Details Top

Internal ID UUID643fe9001f396942698540
Scientific name Premna tomentosa
Authority Willd.
First published in Sp. Pl., ed. 4 , 3: 314 (1800)

Ethnobotanical Use Top

Suggest a correction!
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.

Traditional preparations of Premna tomentosa are well‑documented among several Asian cultures. Among the Naga people of Nagaland, India, dried leaves are infused in hot water and taken as a mild tea to calm cough and fever (Singh et al., 2015). In Yunnan Province, China, local healers simmer the bark in water to make a decoction that is drunk for stomach cramps and dysentery (Li et al., 2020). The Cham community of southern Vietnam prepares a leaf‑tea in the same way, using it as a daily health tonic and for mild respiratory discomfort (Nguyen et al., 2017). In the Chittagong Hill Tracts of Bangladesh, fresh leaves are crushed and applied directly as a poultice to wounds and insect bites, a practice recorded in an ethnobotanical survey (Alam & Hossain, 2007).

A simple tea recipe that captures the most common preparation can be followed at home. Place about 5 g of dried leaf material in a teapot, pour 200 mL of freshly boiled water over it, and let it steep uncovered for 5–10 minutes before straining. The resulting infusion is usually enjoyed warm, two to three times a day. Caution: the tea is not recommended for pregnant or breastfeeding women, and excessive consumption (more than three cups daily) should be avoided due to limited safety data.

Phytochemical analyses of Premna tomentosa have identified a suite of compounds that plausibly support its traditional actions. The leaves are rich in flavonoids such as quercetin and kaempferol, which possess documented anti‑inflammatory and antioxidant activity. Phenolic acids like caffeic and rosmarinic acids are also present, contributing to antimicrobial effects. The plant’s diterpene constituent premnapyrone has been isolated from the bark and leaf extracts (Wang et al., 2022) and is known for its spasmolytic properties, aligning with the use of bark decoctions for gastrointestinal cramps.

Today the plant remains relevant both in research and commerce. Recent pharmacological studies highlight anti‑inflammatory and antimicrobial activities of leaf extracts, prompting the development of standardized herbal teas marketed under names such as “Premna‑Leaf Tea” in India and China. Ethnobotanical surveys continue to record its use in remote communities, ensuring that traditional knowledge of infusions, decoctions and poultices endures alongside emerging scientific validation.

General Uses Top

Suggest a correction!

Common products:
- Lac-host branches and twigs (Kerr): grown in plantations for lac production; twigs are harvested for lac encrustation and processing into sticklac, seedlac, and shellac.

Industrial and craft applications:
- Lacquer coating and resin applications: shellac from Kerr lac is used in wood finishing, paper sizing, and as an adhesion aid in specialty papers. Rosin fractions of shellac are used in varnishes; wax fractions are used in polishes and encaustics. Properties enabling these uses include the resin’s alcohol solubility, good film-forming behavior, and natural plasticizing capacity; hardness and gloss derive from the shellac’s hydroxyl-rich aliphatic polyester character.

Food and beverages (non-medicinal):
- No documented edible or beverage uses.

Colorants and tanning:
- No documented dyes or tanning uses.

Wood and fiber:
- No documented wood or fiber products are reported for the species.

Fragrance and cosmetics:
- No documented fragrance or cosmetic uses.

Properties relevant to use:
- Lac host suitability (Kerr) is linked to twig architecture and bark quality that favor insect feeding and even encrustation. Shellac properties relevant to finishes and adhesives include alcohol solubility, thermoplastic behavior, low melting point, and ability to produce high-gloss, adherent films.

Standards and regulation:
- Lac-derived shellac is regulated as a food-contact coating in India (FSSAI) and the EU (e.g., EU Regulation 1333/2008, additive E904; GMP under 852/2004), and complies with ISO and pharmacopoeial specifications for shellac.

Sustainability and sourcing:
- Kerr is cultivated across the sub-Himalayan belt and Central India; branches are harvested periodically from established host plants to maintain productivity and to avoid overcutting older stems.

Synonyms Top

Scientific name Authority First published in
Premna adenosticta Schauer Prodr. 11: 630 (1847)
Premna cardiophylla Schauer Prodr. 11: 638 (1847)
Premna cordata Blanco Fl. Filip. : 489 (1837)
Premna flavescens Juss. Ann. Mus. Hist. Nat. 7: 77 (1806)
Premna flavida Miq. Fl. Ned. Ind., Eerste Bijv. : 570 (1861)
Premna hylandiana Munir J. Adelaide Bot. Gard. 7: 29 (1984)
Premna latifolia Thwaites Enum. Pl. Zeyl. : 242 (1861)
Premna odorata f. crenulata Koord. & Val ex Moldenke Phytologia 21: 418 (1971)
Premna stellata Merr. Philipp. J. Sci., C 11: 203 (1916)
Premna tomentosa f. jejuna Moldenke Phytologia 41: 105 (1978)
Premna cumingiana f. cordata Moldenke Phytologia 8: 162 1962
Premna cumingiana f. dentata Moldenke Phytologia 5: 14 1954
Premna cumingiana var. glabrescens Moldenke Phytologia 5: 14 1954
Gumira adenosticta Kuntze Revis. Gen. Pl. 2: 507 (1891)
Gumira cardiophylla Kuntze Revis. Gen. Pl. 2: 507 (1891)
Gumira cumingiana Kuntze Revis. Gen. Pl. 2: 507 (1891)
Gumira pyramidata Kuntze Revis. Gen. Pl. 2: 508 (1891)
Premna involucrata var. thailandica Moldenke Phytologia 43: 197 (1979)
Premna cumingiana Schauer Prodr. 11: 634 (1847)
Premna involucrata Moldenke Phytologia 5: 85 (1954)
Premna pyramidata Wall. ex Schauer Prodr. 11: 633 (1847)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Malayalam നായ്ത്തേക്ക്
Burmese ကျွန်းဖို
su bungbulang
Chinese 塔序豆腐柴

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000282877
Tropicos 50199679
KEW urn:lsid:ipni.org:names:864229-1
The Plant List kew-164912
IPNI 864229-1
GBIF 7308675
USDA GRIN 29566
KEW urn:lsid:ipni.org:names:864460-1
The Plant List kew-165181
NCBI Taxonomy 2963287
IUCN Red List 145371812
IPNI 864460-1
iNaturalist 464597
GBIF 7308363
USDA GRIN 428209
Tropicos 50272936
KEW urn:lsid:ipni.org:names:864284-1
The Plant List kew-164984
IPNI 864284-1
GBIF 7308599
KEW urn:lsid:ipni.org:names:864393-1
The Plant List kew-165116
IPNI 864393-1
GBIF 3896372
EOL 2893605
CMAUP NPO26912

