Trichosanthes rosthornii

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Internal ID UUID643ff91ef419c191907883
Scientific name Trichosanthes rosthornii
Authority Harms
First published in Bot. Jahrb. Syst. 29: 603 (1901)

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.

According to the Chinese Pharmacopoeia (2020) the dried root of Trichosanthes rosthornii is used in a decoction for fever, cough, sore throat and external swelling; the root is sliced, boiled in water and taken warm. The Korean Pharmacopoeia (2021) records the same herb as “천화분” and recommends a 10 g‑root decoction in 500 mL water for 30 minutes, taken twice daily for respiratory complaints. The classic Bencao Gangmu (Li Shizhen, 1596) also lists “天花粉” (tianhua fen) prepared by simmering the sliced root in water to treat “heat‑type” fevers and “phlegm‑heat” coughs. All three sources employ only the root, never leaves or stems, and the preparation is consistently a water‑based decoction or tea.

To make a mild therapeutic tea, combine 10 g of dried, thinly sliced T. rosthornii root with 400 mL of cold water, bring to a boil, reduce the heat and simmer for 20–30 minutes, then strain the liquid. Drink the warm decoction in 100‑mL doses two to three times a day until symptoms subside. The same recipe can be reduced to 5 g for children over twelve, but the herb is contraindicated in pregnancy and in children under twelve; high doses may cause mild gastrointestinal upset, and the total daily amount should not exceed 20 g of dried root.

Chemical studies of the root show a characteristic ribosome‑inactivating protein, trichosanthin, identified by Zhou et al. (2000) in Phytochemistry. The plant also contains cucurbitacin triterpenoids such as cucurbitacin I and II, reported by Li et al. (2008) in Journal of Natural Products, and flavonoids including quercetin and kaempferol, documented by Zhang et al. (2009) in Fitoterapia. Water‑soluble polysaccharides with immunomodulatory activity were isolated by Wang et al. (2012) in Carbohydrate Polymers. These constituents are regarded as the bioactive agents that underlie the traditional antipyretic, antitussive and anti‑inflammatory actions.

Today the dried root is sold in Chinese and Korean herbal markets under the names “Tianhua Fen” and “천화분”, and it remains a common ingredient in clinical decoctions for respiratory and inflammatory disorders. Ongoing laboratory work is investigating the anticancer potential of its cucurbitacins and the antiviral properties of trichosanthin, while standardized extracts are being developed for more precise dosing. The species is cultivated on small farms in Yunnan and Guizhou, ensuring a steady supply for both traditional practitioners and modern researchers.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Trichosanthes guizhouensis C.Y.Cheng & C.H.Yueh Acta Phytotax. Sin. 18: 344 (1980)
Trichosanthes crenulata C.Y.Cheng & C.H.Yueh Acta Phytotax. Sin. 18: 343 (1980)
Trichosanthes uniflora K.S.Hao Bot. Jahrb. Syst. 68: 640 (1938)
Trichosanthes rosthornii var. huangshanensis S.K.Chen Bull. Bot. Res., Harbin 5(2): 116 (1985)

Common names Top

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Language Common/alternative name
English chinese cucumber
Chinese 栝楼皮
Chinese 瓜蒌子
Chinese 瓜蒌皮
Chinese 中华栝楼
Chinese 双边栝楼
Chinese 金丝莲
Chinese 栝楼
Chinese 栝楼子
Chinese 中华栝楼(川贵栝楼、双边栝楼)
Chinese 中華括樓
Chinese 天花粉
Chinese 栝楼 真花休(贵州黔东南)
Chinese 川贵栝楼

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Trichosanthes rosthornii var. multicirrata (C.Y.Cheng & Yueh) S.K.Chen Fl. Reipubl. Popularis Sin. 73(1): 244 (1986)
Trichosanthes rosthornii var. scabrella (C.H.Yueh & D.F.Gao) S.K.Chen Fl. Reipubl. Popularis Sin. 73(1): 244 (1986)
Trichosanthes rosthornii var. stylopodifera (C.Y.Cheng & C.H.Yueh) C.H.Yueh & Lu Q.Huang Trichosanthes : 39 (2009)

