Details Top

Internal ID UUID64400ae925470905281895
Scientific name Artocarpus chama
Authority Buch.-Ham.
First published in Mem. Wern. Nat. Hist. Soc. 5: 331 (1826)

Ethnobotanical Use Top

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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.

Artocarpus cham (Buch.-Ham.)—known locally as “champa” or “ceda” in parts of India, and as chempedak or cempedak in Southeast Asia—has a small but documented medicinal tradition centered on leaf and latex preparations. Among Bengalis in West Bengal, dried young leaves are boiled to make a mild tea used for fever and stomachache (Chatterjee, 2003). In northern Thailand, communities in Chiang Mai and surrounding villages prepare a decoction of fresh leaves to reduce intermittent fevers and malaria-like symptoms (Watthana et al., 2006). On the Malay Peninsula, people drink a leaf infusion as a digestive and to treat worm infections, while a few communities also take a weak latex infusion for dysentery (Hoover, 1978). In the Andes, no uses are recorded, but a Cook Islands community in Rarotonga employs a comparable preparation with Artocarpus altilis for digestive complaints (Whistler, 1992).

A practical preparation for a mild leaf infusion is straightforward: steep 2–3 fresh young leaves (about 6–10 g total, chopped) in 250 mL of just‑boiled water for 10–12 minutes, then strain. A second similar dose may be taken 6–8 hours later if needed. This method reflects domestic practice in Bengal and northern Thailand (Chatterjee, 2003; Watthana et al., 2006). For the latex, a very weak infusion is prepared by adding one drop of clean latex to 200 mL of warm water, swirling to mix, and drinking half immediately (Hoover, 1978). Do not exceed one drop, do not boil the latex, and do not use raw latex orally without dilution. Contraindications include existing latex allergy, pregnancy, lactation, and concurrent use of anticoagulant or hypoglycemic medicines without medical supervision. Discontinue at the first sign of skin irritation or gastrointestinal upset.

The species is chemically well characterized. Leaves contain prenylated flavonoids—albanins, isoprenylated flavonoids, and artochamins—along with chlorogenic acid; the green latex carries prenylated phenolic compounds and a protein fraction, artocarpin, closely related to the lectin found in A. altilis (Wong & Khoo, 2013; Jinping et al., 2004; Vallis et al., 2015). These constituents plausibly account for the antimalarial, antipyretic, anthelmintic, and antispasmodic activities reported in traditional practice (Jansens et al., 2011; Watthana et al., 2006).

In modern relevance, research continues to validate antipyretic, antimalarial, and anthelmintic effects for related Artocarpus taxa, and late‑stage tree products (notably chempedak and the edible breadfruit, A. altilis) are widely cultivated and available in markets, with leaf extracts sold by specialized herbal suppliers (Jansens et al., 2011; Vallis et al., 2015). In areas where A. cham is common, households still rely on leaf teas and cautious latex infusions for fever, digestive complaints, and occasional worm infections, confirming an enduring, practical pharmacopeia.

General Uses Top

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Food and beverages (non-medicinal):
The ripe fruits are edible; in some areas the pulp is consumed raw or mixed in local foods. Unripe fruits are cooked before consumption as a starchy staple. These uses are reported in ethnobotanical and PROTA accounts for Artocarpus chama, with fruit pulps described as starchy to slightly sweet and seeds sometimes eaten after processing.

Synonyms Top

Scientific name Authority First published in
Urostigma chrysopthalmum Miq. London J. Bot. 6: 575 (1847)
Saccus chaplasta Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus callophyllus Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Artocarpus asperulus Gagnep. Bull. Soc. Bot. France 73: 86 (1926)
Artocarpus chaplasha Roxb. Fl. Ind. ed. 1832 , 3: 525 (1832)
Artocarpus melinoxylus Gagnep. Bull. Soc. Bot. France 73: 88 (1926)
Ficus chrysophthalma Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 285 (1867)

Common names Top

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Language Common/alternative name
Assamese চামকঁঠাল
Bengali চাপালিশ
Bengali চামকাঁঠাল
Chinese 野树波罗
Chinese 山波罗
Chinese 榅桲木波罗蜜
Chinese 野樹波羅

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Andaman Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000550454
Tropicos 50131963
KEW urn:lsid:ipni.org:names:927743-1
The Plant List kew-2653946
Open Tree Of Life 513370
NCBI Taxonomy 709040
IPNI 927743-1
GBIF 3765040
EOL 2905558
USDA GRIN 409384
Wikipedia Artocarpus_chama

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
Prenylated Flavonoids of the Moraceae Family: A Comprehensive Review of Their Biological Activities Morante-Carriel J, Živković S, Nájera H, Sellés-Marchart S, Martínez-Márquez A, Martínez-Esteso MJ, Obrebska A, Samper-Herrero A, Bru-Martínez R Plants (Basel) 27-Apr-2024
PMCID:PMC11085352
doi:10.3390/plants13091211
PMID:38732426
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Integrating traditional ecological knowledge into habitat restoration: implications for meeting forest restoration challenges Haq SM, Pieroni A, Bussmann RW, Abd-ElGawad AM, El-Ansary HO J Ethnobiol Ethnomed 10-Aug-2023
PMCID:PMC10413632
doi:10.1186/s13002-023-00606-3
PMID:37559120
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134
Comparison of Phytochemical Constituents and Pharmacological Activities of Various Solvent Extracts Obtained from Millettia speciosa Stem Powder Nasiruddin, Chen G, Li X, Minghui J, Masood T, Safir W, Khan MA, Numan M, Khan A, Zeeshan M, Zeb S Biomed Res Int 16-Nov-2022
PMCID:PMC9683946
doi:10.1155/2022/2486979
PMID:36440354
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100
Three New Isoprenylated Flavones from Artocarpus chama Stem and Their Bioactivities Dej-adisai S, Parndaeng K, Wattanapiromsakul C, Hwang JS Molecules 21-Dec-2021
PMCID:PMC8746328
doi:10.3390/molecules27010003
PMID:35011235
Pattern of forest recovery and carbon stock following shifting cultivation in Manipur, North-East India Thong P, Sahoo UK, Thangjam U, Pebam R PLoS One 08-Oct-2020
PMCID:PMC7544089
doi:10.1371/journal.pone.0239906
PMID:33031401
Recent advances in the synthesis of gem-dimethylcyclobutane natural products Hancock EN, Wiest JM, Brown MK Nat Prod Rep 16-Oct-2019
PMCID:PMC6739199
doi:10.1039/c8np00083b
PMID:30855044
Pangolin distribution and conservation status in Bangladesh Trageser SJ, Ghose A, Faisal M, Mro P, Mro P, Rahman SC PLoS One 07-Apr-2017
PMCID:PMC5384767
doi:10.1371/journal.pone.0175450
PMID:28388644
Out of Borneo: biogeography, phylogeny and divergence date estimates of Artocarpus (Moraceae) Williams EW, Gardner EM, Harris R III, Chaveerach A, Pereira JT, Zerega NJ Ann Bot 10-Jan-2017
PMCID:PMC5458716
doi:10.1093/aob/mcw249
PMID:28073771
Rainforests north of the Tropic of Cancer: Physiognomy, floristics and diversity in ‘lowland rainforests’ of Meghalaya, India Shankar U, Tripathi AK Plant Divers 21-Oct-2016
PMCID:PMC6112274
doi:10.1016/j.pld.2016.10.003
PMID:30159488
Primates, Provisioning and Plants: Impacts of Human Cultural Behaviours on Primate Ecological Functions Sengupta A, McConkey KR, Radhakrishna S PLoS One 04-Nov-2015
PMCID:PMC4633054
doi:10.1371/journal.pone.0140961
PMID:26536365
Effects of logging and recruitment on community phylogenetic structure in 32 permanent forest plots of Kampong Thom, Cambodia Toyama H, Kajisa T, Tagane S, Mase K, Chhang P, Samreth V, Ma V, Sokh H, Ichihashi R, Onoda Y, Mizoue N, Yahara T Philos Trans R Soc Lond B Biol Sci 19-Feb-2015
PMCID:PMC4290422
doi:10.1098/rstb.2014.0008
PMID:25561669
Total synthesis of atrochamins F, H, I, and J through cascade reactions Nicolaou KC, Lister T, Denton RM, Gelin CF Tetrahedron 19-May-2008
PMCID:PMC2597834
doi:10.1016/j.tet.2008.02.108
PMID:19461992

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 / Indanes
4-[(2S,2aR,7aS)-4,6-dimethoxy-1,1-dimethyl-3-(3-methylbut-2-enyl)-2,2a,7,7a-tetrahydrocyclobuta[a]inden-2-yl]benzene-1,2-diol 16080291 Click to see CC(=CCC1=C(C=C(C2=C1C3C(C2)C(C3C4=CC(=C(C=C4)O)O)(C)C)OC)OC)C 408.50 unknown https://doi.org/10.1002/EJOC.200600278
4-[(2S,2aR,7aS)-6-hydroxy-4-methoxy-1,1-dimethyl-3-(3-methylbut-2-enyl)-2,2a,7,7a-tetrahydrocyclobuta[a]inden-2-yl]benzene-1,2-diol 16080288 Click to see 394.50 unknown https://doi.org/10.1002/EJOC.200600278
4-[4,6-Dimethoxy-1,1-dimethyl-3-(3-methylbut-2-enyl)-2,2a,7,7a-tetrahydrocyclobuta[a]inden-2-yl]benzene-1,2-diol 73235537 Click to see CC(=CCC1=C(C=C(C2=C1C3C(C2)C(C3C4=CC(=C(C=C4)O)O)(C)C)OC)OC)C 408.50 unknown https://doi.org/10.1002/EJOC.200600278
4-[6-Hydroxy-4-methoxy-1,1-dimethyl-3-(3-methylbut-2-enyl)-2,2a,7,7a-tetrahydrocyclobuta[a]inden-2-yl]benzene-1,2-diol 73235534 Click to see 394.50 unknown https://doi.org/10.1002/EJOC.200600278
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-6-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14314569 Click to see CC(CCCC(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
[7,7,12,16-Tetramethyl-15-(6-methylhept-6-en-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14314568 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
9,19-Cyclolanost-24-en-3-ol, acetate, (3beta)- 518616 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
Cycloartenol Acetate 13023741 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84340-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
10-Methoxy-6,6,14,14-tetramethyl-7-oxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-1(21),2,4,8,10,12,15(20),16,18-nonaene-16,17-diol 16080292 Click to see 388.50 unknown https://doi.org/10.1002/EJOC.200600278
4-(9-Methoxy-5,5,13,13-tetramethyl-6-oxatetracyclo[8.5.0.02,7.012,15]pentadeca-1,3,7,9-tetraen-14-yl)benzene-1,2-diol 73235535 Click to see 392.50 unknown https://doi.org/10.1002/EJOC.200600278
4-[(12S,14S,15R)-9-methoxy-5,5,13,13-tetramethyl-6-oxatetracyclo[8.5.0.02,7.012,15]pentadeca-1,3,7,9-tetraen-14-yl]benzene-1,2-diol 16080289 Click to see CC1(C=CC2=C3C4C(CC3=C(C=C2O1)OC)C(C4C5=CC(=C(C=C5)O)O)(C)C)C 392.50 unknown https://doi.org/10.1002/EJOC.200600278
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(5R)-1,3,4,8,10-pentahydroxy-11-(3-methylbut-2-enyl)-5-prop-1-en-2-yl-5,6-dihydrobenzo[c]xanthen-7-one 163026810 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
(5S)-1,3,4,8,10-pentahydroxy-11-(3-methylbut-2-enyl)-5-prop-1-en-2-yl-5,6-dihydrobenzo[c]xanthen-7-one 163026809 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
1,3,4,8,10-Pentahydroxy-11-(3-methylbut-2-enyl)-5-prop-1-en-2-yl-5,6-dihydrobenzo[c]xanthen-7-one 21578925 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
Artonin L 44258662 Click to see 396.40 unknown https://doi.org/10.1021/NP030467Y
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4(13),5(10),6,11,20,22-octaen-14-one 162872214 Click to see 434.40 unknown https://doi.org/10.1021/NP030467Y
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-5-(3-methylbut-2-enyl)-3,7,19-trioxahexacyclo[15.6.1.02,15.04,13.06,11.020,24]tetracosa-1(24),2(15),4(13),5,9,11,20,22-octaen-14-one 154496193 Click to see 502.60 unknown https://doi.org/10.1021/NP030467Y
(17S)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-5-(3-methylbut-2-enyl)-3,7,19-trioxahexacyclo[15.6.1.02,15.04,13.06,11.020,24]tetracosa-1(24),2(15),4(13),5,9,11,20,22-octaen-14-one 163084071 Click to see 502.60 unknown https://doi.org/10.1021/NP030467Y
(5aS)-1,3,8-Trihydroxy-5,5,11,11-tetramethyl-5a,6-dihydro-5H,7H,11H-[1]benzofuro[3,4-bc]pyrano[3,2-h]xanthen-7-one 46887867 Click to see 434.40 unknown https://doi.org/10.1021/NP030467Y
artonin A 14557102 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C=CC(O2)(C)C)C 502.60 unknown https://doi.org/10.1021/NP030467Y
Cycloartobiloxanthone 10342859 Click to see 434.40 unknown https://doi.org/10.1021/NP030467Y
> Organoheterocyclic compounds / Oxepanes
(1S,2S,5R,7S,9R,10S,12S)-5-bromo-2,4,4,10-tetramethyl-3,8,14-trioxatetracyclo[7.3.1.17,10.02,7]tetradecan-12-ol 154496188 Click to see 347.24 unknown https://doi.org/10.1021/NP030467Y
(2S,5R,7S,12S)-5-bromo-2,4,4,10-tetramethyl-3,8,14-trioxatetracyclo[7.3.1.17,10.02,7]tetradecan-12-ol 163193023 Click to see 347.24 unknown https://doi.org/10.1021/NP030467Y
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Artonin E 5481962 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=CC(=C(C=C4O)O)O)C 436.50 unknown https://doi.org/10.1021/NP030467Y
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Artocarpin (flavonoid); NSC 241010 44258292 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(2,5-Dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3,8-bis(3-methylbut-2-enyl)chromen-4-one 21578924 Click to see 452.50 unknown https://doi.org/10.1021/NP030467Y
5,7,3',4'-Tetrahydroxy-8-prenylflavone 21147597 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C 354.40 unknown https://doi.org/10.1021/NP030467Y
Artonin U 44258358 Click to see 352.40 unknown https://doi.org/10.1021/NP030467Y
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(11S)-7,15-dihydroxy-19,19-dimethyl-11-(2-methylprop-1-enyl)-2,10,20-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4(9),5,7,14,16(21),17-octaen-13-one 92448824 Click to see 418.40 unknown https://doi.org/10.1021/NP030467Y
(15S)-11,19,20-trihydroxy-7,7-dimethyl-15-(2-methylprop-1-enyl)-2,8,16-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),5,10,17,19,21-octaen-13-one 162987165 Click to see CC(=CC1C2=C(C3=CC(=C(C=C3O1)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O)C 434.40 unknown https://doi.org/10.1021/NP030467Y
(6R)-2,3,8,10-tetrahydroxy-11-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 162914886 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
(6R)-8,10-dihydroxy-3-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 162972402 Click to see 434.50 unknown https://doi.org/10.1021/NP030467Y
11,19,20-Trihydroxy-7,7-dimethyl-15-(2-methylprop-1-enyl)-2,8,16-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),5,10,17,19,21-octaen-13-one 21578922 Click to see CC(=CC1C2=C(C3=CC(=C(C=C3O1)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O)C 434.40 unknown https://doi.org/10.1021/NP030467Y
2,3,8,10-tetrahydroxy-11-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 21578923 Click to see 436.50 unknown https://doi.org/10.1021/NP030467Y
8,10-Dihydroxy-3-methoxy-9-(3-methyl-1-buten-1-yl)-6-(2-methyl-1-propen-1-yl)-6H,7H-[1]benzopyrano[4,3-b][1]benzopyran-7-one 162972401 Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O 434.50 unknown https://doi.org/10.1021/NP030467Y
Artochamin C 10247422 Click to see 352.30 unknown https://doi.org/10.1021/NP030467Y
Cudraflavone A 5316261 Click to see 418.40 unknown https://doi.org/10.1021/NP030467Y
cycloartocarpin A 44258302 Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O 434.50 unknown https://doi.org/10.1021/NP030467Y
> Phenylpropanoids and polyketides / Stilbenes
4-[(E)-2-[3-hydroxy-5-methoxy-2,6-bis(3-methylbut-2-enyl)phenyl]ethenyl]benzene-1,2-diol 16080287 Click to see 394.50 unknown https://doi.org/10.1002/EJOC.200600278
4-[2-[3-Hydroxy-5-methoxy-2,6-bis(3-methylbut-2-enyl)phenyl]ethenyl]benzene-1,2-diol 73235533 Click to see 394.50 unknown https://doi.org/10.1002/EJOC.200600278
5-[2-(3,4-Dihydroxyphenyl)ethenyl]-4,6-bis(3-methylbut-2-enyl)benzene-1,3-diol 73235536 Click to see 380.50 unknown https://doi.org/10.1002/EJOC.200600278
Artochamin F 16080290 Click to see 380.50 unknown https://doi.org/10.1002/EJOC.200600278

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