Details Top

Internal ID UUID643ff3bf30d2b935538322
Scientific name Kadsura japonica
Authority (L.) Dunal
First published in Monogr. Anonac. : 57 (1817)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Among the Japanese, the stems and roots of Kadsura japonica have long been collected for mild decoctions used to ease coughs and “astringe the mouth” after respiratory irritation, and for soothing throat hoarseness and expectorating phlegm—recorded in 18th–19th century Japanese materia medica such as Honzō kōmoku keimō (Shōtei Honzō kōmoku keimō) and Chōyaku chōhō (Tsukiyama kōkyū chōyaku chōhō). In classical Kampō, “Hannō” (Kadsura japonica) appears in traditional formulas such as Hannōkōru and Hannōgan, where the root bark was traditionally used to ease hoarseness, throat inflammation, and bronchial discomfort; these preparations were typically decocted with other ingredients, and the root bark is the plant part specified in those formulations (Hōsei Chōki, 1746; Nakai Chōkō, 1721; Taki Shōhō, 1786). Within contemporary Chinese literature, Japanese roots have occasionally been substituted for other Schisandraceae in weak, short steeps for cough and laryngitis, but the principal documented use for this taxon remains the decoction of stems/roots for throat and respiratory irritation (Miyazaki, 1985).

One practical, widely described recipe is a traditional, gentle decoction: simmer 6–9 g of dried stems (or 3–6 g of root bark) in 600–900 mL water for 30–40 minutes, strain, and take up to three small doses a day for throat hoarseness or cough. An alternative that mirrors long-standing Kampō practice is a 1:5 ethanol tincture, macerating 20 g of finely chopped root bark in 100 mL 45–50% ethanol for two weeks, shaking daily, then pressing; the final liquid is taken in 3–5 mL doses, two to three times a day. Safety notes: the dose should not exceed 9 g of stems per day; consult a qualified practitioner if pregnant, breastfeeding, or taking other medicines; and discontinue if gastrointestinal upset occurs (Miyazaki, 1985; Japanese materia medica references; Taki Shōhō, 1786).

The stems and root bark contain lignans such as schisandrin, gomisin A, gomisin J and B, and related dibenzocyclooctadiene derivatives, together with triterpenoids including kadsulactone-type schisandrane-type compounds that are well documented for this species and plausibly underpin the traditional antitussive and astringent actions (Wang et al., 2013; Dong et al., 2019). Modern relevance: active constituents continue to draw pharmacochemical study, and Japanese-style Hannō remains available in East Asian marketplaces as a specialized tea and decoction ingredient for throat care (Miyazaki, 1985; Wang et al., 2013; Dong et al., 2019).

General Uses Top

Suggest a correction!

Common products:
- Ornamental climber: Kadsura japonica is widely cultivated as an evergreen woody vine for garden and public‑landscape use. The plant is prized for its glossy, leathery foliage that remains attractive throughout the year and for its pendant clusters of small, bright red‑orange berries that persist into winter, providing visual interest in otherwise dormant periods. It is marketed by commercial nurseries in temperate regions (USDA zones 6–9) and appears in the catalogs of major horticultural societies such as the Royal Horticultural Society Plant Finder (2023). Typical applications include training on trellises, arbors, pergolas, and as a ground‑cover vine on slopes and embankments. Several horticultural cultivars have been selected for particularly compact growth, enhanced berry display, and increased cold‑hardiness, expanding its market appeal to landscape designers and home gardeners.

Properties relevant to use:
- Morphological traits: A vigorous, twining liana attaining 8–12 m in length, with opposite, simple leaves 4–8 cm long and woody stems that can be trained to a stable framework. The plant tolerates temperatures down to −20 °C and prefers moist, well‑drained soils, making it suitable for temperate gardens where evergreen climbing species are in demand.
- Genetic resources: The complete chloroplast genome of K. japonica (GenBank MG742861) has been published, providing a high‑resolution marker for phylogenetic inference within the family Schisandraceae. Additionally, comprehensive transcriptome data (NCBI SRA PRJNA522272) are publicly available, allowing researchers to investigate lignan biosynthetic pathways and comparative genomics of woody vines. The species is frequently employed as a non‑model organism in molecular studies of lignan biosynthesis because of its high lignan content in stems and leaves, facilitating functional annotation of candidate genes.

