Clausena heptaphylla

Details Top

Internal ID UUID6440119fc0609850233112
Scientific name Clausena heptaphylla
Authority Wight & Arn.
First published in Prodr. Fl. Ind. Orient. : 95 (1834)

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.

Across the northern Thai hills and southern China’s uplands, people prepare strong decoctions of fresh or dried leaves to soothe upset stomachs, diarrhea and abdominal colic. Among the Akha and Lahu of northern Thailand, villagers simmer the leaves and drink the broth for dysentery and upset stomach (Ruangsuttisuk, 1992). In southern China’s Yi, Hani and Dai communities, the leaves are boiled into a bitter decoction taken after meals to ease indigestion, diarrhea and stomach pain (Li et al., 2013). Across the border in northern Myanmar, hill farmers boil fresh leaves as a household tea to relieve gastrointestinal complaints (Anderson, 1986). The plant part used is consistent: leaves, picked fresh or sun‑dried, then boiled for 10–30 minutes. These infusion and decoction practices are recorded in the ethnobotanical literature, though variations in dose and timing are not always specified.

A practical way to prepare a safe, mild leaf decoction is to use the infusion rather than a long simmer. Place 10–15 g of fresh leaves (or 6–9 g dried) in a pot with 300–400 mL of water, bring to a boil, and then remove from heat. Cover and let steep 10–15 minutes, strain, and sip 1/2–1 cup, two to three times daily as needed for gastrointestinal upset. Dose depends on leaf age and variety; begin with smaller amounts and stop if nausea or dizziness occurs. The plant contains carbazole alkaloids (heptaphylline, girinimbine, ekeberine) and coumarins; there is no established safe dose for a tincture or concentrated extract in contemporary practice, and no evidence to support its use during pregnancy or breastfeeding. Keep decoctions mild; avoid long, heavy simmers that concentrate the bitterness and unknown constituents.

Phytochemically, Clausena heptaphylla is noted for carbazole alkaloids and furanocoumarins in the leaves; these classes are well reported for the species and have been studied for antibacterial, anti‑inflammatory and antispasmodic activities in vitro (Wu et al., 1999; Kumar et al., 2007; Reen et al., 2005). While such activity plausibly supports the traditional use for gastrointestinal discomfort, the preparations remain simple household remedies rather than standardized medicines.

Modern relevance includes ongoing laboratory work on the plant’s carbazole alkaloids and furanocoumarins and their antimicrobial and anti‑inflammatory properties, as well as small local tea or tonic markets that still use the leaf decoction for digestive upsets (Wu et al., 1999).

General Uses Top

Suggest a correction!

Common products:
- Leaf essential oil for fragrance applications (e.g., perfume bases and flavorings).

Industrial and craft applications:
- No established non-medicinal industrial uses documented.

Food and beverages (non-medicinal):
- No established non-medicinal food uses documented.

Colorants and tanning:
- No established non-medicinal colorant or tanning uses documented.

Wood and fiber:
- No established non-medicinal timber or fiber uses documented.

Fragrance and cosmetics:
- Leaves yield a volatile oil that is explored for perfumery and flavor use. Chemically, the oil is rich in coumarins (e.g., scopoletin, osthenol) and related phenylpropanoids typical of Rutaceae; sesquiterpenes and esters are present in varying proportions depending on origin and harvest time.

Properties relevant to use:
- Volatile constituents and coumarin-based chemistry confer characteristic odor and flavor notes suitable for blending in fragrance and flavor compositions; quantitative composition varies by habitat and processing.

Standards and regulation:
- No species-specific standards or regulatory frameworks beyond general fragrance and flavor safety and stability guidelines are documented.

Sustainability and sourcing:
- Harvested from wild or cultivated populations in parts of India and Southeast Asia; sustainability data remain limited to broad botanical surveys rather than targeted resource assessments.

Synonyms Top

Scientific name Authority First published in
Amyris anisata Roxb. ex Steud. Nomencl. Bot. , ed. 2, 1: 81 (1840)
Amyris heptaphylla Roxb. ex DC. Prodr. 2: 82 (1825)
Clausena heptaphylla var. engleri (Tanaka) Swingle J. Wash. Acad. Sci. 32: 26 1942
Clausena macrophylla Hook.f. Fl. Brit. India 1: 504 (1875)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

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
      • India
      • Nepal
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000608663
Tropicos 28100020
KEW urn:lsid:ipni.org:names:772136-1
The Plant List kew-2724804
Open Tree Of Life 5762742
NCBI Taxonomy 1392232
IUCN Red List 215235491
IPNI 772136-1
GBIF 3836901
EOL 2877899
USDA GRIN 10809
CMAUP NPO28407

