Page last updated: 2024-12-10
stenusin
Description
stenusin: secretion from collecting bladders of beetles of genus Stenus comma; RN is from 9th CI; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
stenusine : A diastereoisomeric mixture comprising of four stereoisomers, (2'R,3R)-, (2'S,3R)-, (2'S,3S)-, and (2'R,3S)-stenusine. It is a natural product found in Stenus comma, Stenus bimaculatus and Stenus similis. [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]
1-ethyl-3-(2-methylbutyl)piperidine : A member of the class of piperidines that is piperidine substituted by ethyl and 2-methylbutyl groups at positions 1 and 3, respectively. [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]
Cross-References
Synonyms (10)
| Synonym |
|---|
| stenusin |
| n-ethyl-3-(2-methylbutyl)-piperidine |
| 1-ethyl-3-(2-methylbutyl)piperidine |
| CHEBI:194461 |
| n-ethyl-3-(2-methylbutyl)piperidine |
| 54985-88-5 |
| stenusine |
| piperidine, 1-ethyl-3-(2-methylbutyl)- |
| Q21099611 |
| DTXSID40970334 |
Research Excerpts
Overview
Stenusine is a chiral molecule with four stereoisomers.
| Excerpt | Reference | Relevance |
|---|
| "Stenusine is a chiral molecule with four stereoisomers: (2'R,3R)-, (2'S,3R)-, (2'S,3S)-, and (2'R,3S)-stenusine." | ( Intrageneric differences in the four stereoisomers of stenusine in the rove beetle genus, Stenus (Coleoptera, Staphylinidae).
Burkhardt, D; Dettner, K; Gedig, T; Lusebrink, I; Mosandl, A; Seifert, K, 2007) | 1.31 |
Drug Classes (2)
| Class | Description |
|---|
| tertiary amino compound | A compound formally derived from ammonia by replacing three hydrogen atoms by organyl groups. |
| piperidine alkaloid | |
| [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 (7)
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 4 (57.14) | 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 | 7 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |