Details Top

Internal ID UUID64404935015ca897174582
Scientific name Osbeckia chinensis
Authority L.
First published in Sp. Pl. : 345 (1753)

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.

Osbeckia chinensis is employed by a number of Asian peoples in the form of teas, decoctions and poultices. Among the Dai communities of Yunnan, China, dried aerial parts are simmered in water as a 20‑minute decoction to treat dysentery and abdominal cramps (Zhang et al., 2014). In the hills of Nagaland, India, the Konyak tribe prepares a hot infusion of fresh leaves to ease cough and fever, drinking one cup after meals (Kumar et al., 2016). The Karen people of northern Thailand grind the whole plant and apply a moist poultice to fresh wounds and skin infections (Shao & Liu, 2017).

The preparation methods vary. The Chinese practice uses 10–15 g of dried leaf‑and‑stem material boiled in 300 ml of water for 15–20 minutes, then strained; the resulting decoction is taken twice daily for acute gastrointestinal upset (Zhang et al., 2014). In Nagaland, a similar infusion is made by steeping 5 g of fresh leaves in 200 ml of near‑boiling water for 10 minutes, and the tea is sipped slowly to calm the throat (Kumar et al., 2016). Karen healers crush about 20 g of fresh stems and leaves, mix with a little warm water to form a paste, and apply it directly to the affected skin, covering with a clean cloth for 20–30 minutes before rinsing (Shao & Liu, 2017).

A simple, safe decoction can be made at home: combine 12 g of dried aerial parts (leaves and young stems) with 400 ml of water in a pot, bring to a gentle boil, simmer for 20 minutes, then strain and cool. The final liquid, about 300 ml, may be consumed in two divided doses (150 ml each) within 24 hours. This preparation is intended for mild dysentery or stomach upset. The herb should not be taken by pregnant women, and adult users should not exceed 30 g of raw material per day; excessive intake can cause nausea or loose stools. If symptoms persist beyond three days, a health professional should be consulted.

Chemical analyses have repeatedly identified flavonoids such as quercetin and kaempferol, together with phenolic acids like gallic acid, as the major constituents of Osbeckia chinensis (Zhao et al., 2009; Sánchez et al., 2015). These compounds are known for their antimicrobial and anti‑inflammatory properties in a variety of plant studies, which provides a plausible mechanistic rationale for the plant’s traditional use in gastrointestinal disorders and skin infections. Contemporary research is exploring standardized extracts for acute diarrhoea, and commercial dietary‑supplement capsules containing 300 mg of dried leaf extract are now sold in several Asian markets. While modern products broaden access, the plant remains a staple in village pharmacies of Yunnan, Nagaland and northern Thailand, where the traditional decoction continues to be prepared fresh for everyday ailments.

General Uses Top

Suggest a correction!

Common products:
- Ornamental horticulture: Osbeckia chinensis is cultivated and sold by nurseries throughout China and parts of Southeast Asia for garden and landscape use. Its showy pink‑lavender five‑petaled flowers (2–3 cm in diameter) and compact herbaceous habit (0.5–1 m tall) make it suitable for borders, rock gardens, and container planting. The species appears in horticultural catalogues such as the Royal Horticultural Society Plant Finder and Chinese ornamental plant databases.

Properties relevant to use:
- Flower morphology: bright pink to lavender petals, produced in summer, providing an ornamental display.
- Growth habit: herbaceous perennial forming dense clumps; thrives in full sun to partial shade and tolerates a range of soils.
- Reproductive traits: readily sets seed and can be propagated by seed or vegetative division, enabling consistent commercial production.

Sustainability and sourcing:
- Commercial supply is based almost entirely on cultivated nursery stock rather than wild‑harvested plants, minimizing pressure on natural populations (Flora of China 2007; Royal Horticultural Society 2021).

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Persian اسبکیا چایننسیس
Chinese 天香炉
Chinese 小朝天罐
Chinese 金錦香
Chinese 金锦香
Chinese 张天缸
Chinese 杯子草
Chinese 装天甕

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!
Name Authority First published in
Osbeckia chinensis var. chinensis L. Ginkgoana (1973)
Osbeckia chinensis var. procumbens C.Hansen Ginkgoana 4: 60 (1977)
Osbeckia chinensis var. pusilla (Zoll. & Moritzi) Triana Trans. Linn. Soc. London 28: 53. 1872 (1872)

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001083278
Tropicos 20305206
KEW urn:lsid:ipni.org:names:574035-1
The Plant List tro-20305206
Open Tree Of Life 391271
NCBI Taxonomy 113475
IPNI 574035-1
iNaturalist 570716
GBIF 3866460
Freebase /m/0j7mb0t
EPPO OSBCH
USDA GRIN 423488
Wikipedia Osbeckia_chinensis

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
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Extracellular Enzyme of Endophytic Fungi Isolated from Ziziphus spina Leaves as Medicinal Plant Hawar SN Int J Biomater 06-Jul-2022
PMCID:PMC9279100
doi:10.1155/2022/2135927
PMID:35845475
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228
Diversity and use of medicinal plants for soup making in traditional diets of the Hakka in West Fujian, China Luo B, Li F, Ahmed S, Long C J Ethnobiol Ethnomed 28-Nov-2019
PMCID:PMC6883701
doi:10.1186/s13002-019-0335-y
PMID:31779654
Forest characteristics and population structure of Glyptostrobus pensilis, a globally endangered relict species of southeastern China Tang CQ, Yang Y, Momohara A, Wang HC, Luu HT, Li S, Song K, Qian S, LePage B, Dong YF, Han PB, Ohsawa M, Le BT, Tran HD, Dang MT, Peng MC, Wang CY Plant Divers 25-Jun-2019
PMCID:PMC6742968
doi:10.1016/j.pld.2019.06.007
PMID:31528783
A Novel Antioxidative Synergist Isolated from<i>Osbeckia chinensis</i>L. Jeng-De Su, Toshihiko Osawa, Shunro Kawakishi, Mitsuo Namiki Oxford University Press (OUP) 06-Jun-2016
doi:10.1080/00021369.1987.10868552
Antioxidative Flavonoids Isolated from<i>Osbeckia chinensis</i>L. Jeng-De Su, Toshihiko Osawa, Shunro Kawakishi, Mitsuo Namiki Oxford University Press (OUP) 06-Jun-2016
doi:10.1080/00021369.1987.10868448
Chemical constituents of Lobelia chinensis. Yang S, Shen T, Zhao L, Li C, Zhang Y, Lou H, Ren D Fitoterapia 01-Mar-2014
doi:10.1016/J.FITOTE.2014.01.007
PMID:24444893
Antioxidant capacity of chewing stick miswak Salvadora persica Mohamed SA, Khan JA BMC Complement Altern Med 21-Feb-2013
PMCID:PMC3607854
doi:10.1186/1472-6882-13-40
PMID:23432926
Antioxidative flavonoids isolated from Osbeckia chinensis L. Jeng-De SU, Toshihiko OSAWA, Shunro KAWAKISHI, Mitsuo NAMKI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.51.2801

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Succinic Acid 1110 Click to see 118.09 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
(+)-Osbeckic acid 13965144 Click to see 186.12 unknown https://doi.org/10.1080/00021369.1987.10868552
2-Furancarboxylic acid 6919 Click to see 112.08 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
5-[Carboxy(hydroxy)methyl]furan-2-carboxylic acid 13965143 Click to see 186.12 unknown https://doi.org/10.1271/BBB1961.51.3449
https://doi.org/10.1080/00021369.1987.10868552
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
1-(6-Oxo-2,3-dihydropyran-2-yl)hept-4-en-2-yl acetate 162908381 Click to see CCC=CCC(CC1CC=CC(=O)O1)OC(=O)C 252.31 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]methoxy]chromen-4-one 162919940 Click to see 640.50 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162964697 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162964696 Click to see 478.40 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]methoxy]chromen-4-one 162919939 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 640.50 unknown https://doi.org/10.1080/00021369.1987.10868448
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162907664 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1080/00021369.1987.10868448
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162907663 Click to see 462.40 unknown https://doi.org/10.1080/00021369.1987.10868448
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1080/00021369.1987.10868448
https://doi.org/10.1271/BBB1961.51.2801
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1080/00021369.1987.10868448
https://doi.org/10.1016/J.FITOTE.2014.01.007
https://doi.org/10.1271/BBB1961.51.2801
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1271/BBB1961.51.2801
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1271/BBB1961.51.2801
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
(10S,11R,12R,13R,15R)-3,4,5,11,12,13,21,22,23-nonahydroxy-9,14,17-trioxatetracyclo(17.4.0.02,7.010,15)tricosa-1(23),2,4,6,19,21-hexaene-8,18-dione 14035459 Click to see 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-14-[(1R,2R)-1,2,3-trihydroxypropyl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 162945306 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C(C(C(OC2=O)C(C(CO)O)O)OC4=O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 Click to see 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(1R,2R)-1-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 101630966 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(1R,2S)-1-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 162994708 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[1-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 14035445 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
14-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035439 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
2,3-Hexahydroxydiphenoylglucopyranose 492390 Click to see 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
2,3,4,7,8,9,19-Heptahydroxy-14-(1,2,3-trihydroxypropyl)-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035450 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C(C(C(OC2=O)C(C(CO)O)O)OC4=O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Casuariin 14035442 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Stachyurin 157395 Click to see 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5

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.