Bergera kwangsiensis

Details Top

Internal ID UUID68f9145ff4100412841658
Scientific name Bergera kwangsiensis
Authority (C.C.Huang) F.J.Mou
First published in Eur. J. Taxon. 860: 163 2023

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.

Species name: Bergera koenigii (commonly called curry leaf). In several regional treatments the name is listed under the synonym Murraya koenigii; therefore, the traditional records below refer to this same plant (Kumar et al., 2020).

Traditional uses. Across northern India, infusions and decoctions of the leaves are taken to support digestion and ease dyspepsia (Meena et al., 2010; Khare, 2007). In rural Bangladesh and West Bengal, crushed fresh leaves are applied topically as poultices to minor cuts and insect bites, often first sterilizing with warm water (Chanda et al., 2018). In the drier rural north of Thailand and among Tamil-speaking communities in southern India, leaves are infused as a mild diuretic tea for occasional fluid retention (Saundarya et al., 2013). In Sri Lanka’s rural areas, leaf decoctions are used for occasional bouts of diarrhea and to “settle the stomach,” with doses adjusted by age (Kumar et al., 2020). These records all specify the part used as leaves (often fresh, sometimes dried), and the preparation method as infusions, decoctions, or maceration for poultice. Collections that consolidate ethnomedical literature across the subcontinent—Siddiqui et al., 2020; Chanda et al., 2018—report similar leaf-based uses.

One practical recipe. To make a mild leaf infusion, place about 2–3 g of clean fresh leaves (roughly 1 to 1.5 teaspoons, loosely packed) in a cup of near‑boiling water, cover, and steep for 5–10 minutes before straining. Many Indian sources report daily use of a cup or two for digestive support (Khare, 2007). As a topical compress, macerate a handful of fresh leaves, crush to a fine mash, and place between clean cloth layers; apply gently to clean skin for 10–20 minutes, repeating up to twice daily as needed (Chanda et al., 2018). For a 1:5 ethanol tincture, pack a jar loosely with 20 g of chopped fresh leaves, cover with 100 mL of 45% ethanol, seal, and macerate in the dark for 14 days with daily gentle agitation, then strain; commonly used tincture volumes are 10–15 drops taken as needed, and it is generally avoided in pregnancy and lactation because safety data are limited (Khare, 2007; Meena et al., 2010).

Active constituents. Phytochemical studies on this species consistently report essential‑oil terpenoids and related nonvolatile metabolites: limonene, β‑pinene, α‑pinene, caryophyllene, pinenes, β‑phellandrene, and sabinene; along with carbazole alkaloids such as mahanimbine, koenimbine, and mahanine (Miller et al., 2003; Jirovetz et al., 2003; Chanda et al., 2018). These constituents are widely present in leaves and plausibly account for the antimicrobial, spasmolytic, and carminative actions traditionally attributed to leaf infusions and decoctions.

Modern relevance. Indian and Sri Lankan commercial supplies of dried leaves remain common and are used domestically for both culinary and medicinal purposes, while recent lab work continues to profile the essential‑oil components and mahanimbine‑type alkaloids that underpin the species’ documented activities (Jirovetz et al., 2003; Chanda et al., 2018).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Clausena kwangsiensis C.C.Huang Acta Phytotax. Sin. 8: 90 (1959)
Murraya kwangsiensis (C.C.Huang) C.C.Huang Acta Phytotax. Sin. 16(2): 85 (1978)

Common names Top

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Language Common/alternative name
Chinese 广西九里香
Chinese 广西九里香根
Chinese 廣西九里香

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Varieties (abbr. var.) 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
Tropicos 50119332
KEW urn:lsid:ipni.org:names:774434-1
The Plant List tro-50119332
Open Tree Of Life 710089
NCBI Taxonomy 354505
IPNI 774434-1
GBIF 7269468
EOL 2907545
CMAUP NPO16307
World Flora Online wfo-1000057350

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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Title Authors Publication Released IDs
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
Molecular differentiation of the Murraya paniculata Complex (Rutaceae: Aurantioideae: Aurantieae) Nguyen CH, Beattie GA, Haigh AM, Astuti IP, Mabberley DJ, Weston PH, Holford P BMC Evol Biol 30-Dec-2019
PMCID:PMC6937641
doi:10.1186/s12862-019-1555-4
PMID:31888450
Studies on chemical constituents of Rabdosia serra ZHENG Qin China Journal of Chinese Materia Medica 22-Sep-2011
doi:10.4268/CJCMM20111611

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Neral 643779 Click to see 152.23 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
I2-Ionone 638014 Click to see 192.30 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin acetate 92842 Click to see 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid 18413781 Click to see 258.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
[(1E)-2,6-dimethylhepta-1,5-dienyl] acetate 24832062 Click to see 182.26 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see 152.23 unknown via CMAUP database
Hexanal 6184 Click to see 100.16 unknown via CMAUP database
trans-2-Hexenal 5281168 Click to see 98.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4-(2-Aminophenyl)-2-ammonio-4-oxobutanoate 25245862 Click to see 208.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(3R)-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 92153432 Click to see 347.40 unknown via CMAUP database
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/10.4268/CJCMM20111611
3,8-Dimethyl-3-(4-methylpent-3-en-1-yl)-3,11-dihydropyrano(3,2-a)carbazol-9-ol 375148 Click to see 347.40 unknown https://doi.org/10.4268/CJCMM20111611
7-(8-hydroxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-7-yl)-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-8-ol 5318907 Click to see 556.60 unknown https://doi.org/10.4268/CJCMM20111611
Koenine 5318827 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=C(C=C4)O 279.30 unknown https://doi.org/10.4268/CJCMM20111611
Murrayanine 96942 Click to see 225.24 unknown https://doi.org/10.4268/CJCMM20111611
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see 170.25 unknown via CMAUP database
Gamma-dodecalactone, (R)- 10888889 Click to see 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide, cis- 6428573 Click to see 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-[(7R,8S)-8-(hydroxymethyl)-4-methoxy-16,16,19-trimethyl-6,17-dioxa-11-azapentacyclo[10.8.0.02,10.05,9.013,18]icosa-1(12),2,4,9,13(18),14,19-heptaen-7-yl]-2,6-dimethoxyphenol 638195 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C5C(C(OC5=C(C=C24)OC)C6=CC(=C(C(=C6)OC)O)OC)CO 517.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317050 Click to see 544.50 unknown via CMAUP database
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see 544.50 unknown via CMAUP database
(1S,5S,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317051 Click to see 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see 664.60 unknown via CMAUP database
Mahuannin A 5317052 Click to see 544.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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