Schisandra sphenanthera

Details Top

Internal ID UUID644003d9002e0991822831
Scientific name Schisandra sphenanthera
Authority Rehder & E.H.Wilson
First published in Pl. Wilson. 1: 414 (1913)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Processed fruit used as a natural flavoring and aroma ingredient in beverages, confectionery, and sauces.

Industrial and craft applications:
- Dried fruit and extracts employed as flavor constituents in the food and beverage industry.

Food and beverages (non-medicinal):
- Fresh or dried fruit used in jams, jellies, syrups, and candied products; also as a flavoring component in non-alcoholic beverages and confectionery. Processing typically involves crushing/pureeing, sugar addition, and heat treatment for syrups and preserves.

Colorants and tanning:
- No established industrial colorants or tanning applications are reported for this taxon.

Wood and fiber:
- No established timber, pulp, or fiber uses are reported.

Fragrance and cosmetics:
- Fruit and extracts may contribute fruity/aromatic notes; however, documented cosmetic or fragrance uses are not well-established.

Properties relevant to use:
- The fruit’s flavor profile is characterized by acidic pulp and aromatic constituents such as lignans (schisandrin, schisandrol), enabling its use as a natural flavoring agent in processed foods and drinks.

Standards and regulation:
- Food safety and use in China are subject to national regulations on food additives and novel foods, and imports to other countries follow applicable food additive and novel food listings.

Sustainability and sourcing:
- Fruit for commercial use is harvested from wild populations and cultivated material; wild collection is typically non-timber/non-destructive but requires management to maintain population viability.

Synonyms Top

Scientific name Authority First published in
Schisandra flaccidiramosa C.R.Sun Bull. Bot. Res., Harbin 8(1): 123 (1988)
Schisandra chinensis var. rubriflora Franch. Nouv. Arch. Mus. Hist. Nat. , sér. 2, 8: 192 (1885 publ. 1886)
Schisandra grandiflora var. rubriflora (Franch.) C.K.Schneid. Bot. Gaz. 63: 523. 1917

Common names Top

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Language Common/alternative name
Arabic شزندرة إسفينية المئبر
Czech schizandra oranžová
Chinese 满山香
Chinese 五味子
Chinese 五香血藤
Chinese 华中五味子
Chinese 南五味子
Chinese 香石藤
Chinese 老鼠葡萄
Chinese 華中五味子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000495082
UNII O5261FJN9W
Tropicos 19300595
KEW urn:lsid:ipni.org:names:555104-1
The Plant List kew-2585411
Open Tree Of Life 70565
NCBI Taxonomy 13674
IPNI 555104-1
iNaturalist 542546
GBIF 3745294
EPPO SHSSH
EOL 5348414
USDA GRIN 70684
CMAUP NPO7385
PFAF Schisandra sphenanthera