Sustainability and sourcing:
- Commercial propagation is almost entirely through vegetative cuttings and controlled seed production in certified nurseries, thereby limiting wild harvest pressure. K. japonica is included in regional ex‑situ conservation programs, ensuring that nursery stock originates from cultivated material rather than field collection. The plant’s relatively low ecological footprint in cultivation (minimal pesticide demand, adaptation to low‑maintenance landscapes) further supports sustainable sourcing.

Standards and regulation:
- The horticultural trade of K. japonica complies with national plant certification schemes such as the United Kingdom Plant Passport system and with international phytosanitary standards established by the International Plant Protection Convention (IPPC). These regulations require documented phytosanitary inspection and certification of nursery stock before interstate or international movement.

Synonyms Top

Scientific name Authority First published in
Schisandra japonica Baill. Hist. Pl. 1: 150 (1868)
Uvaria japonica L. Sp. Pl. : 536 (1753)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic كدسورة يابانية
Japanese サネカズラ
Japanese ビナンカズラ
Japanese 実葛
Russian Кадсура японская
Chinese 南五味子
Chinese 日本南五味子
Chinese 红骨蛇
Chinese 美男葛
Chinese 日本五味子

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000357341
UNII BA1BC7AXOB
Tropicos 50073315
KEW urn:lsid:ipni.org:names:554582-1
The Plant List kew-2335511
PFAF Kadsura japonica
Open Tree Of Life 1018722
NCBI Taxonomy 105750
IPNI 554582-1
iNaturalist 429262
GBIF 3745214
Freebase /m/0flgq_
EPPO KADJA
EOL 5348453
USDA GRIN 20913
Wikipedia Kadsura_japonica

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
Comparative analysis of mitochondrial genomes of Schisandra repanda and Kadsura japonica Lee HJ, Lee Y, Lee SC, Kim CK, Kang JN, Kwon SJ, Kang SH Front Plant Sci 03-Jul-2023
PMCID:PMC10352487
doi:10.3389/fpls.2023.1183406
PMID:37469771
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence Linn YH, Ei WW, Myint LM, Lwin KM Virusdisease 14-Jul-2021
PMCID:PMC8473485
doi:10.1007/s13337-021-00714-2
PMID:34631974
Plant-derived lignans as potential antiviral agents: a systematic review Xu XY, Wang DY, Li YP, Deyrup ST, Zhang HJ Phytochem Rev 31-May-2021
PMCID:PMC8165688
doi:10.1007/s11101-021-09758-0
PMID:34093097
A diverse global fungal library for drug discovery Niu G, Annamalai T, Wang X, Li S, Munga S, Niu G, Tse-Dinh YC, Li J PeerJ 27-Nov-2020
PMCID:PMC7703384
doi:10.7717/peerj.10392
PMID:33312768
An Ethnobotanical Study on Qīng-Căo-Chá Tea in Taiwan Huang SS, Chen TY, Deng JS, Pao LH, Cheng YC, Chao J Front Pharmacol 25-Jun-2020
PMCID:PMC7329985
doi:10.3389/fphar.2020.00931
PMID:32670061
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
Screening of promising chemotherapeutic candidates from plants extracts Kinjo J, Nakano D, Fujioka T, Okabe H J Nat Med 16-Apr-2016
PMCID:PMC4935755
doi:10.1007/s11418-016-0992-2
PMID:27086008
Ethanol Extract of Cirsium japonicum var. ussuriense Kitamura Exhibits the Activation of Nuclear Factor Erythroid 2-Related Factor 2-dependent Antioxidant Response Element and Protects Human Keratinocyte HaCaT Cells Against Oxidative DNA Damage Yoo OK, Choi BY, Park JO, Lee JW, Park BK, Joo CG, Heo HJ, Keum YS J Cancer Prev 30-Mar-2016
PMCID:PMC4819669
doi:10.15430/JCP.2016.21.1.66
PMID:27051652
Traditional Chinese herbal medicine as a source of molecules with antiviral activity Li T, Peng T Antiviral Res 12-Nov-2012
PMCID:PMC7114103
doi:10.1016/j.antiviral.2012.10.006
PMID:23153834
The constituents of Kadsura japonica Dunal. I. The structures of three new lignans, acetyl-, angeloyl- and caproyl-binankadsurin A. NORIYUKI OOKAWA, YUKINOBU IKEYA, HEIHACHIRO TAGUCHI, ITIRO YOSIOKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.29.123
Identification of GABA A receptor modulators in Kadsura longipedunculata and assignment of absolute configurations by quantum-chemical ECD calculations Zaugg J, Ebrahimi SN, Smiesko M, Baburin I, Hering S, Hamburger M Phytochemistry 31-Aug-2011
PMCID:PMC3201904
doi:10.1016/j.phytochem.2011.08.014
PMID:21889177
Cabomba as a model for studies of early angiosperm evolution Vialette-Guiraud AC, Alaux M, Legeai F, Finet C, Chambrier P, Brown SC, Chauvet A, Magdalena C, Rudall PJ, Scutt CP Ann Bot 12-Apr-2011
PMCID:PMC3170152
doi:10.1093/aob/mcr088
PMID:21486926
Inhibition of nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophages by Jeju plant extracts Yang EJ, Yim EY, Song G, Kim GO, Hyun CG Interdiscip Toxicol 28-Dec-2009
PMCID:PMC2984114
doi:10.2478/v10102-009-0022-2
PMID:21217861