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_040965395.1 ASM4096539v1 Scaffold Iridian Genomes 2024-07-30 60 357.16 Mb

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
Fractionation of Carlina acaulis L. Root Methanolic Extract as a Promising Path towards New Formulations against Bacillus cereus and Methicillin-Resistant Staphylococcus aureus Wnorowska S, Grzegorczyk A, Kurzepa J, Maggi F, Strzemski M Molecules 24-Apr-2024
PMCID:PMC11085459
doi:10.3390/molecules29091939
PMID:38731430
Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry Oliveira GD, McManus C, Vale IR, dos Santos VM Pathogens 18-Mar-2024
PMCID:PMC10974541
doi:10.3390/pathogens13030260
PMID:38535603
Editorial: From classical breeding to modern biotechnological advancement in horticultural crops - trait improvement and stress resilience Kumar P, Irfan M, Siddiqui MW, T R, Liao W Front Plant Sci 11-Oct-2023
PMCID:PMC10603224
doi:10.3389/fpls.2023.1293682
PMID:37900742
Sanitizing Hatching Eggs with Essential Oils: Avian and Microbiological Safety Oliveira GD, McManus C, de Araújo MV, de Sousa DE, de Macêdo IL, de Castro MB, dos Santos VM Microorganisms 26-Jul-2023
PMCID:PMC10456749
doi:10.3390/microorganisms11081890
PMID:37630450
Chemo-enzymatic synthesis and biological activity evaluation of propenylbenzene derivatives Hernik D, Szczepańska E, Ghezzi MC, Brenna E, Włoch A, Pruchnik H, Mularczyk M, Marycz K, Olejniczak T, Boratyński F Front Microbiol 26-Jun-2023
PMCID:PMC10330721
doi:10.3389/fmicb.2023.1223123
PMID:37434714
Use of stability statistics in the selection of Clausena heptaphylla (Roxb.) Wight & Arn for novel anethole rich strain (Jor Lab CH-2) Lal M, Munda S, Gogoi A, Begum T, Baruah J, Chanda SK, Lekhak H Front Plant Sci 14-Dec-2022
PMCID:PMC9794615
doi:10.3389/fpls.2022.1060492
PMID:36589129
3-Methoxy Carbazole Impedes the Growth of Human Breast Cancer Cells by Suppressing NF-κB Signaling Pathway Alanazi J, Unnisa A, Alanazi M, Alharby TN, Moin A, Rizvi SM, Hussain T, Awadelkareem AM, Elkhalifa AO, Faiyaz SS, Khalid M, Gowda DV Pharmaceuticals (Basel) 14-Nov-2022
PMCID:PMC9699412
doi:10.3390/ph15111410
PMID:36422540
Anethole rich Clausena heptaphylla (Roxb.) Wight & Arn., essential oil pharmacology and genotoxic efficiencies Lal M, Begum T, Gogoi R, Sarma N, Munda S, Pandey SK, Baruah J, Tamang R, Saikia S Sci Rep 15-Jun-2022
PMCID:PMC9200763
doi:10.1038/s41598-022-13511-8
PMID:35705583
Phyto-Carbazole Alkaloids from the Rutaceae Family as Potential Protective Agents against Neurodegenerative Diseases Tan MA, Sharma N, An SS Antioxidants (Basel) 01-Mar-2022
PMCID:PMC8944741
doi:10.3390/antiox11030493
PMID:35326143
Synthesis of indole derivatives as prevalent moieties present in selected alkaloids Heravi MM, Amiri Z, Kafshdarzadeh K, Zadsirjan V RSC Adv 15-Oct-2021
PMCID:PMC9042329
doi:10.1039/d1ra05972f
PMID:35497516
Traditional Herbal Medicines Against CNS Disorders from Bangladesh Uddin MJ, Zidorn C Nat Prod Bioprospect 14-Oct-2020
PMCID:PMC7648845
doi:10.1007/s13659-020-00269-7
PMID:33057963
Design, Synthesis and In Vitro Characterization of Novel Antimicrobial Agents Based on 6-Chloro-9H-carbazol Derivatives and 1,3,4-Oxadiazole Scaffolds Bordei Telehoiu AT, Nuță DC, Căproiu MT, Dumitrascu F, Zarafu I, Ioniță P, Bădiceanu CD, Avram S, Chifiriuc MC, Bleotu C, Limban C Molecules 09-Jan-2020
PMCID:PMC7024163
doi:10.3390/molecules25020266
PMID:31936505
Clausmarin A, Potential Immunosuppressant Revealed by Yeast-Based Assay and Interleukin-2 Production Assay in Jurkat T Cells Suauam P, Yingyongnarongkul BE, Palaga T, Miyakawa T, Yompakdee C PLoS One 27-Aug-2015
PMCID:PMC4552291
doi:10.1371/journal.pone.0136804
PMID:26313553
In vitro and in vivo anti-angiogenic activity of girinimbine isolated from Murraya koenigii Iman V, Karimian H, Mohan S, Hobani YH, Noordin MI, Mustafa MR, Noor SM Drug Des Devel Ther 03-Mar-2015
PMCID:PMC4354401
doi:10.2147/DDDT.S71557
PMID:25767375
Simultaneous determination of nine analytes in Clausena harmandiana Pierre. by new developed high-performance liquid chromatography method and the influence of locations in Thailand on level of nordentatin and dentatin Wangboonskul J, Tunsirikongkon A, Sasithornwetchakun W Pharmacogn Mag 01-Jan-2015
PMCID:PMC4329607
doi:10.4103/0973-1296.149666
PMID:25709203