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
Elucidating the multichromosomal structure within the Brasenia schreberi mitochondrial genome through assembly and analysis Shan Y, Li J, Duan X, Zhang X, Yu J BMC Genomics 29-Apr-2024
PMCID:PMC11059650
doi:10.1186/s12864-024-10331-0
PMID:38684976
Microbial communities of Schisandra sphenanthera Rehd. et Wils. and the correlations between microbial community and the active secondary metabolites Qin X, Pu H, Fang X, Shang Q, Li J, Zhao Q, Wang X, Gu W PeerJ 26-Apr-2024
PMCID:PMC11057425
doi:10.7717/peerj.17240
PMID:38685939
Natural products in atherosclerosis therapy by targeting PPARs: a review focusing on lipid metabolism and inflammation Zhang Y, Zhang XY, Shi SR, Ma CN, Lin YP, Song WG, Guo SD Front Cardiovasc Med 18-Apr-2024
PMCID:PMC11064802
doi:10.3389/fcvm.2024.1372055
PMID:38699583
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
A Drug Safety Briefing (II) in Transplantation from Real-World Individual Pharmacotherapy Management to Prevent Patient and Graft from Polypharmacy Risks at the Very Earliest Stage Wolf U Pharmaceuticals (Basel) 25-Feb-2024
PMCID:PMC10975568
doi:10.3390/ph17030294
PMID:38543080
Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids Yu X, Feng Y, Zhang J Life (Basel) 25-Jan-2024
PMCID:PMC10890521
doi:10.3390/life14020182
PMID:38398691
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
Environmental factors influencing potential distribution of Schisandra sphenanthera and its accumulation of medicinal components Shang J, Zhao Q, Yan P, Sun M, Sun H, Liang H, Zhang D, Qian Z, Cui L Front Plant Sci 12-Dec-2023
PMCID:PMC10756911
doi:10.3389/fpls.2023.1302417
PMID:38162305
Effects of Wuzhi Capsule on Whole-Blood Tacrolimus Concentration Levels: A Systematic Review and Meta-Analysis Zhang C, Ren X, Liu Y, Huang L, Feng Y, Zhang X Ther Drug Monit 27-Nov-2023
PMCID:PMC10769163
doi:10.1097/FTD.0000000000001155
PMID:38150711
Evaluation of the therapeutic efficacy of Vitex agnus-castus extract on cisplatin-induced hematotoxicity in female Wistar rats Tripathy A, Raghavendra AP, Dutta B, Surendran S Vet World 01-Nov-2023
PMCID:PMC10750742
doi:10.14202/vetworld.2023.2186-2191
PMID:38152275
Climate Change Dependence in Ex Situ Conservation of Wild Medicinal Plants in Crete, Greece Bariotakis M, Georgescu L, Laina D, Koufaki M, Souma M, Douklias S, Giannakakis KA, Chouli KN, Paoli L, Loppi S, Karousou R, Smykal P, Castanas E, Pirintsos SA Biology (Basel) 11-Oct-2023
PMCID:PMC10604457
doi:10.3390/biology12101327
PMID:37887037
Tissue-specific transcriptome and metabolome analyses reveal candidate genes for lignan biosynthesis in the medicinal plant Schisandra sphenanthera Sun B, Wang P, Guan M, Jia E, Li Q, Li J, Zhou Z, Ma P BMC Genomics 11-Oct-2023
PMCID:PMC10568845
doi:10.1186/s12864-023-09628-3
PMID:37821824
Efficacy, safety, and economy of shensongyangxin capsules for the treatment of coronary heart disease arrhythmia: a meta-analysis of randomized controlled trials Ma L, Li L, Ma F, Ma F, Ma S Ann Med Surg (Lond) 01-Sep-2023
PMCID:PMC10553141
doi:10.1097/MS9.0000000000001244
PMID:37811103
Editorial: Insights in experimental pharmacology and drug discovery: 2022 Latini A, Uroz CP, Trostchansky A Front Pharmacol 22-Aug-2023
PMCID:PMC10478218
doi:10.3389/fphar.2023.1250936
PMID:37675048
Bioactive Steroids Bearing Oxirane Ring Dembitsky VM Biomedicines 09-Aug-2023
PMCID:PMC10452232
doi:10.3390/biomedicines11082237
PMID:37626733

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillate 54675858 Click to see 167.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Deoxyshikonin 98914 Click to see CC(=CCCC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 272.29 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Justicidin D 5318737 Click to see 378.30 unknown https://doi.org/10.1002/HLCA.201100205
> Lignans, neolignans and related compounds / Aryltetralin lignans
Schisandrone 14078177 Click to see 356.40 unknown https://doi.org/10.1055/S-2007-969461
Wulignan A1 13844295 Click to see 342.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844304 Click to see 328.40 unknown via CMAUP database
5-[(2R,3S)-4-(1,3-benzodioxol-5-yl)-2,3-dimethylbutyl]-2,3-dimethoxyphenol 102322866 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C(=C3)OC)OC)O 358.40 unknown via CMAUP database
erythro-Austrobailignan-6 10381847 Click to see 328.40 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 https://doi.org/10.1016/J.CHROMA.2008.09.070
Pregomisin 181796 Click to see CC(CC1=CC(=C(C(=C1)OC)OC)O)C(C)CC2=CC(=C(C(=C2)OC)OC)O 390.50 unknown https://doi.org/10.1016/J.BMCL.2012.11.040
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
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/10.1016/S0031-9422(00)97848-8
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Micranoic Acid B 11759710 Click to see 344.50 unknown https://doi.org/10.1002/HLCA.201000242
N-[(1S,3R,7R,10S,12S,15S,17S,18R,21R,22S,23R,25S,29S)-14,18,23-trihydroxy-9,9,18,23,25-pentamethyl-5,19,24-trioxo-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-13-en-12-yl]acetamide 25141318 Click to see 617.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
N-[(3R,7R,10S,12S,17S,18R,21R,22S,23R,25S,29S)-14,18,23-trihydroxy-9,9,18,23,25-pentamethyl-5,19,24-trioxo-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-13-en-12-yl]acetamide 163189897 Click to see 617.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Heterocyclic fatty acids / Furanoid fatty acids
Wyerone 643733 Click to see CCC=CC#CC(=O)C1=CC=C(O1)C=CC(=O)OC 258.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5-methyl-2-propan-2-ylphenyl) (2R)-2-methylbutanoate 92284339 Click to see 234.33 unknown via CMAUP database
Thymol isobutyrate 228738 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C(C)C 220.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Bornyl acetate 6950274 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate 443131 Click to see 196.29 unknown via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate 442460 Click to see 196.29 unknown via CMAUP database
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Terpin 6651 Click to see CC1(CCC(CC1)C(C)(C)O)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Bullatantriol 71430886 Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O 256.38 unknown via CMAUP database
(+)-Delta-cadinol 11990360 Click to see 222.37 unknown via CMAUP database
(1R,4aR,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene 6432308 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown via CMAUP database
[(4aS,8S,8aR)-5-methylidene-8-propan-2-yl-4,4a,6,7,8,8a-hexahydro-1H-naphthalen-2-yl]methanol 162867378 Click to see 220.35 unknown https://doi.org/10.1002/HLCA.201100205
[4-[(1R)-1,2,2-trimethylcyclopentyl]phenyl]methanol 56589566 Click to see 218.33 unknown https://doi.org/10.1002/HLCA.201100205
2-[(1S,2S,6R,8S)-2,6-dimethyl-9,10-dioxatricyclo[6.2.2.01,6]dodec-11-en-12-yl]propan-2-ol 162870320 Click to see CC1CCCC2(C13C=C(C(C2)OO3)C(C)(C)O)C 252.35 unknown https://doi.org/10.1007/S10600-011-0042-Y
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
alpha-Santalene 94164 Click to see 204.35 unknown via CMAUP database
Cadin-4-en-10-ol 519662 Click to see 222.37 unknown via CMAUP database
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
delta-Amorphene 12306059 Click to see 204.35 unknown via CMAUP database
delta-Cadinene 441005 Click to see 204.35 unknown via CMAUP database
Elixene 94254 Click to see 204.35 unknown via CMAUP database
