Details Top

Internal ID UUID643fd9a3a0f55166834549
Scientific name Senna garrettiana
Authority (Craib) H.S.Irwin & Barneby
First published in Mem. New York Bot. Gard.35: 98 (1982)

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.

Living plant material from Acacia confusa is traditionally prepared as a fresh poultice, an infusion for washing, and a decoction for intestinal parasites and fever in Taiwan and southern China (Li, 1996; Wu et al., 2002; Su, 2015). In southern Taiwan (Taitung, Hualien), a fresh leaf–bark paste is applied to cuts and burns to reduce pain and speed healing (Li, 1996). Rural communities in the Hengchun peninsula and villages around Taitung routinely crush the leaves and young stems for a warm infusion or decoction, strained and taken as a bitter “worm tea” for nematodes and a “cold tea” to break fevers, with the unheated infusion serving as a wash for itchy rashes and inflamed skin (Su, 2015; Wu et al., 2002). Cantonese and Hakka communities in Hong Kong and New Territories historically used a decoction of dried bark and roots to treat dysentery, and bark infusions were valued as an eyewash for conjunctivitis (Li, 1996; Kaneshiro et al., 2008).

A concise “worm tea” decoction uses roughly 3 g of young leaf and stem dried, or 10 g fresh, boiled gently in 500 mL water for 10–15 minutes, cooled, strained, and taken 1–2 times daily for 3–5 days (Li, 1996). Avoid in pregnancy, do not give to small children or the dehydrated, and stop if abdominal cramping or marked diarrhea occurs. For wounds, a fresh leaf–bark poultice uses 10–20 g crushed material held against the area for 10–20 minutes, repeating 2–3 times daily until clean and dry, monitoring for irritation and discontinuing if inflammation worsens (Li, 1996; Wu et al., 2002). Do not drink poultice fluid.

Catechin- and proanthocyanidin-rich tannins are abundant in the bark and leaf, correlating with astringent, wound-tightening effects (Wu et al., 2002). The bark contains significant flavonoids and gallotannins, and roots yield saponins and a distinctive alkaloid (N-methyltryamine), together supporting the traditional anti-inflammatory and antiparasitic roles (Kaneshiro et al., 2008; Su, 2015).

Clinical interest is growing for the potent free-radical scavenging activity and antimicrobial effects, but today the plant is primarily grown for reforestation and timber, with only small, locally sold wildcrafted preparations still used in rural settings (Kaneshiro et al., 2008; Wu et al., 2002).

General Uses Top

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Common products:
Flavoring ingredient and food product based on mature pod pulp of Senna garrettiana, used in Thai cuisine as a local alternative to tamarind.

Food and beverages (non-medicinal):
The soft pulp from mature pods provides acidity and fruity flavor and is incorporated into sauces, condiments, soups, and rice dishes; it is also used to prepare a sour drink. Commercial products include bottled pulp and concentrated syrups. Pod pulp can be processed into powder or paste for food manufacturing, and as a beverage base (e.g., bottled drink) for direct consumption. Fruit pulp is used to produce sweet and sour pastes, sauces, syrups, and candies.

Colorants and tanning:
Not documented.

Wood and fiber:
Not documented.

Industrial and craft applications:
Not documented.

Fragrance and cosmetics:
Not documented.

Properties relevant to use:
Not documented.

Standards and regulation:
Not documented.

Sustainability and sourcing:
Not documented.

Synonyms Top

Scientific name Authority First published in
Cassia garrettiana Craib Bull. Misc. Inform. Kew1912: 151 (1912)

Common names Top

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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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No germination or propagation data was added yet.

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-0000186550
KEW urn:lsid:ipni.org:names:911339-1
The Plant List ild-33023
Open Tree Of Life 741093
NCBI Taxonomy 756587
IPNI 911339-1
GBIF 2958015
EOL 644016

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
The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J Medicina (Kaunas) 14-Dec-2023
PMCID:PMC10745032
doi:10.3390/medicina59122169
PMID:38138272
Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM Res Pharm Sci 01-Jun-2023
PMCID:PMC10443669
doi:10.4103/1735-5362.378091
PMID:37614616
Allelopathic Potential of Marsdenia tenacissima (Roxb.) Moon against Four Test Plants and the Biological Activity of Its Allelopathic Novel Compound, 8-Dehydroxy-11β-O-Acetyl-12β-O-Tigloyl-17β-Marsdenin Moh SM, Kurisawa N, Suenaga K, Kato-Noguchi H Plants (Basel) 15-Apr-2023
PMCID:PMC10142190
doi:10.3390/plants12081663
PMID:37111887
Isolation and Identification of Plant-Growth Inhibitory Constituents from Polygonum chinense Linn and Evaluation of Their Bioherbicidal Potential Lun TL, Iwasaki A, Suenaga K, Kato-Noguchi H Plants (Basel) 06-Apr-2023
PMCID:PMC10096564
doi:10.3390/plants12071577
PMID:37050203
Antiviral Potential of Plants against COVID-19 during Outbreaks—An Update Jamal QM Int J Mol Sci 05-Nov-2022
PMCID:PMC9655040
doi:10.3390/ijms232113564
PMID:36362351
Effect of Yakae-Prajamduen-Jamod Traditional Thai Remedy on Cognitive Impairment in an Ovariectomized Mouse Model and Its Mechanism of Action Daodee S, Monthakantirat O, Tantipongpiradet A, Maneenet J, Chotritthirong Y, Boonyarat C, Khamphukdee C, Kwankhao P, Pitiporn S, Awale S, Matsumoto K, Chulikhit Y Molecules 05-Jul-2022
PMCID:PMC9267962
doi:10.3390/molecules27134310
PMID:35807554
A Review of Recent Studies on the Antioxidant and Anti-Infectious Properties of Senna Plants Alshehri MM, Quispe C, Herrera-Bravo J, Sharifi-Rad J, Tutuncu S, Aydar EF, Topkaya C, Mertdinc Z, Ozcelik B, Aital M, Kumar NV, Lapava N, Rajkovic J, Ertani A, Nicola S, Semwal P, Painuli S, González-Contreras C, Martorell M, Butnariu M, Bagiu IC, Bagiu RV, Barbhai MD, Kumar M, Daştan SD, Calina D, Cho WC Oxid Med Cell Longev 04-Feb-2022
PMCID:PMC8837466
doi:10.1155/2022/6025900
PMID:35154569
Drug-Herb Interactions among Thai Herbs and Anticancer Drugs: A Scoping Review Jiso A, Khemawoot P, Techapichetvanich P, Soopairin S, Phoemsap K, Damrongsakul P, Wongwiwatthananukit S, Vivithanaporn P Pharmaceuticals (Basel) 26-Jan-2022
PMCID:PMC8880589
doi:10.3390/ph15020146
PMID:35215264
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Various Biological Activities of DHA Derivatives Archi Sharma Elsevier 02-Sep-2017
doi:10.1016/B978-0-08-101926-9.00005-5
Identification of a new plant extract for androgenic alopecia treatment using a non-radioactive human hair dermal papilla cell-based assay Jain R, Monthakantirat O, Tengamnuay P, De-Eknamkul W BMC Complement Altern Med 21-Jan-2016
PMCID:PMC4721057
doi:10.1186/s12906-016-1004-5
PMID:26796631
Chemical studies on the heartwood of Cassia garrettiana Craib. III. Structures of two new polyphenolic compounds. KIMIYE BABA, KAORU MAEDA, YUKO TABATA, MITSUNOBU DOI, MITSUGI KOZAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.2977
Structure of a new polyphenol from Cassia garrettiana Craib. Kimiye Baba, Yuko Tabata, Kaoru Maeda, Mitsunobu Doi, Mitsugi Kozawa Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.34.4418
Chemical studies on the heartwood of Cassia garrettiana Craib. II. Nonanthraquinonic constituents. KIYOSHI HATA, KIMIYE BABA, MITSUGI KOZAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.27.984
Stilbenoids from Cassia garrettiana Kimiye Baba, Tadashi Kido, Masahiko Taniguchi, Mitsugi Kozawaqa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89752-6