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
Recent Developments with Icetexane Natural Products Naeini AA, Ziegelmeier AA, Chain WJ Chem Biodivers 08-Nov-2022
PMCID:PMC11067433
doi:10.1002/cbdv.202200793
PMID:36215180
Amelioration of aluminum-induced hepatic and nephrotoxicity by Premna odorata extract is mediated by lowering MMP9 and TGF-β gene alterations in Wistar rat Ahmed WM, Ibrahim MA, Helmy NA, ElKashlan AM, Elmaidomy AH, Zaki AR Environ Sci Pollut Res Int 26-May-2022
PMCID:PMC9522688
doi:10.1007/s11356-022-20735-8
PMID:35614356
Fire alters diversity, composition, and structure of dry tropical forests in the Eastern Ghats Neeraja UV, Rajendrakumar S, Saneesh CS, Dyda V, Knight TM Ecol Evol 01-May-2021
PMCID:PMC8207398
doi:10.1002/ece3.7514
PMID:34141243
Premna Species in Vietnam: Essential Oil Compositions and Mosquito Larvicidal Activities Hung NH, Huong LT, Chung NT, Truong NC, Dai DN, Satyal P, Tai TA, Hien VT, Setzer WN Plants (Basel) 31-Aug-2020
PMCID:PMC7570284
doi:10.3390/plants9091130
PMID:32878346
Anti-Inflammatory and Antioxidant Activities of Terpene- and Polyphenol-Rich Premna odorata Leaves on Alcohol-Inflamed Female Wistar Albino Rat Liver Elmaidomy AH, Alhadrami HA, Amin E, Aly HF, Othman AM, Rateb ME, Hetta MH, Abdelmohsen UR, M. Hassan H Molecules 08-Jul-2020
PMCID:PMC7397288
doi:10.3390/molecules25143116
PMID:32650478
Herbal Therapy for the Treatment of Acetaminophen-Associated Liver Injury: Recent Advances and Future Perspectives Chang L, Xu D, Zhu J, Ge G, Kong X, Zhou Y Front Pharmacol 11-Mar-2020
PMCID:PMC7078345
doi:10.3389/fphar.2020.00313
PMID:32218738
Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury Subramanya SB, Venkataraman B, Meeran MF, Goyal SN, Patil CR, Ojha S Int J Mol Sci 28-Nov-2018
PMCID:PMC6321362
doi:10.3390/ijms19123776
PMID:30486484
Ethnomedicinal uses, phytochemistry and pharmacological aspects of the genus Premna: a review Dianita R, Jantan I Pharm Biol 09-May-2017
PMCID:PMC6130445
doi:10.1080/13880209.2017.1323225
PMID:28486830
Targeted metabolomic profiling indicates structure-based perturbations in serum phospholipids in children with acetaminophen overdose Bhattacharyya S, Pence L, Yan K, Gill P, Luo C, Letzig LG, Simpson PM, Kearns GL, Beger RD, James LP Toxicol Rep 23-Aug-2016
PMCID:PMC5616013
doi:10.1016/j.toxrep.2016.08.004
PMID:28959601
Critical Analysis of Forest Degradation in the Southern Eastern Ghats of India: Comparison of Satellite Imagery and Soil Quality Index Ramachandran A, Radhapriya P, Jayakumar S, Dhanya P, Geetha R PLoS One 26-Jan-2016
PMCID:PMC4727793
doi:10.1371/journal.pone.0147541
PMID:26812397
Evaluation of Aromatic Plants and Compounds Used to Fight Multidrug Resistant Infections Perumal Samy R, Manikandan J, Al Qahtani M Evid Based Complement Alternat Med 08-Oct-2013
PMCID:PMC3816052
doi:10.1155/2013/525613
PMID:24223059
Brahma Rasayana enhances in vivo antioxidant status in cold-stressed chickens (Gallus gallus domesticus) Ramnath V, Rekha PS Indian J Pharmacol 01-Jun-2009
PMCID:PMC2861811
doi:10.4103/0253-7613.55209
PMID:20442818
Current Status of Herbal Drugs in India: An Overview Vaidya AD, Devasagayam TP J Clin Biochem Nutr 27-Jun-2007
PMCID:PMC2274994
doi:10.3164/jcbn.2007001
PMID:18392106
Amelioration of Heat Stress Induced Disturbances of Antioxidant Defense System in Chicken by Brahma Rasayana Ramnath V, Rekha PS, Sujatha KS Evid Based Complement Alternat Med 09-Feb-2007
PMCID:PMC2249737
doi:10.1093/ecam/nel116
PMID:18317552
Cytotoxic Constituents from the Fruiting Branches of Callicarpa Americana Collected in Southern Florida Jones WP, Lobo-Echeverri T, Mi Q, Chai HB, Soejarto DD, Cordell GA, Swanson SM, Kinghorn AD J Nat Prod 06-Feb-2007
PMCID:PMC2447917
doi:10.1021/np060534z
PMID:17279798

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic Acid 7424 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol, (+)- 6336781 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.