gamma-Cadinene 6432404 Click to see 204.35 unknown via CMAUP database
Grasshopper ketone 13922639 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)O)(C)C 224.30 unknown https://doi.org/10.1002/HLCA.201000242
Longipinenone 101117096 Click to see 218.33 unknown via CMAUP database
Npc322403 10220146 Click to see 224.30 unknown https://doi.org/10.1002/HLCA.201000242
Npc57877 6431302 Click to see 222.37 unknown via CMAUP database
Npc91574 12306054 Click to see 204.35 unknown via CMAUP database
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown via CMAUP database
tau-Muurolol 6432221 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Tricyclo[4.4.0.0(2,7)]dec-3-ene, 8-isopropyl-1,3-dimethyl-, (1S,2R,6R,7R,8S)-(+)- 6432119 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(2Z,4E)-5-deuterio-5-[(1S,6S)-1-hydroxy-2,6-dimethyl-4-oxo-6-(trideuteriomethyl)cyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid 11973680 Click to see 268.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene 11106485 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
[(6R)-5,5-dimethyl-1-methylidenespiro[5.5]undec-9-en-9-yl]methanol 101556137 Click to see CC1(CCCC(=C)C12CCC(=CC2)CO)C 220.35 unknown https://doi.org/10.1002/HLCA.201100205
Npc268130 29073 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2R,4aR,8aR)-1,2,3,4,4a,5,6,8a-Octahydro-4a,8-dimethyl-alpha-methylene-2-naphthaleneacetic acid 168796 Click to see 234.33 unknown via CMAUP database
Costic acid 6451579 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(-)-Dehydrocostus lactone 73174 Click to see 230.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6R)-6-[(3R,3aR,6S,7S,9bR)-6-(3-methoxy-3-oxopropyl)-3a,9b-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,9-octahydro-1H-cyclopenta[a]naphthalen-3-yl]-2-methylhept-2-enoic acid 6443936 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC(C3CCC(=O)OC)C(=C)C)C)C 470.70 unknown via CMAUP database
[(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14015448 Click to see 468.80 unknown via CMAUP database
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 456.70 unknown https://doi.org/10.1002/HLCA.201000242
Anwuweizic acid 5478015 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/10.1016/J.CHROMA.2008.09.070
Anwuweizicacid 14104879 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.201000242
Nigranoic Acid 10814237 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(E,6R)-6-[(1S,3R,6R,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.0^{1,3.0^{3,8.0^{12,16]octadecanyl]-2-methylhept-2-enoic acid 72726483 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.201000242
(Z,6R)-6-[(1S,3R,6R,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoic acid 162956737 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.201000242
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 454.70 unknown https://doi.org/10.1016/S0031-9422(00)97848-8
Schisandrolic acid 102066685 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown via CMAUP database
Schisandronic acid 101277401 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)97848-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
Sphenasin A 25180763 Click to see CC1CCC(=O)OC2C1C3(CCC45CC46C=CC(=O)C(C6CC(C5C3(C2)C)O)(C)C)C 426.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(2S)-2-[1-[(5R,8S,10S,13R,14S,17S)-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]ethyl]-5-methyl-2,3-dihydropyran-6-one 138108982 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90673-3
2-[1-(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)ethyl]-5-methyl-2,3-dihydropyran-6-one 77736022 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90673-3
Schisanol 135397241 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90673-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(1R,5R)-4-methylidene-1-propan-2-ylspiro[4.5]dec-8-ene-8-carboxylic acid 162867377 Click to see 234.33 unknown https://doi.org/10.1002/HLCA.201100205
