Page last updated: 2024-12-07
hernandulcin
Description
hernandulcin: sesquiterpene 1000 times sweeter than sucrose from sweet plant Lippia dulcis Trev.; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
| Flora | Rank | Flora Definition | Family | Family Definition |
|---|
| Lippia | genus | A plant genus of the family VERBENACEAE. Lippsidoquinone; TRITERPENES; SESQUITERPENES; and THYMOL have been found in this genus. Plant extracts have cytotoxic activity. It is sometimes called Mexican oregano but that confuses it with real oregano (ORIGANUM).[MeSH] | Verbenaceae | A plant family of the order Lamiales, subclass Asteridae, class Magnoliopsida. The leaves are opposite or whorled. The flowers are aggregated in spikes, clusters, or racemes.[MeSH] |
| Lippia dulcis | species | [no description available] | Verbenaceae | A plant family of the order Lamiales, subclass Asteridae, class Magnoliopsida. The leaves are opposite or whorled. The flowers are aggregated in spikes, clusters, or racemes.[MeSH] |
Cross-References
| ID Source | ID |
|---|
| PubMed CID | 125608 |
| CHEBI ID | 5678 |
| SCHEMBL ID | 110562 |
| MeSH ID | M0129050 |
Synonyms (16)
| Synonym |
|---|
| (s-(r*,r*))-6-(1-hydroxy-1,5-dimethyl-4-hexenyl)-3-methyl-2-cyclohexen-1-one |
| 2-cyclohexen-1-one, 6-(1-hydroxy-1,5-dimethyl-4-hexenyl)-3-methyl-, (s-(r*,r*))- |
| hernandulcin |
| 95602-94-1 |
| C09681 |
| (6s)-6-[(2s)-2-hydroxy-6-methylhept-5-en-2-yl]-3-methylcyclohex-2-en-1-one |
| unii-7v22tjl7nx |
| 7v22tjl7nx , |
| (6s)-6-((2s)-2-hydroxy-6-methylhept-5-en-2-yl)-3-methylcyclohex-2-en-1-one |
| SCHEMBL110562 |
| CHEBI:5678 |
| DTXSID30905099 |
| Q418686 |
| (s)-6-((s)-2-hydroxy-6-methylhept-5-en-2-yl)-3-methylcyclohex-2-en-1-one |
| 2-cyclohexen-1-one, 6-[(1s)-1-hydroxy-1,5-dimethyl-4-hexen-1-yl]-3-methyl-, (6s)- |
| EX-A6121 |
Drug Classes (1)
| Class | Description |
|---|
| sesquiterpenoid | Any terpenoid derived from a sesquiterpene. The term includes compounds in which the C15 skeleton of the parent sesquiterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups). |
| [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 | 3 (42.86) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 26.92
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 | 26.92 (24.57) | | Research Supply Index | 2.08 (2.92) | | Research Growth Index | 4.32 (4.65) | | Search Engine Demand Index | 29.35 (26.88) | | Search Engine Supply Index | 2.00 (0.95) |
| |
Study Types
| Publication Type | This drug (%) | All Drugs (%) |
|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 1 (14.29%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 6 (85.71%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |