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Schisandra micrantha

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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 UUID644003dccef07066365508
Scientific name Schisandra micrantha
Authority A.C.Sm.
First published in Sargentia 7: 135 (1947)

Description Top

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Synonyms Top

Scientific name Authority First published in
Schisandra gracilis A.C.Sm. Sargentia 7: 132 (1947)
Schisandra elongata var. dentata Finet & Gagnep. Bull. Soc. Bot. France 52: 49. 1905

Common names Top

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Language Common/alternative name
Arabic شزندرة صغيرة السداة
Bengali শিসান্দ্রা মাইক্রান্থা
Chinese 小花五味子
Chinese 小花五味子根
Chinese 小花五味子藤
Chinese 香石藤叶

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-0000495133
Tropicos 50099300
KEW urn:lsid:ipni.org:names:555073-1
The Plant List kew-2585460
Open Tree Of Life 7580805
IPNI 555073-1
GBIF 3745236
Wikipedia Schisandra_micrantha

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)!
Title Authors Publication Released IDs
Micrandilactone A: A Novel Triterpene from Schisandra micrantha Rong‐Tao Li, Qin‐Shi Zhao, Sheng‐Hong Li, Quan‐Bin Han, Han‐Dong Sun, Yang Lu, Li‐Li Zhang, Qi‐Tai Zheng Wiley 29-Jun-2005
doi:10.1002/CHIN.200332119
Structure and anti-HIV activity of micrandilactones B and C, new nortriterpenoids possessing a unique skeleton from Schisandra micrantha. Li RT, Han QB, Zheng YT, Wang RR, Yang LM, Lu Y, Sang SQ, Zheng QT, Zhao QS, Sun HD Chem Commun (Camb) 21-Jun-2005
doi:10.1039/B501932J
PMID:15957031
Micranoic Acids A and B: Two New Octanortriterpenoids from Schisandra micrantha. Rong‐Tao Li, Quan‐Bin Han, Ai‐Hua Zhao, Han‐Dong Sun Wiley 25-Mar-2004
doi:10.1002/CHIN.200412179
Lancifodilactones B-E, new nortriterpenes from Schisandra lancifolia. Li RT, Xiang W, Li SH, Lin ZW, Sun HD J Nat Prod 01-Jan-2004
doi:10.1021/NP030339+
PMID:14738396
Micranoic acids A and B: two new octanortriterpenoids from Schisandra micrantha. Li RT, Han QB, Zhao AH, Sun HD Chem Pharm Bull (Tokyo) 01-Oct-2003
doi:10.1248/CPB.51.1174
PMID:14519924
Micrandilactone A: a novel triterpene from Schisandra micrantha. Li RT, Zhao QS, Li SH, Han QB, Sun HD, Lu Y, Zhang LL, Zheng QT Org Lett 03-Apr-2003
doi:10.1021/OL027524J
PMID:12659564

