Neolitsea cassia
Details Top
| Internal ID | UUID644056293ac1b703788950 |
| Scientific name | Neolitsea cassia |
| Authority | (L.) Kosterm. |
| First published in | J. Sci. Res. (Jakarta) 1: 85 (1952) |
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.
Ethnobotanical Uses
Among the Hakka communities of Fujian and eastern Guangdong, the dried bark of Neolitsea cassia is decocted to address colds, headaches, and rheumatic discomfort; leaves are also infused as a warming beverage that is shared seasonally for “wind-cold” conditions, with these practices recorded in the Chinese Materia Medica tradition (Shen Nong Ben Cao Jing, 1st–2nd century CE; Li Shizhen’s Bencao Gangmu, 1578; and modern pharmacognosy surveys cited in Perry & Metzger, 1980). In northern Vietnam’s hill regions, the Ilocano, Tagalog, and Visayan migrants prepare a leaf infusion for menstrual cramps and to relieve flatulence, while in northern Luzon and Cordillera provinces healers recommend a strong decoction of the bark for coughs and fever (Antonio, 1993). In southern India’s Western Ghats, communities use crushed leaves as a poultice for bruises and sprains, and occasionally steep dried leaves to ease digestion and colic; these reports are noted in regional ethnobotanical compendia (Sinha, 1996; Arulappan et al., 2023). Across these regions the plant parts employed are bark for decoctions and infusions, and leaves for infusions and compresses; the indications typically involve respiratory complaints, digestive upset, rheumatic or muscular pain, and topical applications to inflamed tissues.
One practical preparation is a simple leaf infusion traditionally taken for colds and digestive sluggishness: place 2–3 g of dried leaves in 250 mL of just-boiled water, cover and steep for 10 minutes, strain, and drink 1 cup 1–2 times daily. As these preparations are traditionally warming, dose modestly and avoid exceeding this amount; pregnant women should avoid use unless under guidance of a qualified practitioner, and those with liver or kidney disease should consult a healthcare professional before consumption.
The aroma and reported warming effects of Neolitsea cassia stem from an essential oil rich in linalool, 1,8-cineole (eucalyptol), and methyleugenol, complemented by sesquiterpenes such as β-caryophyllene; these constituents show established anti-inflammatory, antispasmodic, and analgesic activities that plausibly underlie the reported applications in colds, cramps, and rheumatic discomfort (Davis & Weldon, 1998; Widyowati et al., 2019).
Today the dried bark and leaves are still available in regional herb shops across Fujian and the Western Ghats, and ongoing work explores the anti-inflammatory potential of leaf essential oils in laboratory models.
General Uses Top
Suggest a correction!Common products:
Fragrance and cosmetics:
Leaves are steam-distilled to yield a leaf essential oil. The oil is used in perfumery as a source of 1,8-cineole and related monoterpenes, contributing a fresh, cineolic note to fragrance compositions.
Properties relevant to use:
The leaf oil is reported to be rich in 1,8-cineole, with sabinene and α-pinene as significant constituents in some samples. These profiles are characteristic of cineole-type laurel leaf oils and explain the oil’s suitability for fragrance applications.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Laurus cassia | L. | Sp. Pl. : 369 (1753) |
| Persea cassia | (L.) Spreng. | Syst. Veg. 2: 267 (1825) |
| Balanopsis cassia | (L.) Raf. | Sylva Tellur. : 134 (1838) |
| Camphorina cassia | (L.) Farw. | Druggists' Circ. 62: 535 (1918) |
| Cinnamomum cassia | (L.) J.Presl | Prir. Rostlin 2: 44 (1825) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | grey bollywood |
| English | smooth-barb bollygum |
| Malayalam | വെള്ളക്കൊടല |
| Telugu | కుక్క కర్పూరమ |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Neolitsea cassia var. cassia | Unknown | |
| Neolitsea cassia var. rigescens | (Meisn.) Chakrab. | Phytotaxa 419(2): 209. 2019 |
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-tropical click to expand
-
Indian Subcontinent
- Assam
- India
- Sri Lanka
-
Indian Subcontinent
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0001248993 |
| Tropicos | 50148283 |
| KEW | urn:lsid:ipni.org:names:466940-1 |
| Open Tree Of Life | 573256 |
| NCBI Taxonomy | 230708 |
| IPNI | 466940-1 |
| iNaturalist | 427240 |
| GBIF | 4180148 |
| Freebase | /m/011f00p0 |
| USDA GRIN | 413303 |
| Wikipedia | Neolitsea_cassia |
| CMAUP | NPO31458 |
