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Schisandra grandiflora

Schisandra grandiflora - 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 UUID644003db5a913595884719
Scientific name Schisandra grandiflora
Authority Hook.f. & Thomson
First published in Fl. Brit. India 1: 44 (1872)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kadsura grandiflora Wall. Tent. Fl. Napal. : 10 (1824)
Sphaerostema grandiflorum (Wall.) Blume Fl. Javae 32-33: 17 (1830)

Common names Top

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Language Common/alternative name
Arabic شزندرة كبيرة الزهرة
Vietnamese ngũ vị tử hoa to
Chinese 大花五味子
Chinese 红花五味子
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
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000495107
Tropicos 19300015
KEW urn:lsid:ipni.org:names:555092-1
The Plant List kew-2585436
PFAF Schisandra grandiflora
PaleoBotany 100413
Open Tree Of Life 533170
NCBI Taxonomy 124788
IPNI 555092-1
iNaturalist 542547
GBIF 3745238
EPPO SHSGR
EOL 2874401
USDA GRIN 70680
Wikipedia Schisandra_grandiflora

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
Comprehensive review of dibenzocyclooctadiene lignans from the Schisandra genus: anticancer potential, mechanistic insights and future prospects in oncology Jafernik K, Motyka S, Calina D, Sharifi-Rad J, Szopa A Chin Med 24-Jan-2024
PMCID:PMC10809469
doi:10.1186/s13020-024-00879-0
PMID:38267965
The potential mechanism of Aidi injection against neuroblastoma—an investigation based on network pharmacology analysis Dai S, Gu Y, Zhan Y, Zhang J, Xie L, Li Y, Lu Y, Yang R, Zhou E, Chen D, Liu S, Zheng S, Shi Z, Dong K, Dong R Front Pharmacol 19-Jan-2024
PMCID:PMC10834740
doi:10.3389/fphar.2024.1310009
PMID:38313313
The Fundamental Role of Oxime and Oxime Ether Moieties in Improving the Physicochemical and Anticancer Properties of Structurally Diverse Scaffolds Fotie J, Matherne CM, Mather JB, Wroblewski JE, Johnson K, Boudreaux LG, Perez AA Int J Mol Sci 28-Nov-2023
PMCID:PMC10705934
doi:10.3390/ijms242316854
PMID:38069175
Schisandra henryi—A Rare Species with High Medicinal Potential Jafernik K, Ekiert H, Szopa A Molecules 25-May-2023
PMCID:PMC10254417
doi:10.3390/molecules28114333
PMID:37298808
Collection calendar: the diversity and local knowledge of wild edible plants used by Chenthang Sherpa people to treat seasonal food shortages in Tibet, China Ding XY, Zhang Y, Wang L, Zhuang HF, Chen WY, Wang YH J Ethnobiol Ethnomed 10-Jun-2021
PMCID:PMC8190990
doi:10.1186/s13002-021-00464-x
PMID:34112198
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Recent advances in natural anti-HIV triterpenoids and analogues Wu HF, Morris-Natschke SL, Xu XD, Yang MH, Cheng YY, Yu SS, Lee KH Med Res Rev 14-Jul-2020
PMCID:PMC7554103
doi:10.1002/med.21708
PMID:32666531
Screen for Potential Candidate Alternatives of Sargentodoxa cuneata from Its Six Adulterants Based on Their Phenolic Compositions and Antioxidant Activities Yang L, Yin P, Cao X, Liu Y Int J Mol Sci 31-Oct-2019
PMCID:PMC6862427
doi:10.3390/ijms20215427
PMID:31683574
Dietary Compounds for Targeting Prostate Cancer Noh S, Choi E, Hwang CH, Jung JH, Kim SH, Kim B Nutrients 08-Oct-2019
PMCID:PMC6835786
doi:10.3390/nu11102401
PMID:31597327
Phytochemicals in Prostate Cancer: From Bioactive Molecules to Upcoming Therapeutic Agents Salehi B, Fokou PV, Yamthe LR, Tali BT, Adetunji CO, Rahavian A, Mudau FN, Martorell M, Setzer WN, Rodrigues CF, Martins N, Cho WC, Sharifi-Rad J Nutrients 29-Jun-2019
PMCID:PMC6683070
doi:10.3390/nu11071483
PMID:31261861
Pharmacological Properties, Molecular Mechanisms, and Pharmaceutical Development of Asiatic Acid: A Pentacyclic Triterpenoid of Therapeutic Promise Nagoor Meeran MF, Goyal SN, Suchal K, Sharma C, Patil CR, Ojha SK Front Pharmacol 04-Sep-2018
PMCID:PMC6131672
doi:10.3389/fphar.2018.00892
PMID:30233358
The Chemical Composition and Functional Properties of Essential Oils from Four Species of Schisandra Growing Wild in the Qinling Mountains, China Wang X, Liu Y, Niu Y, Wang N, Gu W Molecules 05-Jul-2018
PMCID:PMC6100523
doi:10.3390/molecules23071645
PMID:29976902
Diversity and use of wild and non-cultivated edible plants in the Western Himalaya Aryal KP, Poudel S, Chaudhary RP, Chettri N, Chaudhary P, Ning W, Kotru R J Ethnobiol Ethnomed 29-Jan-2018
PMCID:PMC5789610
doi:10.1186/s13002-018-0211-1
PMID:29378614
Chemical diversity and pharmacological significance of the secondary metabolites of nutmeg (Myristica fragrans Houtt.) Abourashed EA, El-Alfy AT Phytochem Rev 10-May-2016
PMCID:PMC5222521
doi:10.1007/s11101-016-9469-x
PMID:28082856
Evaluation of Four Commonly Used DNA Barcoding Loci for Chinese Medicinal Plants of the Family Schisandraceae Zhang J, Chen M, Dong X, Lin R, Fan J, Chen Z PLoS One 04-May-2015
PMCID:PMC4418597
doi:10.1371/journal.pone.0125574
PMID:25938480