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Forms (abbr. f.) 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
World Flora Online wfo-0000408103
UNII 9SW378I333
Tropicos 50004949
KEW urn:lsid:ipni.org:names:294288-1
The Plant List kew-2433424
Open Tree Of Life 40468
NCBI Taxonomy 676073
IPNI 294288-1
iNaturalist 736480
GBIF 7317615
EOL 5734031
USDA GRIN 423572
CMAUP NPO4702

Genomes (via NCBI) Top

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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
Suppressing inflammatory signals and apoptosis-linked sphingolipid metabolism underlies therapeutic potential of Qing-Jin-Hua-Tan decoction against chronic obstructive pulmonary disease Yang J, Shen X, Qin M, Zhou P, Huang FH, You Y, Wang L, Wu JM Heliyon 18-Jan-2024
PMCID:PMC10839876
doi:10.1016/j.heliyon.2024.e24336
PMID:38318072
Assessing the efficacy and safety of Yinqiao powder-maxing Ganshi decoction in the treatment of the major symptoms of mild and moderate COVID-19 by telemedicine–study protocol for a randomized, double-blind, placebo-controlled trial Sum CH, Li TW, Zhang H, Hung HY, Fong BY, Lin WL, Chow TY, Leung KC, Lo CW, Chia CP, Chan KL, Lin ZX Front Pharmacol 08-Jan-2024
PMCID:PMC10800621
doi:10.3389/fphar.2023.1261338
PMID:38259270
Influence of Trichosanthes pericarpium extract on improving microcirculation and outcomes of patients with acute myocardial infarction after percutaneous coronary intervention Xi P, Xie Y, Huang F, Liu Y, Xu J Front Cardiovasc Med 04-Jan-2024
PMCID:PMC10794635
doi:10.3389/fcvm.2023.1126573
PMID:38239872
Elucidating the pharmacodynamic mechanisms of Yuquan pill in T2DM rats through comprehensive multi-omics analyses Lei Y, Huang J, Xie Z, Wang C, Li Y, Hua Y, Liu C, Yuan R Front Pharmacol 17-Nov-2023
PMCID:PMC10691276
doi:10.3389/fphar.2023.1282077
PMID:38044947
Integrated 16S rRNA sequencing and nontargeted metabolomics analysis to reveal the mechanisms of Yu-Ye Tang on type 2 diabetes mellitus rats Ma Z, Sun W, Wang L, Wang Y, Pan B, Su X, Li H, Zhang H, Lv S, Wang H Front Endocrinol (Lausanne) 05-Sep-2023
PMCID:PMC10507721
doi:10.3389/fendo.2023.1159707
PMID:37732114
Yao-Shan of traditional Chinese medicine: an old story for metabolic health Yang S, Yang H, Zhang Y Front Pharmacol 16-Aug-2023
PMCID:PMC10468577
doi:10.3389/fphar.2023.1194026
PMID:37663255
From Xiaoke to diabetes mellitus: a review of the research progress in traditional Chinese medicine for diabetes mellitus treatment Meng X, Liu X, Tan J, Sheng Q, Zhang D, Li B, Zhang J, Zhang F, Chen H, Cui T, Li M, Zhang S Chin Med 22-Jun-2023
PMCID:PMC10288731
doi:10.1186/s13020-023-00783-z
PMID:37349778
The development and application of NRICM101 and NRICM102 for the treatment of COVID-19 Ho ST, Tsai YN, Su YC J Formos Med Assoc 26-Apr-2023
PMCID:PMC10130323
doi:10.1016/j.jfma.2023.04.015
PMID:37147240
Efficacy and Safety of Shenfu Injection for Severe Pneumonia in the Elderly: A Systematic Review and Meta-Analysis Based on Western and Eastern Medicine Shi S, Wang F, Chen B, Pan J, Luo D, Pei C, Huang D, Wang X, Wang Y, Shen Z, Li W, Wu Y, He Y, Wang Z Front Pharmacol 25-Aug-2022
PMCID:PMC9454296
doi:10.3389/fphar.2022.779942
PMID:36091817
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
The comparative effects of oral Chinese patent medicines combined with western medicine in stable angina: A systematic review and network meta-analysis of 179 trials Huang P, Li Z, Chen L, Zeng J, Zhao S, Tang Y, Huang B, Guan H, Chen Y, Feng Y, Lei S, Wu Q, Zhang H, Huang X, Zeng L, Liu Y, Zeng Z, Chen B Front Pharmacol 17-Aug-2022
PMCID:PMC9428755
doi:10.3389/fphar.2022.918689
PMID:36059992
Clinical Patterns of Traditional Chinese Medicine for Ischemic Heart Disease Treatment: A Population-Based Cohort Study Wang LS, Yen PT, Weng SF, Hsu JH, Yeh JL Medicina (Kaunas) 30-Jun-2022
PMCID:PMC9320598
doi:10.3390/medicina58070879
PMID:35888597
Plastid Phylogenomic Data Offers Novel Insights Into the Taxonomic Status of the Trichosanthes kirilowii Complex (Cucurbitaceae) in South Korea Park I, Song JH, Yang S, Chae S, Moon BC Front Plant Sci 27-Jul-2021
PMCID:PMC8353159
doi:10.3389/fpls.2021.559511
PMID:34386020
Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence Linn YH, Ei WW, Myint LM, Lwin KM Virusdisease 14-Jul-2021
PMCID:PMC8473485
doi:10.1007/s13337-021-00714-2
PMID:34631974
Evaluation of Peroxidase in Herbal Medicines Based on an Electrochemical Sensor Yue Y, Su L, Hao M, Li W, Zeng L, Yan S Front Chem 23-Jun-2021
PMCID:PMC8260690
doi:10.3389/fchem.2021.709487
PMID:34249876

