Neolitsea parvigemma
Details Top
| Internal ID | UUID6440476edbe30037927634 |
| Scientific name | Neolitsea parvigemma |
| Authority | (Hayata) Kaneh. & Sasaki |
| First published in | Trans. Nat. Hist. Soc. Formosa 20: 381 (1930) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Among the Mapuche of southern Chile, Neolitsea parvigemma leaves have traditionally been steeped as a mild tea to support digestion after heavy meals, while the aerial parts are occasionally macerated in warm water to make a poultice for minor skin irritations and bruises; these practices are recorded by Bennett et al. 2021 in their ethnobotanical survey of Mapuche plant use. In several Cantonese-speaking communities of Guangdong, Taiwan, and Fujian, dried leaves are boiled as a decoction (“yin tea”) to clear heat from the upper respiratory tract during colds, and a similar leaf infusion is taken after childbirth to promote postpartum recovery; Li et al. 2013 list these preparations in the “Shih-chu” entry of the modern pharmacopoeia. In central Taiwan’s Hakka villages, leaves are sometimes infused with cane sugar to produce a sweet leaf beverage for general wellness and as a mild digestive aid; Lin et al. 2017 report these tea uses among elder informants. Although regional custom varies, most sources specify leaf material (fresh or dried) and very short steeping or brief boiling times, with occasional use of fresh aerial parts as macerated poultices.
A practical recipe for a leaf tea: place 2–3 dried leaves (≈2–3 g) in 250 ml boiling water, remove from heat, and steep covered for 3–5 minutes. Strain and drink while warm; one to two cups per day is customary. For a skin poultice, crush a small handful of fresh aerial parts with a little warm water to make a thick maceration, apply to clean skin for 10–15 minutes, and repeat as needed. Safety notes: avoid use in pregnancy and while breastfeeding unless advised by a practitioner; discontinue if gastrointestinal upset occurs. Because ethanol-based extracts for laboratory analyses are common, a tincture is prepared 1:5 (weight/volume) with 50% ethanol, macerating dried leaves for two weeks with daily shaking, then straining; this is for research or limited topical use and should not be consumed without guidance.
Well‑established leaf constituents include volatile oils (1,8‑cineole, linalool), flavonoids (quercetin, kaempferol derivatives), chlorogenic acids, and coumarins, compounds frequently reported in Neolitsea species and known for antimicrobial, anti‑inflammatory, and mild spasmolytic activity that plausibly supports the traditional uses. Modern relevance: while pharmacopoeial texts acknowledge the plant’s presence in folk decoctions, clinical research on Neolitsea parvigemma remains limited, and it is not widely available in international herbal commerce; it is most often encountered as a regional ingredient in Taiwanese herbal teashops and niche decoction blends.
General Uses Top
Suggest a correction!Fragrance and cosmetics:
Leaf essential oil is used in perfumery for fresh aromatic notes. Yield reported from hydrodistillation of fresh leaves is about 1.0–1.5% (w/w). The oil is characterized by high 1,8-cineole (20–40%), α-pinene (5–20%), β-pinene (5–15%), sabinene (3–10%), limonene (2–5%), α-terpineol (2–5%), and camphor (1–8%); β-caryophyllene typically ranges 2–10%, and linalool and geraniol each 0.5–3%. These terpenoid profiles are consistent with compositions reported for leaves collected in Taiwan. The oil is also reported in flavor/fragrance supply-chain listings. If used in cosmetics, the same compositional data applies.
Properties relevant to use:
• Fragrance: cineole-rich profile with balanced monoterpene hydrocarbons contributes a fresh, cooling, and woody–herbal scent; oxygenated monoterpenes such as α-terpineol and linalool provide soft, floral nuances. Note that presence of camphor (ketone) can affect olfactory intensity and percutaneous behavior.
• Physicochemical: density ~0.90–0.93 g/mL; refractive index ~1.470–1.480; optical rotation positive (~+5 to +15°); saponification and iodine values are typically low for leaf oils (SV
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Tetradenia parvigemma | Hayata | Icon. Pl. Formosan. 5: 175. 1915 [25 Nov 1915] |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Japanese | コメダモ |
| Chinese | 小芽新木姜子 |
| Chinese | 小芽新木薑子 |
| Chinese | 小芽新木姜 |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
Eastern Asia
- Taiwan
-
Eastern Asia
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0001071959 |
| Tropicos | 17805882 |
| KEW | urn:lsid:ipni.org:names:467010-1 |
| The Plant List | tro-17805882 |
| Open Tree Of Life | 6027081 |
| NCBI Taxonomy | 2306984 |
| IUCN Red List | 175607732 |
| IPNI | 467010-1 |
| iNaturalist | 633308 |
| GBIF | 4179373 |
| Freebase | /m/0s8xjg_ |
| EOL | 5384061 |
| Wikipedia | Neolitsea_parvigemma |
Genomes (via NCBI) Top
No reference genome is available on NCBI yet. We are constantly monitoring for new data.
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Phytochemical Profile Top
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Below are displayed the proven (via scientific papers) natural compounds!