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 |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives | |||||
| 3-Phenylpropanal | 7707 | Click to see C1=CC=C(C=C1)CCC=O | 134.17 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives | |||||
| Protocatechuic Acid | 72 | Click to see | 154.12 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives | |||||
| 2-Methoxybenzaldehyde | 8658 | Click to see COC1=CC=CC=C1C=O | 136.15 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Styrenes | |||||
| Styrene | 7501 | Click to see C=CC1=CC=CC=C1 | 104.15 | unknown | via CMAUP database |
| > Benzenoids / Phenol ethers / Anisoles | |||||
| Anethole, (Z)- | 1549040 | Click to see CC=CC1=CC=C(C=C1)OC | 148.20 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Methoxyphenols | |||||
| Cassiferaldehyde | 44178761 | Click to see | 178.18 | unknown | via CMAUP database |
| Coniferaldehyde | 5280536 | Click to see | 178.18 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes | |||||
| Tetradecanal | 31291 | Click to see | 212.37 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Linalool | 6549 | Click to see | 154.25 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds | |||||
| phenylethyl-1-O-beta-D-apiofuranosyl-(1->4)-beta-D-glucopyranoside | 44178762 | Click to see | 416.40 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides | |||||
| Cinnacasolide A | 70692598 | Click to see | 446.40 | unknown | via CMAUP database |
| Cinnacasolide C | 70694646 | Click to see | 586.50 | unknown | via CMAUP database |
| Dihydromelilotoside | 5316728 | Click to see | 328.31 | unknown | via CMAUP database |
| Methyl Dihydromelilotoside | 46881368 | Click to see COC(=O)CCC1=CC=CC=C1OC2C(C(C(C(O2)CO)O)O)O | 342.34 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses | |||||
| Dihydrocinnacasside | 44178764 | Click to see C1=CC=C(C(=C1)CCC(=O)OC2C(C(C(C(O2)CO)O)O)O)O | 328.31 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides | |||||
| (1S,8R,10S)-3,8-dimethyl-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadeca-2(6),3,13(16)-trien-14-one | 163099902 | Click to see | 260.28 | unknown | https://doi.org/10.1016/S0040-4020(01)83309-3 |
| Linderalactone | 6450191 | Click to see | 244.28 | unknown |
https://doi.org/10.1021/NP100874F https://doi.org/10.1016/S0040-4020(01)83308-1 |
| Neolinderan | 595425 | Click to see | 260.28 | unknown | https://doi.org/10.1021/NP100874F |
| > Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes | |||||
| [(1R,4R,6S,7R,13S,14R)-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 | 162966188 | Click to see | 334.30 | unknown | https://doi.org/10.1016/S0040-4020(01)83310-X |
| > Phenylpropanoids and polyketides / Cinnamaldehydes | |||||
| 2-Hydroxycinnamaldehyde | 5318169 | Click to see | 148.16 | unknown | via CMAUP database |
| Cinnamaldehyde | 637511 | Click to see | 132.16 | unknown | via CMAUP database |
| cis-Cinnamaldehyde | 6428995 | Click to see | 132.16 | unknown | via CMAUP database |
| O-Methoxycinnamaldehyde, (E)- | 641298 | Click to see COC1=CC=CC=C1C=CC=O | 162.18 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters | |||||
| Ethyl cinnamate | 637758 | Click to see CCOC(=O)C=CC1=CC=CC=C1 | 176.21 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids | |||||
| Cinnamic acid | 444539 | Click to see C1=CC=C(C=C1)C=CC(=O)O | 148.16 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives / Coumaric acids | |||||
| 2-Methoxycinnamic acid | 734154 | Click to see COC1=CC=CC=C1C=CC(=O)O | 178.18 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| O-Coumaric Acid | 637540 | Click to see | 164.16 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamyl alcohols | |||||
| Cinnamyl Alcohol | 5315892 | Click to see | 134.17 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives | |||||
| Coumarin | 323 | Click to see | 146.14 | unknown | via CMAUP database |
| Thamnosmonin | 312089 | Click to see | 276.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids | |||||
| Procyanidin B | 130556 | Click to see | 578.50 | unknown | via CMAUP database |
| Procyanidin B1 | 11250133 | Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O | 578.50 | unknown | via CMAUP database |
| Procyanidin B2, (+)- | 122738 | Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O | 578.50 | unknown | via CMAUP database |
| Procyanidin C1 | 169853 | Click to see | 866.80 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates | |||||
| (-)-Epicatechin gallate | 107905 | Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O | 442.40 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |