Name	Authority	First published in
Schisandra henryi subsp. henryi
Schisandra henryi subsp. marginalis	(A.C.Sm.) R.M.K.Saunders	Syst. Bot. Monogr. 58: 90 (2000)
Schisandra henryi subsp. yunnanensis	(A.C.Sm.) R.M.K.Saunders	Syst. Bot. Monogr. 58: 89 (2000)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000495123
Tropicos	19300593
KEW	urn:lsid:ipni.org:names:555094-1
The Plant List	kew-2585450
Open Tree Of Life	533172
NCBI Taxonomy	124789
IPNI	555094-1
GBIF	7335130
EPPO	SHSHE

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

Phenolic compound profiling and antioxidant potential of different types of Schisandra henryi in vitro cultures

Jafernik K, Kubica P, Sharafan M, Kruk A, Malinowska MA, Granica S, Szopa A

Appl Microbiol Biotechnol

07-May-2024

PMCID:	PMC11076313
doi:	10.1007/s00253-024-13159-6
PMID:	38713216

Comparative Assessment of Lignan Profiling and Biological Activities of Schisandra henryi Leaf and In Vitro PlantForm Bioreactor-Grown Culture Extracts

Jafernik K, Kubica P, Dziurka M, Kulinowski Ł, Korona-Głowniak I, Elansary HO, Waligórski P, Skalicka-Woźniak K, Szopa A

Pharmaceuticals (Basel)

29-Mar-2024

PMCID:	PMC11053505
doi:	10.3390/ph17040442
PMID:	38675405

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

Discovery and bioinspired total syntheses of unprecedented sesquiterpenoid dimers unveiled bifurcating [4 + 2] cycloaddition and target differentiation of enantiomers

He TB, Yan BC, Zhou YF, Sang YQ, Li XN, Sun HD, Wang C, Xue XS, Puno PT

Chem Sci

29-Nov-2023

PMCID:	PMC10806648
doi:	10.1039/d3sc05233h
PMID:	38274075

Diverse O-methyltransferases catalyze the biosynthesis of floral benzenoids that repel aphids from the flowers of waterlily Nymphaea prolifera

Liu G, Fu J, Wang L, Fang M, Zhang W, Yang M, Yang X, Xu Y, Shi L, Ma X, Wang Q, Chen H, Yu C, Yu D, Chen F, Jiang Y

Hortic Res

06-Nov-2023

PMCID:	PMC10753166
doi:	10.1093/hr/uhad237
PMID:	38156285

Biological Activities of Natural Products III

Ekiert HM, Szopa A

Molecules

19-Jun-2023

PMCID:	PMC10305329
doi:	10.3390/molecules28124854
PMID:	37375409

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

RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review

Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD

Med Chem Res

29-Sep-2022

PMCID:	PMC9520115
doi:	10.1007/s00044-022-02963-2
PMID:	36193545

Functional Differentiation of Floral Color and Scent in Gall Midge Pollination: A Study of a Schisandraceae Plant

Gan SR, Du W, Wang XF

Plants (Basel)

02-Apr-2022

PMCID:	PMC9002483
doi:	10.3390/plants11070974
PMID:	35406954

Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China

Cao Y, Li R, Zhou S, Song L, Quan R, Hu H

J Ethnobiol Ethnomed

27-Oct-2020

PMCID:	PMC7590688
doi:	10.1186/s13002-020-00420-1
PMID:	33109239

The complete chloroplast genome of ‘black tiger 2’ (Kadsura coccinea (lem.) A.C. Smith) in southeast of China and phylogenetic relationshipsAQ1

Yang J, Wang XA, Gao MY, Wei XX

Mitochondrial DNA B Resour

13-Dec-2019

PMCID:	PMC7720960
doi:	10.1080/23802359.2019.1698328
PMID:	33366527

Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China

Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C

J Ethnobiol Ethnomed

19-Aug-2019

PMCID:	PMC6699132
doi:	10.1186/s13002-019-0316-1
PMID:	31426826

Characterization and genetic analysis of the complete chloroplast genome of Schisandra chinensis (Magnoliaceae: Schisandra), an herbal medicine from China

Tian Z

Mitochondrial DNA B Resour

12-Jul-2019

PMCID:	PMC7687546
doi:	10.1080/23802359.2019.1637291
PMID:	33365572

Detecting Schisandrae Chinensis Fructus and Its Chinese Patent Medicines with a Nucleotide Signature

Jiang W, Ren L, Guo M, Mantri N, Zhao S, Pang X

Genes (Basel)

22-May-2019

PMCID:	PMC6562420
doi:	10.3390/genes10050397
PMID:	31121984

Effects of an Endophytic Fungus Umbelopsis dimorpha on the Secondary Metabolites of Host–Plant Kadsura angustifolia

Qin D, Wang L, Han M, Wang J, Song H, Yan X, Duan X, Dong J

Front Microbiol

22-Nov-2018

PMCID:	PMC6262151
doi:	10.3389/fmicb.2018.02845
PMID:	30524412

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
Henricine B	42604341	Click to see CC(COC(=O)C)C(C)C(C1=CC(=C(C=C1)O)OC)C2=CC(=C(C=C2)O)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.405
HenricineB	137347693	Click to see CC(COC(=O)C)C(C)C(C1=CC(=C(C=C1)O)OC)C2=CC(=C(C=C2)O)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.405
> Lignans, neolignans and related compounds / Aryltetralin lignans
4-(3,4-dimethoxyphenyl)-7-hydroxy-6-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	14078175	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)OC)OC)OC)O)C	356.40	unknown	https://doi.org/10.1248/CPB.57.405
6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13844290	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)O)OC)C	342.40	unknown	https://doi.org/10.1248/CPB.57.405
7-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13844293	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)OC)O)C	342.40	unknown	https://doi.org/10.1248/CPB.57.405
8-(4-hydroxy-3-methoxyphenyl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	434449	Click to see CC1C(C(=O)C2=CC3=C(C=C2C1C4=CC(=C(C=C4)O)OC)OCO3)C	340.40	unknown	https://doi.org/10.1016/S0031-9422(00)82627-8
Arisantetralone D	14078176	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)OC)OC)OC)O)C	356.40	unknown	https://doi.org/10.1248/CPB.57.405
Enshicine	13844288	Click to see CC1C(C(=O)C2=CC3=C(C=C2C1C4=CC(=C(C=C4)O)OC)OCO3)C	340.40	unknown	https://doi.org/10.1016/S0031-9422(00)82627-8
EpiwulignanA1	13844294	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)OC)O)C	342.40	unknown	https://doi.org/10.1248/CPB.57.405
Wulignan A1	13844295	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)OC)O)C	342.40	unknown	https://doi.org/10.1248/CPB.57.405
Wulignan a2	13844292	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)O)OC)C	342.40	unknown	https://doi.org/10.1248/CPB.57.405
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
5-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol	15658444	Click to see CC(CC1=CC(=C(C=C1)OC)O)C(C)CC2=CC3=C(C=C2)OCO3	328.40	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
Isoanwulignan	135397589	Click to see CC(CC1=CC(=C(C=C1)OC)O)C(C)CC2=CC3=C(C=C2)OCO3	328.40	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
2,5-Bis(3,4-dimethoxyphenyl)-2-methoxy-3,4-dimethyloxolan-3-ol	74817671	Click to see CC1C(OC(C1(C)O)(C2=CC(=C(C=C2)OC)OC)OC)C3=CC(=C(C=C3)OC)OC	418.50	unknown	https://doi.org/10.1248/CPB.57.405
Galbelgin	609882	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	https://doi.org/10.1248/CPB.57.405
Ganschisandrine	11975478	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	https://doi.org/10.1248/CPB.57.405
Henricine	138108114	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C	386.40	unknown	https://doi.org/10.1055/S-2007-969265
Henricine A	42604340	Click to see CC1C(OC(C1(C)O)(C2=CC(=C(C=C2)OC)OC)OC)C3=CC(=C(C=C3)OC)OC	418.50	unknown	https://doi.org/10.1248/CPB.57.405
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1R,3S,7S,10R,12R,13S,15R,17S,18R,21S,22R,23S,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	162876955	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/10.1002/EJOC.200300560
CID 73086050	73086050	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/10.1002/EJOC.200300560
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R)-2-[(1S)-1-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one	162978286	Click to see CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C	941.10	unknown	https://doi.org/10.1002/EJOC.200300560
JuncosideI	137347208	Click to see CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C	941.10	unknown	https://doi.org/10.1002/EJOC.200300560
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3S,9R,12S,13S,16R,17R)-8,8,13,17-tetramethyl-16-[(1S)-1-[(2R)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-7-oxapentacyclo[10.7.0.01,3.03,9.013,17]nonadec-4-en-6-one	14844615	Click to see CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC6C4(C5)C=CC(=O)OC6(C)C)C)C	466.70	unknown	https://doi.org/10.1002/EJOC.200300560
(Z,6R)-6-[(1S,4R,5R,8S,9S,12S,13R)-13-(2-carboxyethyl)-4,8-dimethyl-12-prop-1-en-2-yl-5-tetracyclo[7.5.0.01,13.04,8]tetradec-10-enyl]-2-methylhept-2-enoic acid	163081373	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2C=CC(C3(C4)CCC(=O)O)C(=C)C)C)C	468.70	unknown	https://doi.org/10.1002/EJOC.200300560
(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/10.1002/EJOC.200300560
(Z,6R)-6-[(4R,5R,8R,12R,13R)-13-(2-carboxyethyl)-4,8-dimethyl-12-prop-1-en-2-yl-5-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]-2-methylhept-2-enoic acid	5320162	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	https://doi.org/10.1007/BF02980199
6-[13-(2-Carboxyethyl)-4,8-dimethyl-12-prop-1-en-2-yl-5-tetracyclo[7.5.0.01,13.04,8]tetradec-10-enyl]-2-methylhept-2-enoic acid	163081371	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2C=CC(C3(C4)CCC(=O)O)C(=C)C)C)C	468.70	unknown	https://doi.org/10.1002/EJOC.200300560
6-[13-(2-Carboxyethyl)-4,8-dimethyl-12-prop-1-en-2-yl-5-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]-2-methylhept-2-enoic acid	75183620	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	https://doi.org/10.1002/EJOC.200300560
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/10.1002/EJOC.200300560
8,8,13,17-Tetramethyl-16-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-7-oxapentacyclo[10.7.0.01,3.03,9.013,17]nonadec-4-en-6-one	14844614	Click to see CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC6C4(C5)C=CC(=O)OC6(C)C)C)C	466.70	unknown	https://doi.org/10.1002/EJOC.200300560
Nigranoic Acid	10814237	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	https://doi.org/10.1002/EJOC.200300560 https://doi.org/10.1007/BF02980199
> 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/10.1002/EJOC.200300560
Mangiferonic Acid	14034474	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/10.1002/EJOC.200300560
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[1-(4-Oxo-3-oxabicyclo[3.1.1]heptan-2-yl)-1-(8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.03,9.013,17]nonadeca-1(12),2,4-trien-16-yl)ethyl] acetate	77915999	Click to see CC(=O)OC(C)(C1CCC2(C1(CCC3=C2CCC4C(=C3)C=CC(=O)OC4(C)C)C)C)C5C6CC(C6)C(=O)O5	522.70	unknown	https://doi.org/10.1002/EJOC.200300560
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
1-[2-[2-[4a-hydroxy-6-[4-hydroxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-8a-methyl-2-oxo-5,6,7,8-tetrahydro-1H-naphthalen-1-yl]-1-benzoyloxyethyl]-1-hydroxy-2-methyl-3-oxocyclopentyl]ethyl benzoate	85150748	Click to see CC1C(C(CC(O1)OC2CCC3(C(C(=O)C=CC3(C2)O)CC(C4(C(=O)CCC4(C(C)OC(=O)C5=CC=CC=C5)O)C)OC(=O)C6=CC=CC=C6)C)O)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC	1185.30	unknown	https://doi.org/10.1002/EJOC.200300560
> Organoheterocyclic compounds / Furopyrans
(1R,3S,7S,10R,15R,17S,18R,21R,22S,23S,25R,29S)-22,23-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]nonacos-12-ene-5,14,19,24-tetrone	12080813	Click to see CC1C2C(C3(C4C(CCC56CC78C(CC=C5C(=O)C4(O2)O6)C(OC7CC(=O)O8)(C)C)(C(=O)C3(C)O)C)O)OC1=O	558.60	unknown	https://doi.org/10.1002/EJOC.200300560
(1R,3S,7S,10R,15R,17S,18R,21S,22R,23S,25R,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	12080812	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/10.1002/EJOC.200300560
(1R,3S,7S,10R,15R,17S,18R,21S,22R,23S,25R,29R)-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	101362629	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/10.1002/EJOC.200300560
22,23-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]nonacos-12-ene-5,14,19,24-tetrone	162914299	Click to see CC1C2C(C3(C4C(CCC56CC78C(CC=C5C(=O)C4(O2)O6)C(OC7CC(=O)O8)(C)C)(C(=O)C3(C)O)C)O)OC1=O	558.60	unknown	https://doi.org/10.1002/EJOC.200300560
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	85422652	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/10.1002/EJOC.200300560
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	73307279	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/10.1002/EJOC.200300560
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(9R,13R,16R,17R)-8,8,13,17-tetramethyl-16-[(1S)-1-[(2R)-6-oxo-2,3-dihydropyran-2-yl]ethyl]-7-oxatetracyclo[10.7.0.03,9.013,17]nonadeca-1(12),2,4-trien-6-one	162883830	Click to see CC(C1CCC2(C1(CCC3=C2CCC4C(=C3)C=CC(=O)OC4(C)C)C)C)C5CC=CC(=O)O5	450.60	unknown	https://doi.org/10.1002/EJOC.200300560
8,8,13,17-Tetramethyl-16-[1-(6-oxo-2,3-dihydropyran-2-yl)ethyl]-7-oxatetracyclo[10.7.0.03,9.013,17]nonadeca-1(12),2,4-trien-6-one	162883829	Click to see CC(C1CCC2(C1(CCC3=C2CCC4C(=C3)C=CC(=O)OC4(C)C)C)C)C5CC=CC(=O)O5	450.60	unknown	https://doi.org/10.1002/EJOC.200300560
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10-Hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) benzoate	10007357	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
(9-Hydroxy-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) benzoate	14605163	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1(C)O)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)OC	552.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
(9S,10S,11S)-3,4,5,19-tetramethoxy-9,10-dimethyl-11-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-10-ol	5317802	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC5=CC=CC=C5)OCO4)OC)OC)OC)OC	508.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
(9S,10S)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene	9802006	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/CPB.57.405
[(8R,9S,10S)-9-hydroxy-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] benzoate	14605165	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1(C)O)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)OC	552.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
[(8R,9S,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] benzoate	6713205	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
[(9S,10S,11R)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate	3001661	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
Arisanschinin K	332607	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012 https://doi.org/10.1248/CPB.57.405
Deoxyschizandrin	43595	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/CPB.57.405
Gomisin G	14992067	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012
Schisandrin	3001664	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1248/CPB.57.405
schisandrin A	155256	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/CPB.57.405
Schisandrol A	11102092	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1248/CPB.57.405
Schisantherin A	151529	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1016/J.FITOTE.2005.03.012 https://doi.org/10.1248/CPB.57.405
Schizandrin	23915	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1248/CPB.57.405

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Schisandra henryi

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