(3r,4r,5r,6r)-6-(hydroxymethyl)tetrahydro-2h-pyran-2,3,4,5-tetraol
Q27106313
dtxcid201474034
gulo-hexose
chebi:37691
dtxcid3095191
wurcs=2.0/1,1,0/(a2212h-1x_1-5)/1/
chebi:27611
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
D-aldohexoseAny D-aldose having a chain of six carbon atoms in the molecule.
D-gulose
gulopyranoseThe pyranose form of gulose.
[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
AID30427Compound was tested for inhibition of Human acrosin by aldohexoses1981Journal of medicinal chemistry, Nov, Volume: 24, Issue:11
Inhibition of human acrosin by monosaccharides and related compounds: structure-activity relationships.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (37)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (10.81)18.7374
1990's5 (13.51)18.2507
2000's7 (18.92)29.6817
2010's15 (40.54)24.3611
2020's6 (16.22)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 (%)
Trials0 (0.00%)5.53%
Reviews1 (2.70%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other36 (97.30%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]