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Internal ID UUID68f8f5f96d242338629645
Scientific name Paris chinensis
Authority Franch.
First published in Nouv. Arch. Mus. Hist. Nat. , sér. 2, 10: 97 (1887 publ. 1888)

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Synonyms Top

Scientific name Authority First published in
Paris formosana Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 367 (1911)
Paris brachysepala Pamp. Nuovo Giorn. Bot. Ital. , n.s., 22: 266 (1915)
Daiswa chinensis (Franch.) Takht. Brittonia 35: 259 (1983)
Daiswa chinensis subsp. brachysepala (Pamp.) Takht. Brittonia 35: 262 (1983)
Paris polyphylla var. chinensis (Franch.) H.Hara J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 10: 176 (1969)
Daiswa polyphylla var. chinensis (Franch.) M.N.Tamura Fl. Thailand 13(3): 524 (2017)

Common names Top

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Language Common/alternative name
Chinese 七叶一枝花
Chinese 蚤休
Chinese 华重楼
Chinese 华重楼(七叶一枝花、海南重楼)

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 18405723
KEW urn:lsid:ipni.org:names:77188961-1
The Plant List kew-310565
Open Tree Of Life 329813
NCBI Taxonomy 221254
IPNI 77188961-1
iNaturalist 733163
GBIF 5295939
USDA GRIN 423827
World Flora Online wfo-0000714925
Tropicos 18406999
KEW urn:lsid:ipni.org:names:539692-1
IPNI 539692-1
GBIF 5295940
USDA GRIN 423489

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
Novel Insights on Ferroptosis Modulation as Potential Strategy for Cancer Treatment: When Nature Kills Consoli V, Fallica AN, Sorrenti V, Pittalà V, Vanella L Antioxid Redox Signal 17-Jan-2024
PMCID:PMC10824235
doi:10.1089/ars.2022.0179
PMID:37132605
Genome skimming as an efficient tool for authenticating commercial products of the pharmaceutically important Paris yunnanensis (Melanthiaceae) Zhou N, Tang L, Xie P, Miao K, Yang C, Liu H, Ji Y BMC Plant Biol 29-Jun-2023
PMCID:PMC10308783
doi:10.1186/s12870-023-04365-x
PMID:37380980
Revision on the Genus Paris in Thailand, with a New Species Paris siamensis Ruchisansakun S, Sraphet S, Yothawut C, Thamanukornsri C, Suksee N, Kongsawadworakul P, Srisawad N, Thawara N, Umpunjun P, Rodpradit S, Sangkaew W, Triwitayakorn K Plants (Basel) 17-Jan-2023
PMCID:PMC9919091
doi:10.3390/plants12030430
PMID:36771515
Anti-tumor pharmacology of natural products targeting mitosis Huang M, Liu C, Shao Y, Zhou S, Hu G, Yin S, Pu W, Yu H Cancer Biol Med 15-Jun-2022
PMCID:PMC9257311
doi:10.20892/j.issn.2095-3941.2022.0006
PMID:35699421
Ultra-Barcoding Discovers a Cryptic Species in Paris yunnanensis (Melanthiaceae), a Medicinally Important Plant Ji Y, Liu C, Yang J, Jin L, Yang Z, Yang JB Front Plant Sci 22-Apr-2020
PMCID:PMC7189017
doi:10.3389/fpls.2020.00411
PMID:32391031
An Exploration of Traditional Chinese Medicinal Plants with Anti-Inflammatory Activities Fan C, Jin HZ, Wu L, Zhang Y, Ye RD, Zhang W, Zhang Y Evid Based Complement Alternat Med 04-Apr-2017
PMCID:PMC5394394
doi:10.1155/2017/1231820
PMID:28473862
Studies on the Constituents of <i>Paris Formosana Hayata</i> Part II Pen‐Ho Yeh, Hsüch‐Ching Chiang Wiley 04-Jun-2015
doi:10.1002/JCCS.198200006
Paris chinensis dioscin induces G2/M cell cycle arrest and apoptosis in human gastric cancer SGC-7901 cells Gao LL, Li FR, Jiao P, Yang MF, Zhou XJ, Si YH, Jiang WJ, Zheng TT World J Gastroenterol 21-Oct-2011
PMCID:PMC3218152
doi:10.3748/wjg.v17.i39.4389
PMID:22110264
Separation and identification of steroidal compounds with cytotoxic activity against human gastric cancer cell lines in vitro from the rhizomes of Paris polyphylla var. chinensis Huang Yun, Cui Lijian, Zhan Wenhong, Dou Yuhong, Wang Yongli, Wang Qiang, Zhao Ding Springer Science and Business Media LLC 23-Feb-2008
doi:10.1007/S10600-007-0225-8
Structure characterization of haemostatic diosgenin glycosides from paris polyphylia James C.N. Ma, F.W. Lau Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81066-3

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 / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1002/JCCS.198200006
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1002/JCCS.198200006
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Spirost-5-en-3,17-diol 581098 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)O)C)OC1 430.60 unknown https://doi.org/10.1007/S10600-007-0225-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
2,3,14,20,22,25-Hexahydroxycholest-7-en-6-one 271605 Click to see 480.60 unknown https://doi.org/10.1007/S10600-007-0225-8
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown https://doi.org/10.1002/JCCS.198200006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(1S,2S,4S,7S,8R,9S,12S,13R,14S,16R)-16-hydroxy-14-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-7-(hydroxymethyl)-9,13-dimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-one 163085946 Click to see 816.90 unknown https://doi.org/10.1007/S10600-007-0225-8
16-Hydroxy-14-[5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-7-(hydroxymethyl)-9,13-dimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-one 74317168 Click to see 816.90 unknown https://doi.org/10.1007/S10600-007-0225-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 271916 Click to see 869.00 unknown https://doi.org/10.1016/S0031-9422(00)81066-3
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 14776074 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)C)OC1 738.90 unknown https://doi.org/10.1007/S10600-007-0225-8
2-[5-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 72960700 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 855.00 unknown https://doi.org/10.1016/S0031-9422(00)81066-3
https://doi.org/10.1007/S10600-007-0225-8
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1002/JCCS.198200006
Gracillin 159861 Click to see 885.00 unknown https://doi.org/10.1007/S10600-007-0225-8
Ophiopogonin C' 4483248 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown https://doi.org/10.1007/S10600-007-0225-8
Prosapogenin A 11061578 Click to see 722.90 unknown https://doi.org/10.1007/S10600-007-0225-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.1002/JCCS.198200006
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.198200006
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.198200006
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1002/JCCS.198200006
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1002/JCCS.198200006
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1002/JCCS.198200006
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
1,8-dihydroxy-6-methyl-2,3-dihydro-1H-cyclopenta[b]chromen-9-one 10966363 Click to see 232.23 unknown https://doi.org/10.1007/S10600-007-0225-8

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