Compounds > abscisic acid-beta-d-glucopyranosyl ester
Page last updated: 2024-11-13
abscisic acid-beta-d-glucopyranosyl ester
Description
abscisic acid-beta-D-glucopyranosyl ester: from Citrus junos fruit waste from food processing industry; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
(+)-abscisic acid beta-D-glucopyranosyl ester : A (+)-abscisic acid D-glucopyranosyl ester that is derived from beta-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]
Flora | Rank | Flora Definition | Family | Family Definition |
Citrus | genus | A plant genus of the family RUTACEAE. They bear the familiar citrus fruits including oranges, grapefruit, lemons, and limes. There are many hybrids which makes the nomenclature confusing.[MeSH] | Rutaceae | A plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH] |
Cross-References
Synonyms (26)
Synonym |
abscisic acid-beta-d-glucopyranosyl ester |
abscisic acid glucose ester |
beta-d-glucopyranosyl abscisate |
(+)-a-aba glucose ester |
aba glucosyl ester |
(+)-aba glucose ester |
(+)-abscisyl beta-d-glucopyranoside |
CHEBI:22151 |
aba-beta-ge |
abscisic acid 1'-o-beta-glucoside |
(+)-s-aba-beta-ge |
beta-d-glucopyranosyl cis-(+)-abscisate |
(+)-beta-d-glucopyranosyl abscisate |
1-o-{(2z,4e)-5-[(1s)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoyl}-beta-d-glucopyranose |
(+)-abscisic acid beta-d-glucopyranosyl ester |
(+)-(s)-aba-beta-ge |
abscisic acid-1'-o-beta-glucoside |
LMPR0103050011 |
Q27109428 |
MS-27522 |
CS-0094773 |
HY-111974 |
21414-42-6 |
DTXSID701343860 |
??-d-glucopyranosyl abscisate |
AKOS040757340 |
Drug Classes (1)
Class | Description |
(+)-abscisic acid D-glucopyranosyl ester | A carboxylic ester resulting from the condensation of the carboxylic acid group of (+)-abscisic acid with the anomeric hydroxy group of D-glucopyranose. |
[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 (5)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (60.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 12.50
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.
Metric | This Compound (vs All) |
---|
Research Demand Index | 12.50 (24.57) | Research Supply Index | 1.79 (2.92) | Research Growth Index | 4.30 (4.65) | Search Engine Demand Index | 0.00 (26.88) | Search Engine Supply Index | 0.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |