Page last updated: 2024-12-08

taiwanin c

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

Description

taiwanin C: were isolated from the root of Acanthopanax chiisanensis; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

taiwanin C : A furonaphthodioxole that is furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8H)-one substituted by a 1,3-benzodioxol-5-yl group at position 5. It is a naturally occurring lignan extracted from Taiwania cryptomerioides and found to be a potential inhibitor of COX2 expression. [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
Taiwaniagenus[no description available]CupressaceaeA plant family of the order Pinales, class Pinopsida, division Tracheophyta. They are mainly resinous, aromatic evergreen trees.[MeSH]
Acanthopanaxgenus[no description available]AraliaceaeThe ginseng plant family of the order Apiales, subclass Rosidae, class Magnoliopsida. Leaves are generally alternate, large, and compound. Flowers are five-parted and arranged in compound flat-topped umbels. The fruit is a berry or (rarely) a drupe (a one-seeded fruit). It is well known for plant preparations used as adaptogens (immune support and anti-fatigue).[MeSH]
Taiwania cryptomerioidesspecies[no description available]CupressaceaeA plant family of the order Pinales, class Pinopsida, division Tracheophyta. They are mainly resinous, aromatic evergreen trees.[MeSH]

Cross-References

ID SourceID
PubMed CID363127
CHEMBL ID65755
CHEBI ID191411
MeSH IDM0441905

Synonyms (14)

Synonym
furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(8h)-one, 5-(1,3-benzodioxol-5-yl)-
5-(1,3-benzodioxol-5-yl)-8h-isobenzofuro[5,6-f][1,3]benzodioxol-6-one
taiwanin c
bdbm50280971
CHEMBL65755 ,
5-(2h-1,3-benzodioxol-5-yl)-2h-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8h)-one
5-(1,3-benzodioxol-5-yl)-8h-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one
14944-34-4
5-(1,3-benzodioxol-5-yl)furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8h)-one
6,7-(epoxymethanoxy)-9-(1,3-benzodioxole-5-yl)-1,3-dihydronaphtho[2,3-c]furan-1-one
CHEBI:191411
5-benzo[1,3]dioxol-5-yl-8h-furo[3'',4'':6,7]naphtho[2,3-d][1,3]dioxol-6-one
DTXSID201318393
AKOS040763332
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antineoplastic agentA substance that inhibits or prevents the proliferation of neoplasms.
platelet aggregation inhibitorA drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
[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 (3)

ClassDescription
furonaphthodioxole
benzodioxoles
lignanAny phenylpropanoid derived from phenylalanine via dimerization of substituted cinnamic alcohols, known as monolignols, to a dibenzylbutane skeleton. Note that while individual members of the class have names ending ...lignane, ...lignene, ...lignadiene, etc., the class names lignan, neolignan, etc., do not end with an "e".
[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 (9)

Assay IDTitleYearJournalArticle
AID385091Antiviral activity against deltaTat/Rev deffective HIV1 in 1A2 cells assessed as inhibition of metabolic activity in uninfected cells2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID384925Cytotoxicity against human MCF7 cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID384924Cytotoxicity against human Col2 cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID384923Cytotoxicity against human KB cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID385092Antiviral activity against deltaTat/Rev deffective HIV1 in 1A2 cells assessed as reduction of syncytium formation2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID384922Cytotoxicity against mouse P388 cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID385089Cytotoxicity against human Lu1 cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID385094Inhibition of HIV1 reverse transcriptase at 200 ug/ml2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
AID385090Cytotoxicity against rat ASK cells after 72 hrs by sulforhodamine B assay2008Journal of natural products, Apr, Volume: 71, Issue:4
Dichapetalin-type triterpenoids and lignans from the aerial parts of Phyllanthus acutissima.
[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's5 (41.67)29.6817
2010's6 (50.00)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: 11.97

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 Index11.97 (24.57)
Research Supply Index2.56 (2.92)
Research Growth Index4.53 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.97)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other12 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]