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Fritillaria ebeiensis

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 UUID644026496c5f7031925647
Scientific name Fritillaria ebeiensis
Authority G.D.Yu & G.Q.Ji
First published in J. Nanjing Coll. Pharm. 16(3): 29 (1985)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Fritillaria ebeiensis var. purpurea G.D.Yu & P.Li J. Nanjing Coll. Pharm. 16(3): 30 (1985)

Common names Top

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000767773
KEW urn:lsid:ipni.org:names:957832-1
Open Tree Of Life 7047022
NCBI Taxonomy 2109891
iNaturalist 859904
GBIF 5300666
IPNI 957832-1

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
Chemistry and bioactivities of natural steroidal alkaloids Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD Nat Prod Bioprospect 15-Jun-2022
PMCID:PMC9198197
doi:10.1007/s13659-022-00345-0
PMID:35701630
Evaluation of antitumor property of extracts and steroidal alkaloids from the cultivated Bulbus Fritillariae ussuriensis and preliminary investigation of its mechanism of action Wang D, Jiang Y, Wu K, Wang S, Wang Y BMC Complement Altern Med 21-Feb-2015
PMCID:PMC4337094
doi:10.1186/s12906-015-0551-5
PMID:25880867
Studies on the Chemical Constituents of <i>Fritillaria monanth</i> Yong Ming Luo, Fei Li, Hong Ning Liu, Wei Feng Zhu, Dong Mei Yan Trans Tech Publications, Ltd. 04-Sep-2013
doi:10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
Structures of Three New Diterpenoids, Fritillebic Acid and Fritillebins A and B, from Bulbs of Fritillaria ebeiensis G. D. Yu et G. Q. JI. Ji-Zhou WU, Chikako MORIZANE, Akira IIDA, Shin-ichi UEDA, Zuo-Ling ZHOU, Min XU, Min ZHANG, Rei-Min LI, Tetsuro FUJITA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.43.1448
The structural elucidation of fritillaria alkaloids from Fritillaria ebeiensis var. purpurea. I. The structures of ebeienine, ebeiedine and ebeiedinone. PING LEE, YUKIE KITAMURA, KOH KANEKO, MOTOO SHIRO, GUO-JUN XU, YUH-PAN CHEN, HONG-YEN HSU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.4316
Active constituents of the bulbs of <i>Fritillaria ebeiensis</i> and their antitumour activity in mice Li Ping, Xu Guojun, Xu Luoshan, Wang Yixian Wiley 18-Oct-2006
doi:10.1002/PTR.2650090617
Structures of two diterpenoid dimers from bulbs of Fritillaria ebeiensis. Wu JZ, Ruan HL, Yao NH, Zhao QS, Sun HD, Morizane C, Iida A, Fujita T J Asian Nat Prod Res 01-Jan-2000
doi:10.1080/10286020008039907
PMID:11256689

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 / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(14-Hydroxy-5,5,9-trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl 6-acetyloxy-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylate 74344316 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CCC2C1(C)C)CC4C(=O)OCC5(CC67CCC8C(CCCC8(C6CCC5C7)C)(C)C)O)C 651.00 unknown https://doi.org/10.1248/CPB.43.1448
(1S,4S,6R,9S,10R,13R,14R)-6-acetyloxy-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylic acid 101682665 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CCC2C1(C)C)CC4C(=O)O)C 362.50 unknown https://doi.org/10.1248/CPB.43.1448
[(1S,4R,9R,10R,13R,14R)-14-hydroxy-5,5,9-trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl (1S,4S,6R,9S,10R,13R,14R)-6-acetyloxy-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylate 101682666 Click to see 651.00 unknown https://doi.org/10.1248/CPB.43.1448
Fritillebinide C 102157321 Click to see 635.00 unknown https://doi.org/10.1080/10286020008039907
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(1R,2S,6S,9S,10R,11S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol 5316983 Click to see 415.70 unknown https://doi.org/10.1248/CPB.36.4316
(1R,2S,6S,9S,11S,14S,15S,18S,20S,23R,24S)-10,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 102063129 Click to see 429.60 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
(1R,2S,6S,9S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 102062796 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1248/CPB.36.4316
(5alpha,8xi,10xi,13xi,25xi)-Cevane-3,6,20-triol 139291898 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1248/CPB.36.4316
CID 14240939 14240939 Click to see 413.60 unknown https://doi.org/10.1248/CPB.36.4316
Ebeiedinone 5316984 Click to see 413.60 unknown https://doi.org/10.1248/CPB.36.4316
Isoverticine 21573744 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1248/CPB.36.4316
Kashmirine 5221 Click to see 429.60 unknown https://doi.org/10.1248/CPB.36.4316
Peimine 131900 Click to see 431.70 unknown https://doi.org/10.1002/PTR.2650090617
https://doi.org/10.1248/CPB.36.4316
> Organoheterocyclic compounds / Piperidines
(1R,6R,9S,10R,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-2(11)-ene-17,20-diol 5316980 Click to see CC1CCC2C(C3=C(CN2C1)C4CC5C(C4CC3)CC(C6C5(CCC(C6)O)C)O)C 413.60 unknown https://doi.org/10.1248/CPB.36.4316
Ebeinone 180322 Click to see 411.60 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
Ziebeimine 3083151 Click to see 413.60 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134

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