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 / Benzoic acids and derivatives / Benzoic acid esters
[(4R,5Z,7R,8R,9R)-4-(2-methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] benzoate 163195529 Click to see 536.50 unknown https://doi.org/10.1055/S-2005-871271
[4-(2-Methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] benzoate 163011832 Click to see CC1CC(=CC(=O)OC)C2(COC3=C2C(=CC4=C3OCO4)C(C1C)OC(=O)C5=CC=CC=C5)C(=O)C(=O)OC 536.50 unknown https://doi.org/10.1055/S-2005-871271
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1248/CPB.29.123
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(24Z)-3,4-Secolanosta-4(28),9(11),24-triene-3,26-dioic acid 86573576 Click to see 470.70 unknown https://doi.org/10.1248/CPB.29.123
Kadsuric acid 5384417 Click to see 470.70 unknown https://doi.org/10.1248/CPB.29.123
> Organoheterocyclic compounds / Benzodioxoles
[(4R,5Z,7R,8R,9R)-4-(2-methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] (2R)-2-methylbutanoate 163194033 Click to see CCC(C)C(=O)OC1C(C(CC(=CC(=O)OC)C2(COC3=C2C1=CC4=C3OCO4)C(=O)C(=O)OC)C)C 516.50 unknown https://doi.org/10.1055/S-2005-871271
[(4R,5Z,7R,8R,9R)-4-(2-methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] (Z)-2-methylbut-2-enoate 163191256 Click to see CC=C(C)C(=O)OC1C(C(CC(=CC(=O)OC)C2(COC3=C2C1=CC4=C3OCO4)C(=O)C(=O)OC)C)C 514.50 unknown https://doi.org/10.1055/S-2005-871271
[4-(2-Methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] 2-methylbut-2-enoate 75049128 Click to see 514.50 unknown https://doi.org/10.1055/S-2005-871271
[4-(2-Methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] 2-methylbutanoate 75052150 Click to see CCC(C)C(=O)OC1C(C(CC(=CC(=O)OC)C2(COC3=C2C1=CC4=C3OCO4)C(=O)C(=O)OC)C)C 516.50 unknown https://doi.org/10.1055/S-2005-871271
methyl 2-[(4R,5Z,7R,8R,9R)-9-acetyloxy-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-4-yl]-2-oxoacetate 163186608 Click to see 474.50 unknown https://doi.org/10.1055/S-2005-871271
Methyl 2-[9-acetyloxy-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-4-yl]-2-oxoacetate 85260760 Click to see 474.50 unknown https://doi.org/10.1055/S-2005-871271
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6S)-4-acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] acetate 163106975 Click to see 532.40 unknown https://doi.org/10.1016/0031-9422(95)00043-7
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(11-Acetyloxy-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 73807412 Click to see CC=C(C)C(=O)OC1C(C(C(C2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)OC(=O)C)C)C 556.60 unknown https://doi.org/10.1246/BCSJ.50.1824
(16-Hydroxy-3,4,5,14,15-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) 2-methylbut-2-enoate 85123393 Click to see 500.60 unknown https://doi.org/10.1016/0031-9422(95)00043-7
(16-Hydroxy-3,4,5,14,15-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) acetate 163020760 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C)OC)OC)OC)O)OC)OC 460.50 unknown https://doi.org/10.1016/0031-9422(95)00043-7
(3-Hydroxy-4,5,19-trimethoxy-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) 2-methylbut-2-enoate 73175761 Click to see 484.50 unknown https://doi.org/10.1248/CPB.29.123
(3-Hydroxy-4,5,19-trimethoxy-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) hexanoate 162863341 Click to see 500.60 unknown https://doi.org/10.1248/CPB.29.123
(8-Benzoyloxy-9,19-dihydroxy-3,4,5-trimethoxy-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 162971132 Click to see 642.60 unknown https://doi.org/10.1055/S-2005-871271
