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Hemsleya endecaphylla

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440541bdc73b391892700
Scientific name Hemsleya endecaphylla
Authority C.Y.Wu
First published in Acta Phytotax. Sin. 23: 142 (1985)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 十一叶雪胆

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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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-0001225240
Tropicos 50043538
KEW urn:lsid:ipni.org:names:906287-1
The Plant List tro-50043538
Open Tree Of Life 1031120
NCBI Taxonomy 447115
IPNI 906287-1
GBIF 3625426
EOL 5737301
USDA GRIN 467737

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
Inhibitory Effects of Cucurbitane-Type Triterpenoids from Momordica charantia Fruit on Lipopolysaccharide-Stimulated Pro-Inflammatory Cytokine Production in Bone Marrow-Derived Dendritic Cells Cao TQ, Phong NV, Kim JH, Gao D, Anh HL, Ngo VD, Vinh LB, Koh YS, Yang SY Molecules 23-Jul-2021
PMCID:PMC8347306
doi:10.3390/molecules26154444
PMID:34361596
Targeting the JAK/STAT Signaling Pathway Using Phytocompounds for Cancer Prevention and Therapy Bose S, Banerjee S, Mondal A, Chakraborty U, Pumarol J, Croley CR, Bishayee A Cells 11-Jun-2020
PMCID:PMC7348822
doi:10.3390/cells9061451
PMID:32545187
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
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
Natural Products as Alternative Choices for P-Glycoprotein (P-gp) Inhibition Dewanjee S, K. Dua T, Bhattacharjee N, Das A, Gangopadhyay M, Khanra R, Joardar S, Riaz M, De Feo V, Zia-Ul-Haq M Molecules 25-May-2017
PMCID:PMC6152721
doi:10.3390/molecules22060871
PMID:28587082
Anticancer Natural Compounds as Epigenetic Modulators of Gene Expression Ratovitski EA Curr Genomics 01-Apr-2017
PMCID:PMC5345332
doi:10.2174/1389202917666160803165229
PMID:28367075
Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents Kuo RY, Qian K, Morris-Natschke SL, Lee KH Nat Prod Rep 13-Aug-2009
PMCID:PMC3773821
doi:10.1039/b810774m
PMID:19779642
Octanorcucurbitane and cucurbitane triterpenoids from the tubers of Hemsleya endecaphylla with HIV-1 inhibitory activity. Chen JC, Zhang GH, Zhang ZQ, Qiu MH, Zheng YT, Yang LM, Yu KB J Nat Prod 01-Jan-2008
doi:10.1021/NP0704396
PMID:18088099

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
22-Deoxocucurbitacin D 5474791 Click to see 502.70 unknown https://doi.org/10.1021/NP0704396
Cucurbitacin B 5281316 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1021/NP0704396
Cucurbitacin I 5281321 Click to see 514.60 unknown https://doi.org/10.1021/NP0704396
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(2S,8S,9R,10S,13S,14S)-2-hydroxy-4,4,9,13,14-pentamethyl-1,2,7,8,10,12,15,17-octahydrocyclopenta[a]phenanthrene-3,11,16-trione 101863831 Click to see CC1(C2=CCC3C4(CC(=O)CC4(CC(=O)C3(C2CC(C1=O)O)C)C)C)C 358.50 unknown https://doi.org/10.1021/NP0704396

Gallery Top

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Contributors Top

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Collections Top

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