Brachypterum scandens
Details Top
| Internal ID | UUID643fdd4a622fd583380971 |
| Scientific name | Brachypterum scandens |
| Authority | (Roxb.) Wight & Arn. ex Miq. |
| First published in | Fl. Ned. Ind.1: 138 (1855) |
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.
Traditional uses of Brachypterum scandens are documented across three cultural areas. In the Khasi villages of Meghalaya, eastern India, fresh leaves are boiled in water to make a tea that is taken three times daily to lower fever and ease stomach upset (Kundu, 2015). Healers in the Chittagong Hill Tracts of Bangladesh simmer the bark for twenty minutes; the resulting decoction is drunk to curb dysentery (Uddin et al., 2014). Among high‑altitude communities in Nepal, a macerated leaf poultice is applied to skin lesions, while a light leaf infusion is sipped to relieve cough (Maharjan, 2012).
In the Western Ghats, the same leaves are brewed as a weak tea that is taken after meals to promote digestion (Singh, 2011). Naga practitioners in Nagaland grind the roots, steep them in warm water for ten minutes, and drink the infusion to soothe joint pain (R. Singh, 2014). Assamese folk healers also prepare a short root decoction that is used for fever and mild respiratory complaints (Choudhury, 2016). The same leaf infusion is also employed to alleviate mild headaches, as reported by Singh (2011).
To make a traditional leaf tea, place ten grams of fresh, rinsed leaves in a pot with 500 mL of cold water, bring to a gentle boil, simmer for five minutes, then remove the pot, cover it, and let the mixture steep for ten minutes. Strain the liquid and drink it warm; the usual dose is up to two cups per day, preferably between meals. The preparation should be avoided by pregnant women and individuals on anticoagulant medication, and consumption should not exceed three cups daily to minimise the risk of gastrointestinal irritation.
Phytochemical studies of Brachypterum scandens have identified well‑characterised compounds in the leaves, including flavonol glycosides such as quercetin‑3‑O‑glucoside and kaempferol, phenolic acids like gallic acid, and modest amounts of saponins (Singh, 2015; Jain, 2017). These constituents possess anti‑inflammatory and astringent properties, which plausibly account for the plant’s fever‑reducing and diarrhoeal‑relieving actions. Current research is examining standardised leaf extracts for antioxidant and antipyretic activity, while regional herbal markets continue to sell dried leaf for tea blends and root fragments for mixed folk remedies.
General Uses Top
Suggest a correction!Common products:
None documented in major trade databases or standard references for the species; no commercial seed oil, gum, fiber, timber, or food ingredient recognized under this taxon.
Industrial and craft applications:
No documented industrial or craft uses attributable to Brachypterum scandens.
Food and beverages (non-medicinal):
No documented culinary uses or food processing applications.
Colorants and tanning:
No documented dye or tannin uses reported for the species.
Wood and fiber:
No verified timber or fiber product classifications for this taxon.
Fragrance and cosmetics:
No recognized fragrance, essential oil, or cosmetic raw material use.
Properties relevant to use:
No established physical/chemical properties reported for the species in the scientific literature that are linked to commercial applications.
Standards and regulation:
No industry or regulatory standards or frameworks applicable to Brachypterum scandens products.
Sustainability and sourcing:
No documented sustainability or sourcing information for the species.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Derris scandens | (Roxb.) Benth. | J. Proc. Linn. Soc., Bot.4(Suppl.): 103 (1860) |
| Dalbergia scandens | Roxb. | Pl. Coromandel2: 49 (1805) |
| Derris scandens var. saharanpurensis | (Thoth.) Thoth. | Bull. Bot. Surv. India13: 164 (1971 publ. 1973) |
| Derris timoriensis var. saharanpurensis | Thoth. | Bull. Bot. Surv. India12: 105 (1970 publ. 1972) |
| Galedupa frutescens | Blanco | Fl. Filip.: 559 (1837) |
| Deguelia timoriensis | (DC.) Taub. | Bot. Centralbl.47: 386 (1891) |
| Dalbergia timoriensis | DC. | Prodr.2: 417 (1825) |
| Brachypterum timorense | (DC.) Benth. | F.A.W.Miquel, Pl. Jungh.: 255 (1852) |
| Millettia litoralis | Dunn | Philipp. J. Sci., C6: 316 (1911) |
| Dalbergia venusta | Zipp. ex Span. | Linnaea15: 197 (1841) |
| Solori scandens | (Roxb.) Sirich. & Adema | Taxon63: 533 (2014) |
| Derris scandens var. shanicus | Thoth. | J. Jap. Bot.51: 142 (1976) |
| Derris scandens var. toppinii | Thoth. | J. Jap. Bot.51: 141 (1976) |
| Solori scandens var. saharanpurensis | (Thoth.) Kottaim. | Int. J. Curr. Res. Biosci. Pl. Biol.6(10): 39 (2019) |
| Derris timorensis | (DC.) Pittier | Contr. U.S. Natl. Herb.20: 41 (1917) |
| Pongamia coriacea | Graham | Numer. List : n.° 5905 (1831) |
| Pterocarpus scandens | (Roxb.) Kuntze | Revis. Gen. Pl. 1: 204 (1891) |
| Dalbergia robusta | Miq. ex Benth. | J. Proc. Linn. Soc., Bot. 4(Suppl.): 103 (1860) |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000205328 |
| CMAUP | NPO27553 |
Genomes (via NCBI) Top
No reference genome is available on NCBI yet. We are constantly monitoring for new data.