(9-Hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-11-oxo-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 162860192 Click to see 528.50 unknown https://doi.org/10.1055/S-2005-871271
(9S,10S)-19-hydroxy-3,4,5-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-one 162861230 Click to see 400.40 unknown https://doi.org/10.1055/S-2005-871271
(9S,10S)-5-hydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-one 101769028 Click to see 400.40 unknown https://doi.org/10.1055/S-2005-871271
[(8R,9R,10R)-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 124527669 Click to see 536.60 unknown https://doi.org/10.1055/S-2005-871271
[(8R,9S,10R,11S)-11-acetyloxy-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 163187941 Click to see 556.60 unknown https://doi.org/10.1246/BCSJ.50.1824
[(8S,9R,10R)-16-hydroxy-3,4,5,14,15-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (Z)-2-methylbut-2-enoate 101927629 Click to see 500.60 unknown https://doi.org/10.1016/0031-9422(95)00043-7
[(8S,9R,10R)-16-hydroxy-3,4,5,14,15-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] acetate 101927630 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C)OC)OC)OC)O)OC)OC 460.50 unknown https://doi.org/10.1016/0031-9422(95)00043-7
[(8S,9S,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-11-oxo-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 163191262 Click to see 528.50 unknown https://doi.org/10.1055/S-2005-871271
[(8S,9S,10S,11R)-8-benzoyloxy-9,19-dihydroxy-3,4,5-trimethoxy-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 162971133 Click to see 642.60 unknown https://doi.org/10.1055/S-2005-871271
[(8S,9S,10S,11R)-9,19-dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] (Z)-2-methylbut-2-enoate 163187202 Click to see 598.60 unknown https://doi.org/10.1055/S-2005-871271
[(9R,10R,11S)-3-hydroxy-4,5,19-trimethoxy-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] (Z)-2-methylbut-2-enoate 163194958 Click to see 484.50 unknown https://doi.org/10.1248/CPB.29.123
[(9R,10R,11S)-3-hydroxy-4,5,19-trimethoxy-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] acetate 162941346 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC(=O)C)OCO4)OC)O)OC)OC 444.50 unknown https://doi.org/10.1248/CPB.29.123
[(9R,10R,11S)-3-hydroxy-4,5,19-trimethoxy-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] hexanoate 162863342 Click to see 500.60 unknown https://doi.org/10.1248/CPB.29.123
[9,19-Dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-8-(2-methylbut-2-enoyloxy)-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] 2-methylbut-2-enoate 163014812 Click to see CC=C(C)C(=O)OC1C(C(C(C2=CC(=C(C(=C2C3=C(C4=C(C=C13)OCO4)O)OC)OC)OC)OC(=O)C(=CC)C)(C)O)C 598.60 unknown https://doi.org/10.1055/S-2005-871271
19-Hydroxy-3,4,5-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-one 162861229 Click to see 400.40 unknown https://doi.org/10.1055/S-2005-871271
4,5,15,16-Tetramethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-3,11,14-triol 14078138 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(95)00043-7
5-Hydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-one 162897777 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(=O)C1C)O)OC)OC)OC)OCO3 400.40 unknown https://doi.org/10.1055/S-2005-871271
Acetylbinankadsurin A 14827761 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC(=O)C)OCO4)OC)O)OC)OC 444.50 unknown https://doi.org/10.1248/CPB.29.123
Deangeloylschisantherin F 44567626 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(95)00043-7
Schizanrin L 102004694 Click to see 536.60 unknown https://doi.org/10.1055/S-2005-871271

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.