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1S,3R,7R,10S,12S,13R,15R,17S,18R,21R,22S,23S,25S,29S)-12,18-dihydroxy-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,14,19,24-tetrone 102185242 Click to see CC1C2C3C(C(C(=O)O3)(C)O)OC45C2C(C1=O)(CCC6(O4)CC78C(CC(C6C5=O)O)C(OC7CC(=O)O8)(C)C)C 560.60 unknown https://doi.org/10.1021/NP900292E
(1S,3S,7S,10R,12R,13S,15S,17S,18R,21S,22R,23R,25R,29R)-12-hydroxy-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,14,19,24-tetrone 134715168 Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC(C6C5=O)O)C(OC7CC(=O)O8)(C)C)C 544.60 unknown https://doi.org/10.1021/NP900292E
13-Hydroxy-9-(hydroxymethyl)-3',9,19,21-tetramethylspiro[4,8,16,24-tetraoxaheptacyclo[13.8.1.115,18.01,13.03,7.03,10.021,25]pentacosane-17,5'-oxolane]-2',5,14,20-tetrone 75034293 Click to see CC1CC2(C3C(C(=O)C4(C3C5(O2)C(=O)C6(CCC7C(OC8C7(CC6(O5)CC4)OC(=O)C8)(C)CO)O)C)C)OC1=O 560.60 unknown https://doi.org/10.1021/NP900292E
8-(Hydroxymethyl)-3',8,19,21-tetramethylspiro[4,9,13,24,25-pentaoxaoctacyclo[14.8.1.11,19.03,5.03,16.07,14.010,14.022,26]hexacosane-23,5'-oxolane]-2,2',12,20-tetrone 75034294 Click to see CC1CC2(C3C(C(=O)C4(C3C5(O2)C(=O)C67C(O6)CC8C(OC9C8(CC7(O5)CC4)OC(=O)C9)(C)CO)C)C)OC1=O 558.60 unknown https://doi.org/10.1021/NP900292E
Micrandilactone A 101240964 Click to see CC1C2C(C3(C4C(CCC56CC78C(CC(C5C(=O)C4(O2)O6)O)C(OC7CC(=O)O8)(C)C)(C(=O)C3(C)O)C)O)OC1=O 576.60 unknown https://doi.org/10.1021/NP900292E
Schigrandilactone A 44482062 Click to see CC1CC2(C3C(C(=O)C4(C3C5(O2)C(=O)C6(CCC7C(OC8C7(CC6(O5)CC4)OC(=O)C8)(C)CO)O)C)C)OC1=O 560.60 unknown https://doi.org/10.1021/NP900292E
Schigrandilactone B 44482063 Click to see CC1CC2(C3C(C(=O)C4(C3C5(O2)C(=O)C67C(O6)CC8C(OC9C8(CC7(O5)CC4)OC(=O)C9)(C)CO)C)C)OC1=O 558.60 unknown https://doi.org/10.1021/NP900292E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Altaicalarin D 46186621 Click to see CC=C(C)C(=O)OC1C(C(C(=O)C2(C1O2)C)OC(=O)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 504.60 unknown https://doi.org/10.1021/NP900292E