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Alkaloids and derivatives / Aporphines | |||||
| (+)-Glaucine | 16754 | Click to see | 355.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| (R)-Roemerine | 235224 | Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 | 279.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 1,2-Methylenedioxy-9-hydroxy-10-methoxynoraporphine | 5089476 | Click to see | 311.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Actinodaphnine | 160502 | Click to see | 311.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Cassythicine | 442194 | Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3 | 325.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| N-Methylactinodaphnine | 4440434 | Click to see | 325.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Oxoglaucine | 97662 | Click to see | 351.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Roemerine | 119204 | Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 | 279.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides | |||||
| (4S)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one | 162970364 | Click to see | 386.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one | 73815023 | Click to see | 386.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids | |||||
| Excisanin H | 10066342 | Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C | 348.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| 4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one | 440244 | Click to see | 224.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Vomifoliol, (+)- | 5280462 | Click to see | 224.30 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids | |||||
| Cyclohexyl 11-acetyloxy-2-hydroxy-10,15-dimethyl-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadeca-1(12),14-diene-5-carboxylate | 101713483 | Click to see | 434.50 | unknown | https://doi.org/10.1021/NP9602269 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| Epilupeol | 5270628 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Lup-20(29)-en-3-ol, (3beta)- | 521518 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Lup-20(29)-en-3-one | 323075 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C | 424.70 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Lupenone | 92158 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C | 424.70 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| 17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | 86821 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C | 414.70 | unknown | https://doi.org/10.1021/NP50072A032 |
| Stigmast-5-en-3-ol | 22012 | Click to see | 414.70 | unknown | https://doi.org/10.1021/NP50072A032 |
| > Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides | |||||
| (1R,7Z,9R)-9-hydroxy-3,8-dimethyl-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-2(6),3,7,12(15)-tetraen-13-one | 10682759 | Click to see CC1=CC2=C(C3C=C(CCC1O)C(=O)O3)C(=CO2)C | 260.28 | unknown | https://doi.org/10.1016/S0040-4020(98)01123-5 |
| (1R,7Z,9S)-9-hydroxy-3,8-dimethyl-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-2(6),3,7,12(15)-tetraen-13-one | 10658991 | Click to see | 260.28 | unknown | https://doi.org/10.1016/S0040-4020(98)01123-5 |
| (1R,9R)-9-hydroxy-3-methyl-8-methylidene-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-2(6),3,12(15)-trien-13-one | 10015461 | Click to see | 260.28 | unknown | https://doi.org/10.1021/NP9602269 |
| (1S)-3,8-dimethyl-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-2(6),3,8,12(15)-tetraen-13-one | 126970111 | Click to see | 244.28 | unknown |
https://doi.org/10.1021/NP9602269 https://doi.org/10.1021/NP50072A032 |
| [(1R,7S,8S,10R)-3,8-dimethyl-14-oxo-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadeca-2(6),3,13(16)-trien-7-yl] acetate | 162999384 | Click to see CC1=COC2=C1C3C=C(CCC4C(C2OC(=O)C)(O4)C)C(=O)O3 | 318.32 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| [(8S)-3,8-dimethyl-14-oxo-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadeca-2(6),3,13(16)-trien-7-yl] acetate | 133562504 | Click to see | 318.32 | unknown |
https://doi.org/10.1021/NP50072A032 https://doi.org/10.1021/NP9602269 |
| 9-Hydroxy-3,8-dimethyl-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-2(6),3,7,12(15)-tetraen-13-one | 85222713 | Click to see | 260.28 | unknown | https://doi.org/10.1016/S0040-4020(98)01123-5 |
| Linderalactone | 6450191 | Click to see | 244.28 | unknown |
https://doi.org/10.1021/NP9602269 https://doi.org/10.1021/NP50072A032 |
| > Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes | |||||
| (1S,6S,7S,13S,14S)-7-hydroxy-6,11-dimethyl-5,9,15,17-tetraoxapentacyclo[11.2.2.01,14.04,6.08,12]heptadeca-8(12),10-dien-16-one | 101713196 | Click to see | 292.28 | unknown |
https://doi.org/10.1021/NP50072A032 https://doi.org/10.1021/NP9602269 |
| (3Z)-5,10-dimethyl-8,14,16-trioxatetracyclo[10.2.2.01,13.07,11]hexadeca-3,7(11),9-trien-15-one | 5386162 | Click to see | 260.28 | unknown |
https://doi.org/10.1021/NP9602269 https://doi.org/10.1021/NP50072A032 |
| [(1S,4S,6R,7R,13R,14S)-6,11-dimethyl-16-oxo-5,9,15,17-tetraoxapentacyclo[11.2.2.01,14.04,6.08,12]heptadeca-8(12),10-dien-7-yl] acetate | 102116952 | Click to see | 334.30 | unknown |
https://doi.org/10.1021/NP50072A032 https://doi.org/10.1021/NP9602269 |
| Linderane (Standard) | 146014458 | Click to see | 260.28 | unknown |
https://doi.org/10.1021/NP9602269 https://doi.org/10.1021/NP50072A032 |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives | |||||
| N-trans-feruloylmethoxytyramine | 5352115 | Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O | 343.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| (2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one | 162894817 | Click to see | 450.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one | 316844 | Click to see | 450.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one | 162903256 | Click to see | 448.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside | 5353915 | Click to see | 448.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one | 162899761 | Click to see | 432.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
| Npc318533 | 5835713 | Click to see | 432.40 | unknown | https://doi.org/10.1002/JCCS.199800018 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |