Page last updated: 2024-11-13

taccalonolide aj

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

Description

taccalonolide AJ: isolated from plants of the genus Tacca; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID56926890
CHEMBL ID2408398
MeSH IDM0571891

Synonyms (9)

Synonym
CHEMBL2408398
taccalonolide aj
1349904-82-0
[(1s,2s,3r,5s,7s,9s,10r,11r,12s,13s,14r,15r,16s,17s,18s,20s,23s,24s,25r,26r)-10,14-diacetyloxy-3,23,26-trihydroxy-11,15,17,23,24-pentamethyl-4,22-dioxo-8,19,21-trioxaoctacyclo[13.11.0.02,12.05,11.07,9.016,25.018,20.020,24]hexacosan-13-yl] acetate
HY-N4208
CS-0032438
MS-31071
PD125320
AKOS040760730

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The hypothesis that pharmacokinetic differences underlie the differential efficacies of taccalonolides AF and AJ was tested."( Pharmacokinetic Analysis and in Vivo Antitumor Efficacy of Taccalonolides AF and AJ.
Benavides, R; Cichewicz, RH; Du, L; Kuhn, JG; Li, J; Mooberry, SL; Risinger, AL; Robles, AJ, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID1177715Antiproliferative activity against human HeLa cells by SRB assay2014Bioorganic & medicinal chemistry, Sep-15, Volume: 22, Issue:18
Taccalonolide microtubule stabilizers.
AID1180503Antiproliferative activity against human HeLa cells by SRB assay2014Journal of medicinal chemistry, Jul-24, Volume: 57, Issue:14
Synthetic reactions with rare taccalonolides reveal the value of C-22,23 epoxidation for microtubule stabilizing potency.
AID1625143Induction of porcine tubulin polymerization measured at 1 min interval for 1 hr2019Journal of natural products, 03-22, Volume: 82, Issue:3
Identification of C-6 as a New Site for Linker Conjugation to the Taccalonolide Microtubule Stabilizers.
AID1180516Ratio of taccalonolide B IC50 to compound IC50 for human HeLa cells by SRB assay2014Journal of medicinal chemistry, Jul-24, Volume: 57, Issue:14
Synthetic reactions with rare taccalonolides reveal the value of C-22,23 epoxidation for microtubule stabilizing potency.
AID762821Antiproliferative activity against human HeLa cells2013Journal of natural products, Jul-26, Volume: 76, Issue:7
Hydrolysis reactions of the taccalonolides reveal structure-activity relationships.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's11 (91.67)24.3611
2020's1 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.94

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 Index11.94 (24.57)
Research Supply Index2.56 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (8.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (91.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]