Page last updated: 2024-12-10

falcarindiol

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

Description

falcarindiol: from leaves of Schefflera digitata (Araliaceae) and in carrots; inhibits germination of spores of most common dermatophyte fungi [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
ScheffleragenusA plant genus of the family ARALIACEAE that contains oleanane and ursane glycosides and triterpenoid SAPONINS.[MeSH]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]
Schefflera digitataspecies[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]

Cross-References

ID SourceID
PubMed CID6436239
CHEMBL ID425677
CHEBI ID69236
MeSH IDM0105987

Synonyms (22)

Synonym
ACON1_000065
55297-87-5
falcarindiol
(3s,8s,9z)-heptadeca-1,9-dien-4,6-diyne-3,8-diol
1,9-heptadecadiene-4,6-diyne-3,8-diol
MEGXP0_000391
NCGC00168828-01
chebi:69236 ,
CHEMBL425677
heptadeca-1,9-diene-4,6-diyne-3,8-diol
unii-8g3aw3gyu8
8g3aw3gyu8 ,
falcalindiol
1,9-heptadecadiene-4,6-diyne-3,8-diol, (3s,8s,9z)-
Q60998696
(z)-falcarindiol
MS-23672
CS-0008913
HY-N0364
1,9-heptadecadiene-4,6-diyne-3,8-diol, [s-[r*,r*-(z)]]-
(3s,8s,9z)-1,9-heptadecadiene-4,6-diyne-3,8-diol
(+)-falcarindiol
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
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 (1)

ClassDescription
organic molecular entityAny molecular entity that contains carbon.
[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 (7)

Assay IDTitleYearJournalArticle
AID1423206Cytotoxicity against HEK293 cells assessed as decrease in cell viability at 10 uM after 24 hrs by resazurin based assay2018Journal of natural products, 11-26, Volume: 81, Issue:11
Stereoselective Synthesis of the Isomers of Notoincisol A: Assigment of the Absolute Configuration of this Natural Product and Biological Evaluation.
AID1756182Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production preincubated for 1 hr followed by LPS stimulation and measured after 24 hrs by Griess reagent based assay2021Journal of natural products, 02-26, Volume: 84, Issue:2
Diterpenoids and Diacetylenes from the Roots of
AID1423208Transactivation of human full length PPARgamma expressed in HEK293 cells up to 3 uM after 18 hrs by luciferase reporter gene based luminescence assay2018Journal of natural products, 11-26, Volume: 81, Issue:11
Stereoselective Synthesis of the Isomers of Notoincisol A: Assigment of the Absolute Configuration of this Natural Product and Biological Evaluation.
AID1651574Cytotoxicity against HEK293 cells assessed as cell viability at 10 uM after 24 hrs by resazurin conversion assay2020Journal of natural products, 04-24, Volume: 83, Issue:4
Polyacetylenes from
AID1651573Cytotoxicity against HEK293 cells assessed as cell viability at 3 uM after 18 hrs by luciferase assay relative to control2020Journal of natural products, 04-24, Volume: 83, Issue:4
Polyacetylenes from
AID1651571Activation of human PPARgamma expressed in HEK293 cells at 3 uM incubated for 18 hrs by luciferase reporter assay relative to control2020Journal of natural products, 04-24, Volume: 83, Issue:4
Polyacetylenes from
AID1756183Cytotoxicity against mouse RAW264.7 cells assessed as reduction in cell viability by MTT assay2021Journal of natural products, 02-26, Volume: 84, Issue:2
Diterpenoids and Diacetylenes from the Roots of
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (73)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (2.74)18.7374
1990's7 (9.59)18.2507
2000's16 (21.92)29.6817
2010's40 (54.79)24.3611
2020's8 (10.96)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 Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other73 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]