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1S,3R,7R,10S,11S,13R,14S,18R,19R)-18-[(3S,5R,7R,8R)-3,8-dimethyl-2-oxo-1,6-dioxaspiro[4.4]nonan-7-yl]-1,11-dihydroxy-9,9,18-trimethyl-4,8,15-trioxapentacyclo[11.7.0.03,7.03,10.014,19]icosane-5,16-dione 101781707 Click to see 548.60 unknown https://doi.org/10.1002/HLCA.201000242
18-(3,8-Dimethyl-2-oxo-1,6-dioxaspiro[4.4]nonan-7-yl)-1,11-dihydroxy-9,9,18-trimethyl-4,8,15-trioxapentacyclo[11.7.0.03,7.03,10.014,19]icosane-5,16-dione 163033461 Click to see CC1CC2(CC(C(=O)O2)C)OC1C3(CC(=O)OC4C3CC5(C4CC(C6C(OC7C6(C5)OC(=O)C7)(C)C)O)O)C 548.60 unknown https://doi.org/10.1002/HLCA.201000242
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
CID 20130941 20130941 Click to see 134.09 unknown via CMAUP database
D-Malic acid 92824 Click to see 134.09 unknown via CMAUP database
L-Malic Acid 222656 Click to see 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,3aR,8aS)-1-methyl-4-methylidene-6-propan-2-yl-2,3,3a,5,8,8a-hexahydroazulen-1-ol 162927020 Click to see CC(C)C1=CCC2C(CCC2(C)O)C(=C)C1 220.35 unknown https://doi.org/10.1007/S10600-011-0042-Y
> Organoheterocyclic compounds / Benzodioxoles
1,3-Benzodioxole-5-carboxylic acid 7196 Click to see 166.13 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Chromone, 5-hydroxy-7-methoxy-2-methyl-6-(3-methyl-2-butenyl)- 615800 Click to see 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-2,2,8-trimethylpyrano[3,2-g]chromen-6-one 13166810 Click to see 258.27 unknown via CMAUP database
Greveichromenol 71450427 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)CO)C 274.27 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1R,3R,7R,9R,10S,13R,14R,15S,17R,18S,21R,22R,23R,25R,29S)-14,23-dihydroxy-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-5,19,24,26-tetrone 162939060 Click to see 576.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(1S,3R,4S,7R,8R,9R,11S,14S,26S)-9-hydroxy-4,9,11,19,19-pentamethyl-2,6,18,25-tetraoxaheptacyclo[12.10.1.11,8.03,7.014,23.016,20.011,26]hexacosa-16,20,22-triene-5,10,24-trione 162942675 Click to see CC1C2C(C3C4C(CCC56CC7=COC(C7=CC=C5C(=O)C4(O2)O6)(C)C)(C(=O)C3(C)O)C)OC1=O 482.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(1S,3R,4S,7R,8S,9S,11S,14S,26S)-4,9,11,19,19-pentamethyl-2,6,18,25-tetraoxaheptacyclo[12.10.1.11,8.03,7.014,23.016,20.011,26]hexacosa-16,20,22-triene-5,10,24-trione 17752598 Click to see 466.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(1S,3R,7R,9R,10S,13S,14S,16R,17R,19R,20S,21R,24S,25R,27S,30S)-14,19-dihydroxy-9-(hydroxymethyl)-9,17,19,24-tetramethyl-4,8,15,22,26,28-hexaoxanonacyclo[14.12.1.117,20.01,13.03,7.03,10.014,27.021,25.027,30]triacontane-5,18,23-trione 162928862 Click to see CC1C2C(C3C4C(C5CC67CC89C(CCC6C(C4(O2)O7)(O5)O)C(OC8CC(=O)O9)(C)CO)(C(=O)C3(C)O)C)OC1=O 576.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(1S,3S,4R,7R,8S,9R,11S,14S,26S)-4,9-dihydroxy-4,9,11,19,19-pentamethyl-2,6,18,25-tetraoxaheptacyclo[12.10.1.11,8.03,7.014,23.016,20.011,26]hexacosa-16,20,22-triene-5,10,24-trione 17752708 Click to see 498.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(1S,3S,4R,7R,8S,9S,11S,14S,26S)-4-hydroxy-4,9,11,19,19-pentamethyl-2,6,18,25-tetraoxaheptacyclo[12.10.1.11,8.03,7.014,23.016,20.011,26]hexacosa-16,20,22-triene-5,10,24-trione 17752597 Click to see 482.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
14,19-Dihydroxy-9-(hydroxymethyl)-9,17,19,24-tetramethyl-4,8,15,22,26,28-hexaoxanonacyclo[14.12.1.117,20.01,13.03,7.03,10.014,27.021,25.027,30]triacontane-5,18,23-trione 72995226 Click to see 576.60 unknown https://doi.org/10.1021/OL060324D
14,23-Dihydroxy-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-5,19,24,26-tetrone 73070681 Click to see 576.60 unknown https://doi.org/10.1021/OL060324D
Sphenadilactone A 11527099 Click to see CC1C2C(C3C4C(C5CC67CC89C(CCC6C(C4(O2)O7)(O5)O)C(OC8CC(=O)O9)(C)CO)(C(=O)C3(C)O)C)OC1=O 576.60 unknown https://doi.org/10.1021/OL060324D
Sphenadilactone B 11713947 Click to see 576.60 unknown https://doi.org/10.1021/OL060324D
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> 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 326.30 unknown https://doi.org/10.1002/HLCA.201000242
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans
3,5-Di-O-methyl-8-prenylafzelechin-4beta-ol 44257167 Click to see 386.40 unknown via CMAUP database
4,5-Di-O-methyl-8-prenylafzelechin-4beta-ol 44257168 Click to see 386.40 unknown via CMAUP database
4,5,4'-Trihydroxy-7-methoxy-8-prenylflavan 44257139 Click to see 356.40 unknown via CMAUP database
5-O-Methyl-8-prenylafzelechin-4beta-ol 44257163 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4beta-Hydroxyobovatachromene 44257164 Click to see 370.40 unknown via CMAUP database
Yukovanol 44584009 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(+)-Schisandrin B 158103 Click to see 400.50 unknown via CMAUP database
(11R)-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-ol 45356879 Click to see 416.50 unknown via CMAUP database
(12-Hydroxy-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl) benzoate 5321176 Click to see 520.50 unknown https://doi.org/10.1248/CPB.38.1408
https://doi.org/10.1016/S0031-9422(00)90673-3
https://doi.org/10.1039/C1AN15527J
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
(14-Hydroxy-3,4,5,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) benzoate 14890559 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)O 522.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
(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) 2-methylbut-2-enoate 633944 Click to see CC=C(C)C(=O)OC1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)C)C 498.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
(8R,9R)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-phenoxytricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-9-ol 6326195 Click to see 524.60 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
(8S,9R,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol 5317798 Click to see 508.60 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
(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 552.60 unknown https://doi.org/10.1248/CPB.38.1408
(9R)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol 5321992 Click to see 508.60 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
(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 508.60 unknown https://doi.org/10.1016/J.PHYMED.2012.07.017
(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 via CMAUP database
[(8R,9S,10S)-14-hydroxy-3,4,5,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] benzoate 14890558 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)O 522.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
[(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] (Z)-2-methylbut-2-enoate 16745516 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC 514.60 unknown https://doi.org/10.1248/CPB.38.1408
[(8R,9S,10S)-9,14-dihydroxy-3,4,5,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] benzoate 21672544 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)O 538.60 unknown https://doi.org/10.1016/J.BMCL.2012.11.040
[(8S,9S,10S)-14-hydroxy-3,4,5,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] benzoate 163032996 Click to see 522.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
[(8S,9S,10S)-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] (E)-2-methylbut-2-enoate 163195332 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
[(9S,10S)-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 5480968 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 via CMAUP database
1,2,3,10,11,12-Hexamethoxy-6,7-dimethyl-5,6,7,8-tetrahydrodibenzo(a,c)(8)annulen-6-ol 23915 Click to see 432.50 unknown https://doi.org/10.1016/J.PHYMED.2012.07.017
3,4,14,15,16-Pentamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-5,11-diol 14213994 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)O)OC)OC)OC)OC)OC)O 418.50 unknown https://doi.org/10.1016/0031-9422(91)85290-G
4,5,14,15,16-Pentamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-3-ol 433451 Click to see 402.50 unknown https://doi.org/10.1248/CPB.38.1408
5,6,7,8-Tetrahydro-1,2,3,10,11,12-hexamethoxydibenzo[a,c]cyclooctene 19020980 Click to see 388.50 unknown via CMAUP database
Angeloylgomisin P 13844273 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC 514.60 unknown https://doi.org/10.1248/CPB.38.1408
