Page last updated: 2024-12-07

6-tuliposide a

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

Description

6-tuliposide A: from Alstroemeria ligtu L.; structure given in first source; RN given from Chem Abstr. Index Guide 1985; RN not Chemline 9/85 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

6-tuliposide A : A 6-O-acyl-D-glucose that is the 6-O-(4-hydroxy-2-methylenebutanoyl) derivative of D-glucopyranose. [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]

FloraRankFlora DefinitionFamilyFamily Definition
AlstroemeriagenusA plant genus of the family Alstroemeriaceae. Members contain allergens, tuliposide A and tulipalin A.[MeSH]AlstroemeriaceaeA family of the order Liliales.[MeSH]
Alstroemeria ligtuspecies[no description available]AlstroemeriaceaeA family of the order Liliales.[MeSH]

Cross-References

ID SourceID
PubMed CID21119819
CHEBI ID72781
MeSH IDM0133891

Synonyms (7)

Synonym
CHEBI:72781
6-o-(4-hydroxy-2-methylenebutanoyl)-d-glucopyranose
6-tuliposide a
6-o-(4-hydroxy-2-methylenebutanoyl)-d-glucose
C20577
Q27140142
[(2r,3s,4s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 4-hydroxy-2-methylidenebutanoate
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
allergenA chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role 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]

Drug Classes (2)

ClassDescription
6-O-acyl-D-glucoseA monosaccharide derivative that is a D-glucose derivative having an acyl group at the O-6 position.
homoallylic alcoholAn aliphatic alcohol where the hydroxy carbon is beta to a double bond.
[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 (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (25.00)18.7374
1990's1 (12.50)18.2507
2000's1 (12.50)29.6817
2010's3 (37.50)24.3611
2020's1 (12.50)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%
Reviews0 (0.00%)6.00%
Case Studies1 (12.50%)4.05%
Observational0 (0.00%)0.25%
Other7 (87.50%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]