Page last updated: 2024-11-13
thiocoraline
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
thiocoraline: a depsipeptide from marine actinomycete, Micromonospora; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 70698112 |
CHEBI ID | 69052 |
MeSH ID | M0283010 |
Synonyms (4)
Synonym |
---|
173046-02-1 |
thiocoraline |
CHEBI:69052 |
Q27137393 |
Research Excerpts
Overview
Thiocoraline is a potent Notch pathway activator and an inhibitor of MTC-TT cell proliferation at low nanomolar concentrations. It belongs to the family of bisintercalator natural products that bind duplex DNA.
Actions
Excerpt | Reference | Relevance |
---|---|---|
"Thiocoraline does not inhibit DNA-topoisomerase II enzymes in vitro, nor does it induce DNA breakage in cells exposed to effective drug concentrations." | ( Mode of action of thiocoraline, a natural marine compound with anti-tumour activity. Bergamaschi, D; Bonfanti, M; Catapano, CV; D'Incalci, M; Erba, E; Faircloth, G; Faretta, M; Jimeno, J; Ronzoni, S; Taverna, S, 1999) | 1.36 |
Treatment
Excerpt | Reference | Relevance |
---|---|---|
"Thiocoraline treatment decreased cell proliferation in a dose- and time-dependent manner." | ( Thiocoraline alters neuroendocrine phenotype and activates the Notch pathway in MTC-TT cell line. Bugni, TS; Chen, H; Dammalapati, A; Eide, J; Jaskula-Sztul, R; Korlesky, C; Tesfazghi, S; Wyche, TP, 2013) | 2.55 |
Dosage Studied
Excerpt | Relevance | Reference |
---|---|---|
" Pharmacokinetic analysis showed that thiocoraline has distinct pharmacokinetic profiling when dosed in different formulation solutions." | ( Validation of a sensitive assay for thiocoraline in mouse plasma using liquid chromatography-tandem mass spectrometry. Aviles, P; Calvo, P; Faircloth, G; Guillen, MJ; Lee, W; Ly, C; Manzanares, I; Yin, J, 2003) | 0.86 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Drug Classes (1)
Class | Description |
---|---|
peptide | Amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another with formal loss of water. The term is usually applied to structures formed from alpha-amino acids, but it includes those derived from any amino carboxylic acid. X = OH, OR, NH2, NHR, etc. |
[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] |
Pathways (1)
Pathway | Proteins | Compounds |
---|---|---|
thiocoraline biosynthesis | 4 | 15 |
Research
Studies (30)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 5 (16.67) | 18.2507 |
2000's | 10 (33.33) | 29.6817 |
2010's | 14 (46.67) | 24.3611 |
2020's | 1 (3.33) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 21.88
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.
| This Compound (21.88) All Compounds (24.57) |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (3.33%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 29 (96.67%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |