Neolitsea parvigemma

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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

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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

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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

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M Heliyon 07-Dec-2022
PMCID:PMC9801090
doi:10.1016/j.heliyon.2022.e12013
PMID:36590503
Molecular Phylogeny Revealing the Single Origin of Cinnamomum-associated Bruggmanniella (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan Lin SF, Yang MM, Tokuda M Zool Stud 30-Nov-2020
PMCID:PMC8181171
doi:10.6620/ZS.2020.59-66
PMID:34140983
Cladistic analysis of the genus Bruggmanniella Tavares (Diptera, Cecicomyiidae, Asphondyliini) with evolutionary inferences on the gall inducer-host plant association and description of a new Brazilian species Garcia CD, Lamas CJ, Urso-Guimarães MV PLoS One 05-Feb-2020
PMCID:PMC7001989
doi:10.1371/journal.pone.0227853
PMID:32023290
Antagonism of Human Formyl Peptide Receptor 1 with Natural Compounds and their Synthetic Derivatives Schepetkin IA, Khlebnikov AI, Kirpotina LN, Quinn MT Int Immunopharmacol 15-Sep-2015
PMCID:PMC4791210
doi:10.1016/j.intimp.2015.08.036
PMID:26382576
Chemical Constituents of <i>Neolitsea parvigemma</i> and <i>Neolitsea konishii</i> Keh‐Shaw Chen, Fang‐Rong Chang, Yi‐Chen Chia, Tian‐Shung Wu, Yang‐Chang Wu Wiley 01-May-2015
doi:10.1002/JCCS.199800018
Chemical Constituents of Neolitsea parvigemma Wen-Shyong Li, James D. McChesney American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50072A032
Sesquiterpenoids from Neolitsea parvigemma: Isolation, oxidation products and antiplatelet actions Keh-Shaw Chen, Yang-Chang Wu Elsevier BV 23-Apr-2003
doi:10.1016/S0040-4020(98)01123-5
Two Novel Sesquiterpenes from <i>Neolitsea parvigemma</i> Keh-Shaw Chen, Fang-Rong Chang, Ting-Ting Jong, Yang-Chang Wu American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP9602269

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

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