thyrsiferol

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

Description

thyrsiferol: RN given for (2R-(2alpha(S*(S*(2R*,5R*))),4abeta,(alpha(2S*,5R*),8aalpha)-isomer; a marine algae metabolite; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	10984902
CHEMBL ID	2272771
SCHEMBL ID	12084163
MeSH ID	M0365742

Synonyms (6)

Synonym
66873-39-0
2,5-furandimethanol, alpha2-(3-(6-(5-bromotetrahydro-2,6,6-trimethyl-2h-pyran-2-yl)octahydro-8a-methylpyrano(3,2-b)pyran-2-yl)-3-hydroxybutyl)tetrahydro-alpha5,alpha5,2-trimethyl-, (2r-(2alpha(s(s(2r,5r))),4abeta,6alpha(2s,5r),8aalpha))-
thyrsiferol
CHEMBL2272771
SCHEMBL12084163
(1s,4s)-4-[(2r,4as,6r,8ar)-2-[(2s,5r)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2h-pyrano[3,2-b]pyran-6-yl]-1-[(2r,5r)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]pentane-1,4-diol

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

Bioassays (1)

Assay ID	Title	Year	Journal	Article
AID1105423	Inhibition of mitochondrial complex 1 in Homo sapiens (human) T47D cells by Clark's electrode method	2013	Molecules (Basel, Switzerland), Jan-09, Volume: 18, Issue:1	Tricolorin A as a natural herbicide.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	1 (12.50)	18.2507
2000's	4 (50.00)	29.6817
2010's	3 (37.50)	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]

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	8 (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
colchicine (S)-colchicine : A colchicine that has (S)-configuration. It is a secondary metabolite, has anti-inflammatory properties and is used to treat gout, crystal-induced joint inflammation, familial Mediterranean fever, and many other conditions.	2.03	1	alkaloid; colchicine	anti-inflammatory agent; gout suppressant; mutagen
titanium Titanium: A dark-gray, metallic element of widespread distribution but occurring in small amounts with atomic number, 22, atomic weight, 47.867 and symbol, Ti; specific gravity, 4.5; used for fixation of fractures.	7.02	1	titanium group element atom
glycosides [no description available]	7.02	1
squalene Addavax: an oil-water nanoemulsion and adjuvant containing squalene, Tween 80, and sorbitane trioleate	2.21	1	triterpene	human metabolite; mouse metabolite; plant metabolite; Saccharomyces cerevisiae metabolite
dehydrothyrsiferol dehydrothyrsiferol: structure in first source	2.21	1

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