Page last updated: 2024-11-12

fuscol

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

Description

fuscol: isolated from the shallow water octocoral Eunicea fusca; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	10891538
CHEMBL ID	476288
MeSH ID	M000603878

Synonyms (3)

Synonym
fuscol
CHEMBL476288
(3e,5e)-6-[(1s,3r,4r)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl]-2-methylhepta-3,5-dien-2-ol

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (11)

Assay ID	Title	Year	Journal	Article
AID621753	Antiinflammatory activity in mouse assessed as inhibition of TPA-induced mouse ear edema at 0.5 mg/ear administered relative to untreated control	2011	Bioorganic & medicinal chemistry letters, Oct-01, Volume: 21, Issue:19	Fuscoside E: a strong anti-inflammatory diterpene from Caribbean octocoral Eunicea fusca.
AID400412	Antifungal activity against Cladosporium cucumerinum at 0.2 umol after 2 days	1998	Journal of natural products, Mar, Volume: 61, Issue:3	Four new bioactive lobane diterpenes of the soft coral Lobophytum pauciflorum from Mindoro, Philippines.
AID1165102	Antiinflammatory activity in mouse assessed as reduction in PMA-induced ear edema at 0.1 mg/ear administered topically measured after 24 hrs relative to control	2014	Bioorganic & medicinal chemistry letters, Oct-15, Volume: 24, Issue:20	Synthesis and evaluation of anti-inflammatory activity of derivatives of the marine natural products fuscol and eunicol.
AID636132	Cytotoxicity against human A431 cells after 4 days by coulter counting	2012	Bioorganic & medicinal chemistry, Jan-15, Volume: 20, Issue:2	Cyclolobatriene, a novel prenylated germacrene diterpene, from the soft coral Lobophytum pauciflorum.
AID400414	Toxicity in Artemia salina after 48 hrs	1998	Journal of natural products, Mar, Volume: 61, Issue:3	Four new bioactive lobane diterpenes of the soft coral Lobophytum pauciflorum from Mindoro, Philippines.
AID400411	Antifungal activity against Cladosporium cucumerinum at 0.4 umol after 2 days	1998	Journal of natural products, Mar, Volume: 61, Issue:3	Four new bioactive lobane diterpenes of the soft coral Lobophytum pauciflorum from Mindoro, Philippines.
AID678054	Antiinflammatory activity in CD1 mouse ear edema model assessed as reduction in phorbol myristate acetate-induced edema at 0.1 mg/ear administered topically at right ear 1 hr before phorbol myristate acetate challenge and measured 24 hrs post dose	2012	Journal of natural products, Jul-27, Volume: 75, Issue:7	Eunicidiol, an anti-inflammatory dilophol diterpene from Eunicea fusca.
AID678056	Toxicity in CD1 mouse model phorbol myristate acetate-induced ear edema model at 0.1 mg/ear administered topically at right ear 1 hr before phorbol myristate acetate challenge and measured 24 hrs post dose	2012	Journal of natural products, Jul-27, Volume: 75, Issue:7	Eunicidiol, an anti-inflammatory dilophol diterpene from Eunicea fusca.
AID1165103	Toxicity in mouse at 0.1 mg/ear administered topically	2014	Bioorganic & medicinal chemistry letters, Oct-15, Volume: 24, Issue:20	Synthesis and evaluation of anti-inflammatory activity of derivatives of the marine natural products fuscol and eunicol.
AID400413	Antifungal activity against Cladosporium cucumerinum at 0.1 umol after 2 days	1998	Journal of natural products, Mar, Volume: 61, Issue:3	Four new bioactive lobane diterpenes of the soft coral Lobophytum pauciflorum from Mindoro, Philippines.
AID400410	Antifungal activity against Cladosporium cucumerinum at 0.8 umol after 2 days	1998	Journal of natural products, Mar, Volume: 61, Issue:3	Four new bioactive lobane diterpenes of the soft coral Lobophytum pauciflorum from Mindoro, Philippines.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	1 (20.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	4 (80.00)	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: 21.83

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.

Metric	This Compound (vs All)
Research Demand Index	21.83 (24.57)
Research Supply Index	1.79 (2.92)
Research Growth Index	4.32 (4.65)
Search Engine Demand Index	18.60 (26.88)
Search Engine Supply Index	2.00 (0.95)

This Compound (21.83)

All Compounds (24.57)

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]

Substance	Relationship Strength	Studies	Classes	Roles
indomethacin Indomethacin: A non-steroidal anti-inflammatory agent (NSAID) that inhibits CYCLOOXYGENASE, which is necessary for the formation of PROSTAGLANDINS and other AUTACOIDS. It also inhibits the motility of POLYMORPHONUCLEAR LEUKOCYTES.. indometacin : A member of the class of indole-3-acetic acids that is indole-3-acetic acid in which the indole ring is substituted at positions 1, 2 and 5 by p-chlorobenzoyl, methyl, and methoxy groups, respectively. A non-steroidal anti-inflammatory drug, it is used in the treatment of musculoskeletal and joint disorders including osteoarthritis, rheumatoid arthritis, gout, bursitis and tendinitis.	2.77	3	aromatic ether; indole-3-acetic acids; monochlorobenzenes; N-acylindole	analgesic; drug metabolite; EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor; environmental contaminant; gout suppressant; non-steroidal anti-inflammatory drug; xenobiotic metabolite; xenobiotic
tetradecanoylphorbol acetate Tetradecanoylphorbol Acetate: A phorbol ester found in CROTON OIL with very effective tumor promoting activity. It stimulates the synthesis of both DNA and RNA.. phorbol ester : Esters of phorbol, originally found in croton oil (from Croton tiglium, of the family Euphorbiaceae). A number of phorbol esters possess activity as tumour promoters and activate the mechanisms associated with cell growth. Some of these are used in experiments as activators of protein kinase C.. phorbol 13-acetate 12-myristate : A phorbol ester that is phorbol in which the hydroxy groups at the cyclopropane ring juction (position 13) and the adjacent carbon (position 12) have been converted into the corresponding acetate and myristate esters. It is a major active constituent of the seed oil of Croton tiglium. It has been used as a tumour promoting agent for skin carcinogenesis in rodents and is associated with increased cell proliferation of malignant cells. However its function is controversial since a decrease in cell proliferation has also been observed in several cancer cell types.	2.1	1	acetate ester; diester; phorbol ester; tertiary alpha-hydroxy ketone; tetradecanoate ester	antineoplastic agent; apoptosis inducer; carcinogenic agent; mitogen; plant metabolite; protein kinase C agonist; reactive oxygen species generator
5,22-cholestadien-3beta-ol 5,22-cholestadien-3beta-ol: RN given refers to ((3beta)-(22E))-isomer	2.06	1	cholestanoid

Condition	Relationship Strength	Studies
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases.	2.06	1
Anasarca [description not available]	2.77	3
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE.	2.77	3

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