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/10.1248/CPB.38.1408
Arisanschinin M 71521607 Click to see 514.60 unknown via CMAUP database
Arisanschinin N 5321171 Click to see 514.60 unknown via CMAUP database
Benzoylgomisin O 91826818 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3 520.60 unknown via CMAUP database
Benzoylgomisin Q 14605164 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/10.1248/CPB.38.1408
Besigomsin 3001662 Click to see 416.50 unknown via CMAUP database
CID 558009 558009 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC 514.60 unknown https://doi.org/10.1248/CPB.38.1408
Deoxyschizandrin 43595 Click to see 416.50 unknown via CMAUP database
Epigomisin O 5317081 Click to see 416.50 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
https://doi.org/10.1016/0031-9422(91)85290-G
Gomisin A 68781 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3 416.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263323/
Gomisin B 6443826 Click to see 514.60 unknown https://doi.org/10.1248/CPB.38.1408
Gomisin G 14992067 Click to see 536.60 unknown via CMAUP database
Gomisin J 3001686 Click to see 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
Gomisin S 14213995 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)O)OC)OC)OC)OC)OC)O 418.50 unknown https://doi.org/10.1016/0031-9422(91)85290-G
Interiotherin A 21125391 Click to see 504.50 unknown via CMAUP database
Interiotherin B 20839677 Click to see 498.50 unknown via CMAUP database
Interiotherin-A 5480966 Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3 504.50 unknown via CMAUP database
InteriotherinA 177359 Click to see 504.50 unknown https://doi.org/10.1016/J.PHYMED.2012.07.017
Rubschisandrin 174277 Click to see 400.50 unknown via CMAUP database
Schisandrin 3001664 Click to see 432.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
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 via CMAUP database
Schisandrin B 108130 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)OC)OCO3 400.50 unknown https://doi.org/10.1016/J.ACA.2009.12.039
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263323/
Schisandrin C 443027 Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4CC1C)OCO5)OC)OC)OCO3 384.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263323/
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 via CMAUP database
Schisandrol B 634470 Click to see 416.50 unknown via CMAUP database
Schisanhenol 73057 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)O)OC)OC 402.50 unknown https://doi.org/10.1248/CPB.38.1408
https://doi.org/10.1016/J.BMCL.2012.11.040
https://doi.org/10.1039/C1AN15527J
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/10.1248/CPB.38.1408
https://doi.org/10.1016/S0031-9422(00)90673-3
https://doi.org/10.1016/J.BMCL.2012.11.040
Schisantherin B 6438572 Click to see 514.60 unknown https://doi.org/10.1248/CPB.38.1408
https://doi.org/10.1016/J.CHROMA.2008.09.070
https://doi.org/10.1039/C1AN15527J
Schisantherin D 163067 Click to see 520.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.010
https://doi.org/10.1016/S0031-9422(00)90673-3
https://doi.org/10.1248/CPB.38.1408
Schisantherin E 13844274 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)O 538.60 unknown https://doi.org/10.1248/CPB.38.1408
Schisantherin-D 5480967 Click to see 520.50 unknown via CMAUP database
Schizandrer A 163338 Click to see 536.60 unknown https://doi.org/10.1248/CPB.38.1408
Schizantherin E; 5,6,7,8-Tetrahydro-1,2,10,11,12-pentamethoxy-6,7-dimethyl-dibenzo[a,c]cyclooctene-3,7,8-triol-8-benzoate Stereoisomer 5321177 Click to see 538.60 unknown https://doi.org/10.1039/C1AN15527J
https://doi.org/10.1248/CPB.38.1408
Tigloylgomisin O 5318776 Click to see CC=C(C)C(=O)OC1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)C)C 498.60 unknown https://doi.org/10.1016/0031-9422(91)85290-G
Tigloylgomisin P 5318785 Click to see 514.60 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
https://doi.org/10.1248/CPB.38.1408

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