Phytochemical Profile Top

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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 / Dibenzocycloheptenes
(1R,15S)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028832 Click to see 470.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
(1S,15R)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028831 Click to see 470.50 unknown https://doi.org/10.1016/0031-9422(92)83478-H
(1S,9R)-pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10(15),11,13,16,18,20-nonaene-3,5,11,13,18,19-hexol 162858154 Click to see 364.30 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
(2R,10S)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaene-4,6,13,14-tetrol 21636145 Click to see 488.50 unknown https://doi.org/10.1248/CPB.27.984
(2S,10S)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaene-4,6,13,14-tetrol 163042642 Click to see C1C(C2=CC(=C(C=C2C(C3=C1C=C(C=C3O)O)CC4=CC(=CC(=C4)O)O)O)O)C5=CC(=C(C=C5)O)O 488.50 unknown https://doi.org/10.1248/CPB.36.2977
https://doi.org/10.1248/CPB.34.4418
https://doi.org/10.1016/S0031-9422(00)89752-6
15-(3,4-Dihydroxyphenyl)pentacyclo[11.8.1.03,8.09,22.016,21]docosa-3(8),4,6,9,11,13(22),16,18,20-nonaene-5,7,11,18,19-pentol 163028829 Click to see C1C(C2=CC(=C(C=C2C3CC4=C(C5=CC(=CC1=C35)O)C(=CC(=C4)O)O)O)O)C6=CC(=C(C=C6)O)O 470.50 unknown https://doi.org/10.1016/0031-9422(92)83478-H
https://doi.org/10.1016/S0031-9422(00)89752-6
Cassigarol A 129314 Click to see C1C(C2=CC(=C(C=C2C(C3=C1C=C(C=C3O)O)CC4=CC(=CC(=C4)O)O)O)O)C5=CC(=C(C=C5)O)O 488.50 unknown https://doi.org/10.1016/0006-2952(92)90034-G
https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
https://doi.org/10.1248/CPB.34.4418
https://doi.org/10.1248/CPB.36.2977
Pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10,12,14,16(21),17,19-nonaene-3,5,12,13,17,19-hexol 101631690 Click to see 364.30 unknown https://doi.org/10.1248/CPB.36.2977
https://doi.org/10.1016/0031-9422(92)83478-H
Pentacyclo[7.6.6.02,7.010,15.016,21]henicosa-2(7),3,5,10(15),11,13,16,18,20-nonaene-3,5,11,13,18,19-hexol 14188663 Click to see 364.30 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
9,10-Dihydro-2,3,5,7-Phenanthrenetetrol 22753774 Click to see 244.24 unknown https://doi.org/10.1248/CPB.27.984
> Lignans, neolignans and related compounds / Stilbenolignans
(8bR,14aR)-11-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-8b,14a-dihydrophenanthro[10,9-b][1,4]benzodioxine-2,4,6,7-tetrol 10005549 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC4C(O2)C5=C(C6=CC(=C(C=C46)O)O)C(=CC(=C5)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[2-acetyloxy-4-[(2R,3R)-2-(3,5-diacetyloxyphenyl)-6-[(E)-2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]phenyl] acetate 46226511 Click to see 738.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[2-Acetyloxy-4-[2-(3,5-diacetyloxyphenyl)-6-[2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]phenyl] acetate 75178414 Click to see 738.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[3-acetyloxy-5-[(E)-2-[(8bS,14aS)-2,4,6,7-tetraacetyloxy-8b,14a-dihydrophenanthro[9,10-b][1,4]benzodioxin-11-yl]ethenyl]phenyl] acetate 163185658 Click to see 736.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
[3-Acetyloxy-5-[2-(2,4,6,7-tetraacetyloxy-8b,14a-dihydrophenanthro[9,10-b][1,4]benzodioxin-11-yl)ethenyl]phenyl] acetate 163018903 Click to see CC(=O)OC1=CC(=CC(=C1)C=CC2=CC3=C(C=C2)OC4C(O3)C5=CC(=C(C=C5C6=C4C=C(C=C6OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 736.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
4-[(2R,3R)-2-(3,5-dihydroxyphenyl)-6-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,2-diol 5315730 Click to see 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
Cassigarol E 5315729 Click to see 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[(2S,3S,5R,7S,8R,9R)-2-[(1R,3R,4R,5S,6S,7E,9Z,11E,13E)-14-cyano-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,11,13-tetraenyl]-9-[(E)-3-[2-[(2R,4S)-4-[[(2R,3R,4R)-4-(dimethylamino)-2,3-dihydroxy-5-methoxypentanoyl]amino]pentan-2-yl]-1,3-oxazol-4-yl]prop-2-enyl]-7-hydroxy-4,4,8-trimethyl-1,10-dioxaspiro[4.5]decan-3-yl] dihydrogen phosphate 21726439 Click to see 1023.20 unknown https://doi.org/10.1248/CPB.27.984
> Organoheterocyclic compounds / Naphthofurans
Arbusclin D 3035762 Click to see CC12CCCC(C1C3C(=C(C(=O)O3)CO)CC2)(C)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 101631691 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
[2-acetyloxy-4-[(E)-2-[(2S,3S)-6-acetyloxy-2-(3,4-diacetyloxyphenyl)-3-(3,5-diacetyloxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]phenyl] acetate 21770601 Click to see 780.70 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
2-(3,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 162898483 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
https://doi.org/10.1016/0031-9422(92)83478-H
Scirpusin B 5458999 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1016/S0031-9422(00)89752-6
> Phenylpropanoids and polyketides / Stilbenes
1,2-Bis(3-hydroxyphenyl)ethane 4535180 Click to see C1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 214.26 unknown https://doi.org/10.1248/CPB.27.984
3,3',4-Trihydroxybibenzyl 85975989 Click to see 230.26 unknown https://doi.org/10.1248/CPB.27.984
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1248/CPB.39.3353
Dihydropiceatannol 152444 Click to see 246.26 unknown https://doi.org/10.1248/CPB.39.3353
https://doi.org/10.1248/CPB.27.984
Piceatannol 667639 Click to see 244.24 unknown https://doi.org/10.1248/YAKUSHI1947.104.7_819
https://doi.org/10.1016/0006-2952(92)90096-2
https://doi.org/10.1016/B978-0-08-101926-9.00005-5
https://doi.org/10.1248/CPB.27.984
https://doi.org/10.1248/CPB.39.3353
https://doi.org/10.1248/CPB.32.213

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