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Trichosanthes ovigera

Trichosanthes ovigera - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff931105e0336367250
Scientific name Trichosanthes ovigera
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 934 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Platygonia himalensis Naudin ex C.B.Clarke Fl. Brit. India 2: 608 (1879)
Trichosanthes himalensis C.B.Clarke Fl. Brit. India 2: 608 (1879)
Trichosanthes horsfieldii Miq. Fl. Ned. Ind. 1(1): 677 (1856)
Anguina himalensis Kuntze Revis. Gen. Pl. 1: 254 (1891)
Anguina horsfieldii Kuntze Revis. Gen. Pl. 1: 254 (1891)
Anguina ovigera Kuntze Revis. Gen. Pl. 1: 254 (1891)

Common names Top

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Language Common/alternative name
Chinese 全緣括樓
Chinese 栝楼
Chinese 全缘栝楼

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000408670
Tropicos 50043851
KEW urn:lsid:ipni.org:names:294254-1
Open Tree Of Life 157091
Observations.org 315571
NCBI Taxonomy 386244
IPNI 294254-1
GBIF 7317673
Elurikkus 587817
USDA GRIN 319707

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
Melon Fly, Bactrocera cucurbitae (Diptera: Tephritidae), Infestation in Host Fruits in the Southwestern Islands of Japan Before the Initiation of Island-wide Population Suppression, as Recorded in Publications of Japanese Public Institutions McQuate GT, Teruya T Int J Insect Sci 07-Jun-2015
PMCID:PMC4722880
doi:10.4137/IJIS.S24582
PMID:26816487
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
Studies on the constituents of Trichosanthes species. I. On the neutral ether extracts of the dried roots of Trichosanthes japonica Regel, Trichosanthes kirilowii Maxim. and Trichosanthes cucumeroides Maxim.. MATAO KANAOKA, MASAO YOSHIZAKI, HIROHARU FUJINO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.30.2570
7-OX0-10α-Cucurbitadienol from the seeds of Trichosanthes kirilowii and its anti-inflammatory effect Toshihiro Akihisa, Ken Yasukawa, Yumiko Kimura, Michio Takido, Wilhelmus C.M.C. Kokke, Toshitake Tamura Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97029-8
A chemotaxonomic study of flavonoids in the leaves of six Trichosanthes species Masao Yoshizaki, Hiroharu Fujino, Mihoko Masuyama, Munehisa Arisawa, Naokata Morita Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83876-5
[Studies on the constituents of trichosanthes root. II. Constituents of roots of Trichosanthes cucumeroides Maxim]. Kitajima J, Tanaka Y Yakugaku Zasshi 01-Apr-1989
doi:10.1248/YAKUSHI1947.109.4_256
PMID:2760812

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 / Benzoic acids and derivatives / Benzoic acid esters
[(3R,4aR,6aS,6bS,8aS,11R,12aR,14bS)-11-(acetyloxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-6-oxo-2,3,4a,5,7,8,9,10,12,12a,13,14-dodecahydro-1H-picen-3-yl] benzoate 162929088 Click to see CC(=O)OCC1(CCC2(CCC3(C4=C(CCC3(C2C1)C)C5(CCC(C(C5CC4=O)(C)C)OC(=O)C6=CC=CC=C6)C)C)C)C 602.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1248/YAKUSHI1947.109.4_256
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(2R,4aS,6aS,10R,12aR,14aS,14bR)-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 10098262 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
[(3R,4aR,6aS,6bS,8aS,11R,12aR,14bS)-11-(acetyloxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-1,2,3,4a,5,7,8,9,10,12,12a,13-dodecahydropicen-3-yl] benzoate 163021080 Click to see CC(=O)OCC1(CCC2(CCC3(C4=CCC5C(C(CCC5(C4=CCC3(C2C1)C)C)OC(=O)C6=CC=CC=C6)(C)C)C)C)C 586.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
[11-(Acetyloxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-1,2,3,4a,5,7,8,9,10,12,12a,13-dodecahydropicen-3-yl] benzoate 163021079 Click to see CC(=O)OCC1(CCC2(CCC3(C4=CCC5C(C(CCC5(C4=CCC3(C2C1)C)C)OC(=O)C6=CC=CC=C6)(C)C)C)C)C 586.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
[17-(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-yl] acetate 347368 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 454.70 unknown https://doi.org/10.1248/CPB.30.2570
[17-(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 162869189 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-[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-acetoxy-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]allyl acetate 122179233 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
5alpha-Stigmast-7-en-3beta-ol, acetate 22296968 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1248/CPB.30.2570
Betulin diacetate 236415 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)COC(=O)C 526.80 unknown https://doi.org/10.1016/S0031-9422(00)97029-8
Spinasteryl acetate 6452058 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 454.70 unknown https://doi.org/10.1248/CPB.30.2570
Stigmast-7-en-3-ol, acetate, (3beta,5alpha)- 635170 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1248/CPB.30.2570
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-17-(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 137706369 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
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-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 14353035 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
[(2R,4aS,6aS,8aR,10S,12aS,14aS,14bR)-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 14353037 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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)83876-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Lespedin 5486199 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

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