Trichosanthes cucumeroides - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID643ff91bd7c7f786966588
Scientific name Trichosanthes cucumeroides
Authority Maxim.
First published in Enum. Pl. Jap. 1: 172 (1873)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Trichosanthes dicoelosperma C.B.Clarke Fl. Brit. India 2: 609 (1879)
Anguina dicaelosperma Kuntze Revis. Gen. Pl. 1: 254 (1891)
Bryonia cucumeroides Ser. Prodr. 3: 308 (1828)
Trichosanthes ovigera subsp. cucumeroides (Ser.) C.Jeffrey Mansfeld's Encycl. 3: 1528 (2001)
Trichosanthes cucumeroides var. dicoelosperma (C.B.Clarke) S.K.Chen Bull. Bot. Res., Harbin 5(2): 118 (1985)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Japanese カラスウリ
Chinese 王瓜
Chinese 王瓜子
Chinese 王瓜根
Chinese 一种维管植物

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

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-0000408021
Tropicos 9201113
KEW urn:lsid:ipni.org:names:294179-1
Open Tree Of Life 525476
Observations.org 315559
NCBI Taxonomy 685054
IPNI 294179-1
iNaturalist 452203
iNaturalist 452204
iNaturalist 452206
GBIF 7317828
Elurikkus 587839
USDA GRIN 40107

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
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
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
The Updated Review on Plant Peptides and Their Applications in Human Health Mani S, Bhatt SB, Vasudevan V, Prabhu D, Rajamanikandan S, Velusamy P, Ramasamy P, Raman P Int J Pept Res Ther 27-Jul-2022
PMCID:PMC9326430
doi:10.1007/s10989-022-10437-7
PMID:35911180
Nocturnal ambush predators and their potential impact on flower‐visiting moths Sakagami K, Funamoto D, Sugiura S Ecology 16-Oct-2021
PMCID:PMC9286552
doi:10.1002/ecy.3482
PMID:34289091
23,24-Dihydrocucurbitacin B promotes lipid clearance by dual transcriptional regulation of LDLR and PCSK9 Li HH, Li J, Zhang XJ, Li JM, Xi C, Wang WQ, Lu YL, Xuan LJ Acta Pharmacol Sin 29-Jul-2019
PMCID:PMC7471448
doi:10.1038/s41401-019-0274-0
PMID:31358898
Procoagulant serine glycoprotease from Cucumis sativus L.: action on human fibrinogen and fibrin clot Nafeesa Z, Shivalingu BR, Neema KN, Achar RR, Venkatesh BK, Hanchinal V, Priya BS, Nanjunda Swamy S 3 Biotech 29-May-2017
PMCID:PMC5447519
doi:10.1007/s13205-017-0686-9
PMID:28555432
Plants Producing Ribosome-Inactivating Proteins in Traditional Medicine Polito L, Bortolotti M, Maiello S, Battelli MG, Bolognesi A Molecules 18-Nov-2016
PMCID:PMC6273415
doi:10.3390/molecules21111560
PMID:27869738
Ribosome-Inactivating and Related Proteins Schrot J, Weng A, Melzig MF Toxins (Basel) 08-May-2015
PMCID:PMC4448163
doi:10.3390/toxins7051556
PMID:26008228
Immunotoxins Constructed with Ribosome-Inactivating Proteins and their Enhancers: A Lethal Cocktail with Tumor Specific Efficacy Gilabert-Oriol R, Weng A, von Mallinckrodt B, Melzig MF, Fuchs H, Thakur M Curr Pharm Des 01-Dec-2014
PMCID:PMC4296666
doi:10.2174/1381612820666140826153913
PMID:25341935
Revision of the genus Paridea Baly, 1886 from Taiwan (Coleoptera, Chrysomelidae, Galerucinae) Lee CF, Bezděk J Zookeys 28-Apr-2014
PMCID:PMC4023269
doi:10.3897/zookeys.405.7458
PMID:24843276
The Cucurbitaceae of India: Accepted names, synonyms, geographic distribution, and information on images and DNA sequences Renner SS, Pandey AK PhytoKeys 11-Mar-2013
PMCID:PMC3652411
doi:10.3897/phytokeys.20.3948
PMID:23717193
Synopsis of Trichosanthes (Cucurbitaceae) based on recent molecular phylogenetic data de Boer HJ, Thulin M PhytoKeys 19-Apr-2012
PMCID:PMC3349053
doi:10.3897/phytokeys.12.2952
PMID:22645411
Extensive screening for herbal extracts with potent antioxidant properties Niwano Y, Saito K, Yoshizaki F, Kohno M, Ozawa T J Clin Biochem Nutr 28-Dec-2010
PMCID:PMC3022069
doi:10.3164/jcbn.11-013FR
PMID:21297917
Diensynthesen auf dem Fettgebiet, V.: Die Zusammensetzung des Samenfettes von Trichosanthes cucumeroides (Studien auf dem Fettgebiet, 44. Mitteil.) Hans Paul Kaufmann, Josef Baltes, Heinz Büter Wiley 20-Jul-2007
doi:10.1002/CBER.19370701233
Sterols from fruits of Trichosanthes cucumeroides and T. japonica Takao Matsuno, Seiichi Nagata Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86475-4