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Lancifodilactone K 11598937 Click to see CC1C(C2C(C1=O)(CCC34CC56C(CC=C3C(=O)C2(O4)O)C(OC5CC(=O)O6)(C)C)C)C7C=C(C(=O)O7)C 526.60 unknown https://doi.org/10.1021/NP900292E
> Organoheterocyclic compounds / Furofurans
(1S,3R,3'S,7R,9R,10S,11S,13R,15R,17R,18S,19S,21S,25S)-11-hydroxy-9-(hydroxymethyl)-3',9,19,21-tetramethylspiro[4,8,16,24-tetraoxaheptacyclo[13.8.1.115,18.01,13.03,7.03,10.021,25]pentacosane-17,5'-oxolane]-2',5,14,20-tetrone 46883066 Click to see CC1CC2(C3C(C(=O)C4(C3C5(O2)C(=O)C6CC(C7C(OC8C7(CC6(O5)CC4)OC(=O)C8)(C)CO)O)C)C)OC1=O 560.60 unknown https://doi.org/10.1021/NP900292E
> Organoheterocyclic compounds / Furopyrans
(1S,3aR,3bS,4S,5aS,7aS,8aR,11aR,13R,13aS,14S,15aR,16aS,16bS,17aR)-14-Hydroxy-13-(hydroxymethyl)-1,4,5a,13-tetramethyltetradecahydro-2H,10H-7a,16a-epoxy-3,9,12,17-tetraoxacyclopenta[3',3a']azuleno[6',5':5,6]cycloocta[1,2,3-cd]-as-indacene-2,5,10,16(1H,8H,13H)-tetrone 44482064 Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC(=O)O7)OC(C8C(CC6C5=O)O)(C)CO)C 560.60 unknown https://doi.org/10.1021/NP900292E
(1S,3R,10R,15S,17S,21S,22R,23R,25S,29R)-23-hydroxy-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-12-ene-5,14,19,24-tetrone 138108831 Click to see CC1C2C(C3C4C(CCC56CC78C(CC=C5C(=O)C4(O2)O6)C(OC7CC(=O)O8)(C)C)(C(=O)C3(C)O)C)OC1=O 542.60 unknown https://doi.org/10.1021/NP900292E
(1S,3R,7R,10S,15R,17S,18R,21R,22S,23S,25S,29S)-18-hydroxy-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-12-ene-5,14,19,24-tetrone 102185244 Click to see CC1C2C3C(C(C(=O)O3)(C)O)OC45C2C(C1=O)(CCC6(O4)CC78C(CC=C6C5=O)C(OC7CC(=O)O8)(C)C)C 542.60 unknown https://doi.org/10.1021/NP900292E
11-Hydroxy-9-(hydroxymethyl)-9,18,23,25-tetramethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,14,19,24-tetrone 75034295 Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC(=O)O7)OC(C8C(CC6C5=O)O)(C)CO)C 560.60 unknown https://doi.org/10.1021/NP900292E
Lancifodilactone D 12080814 Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC=C6C5=O)C(OC7CC(=O)O8)(C)C)C 526.60 unknown https://doi.org/10.1021/NP900292E

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