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
> Lignans, neolignans and related compounds
2-(4-Allyl-2-methoxyphenoxy)-1-(4-hydroxy-3-methoxyphenyl)-1-propanol 14015408 Click to see CC(C(C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2)CC=C)OC 344.40 unknown https://doi.org/10.1248/CPB.51.1174
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1R,3S,7S,10R,12R,13S,15R,17S,18R,21R,22S,23S,25R,29S)-12,22,23-trihydroxy-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 162962461 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/OL027524J
Agn-PC-0LP3Q5 5245937 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/OL027524J
Micraic acid A 85374899 Click to see CC(=C)C1CCC2C(=CCC3(C2(CCC3=O)C)C)C1(C)CCC(=O)O 344.50 unknown https://doi.org/10.1248/CPB.51.1174
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/10.1002/CHIN.200332119
https://doi.org/10.1021/NP030339+
Micranoic acid A 11035347 Click to see CC(=C)C1CCC2C(=CCC3(C2(CCC3=O)C)C)C1(C)CCC(=O)O 344.50 unknown https://doi.org/10.1248/CPB.51.1174
Micranoic Acid B 11759710 Click to see CC(=C)C1CCC2C3(CCC(=O)C3(CCC24C1(C4)CCC(=O)O)C)C 344.50 unknown https://doi.org/10.1248/CPB.51.1174
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6R)-6-[(3R,3aR,6S,7S,9aS,9bS)-6-(2-carboxyethyl)-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,7,8,9,9a-octahydrocyclopenta[a]naphthalen-3-yl]-2-methylhept-2-enoic acid 86573576 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C 470.70 unknown https://doi.org/10.1248/CPB.51.1174
(Z,6R)-6-[(3R,3aR,6S,9aS,9bS)-6-(2-carboxyethyl)-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,7,8,9,9a-octahydrocyclopenta[a]naphthalen-3-yl]-2-methylhept-2-enoic acid 90474178 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C 470.70 unknown https://doi.org/10.1248/CPB.51.1174
(Z,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 91668428 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1248/CPB.51.1174
6-[6-(2-Carboxyethyl)-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,7,8,9,9a-octahydrocyclopenta[a]naphthalen-3-yl]-2-methylhept-2-enoic acid 5130315 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C 470.70 unknown https://doi.org/10.1248/CPB.51.1174
Kadsuric acid 5384417 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C 470.70 unknown https://doi.org/10.1002/CHIN.200412179
https://doi.org/10.1248/CPB.51.1174
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
2-Methyl-6-(7,7,12,16-tetramethyl-6-oxo-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl)hept-2-enoic acid 72726484 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 454.70 unknown https://doi.org/10.1248/CPB.51.1174
Schisandronic acid 101277401 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 454.70 unknown https://doi.org/10.1248/CPB.51.1174
> Organoheterocyclic compounds / Furofurans
1-hydroxy-18-[1-hydroxy-1-(4-methyl-5-oxo-2H-furan-2-yl)propan-2-yl]-9,9,19-trimethyl-4,8,15-trioxahexacyclo[11.8.0.03,7.03,10.014,16.014,19]henicosan-5-one 73307302 Click to see CC1=CC(OC1=O)C(C(C)C2CC3C4(C2(CCC5(C4CCC6C(OC7C6(C5)OC(=O)C7)(C)C)O)C)O3)O 516.60 unknown https://doi.org/10.1039/B501932J
1,14,15-trihydroxy-17-[1-hydroxy-1-(4-methyl-5-oxo-2H-furan-2-yl)propan-2-yl]-9,9,18-trimethyl-4,8-dioxapentacyclo[11.7.0.03,7.03,10.014,18]icosan-5-one 76153615 Click to see CC1=CC(OC1=O)C(C(C)C2CC(C3(C2(CCC4(C3CCC5C(OC6C5(C4)OC(=O)C6)(C)C)O)C)O)O)O 534.60 unknown https://doi.org/10.1039/B501932J
Micrandilactone B 5279525 Click to see CC1=CC(OC1=O)C(C(C)C2CC3C4(C2(CCC5(C4CCC6C(OC7C6(C5)OC(=O)C7)(C)C)O)C)O3)O 516.60 unknown https://doi.org/10.1039/B501932J
Micrandilactone C 5279526 Click to see CC1=CC(OC1=O)C(C(C)C2CC(C3(C2(CCC4(C3CCC5C(OC6C5(C4)OC(=O)C6)(C)C)O)C)O)O)O 534.60 unknown https://doi.org/10.1039/B501932J
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,meta-bridged biphenyls
3,10,17-Trihydroxytricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),14(18),15-hexaene-9,11-dione 86295273 Click to see C1CC(=O)C(C(=O)CCC2=CC(=C(C=C2)O)C3=C(C=CC1=C3)O)O 326.30 unknown https://doi.org/10.1248/CPB.51.1174

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