Page last updated: 2024-12-06

thiarubrine a

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

Description

Thiarubrine A is a natural product with a unique structure containing a thiazole ring fused to a pyridone ring. It has been isolated from various Streptomyces species and exhibits potent biological activities, including antimicrobial, anti-inflammatory, and anticancer effects. The compound's synthesis has been studied extensively, leading to several synthetic routes, including a biomimetic approach. Thiarubrine A is a promising lead compound for drug development, particularly for the treatment of infections and inflammatory diseases. Its unique mechanism of action, involving the inhibition of bacterial DNA synthesis and the modulation of inflammatory pathways, has sparked significant research interest. The compound's ability to disrupt bacterial cell wall formation and inhibit the production of pro-inflammatory cytokines makes it a potential candidate for a new class of therapeutic agents.'

thiarubrine A: dithiin polyacetylene; bioactive constituent of Aspilia (Asteraceae); structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
AspiliagenusA plant genus of the family ASTERACEAE. Members contain thiarubrine A and diterpenes.[MeSH]AsteraceaeA large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH]

Cross-References

ID SourceID
PubMed CID72386
CHEBI ID9538
SCHEMBL ID1653142
MeSH IDM0130703

Synonyms (20)

Synonym
3-hex-5-en-1,3-diynyl-6-prop-1-ynyl-dithiine
thiarubrine a
thiarubrin a
63543-09-9
C08461
3-(5-hexene-1,3-diynyl)-6-(1-propynyl)-1,2-dithiin
1,2-dithiin, 3-(5-hexene-1,3-diynyl)-6-(1-propynyl)-
unii-dvv5w0eg1z
dvv5w0eg1z ,
thiarubrin(e) a
1-(2-methyleth-1-yn)-4-(hex-1,3-diyn-5-ene)-2,3-dithiacyclohex-1,3-diene
1,2-dithiin, 3-(5-hexene-1,3-diyn-1-yl)-6-(1-propyn-1-yl)-
thiarubrine a [mi]
SCHEMBL1653142
CHEBI:9538
DTXSID80212947
LMFA12000371
thiorubrine a
3-(hexa-5-en-1,3-diyn-1-yl)-6-(prop-1-yn-1-yl)-1,2-dithiine
Q27108431
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
organosulfur heterocyclic compound
[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]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (62.50)18.7374
1990's1 (12.50)18.2507
2000's2 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (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: 19.55

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 Index19.55 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.11 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (19.55)

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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]