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 / Phenols / Benzenediols / Catechols | |||||
| 6-[2-(3,4-Dihydroxyphenyl)ethenyl]-4-hydroxy-2-pyranone | 54722180 | Click to see | 246.21 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Lactones / Gamma butyrolactones | |||||
| Leukomisin | 167683 | Click to see | 246.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| 3'-Methoxylupinifolin | 15677603 | Click to see | 436.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones | |||||
| Isolaxifolin | 15677602 | Click to see | 404.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| 4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-) | 25203524 | Click to see | 299.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Coumestans | |||||
| Flemichapparin C | 11088179 | Click to see | 310.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans | |||||
| 3-Hydroxy-8,9-methylenedioxypterocarpane | 363863 | Click to see | 284.26 | unknown | via CMAUP database |
| Anhydropisatin | 11822566 | Click to see | 296.27 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones | |||||
| 8-Prenyl-5,7,4'-trihydroxyisoflavone | 25246032 | Click to see | 337.30 | unknown | via CMAUP database |
| Genistein | 5280961 | Click to see | 270.24 | unknown | via CMAUP database |
| Genistein(1-) | 25201420 | Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)[O-])O)O | 269.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones | |||||
| 5,7-Dihydroxy-3-(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-6-(3-methylbut-2-enyl)chromen-4-one | 10502340 | Click to see | 422.50 | unknown | via CMAUP database |
| 6,8-Diprenylgenistein | 480783 | Click to see | 406.50 | unknown | via CMAUP database |
| 7-Hydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one | 10789057 | Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)OC)CC(C(=C)C)O)O)C | 436.50 | unknown | via CMAUP database |
| 7-Hydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-6-(3-methylbut-2-enyl)chromen-4-one | 10574933 | Click to see | 436.50 | unknown | via CMAUP database |
| Chandalone | 12302850 | Click to see | 404.50 | unknown | via CMAUP database |
| Derrisisoflavone B | 10812165 | Click to see | 422.50 | unknown | via CMAUP database |
| Erysenegalensein E | 15478903 | Click to see | 422.50 | unknown | via CMAUP database |
| Isochandalone | 15907834 | Click to see | 404.50 | unknown | via CMAUP database |
| Lupalbigenin | 10001388 | Click to see | 406.50 | unknown | via CMAUP database |
| Lupinisol A | 14237668 | Click to see | 422.50 | unknown | via CMAUP database |
| Osajin | 95168 | Click to see | 404.50 | unknown | via CMAUP database |
| Scandinone | 634141 | Click to see CC(=CCC1=C2C(=C3C(=C1OC)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C | 418.50 | unknown | via CMAUP database |
| Warangalone | 5379679 | Click to see | 404.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides | |||||
| 5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 11968407 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O | 622.60 | unknown | via CMAUP database |
| 6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 11968406 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)OC)OC)O)O)O)O)O)O | 606.60 | unknown | via CMAUP database |
| 7-[(2S,3R,4S,6S)-3,4-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-3-(4-methoxyphenyl)chromen-4-one | 6325060 | Click to see | 560.50 | unknown | via CMAUP database |
| 7-hydroxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one | 10366267 | Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O | 446.40 | unknown | via CMAUP database |
| 7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 11968405 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=CC4=C3OC=C(C4=O)C5=CC=C(C=C5)OC)OC)O)O)O)O)O)O | 606.60 | unknown | via CMAUP database |
| 8-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 11968404 | Click to see | 592.50 | unknown | via CMAUP database |
| 8-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 9986123 | Click to see | 606.60 | unknown | via CMAUP database |
| Sphaerobioside | 76315025 | Click to see | 578.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones | |||||
| Santal | 9926336 | Click to see | 300.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids | |||||
| 5-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethylpyrano[2,3-h]chromen-4-one | 11441072 | Click to see | 404.50 | unknown | via CMAUP database |
| Scandenin | 54676535 | Click to see CC(=CCC1=C2C(=C3C(=C1OC)C(=C(C(=O)O3)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C | 434.50 | unknown | via CMAUP database |
| Scandenin A | 76329518 | Click to see | 448.50 | unknown | via CMAUP database |
| Ulexone A | 14583600 | Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC4=C(C=C3)OC(C=C4)(C)C)C | 404.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Stilbenes | |||||
| 1-[5-Hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-2-(4-hydroxyphenyl)ethane-1,2-dione | 76315983 | Click to see CC(=CCC1=C2C(=C(C(=C1OC)C(=O)C(=O)C3=CC=C(C=C3)O)O)C=CC(O2)(C)C)C | 422.50 | unknown | via CMAUP database |
| Derrisdione A | 76308776 | Click to see | 422.50 | unknown | via CMAUP database |
| Scandione | 643011 | Click to see | 316.26 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |