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Schisandra glaucescens

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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 UUID644003dc795a7097293986
Scientific name Schisandra glaucescens
Authority Diels
First published in Bot. Jahrb. Syst. 29: 323 (1900)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic شزندرة جلكاء
Chinese 花血藤
Chinese 金山五味子

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000495130
Tropicos 19300592
KEW urn:lsid:ipni.org:names:555091-1
The Plant List kew-2585458
Open Tree Of Life 533183
NCBI Taxonomy 124787
IPNI 555091-1
GBIF 3745254
EPPO SHSGL
EOL 5348421
CMAUP NPO19979

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
Biological Activity of Oleanolic Acid Derivatives HIMOXOL and Br-HIMOLID in Breast Cancer Cells Is Mediated by ER and EGFR Lisiak N, Dzikowska P, Wisniewska U, Kaczmarek M, Bednarczyk-Cwynar B, Zaprutko L, Rubis B Int J Mol Sci 07-Mar-2023
PMCID:PMC10048893
doi:10.3390/ijms24065099
PMID:36982173
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA Pharmaceuticals (Basel) 11-Nov-2022
PMCID:PMC9699253
doi:10.3390/ph15111392
PMID:36422521
Natural Products Targeting Liver X Receptors or Farnesoid X Receptor She J, Gu T, Pang X, Liu Y, Tang L, Zhou X Front Pharmacol 05-Jan-2022
PMCID:PMC8766425
doi:10.3389/fphar.2021.772435
PMID:35069197
Phenolics from Medicinal and Aromatic Plants: Characterisation and Potential as Biostimulants and Bioprotectants Kisiriko M, Anastasiadi M, Terry LA, Yasri A, Beale MH, Ward JL Molecules 20-Oct-2021
PMCID:PMC8588183
doi:10.3390/molecules26216343
PMID:34770752
Natural Compounds in Sex Hormone-Dependent Cancers: The Role of Triterpenes as Therapeutic Agents Şoica C, Voicu M, Ghiulai R, Dehelean C, Racoviceanu R, Trandafirescu C, Roșca OJ, Nistor G, Mioc M, Mioc A Front Endocrinol (Lausanne) 21-Jan-2021
PMCID:PMC7859451
doi:10.3389/fendo.2020.612396
PMID:33552000
Pharmacological Modulation of Steroid Activity in Hormone-Dependent Breast and Prostate Cancers: Effect of Some Plant Extract Derivatives Bayala B, Zoure AA, Baron S, de Joussineau C, Simpore J, Lobaccaro JM Int J Mol Sci 23-May-2020
PMCID:PMC7279356
doi:10.3390/ijms21103690
PMID:32456259
Naturally Lignan-Rich Foods: A Dietary Tool for Health Promotion? Rodríguez-García C, Sánchez-Quesada C, Toledo E, Delgado-Rodríguez M, Gaforio JJ Molecules 06-Mar-2019
PMCID:PMC6429205
doi:10.3390/molecules24050917
PMID:30845651
In Vivo and In Vitro Anti-Arthritic Effects of Cardenolide-Rich and Caffeoylquinic Acid-Rich Fractions of Periploca forrestii Liu T, Wang X, He YL, Wang Y, Dong L, Ma X, Zheng L, Liu CH, Wang GC, Zheng J, Lan YY, Li YJ Molecules 09-Aug-2018
PMCID:PMC6222661
doi:10.3390/molecules23081988
PMID:30096961
Triterpenoids from the Stems of <i>Schisandra glaucescens</i> Fan‐Yu Meng, Jia‐Xiang Sun, Xue Li, Hui‐Fang Pi, Peng Zhang, Han‐Li Ruan Wiley 17-Oct-2011
doi:10.1002/HLCA.201100033

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
> Lignans, neolignans and related compounds / Aryltetralin lignans
(5R,6S)-5-(4-hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6-dihydronaphthalen-2-ol 50900853 Click to see CC1C(C2=CC(=C(C=C2C=C1C)O)OC)C3=CC(=C(C=C3)O)OC 326.40 unknown via CMAUP database
Phenol, 2-methoxy-4-[(5R,6R,7S)-5,6,7,8-tetrahydro-6,7-dimethylnaphtho[2,3-d]-1,3-dioxol-5-yl]-, rel- 44447181 Click to see CC1CC2=CC3=C(C=C2C(C1C)C4=CC(=C(C=C4)O)OC)OCO3 326.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
6-[2,3-Dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4-methoxy-1,3-benzodioxole 78385328 Click to see CC1C(C(C1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C=C4OC)OC)OC)C 400.50 unknown https://doi.org/10.1002/HLCA.201100033
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Dihydroguaiaretic acid, meso- 476856 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC 330.40 unknown via CMAUP database
Macelignan 10404245 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC 328.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Machilusin 45268387 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
(-)-Zuonin A 12310041 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown via CMAUP database
Chicanine 53360432 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 435761 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.201100033
Anwuweizicacid 14104879 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.201100033
Manwuweizic acid 14104874 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C 470.70 unknown https://doi.org/10.1002/HLCA.201100033
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
2-Oxo-2-oxonioacetate 18676629 Click to see [H+].[H+].C(=O)(C(=O)[O-])[O-] 90.03 unknown via CMAUP database

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