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 / Anthracenes / Anthraquinones
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1016/S0031-9422(00)88768-3
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.1002/RECL.19470660608
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
1-(p-Methoxyphenyl)-2-propanone 31231 Click to see 164.20 unknown https://doi.org/10.1002/RECL.19470660608
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see 148.20 unknown https://doi.org/10.1080/10412905.1992.9698154
https://doi.org/10.1002/RECL.19470660608
Estragole 8815 Click to see 148.20 unknown https://doi.org/10.1002/RECL.19470660608
https://doi.org/10.1080/10412905.1992.9698154
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Neranic acid 5312583 Click to see 168.23 unknown https://doi.org/10.1080/10575639908045434
https://doi.org/10.1016/S0367-326X(00)00320-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Boydone B 73346125 Click to see CCC(C)C1=C(C(C(C1=O)(C)CC)O)OC 226.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Elemene 80048 Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1002/RECL.19470660608
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Pseudacyclin A 46848855 Click to see 739.90 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
D-Lactic Acid 61503 Click to see 90.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3S,4R,5S)-4-Hydroxy-5-methoxy-4-((2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl)-1-oxaspiro(2.5)octan-6-one 10957430 Click to see 296.36 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
1-Methoxy-3-methyl-9H-carbazole 375150 Click to see CC1=CC2=C(C(=C1)OC)NC3=CC=CC=C32 211.26 unknown https://doi.org/10.1016/0031-9422(73)80423-6
10-hydroxy-3,3-dimethyl-2,11-dihydro-1H-pyrano[3,2-a]carbazole-5-carbaldehyde 14282355 Click to see 295.30 unknown https://doi.org/10.1016/S0031-9422(00)80575-0
3-Methylcarbazole 20746 Click to see 181.23 unknown https://doi.org/10.1016/S0031-9422(00)91444-4
Clausenal 10377645 Click to see COC1=CC=CC2=C1NC3=C2C=C(C=C3OC)C=O 255.27 unknown https://doi.org/10.1016/0031-9422(94)00666-H
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Mevalonolactone 6419891 Click to see 130.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-hydroxy-2,2-dimethyl-6-(2-methylbut-3-en-2-yl)-3H-pyrano[2,3-h]chromene-4,8-dione 10404227 Click to see 328.40 unknown https://doi.org/10.1016/S0040-4039(01)89728-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(3R,6R,8R)-6-(2-hydroxypropan-2-yl)-3-methyl-14-(2-methylbut-3-en-2-yl)-2,7,16-trioxatetracyclo[8.8.0.03,8.012,17]octadeca-1(10),11,13,17-tetraen-15-one 92272919 Click to see 398.50 unknown https://doi.org/10.1016/S0367-326X(00)00320-8
5-hydroxy-2,2-dimethyl-3H-pyrano[3,2-g]chromene-4,8-dione 5315948 Click to see 260.24 unknown https://doi.org/10.1016/S0040-4039(01)89728-8
Clausmarin A 49940 Click to see CC12CCC(OC1CC3=C(O2)C=C4C(=C3)C=C(C(=O)O4)C(C)(C)C=C)C(C)(C)O 398.50 unknown https://doi.org/10.1016/S0305-1978(99)00035-6
https://doi.org/10.1016/S0367-326X(00)00320-8
> Phenylpropanoids and polyketides / Depsides and depsidones
Botryorhodine C 46916752 Click to see CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C(=CC(=C3C)O)C)CO)O 316.30 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.