Page last updated: 2024-11-12

eudesmanolide

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

Description

eudesmanolide: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12443309
CHEMBL ID406233
CHEBI ID181502
MeSH IDM0453396

Synonyms (15)

Synonym
telekin
(3ar,4ar,8ar,9ar)-4a-hydroxy-8a-methyl-3,5-dimethylidene-4,6,7,8,9,9a-hexahydro-3ah-benzo[][1]benzouran-2-one
CHEBI:181502
eudesmanolide
CHEMBL406233
NCGC00384720-01
ncgc00384720-01_c15h20o3_(3ar,4ar,8ar,9ar)-4a-hydroxy-8a-methyl-3,5-bis(methylene)decahydronaphtho[2,3-b]furan-2(3h)-one
5alpha-hydroxyeudesm-4(15),11(13)-dien-8beta,12-olide
(3ar,4ar,8ar,9ar)-4a-hydroxy-8a-methyl-3,5-dimethylenedecahydronaphtho[2,3-b]furan-2(3h)-one
CS-0564736
HY-N10483
STARBLD0028755
(3ar,4ar,8ar,9ar)-4a-hydroxy-8a-methyl-3,5-dimethylidene-4,6,7,8,9,9a-hexahydro-3ah-benzo[f][1]benzofuran-2-one
AKOS040739215
compound np-009716

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
sesquiterpene lactoneAny member of a diverse class of complex, multicyclic phytochemicals showing a variety of skeleton arrangements and bioactivities, and having in common a sesquiterpenoid structure including a lactone ring.
[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 (16)

Assay IDTitleYearJournalArticle
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347159Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347160Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID320961Inhibition of serotonin release in bovine platelets2008Journal of medicinal chemistry, Mar-13, Volume: 51, Issue:5
Neural networks as valuable tools to differentiate between sesquiterpene lactones' inhibitory activity on serotonin release and on NF-kappaB.
AID735829Antiproliferative activity against human A549 cells assessed as inhibition of cell proliferation after 72 hrs by CCK8 assay2013Journal of natural products, Apr-26, Volume: 76, Issue:4
Structural investigation and biological activity of sesquiterpene lactones from the traditional Chinese herb Inula racemosa.
AID1675636Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
AID551551Cell cycle arrest in human MCF7 cells assessed as accumulation at G2/M phase at IC50 concentration after 24 hrs using propidium iodide staining by flow cytometry2011Bioorganic & medicinal chemistry letters, Jan-01, Volume: 21, Issue:1
Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi.
AID1675634Cytotoxicity against human SMMC-7721 cells assessed as reduction in cell viability after 48 hrs by MTT assay
AID1252949Antifungal activity against Candida albicans SC5314 assessed as inhibition of yeast cell to hyphae transition after 4 hrs by microscopic analysis2015Bioorganic & medicinal chemistry letters, Nov-15, Volume: 25, Issue:22
Sesquiterpenes from Carpesium macrocephalum inhibit Candida albicans biofilm formation and dimorphism.
AID1252948Antifungal activity against Candida albicans SC5314 assessed as inhibition of biofilm formation by XTT assay2015Bioorganic & medicinal chemistry letters, Nov-15, Volume: 25, Issue:22
Sesquiterpenes from Carpesium macrocephalum inhibit Candida albicans biofilm formation and dimorphism.
AID551550Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay2011Bioorganic & medicinal chemistry letters, Jan-01, Volume: 21, Issue:1
Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi.
AID1675635Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability after 48 hrs by MTT assay
AID735827Antiproliferative activity against human HT1080 cells assessed as inhibition of cell proliferation after 72 hrs by CCK8 assay2013Journal of natural products, Apr-26, Volume: 76, Issue:4
Structural investigation and biological activity of sesquiterpene lactones from the traditional Chinese herb Inula racemosa.
AID735828Antiproliferative activity against human HepG2 cells assessed as inhibition of cell proliferation after 72 hrs by CCK8 assay2013Journal of natural products, Apr-26, Volume: 76, Issue:4
Structural investigation and biological activity of sesquiterpene lactones from the traditional Chinese herb Inula racemosa.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (45)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's8 (17.78)29.6817
2010's29 (64.44)24.3611
2020's8 (17.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.51

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index24.51 (24.57)
Research Supply Index3.83 (2.92)
Research Growth Index5.01 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (24.51)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.22%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other44 (97.78%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]