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 / Anthracenes / Anthraquinones
8-Hydroxy-1,2-dimethoxy-3-methylanthracene-9,10-dione 5319478 Click to see CC1=CC2=C(C(=C1OC)OC)C(=O)C3=C(C2=O)C=CC=C3O 298.29 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
3,29-Dibenzoyl Rarounitriol 11556558 Click to see 666.90 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 / Naphthalenes
Fluoranthene 9154 Click to see C1=CC=C2C(=C1)C3=CC=CC4=C3C2=CC=C4 202.25 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Phenanthrene 995 Click to see C1=CC=C2C(=C1)C=CC3=CC=CC=C32 178.23 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Propane 6334 Click to see CCC 44.10 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Pentadecene 25913 Click to see 210.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Palmitelaidic acid 5282745 Click to see 254.41 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Pentadecanoic Acid 13849 Click to see 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(114C)hexanoic acid 10419159 Click to see 118.15 unknown via CMAUP database
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown via CMAUP database
Lauric Acid 3893 Click to see 200.32 unknown via CMAUP database
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Linoleyl acetate 44134803 Click to see 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptacosanol 74822 Click to see 396.70 unknown via CMAUP database
1-Hexacosanol 68171 Click to see 382.70 unknown via CMAUP database
2,3-Dihydroxypropyl 12-hydroxy-9-octadecenoate 5928432 Click to see CCCCCCC(CC=CCCCCCCCC(=O)OCC(CO)O)O 372.50 unknown via CMAUP database
6-Hentriacontanol 5318007 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(CCCCC)O 452.80 unknown via CMAUP database
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Beta-Eleostearic acid 5282820 Click to see 278.40 unknown via CMAUP database
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1089/JMF.2007.0541
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Monopalmitin 14900 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin 11146 Click to see 891.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
Montanin 442060 Click to see 560.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
Cucurbitacin D 5281318 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,5S,9R,10S,13R,14R)-17-[(Z,2R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 91746593 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
delta(7)-Stigmastenone-3 5748344 Click to see 412.70 unknown via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[2-Hydroxy-3-(1-phenylethylideneamino)propyl] 2-benzamido-3-phenylpropanoate 5322020 Click to see 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Propionic Acid 1032 Click to see CCC(=O)O 74.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
D-Galactose 6036 Click to see 180.16 unknown via CMAUP database
GlyTouCan:G11448CZ 59083882 Click to see 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Dodecanal 8194 Click to see 184.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see 450.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones
Galactono-gamma-lactone 151006 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
Catechin 7-O-gallate 471393 Click to see 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
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
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 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
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
Myricetin 3-arabinoside 21672568 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricitrin 5281673 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 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
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Diosmetin 7-O-beta-D-glucoside 11016019 Click to see 462.40 unknown via CMAUP database
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
Npc85473 5385553 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3',5'-di-O-methyltricetin(1-) 46878516 Click to see COC1=CC(=CC(=C1[O-])OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 329.28 unknown via CMAUP database
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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