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 / 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 https://doi.org/10.1248/YAKUSHI1947.109.4_256
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1248/YAKUSHI1947.109.4_256
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(11E)-octadeca-9,11,13-trienoic acid 160046675 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1002/CBER.19370701233
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1002/CBER.19370701233
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3S,4S,5R,6S)-2-(2-methylbut-3-en-2-yloxymethyl)-6-[[(1E,3R,4S,8R,9R,10R,11S,14R)-4,9,14-trihydroxy-14-(methoxymethyl)-3,10-dimethyl-6-propan-2-yl-8-tricyclo[9.3.0.03,7]tetradeca-1,6-dienyl]oxy]oxane-3,4,5-triol 163029042 Click to see CC1C2CCC(C2=CC3(C(CC(=C3C(C1O)OC4C(C(C(C(O4)COC(C)(C)C=C)O)O)O)C(C)C)O)C)(COC)O 596.70 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10-Acetyloxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,10,11,12,14,14b-decahydropicen-2-yl)methyl acetate 163007990 Click to see CC(=O)OCC1(CCC2(CCC3(C4=CC=C5C(C(CCC5(C4=CCC3(C2C1)C)C)OC(=O)C)(C)C)C)C)C 522.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
[(3S,5R,8R,9S,10R,13R,14S,17R)-17-[(E,2R)-6-acetyloxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162869190 Click to see CC(CC=CC(C)(C)OC(=O)C)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 528.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
2-(9-Acetyloxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl)prop-2-enyl acetate 162991821 Click to see CC(=O)OCC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 526.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
Erythrodiol diacetate 21633449 Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)(C)C 526.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
Olean-12-ene-3beta,28-diol, diacetate 609029 Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)(C)C 526.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,9R,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12315384 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)86475-4
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/YAKUSHI1947.109.4_256
delta7Stigmastenol 521367 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)86475-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(10-Acetyloxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,13,14,14b-tetradecahydropicen-2-yl)methyl acetate 14353036 Click to see CC(=O)OCC1(CCC2(CCC3(C4=C(CCC3(C2C1)C)C5(CCC(C(C5CC4)(C)C)OC(=O)C)C)C)C)C 526.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
(10-Acetyloxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl)methyl acetate 85123631 Click to see CC(=O)OCC1(CCC2(CCC3(C4=C(CCC3(C2C1)C)C5(CCC(C(C5C=C4)(C)C)OC(=O)C)C)C)C)C 524.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
Isokarounidiol diacetate 10369552 Click to see CC(=O)OCC1(CCC2(CCC3(C4=C(CCC3(C2C1)C)C5(CCC(C(C5C=C4)(C)C)OC(=O)C)C)C)C)C 524.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)83876-5
Kaempferol-3-O-glucoside-7-O-rhamnoside 14035324 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)83876-5
Lespedin;Lespenephryl 12305415 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83876-5

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

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.