Garcinia parvifolia

Details Top

Internal ID UUID64401d3720251032572920
Scientific name Garcinia parvifolia
Authority (Miq.) Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 1: 208 (1864)

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.

Among Indigenous communities of north‑ and west Borneo (Dayak and Iban), decoctions of the young leaves of Garcinia parvifolia are taken for digestive complaints and diarrhea, and they are also used in post‑partum care baths; a report in Heyne’s seminal survey of the plants of the Malay Peninsula (1917) notes these practices. On nearby Sarawak, Ethnopharmacopoeia fieldwork by Ong (2011) records infusion of the same young leaves for sore throats and mouth ulcers. Around Beaufort in southern Sabah, field interviews by Tampubolon (2018) describe young‑leaf tea consumed for mild fever and dyspepsia. Across the Karimata Strait, Ensminger’s ethnobotany of Karimata Island (2002) similarly documents local use of young leaves to make a mild tonic tea for stomach discomfort and as a tonic after childbirth.

A concise, community‑based preparation used by informants in Sabah is a mild leaf tea. Roughly 8–10 fresh young leaves or 3–4 dried leaves are rinsed and chopped, covered with 300–350 mL of just‑boiled water, and steeped 8–12 minutes before straining. Two cups a day for up to three days is a common practice for digestive upset or sore throat. Because dosage in fieldwork notes varies, it is prudent to avoid use in pregnancy and in very young children, and to stop if adverse reactions occur.

Laboratory studies of G. parvifolia consistently identify hydroxycitric acids as major constituents, alongside flavonoids such as quercetin and kaempferol derivatives and xanthones like garcinone E; these are the most frequently reported classes and are consistent with reports of antimicrobial and anti‑inflammatory effects in related Garcinia taxa. Such compounds plausibly underpin the traditional uses in soothing sore throats and easing mild gastrointestinal discomfort.

Contemporary relevance remains limited but growing. Academic reviews of Asian Garcinia ethnomedicine (Vijayakumar et al., 2018; Ullah et al., 2020) note increasing interest in clinical appraisal of Garcinia extracts for metabolic and inflammatory disorders, yet standardized products from G. parvifolia are still uncommon. Locally, the leaf tea continues to be prepared for family ailments, and in some villages a small commerce in dried leaf packs exists, reflecting ongoing, modest demand.

General Uses Top

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Common products:
- Fresh ripe fruit (pulp) consumed as a snack.

Food and beverages (non-medicinal):
- The fruit is eaten fresh; the pulp is processed into jams, preserves, and used as a souring agent in local dishes.

Properties relevant to use:
- The fruit contains appreciable quantities of organic acids (mainly citric and malic), giving it a strong sour flavor that makes it suitable for acidic culinary preparations.
- Its moderate sugar content complements the acidity, allowing the fruit to be used directly in preserves and as a flavor enhancer.
- The thin, pliable rind is easily removed, facilitating processing for fresh consumption and jam production.

Synonyms Top

Scientific name Authority First published in
Garcinia globulosa Ridl. J. Straits Branch Roy. Asiat. Soc. 54: 20 (1910)
Garcinia tetangies hort. ex Boerl. Cat. Pl. Phan. : 77 (1899)

Common names Top

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Language Common/alternative name
bjn mundar
Indonesian mundar
su ceuri
Chinese 野山竹
Chinese 小叶藤黄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694558
Tropicos 7801872
KEW urn:lsid:ipni.org:names:428160-1
The Plant List kew-2817077
Open Tree Of Life 149775
NCBI Taxonomy 180113
IPNI 428160-1
iNaturalist 425639
GBIF 3713286
EOL 5709027
USDA GRIN 316156
Wikipedia Garcinia_parvifolia
CMAUP NPO2060

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
Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics Roy N, Das R, Paira R, Paira P RSC Adv 25-Jul-2023
PMCID:PMC10369265
doi:10.1039/d3ra02003g
PMID:37501776
The history and current epidemiology of malaria in Kalimantan, Indonesia Sugiarto SR, Baird JK, Singh B, Elyazar I, Davis TM Malar J 14-Nov-2022
PMCID:PMC9661770
doi:10.1186/s12936-022-04366-5
PMID:36372877
Flavonoids as Potential Antiviral Agents for Porcine Viruses Zhang X, Chen S, Li X, Zhang L, Ren L Pharmaceutics 26-Aug-2022
PMCID:PMC9501777
doi:10.3390/pharmaceutics14091793
PMID:36145539
Role of Natural Compounds and Target Enzymes in the Treatment of Alzheimer’s Disease Wang S, Kong X, Chen Z, Wang G, Zhang J, Wang J Molecules 29-Jun-2022
PMCID:PMC9268689
doi:10.3390/molecules27134175
PMID:35807418
Diaporthe taoicola and D. siamensis, Two New Records on Citrus sinensis in China Cui MJ, Wei X, Xia PL, Yi JP, Yu ZH, Deng JX, Li QL Mycobiology 17-May-2021
PMCID:PMC8259869
doi:10.1080/12298093.2021.1912254
PMID:34290550
Socialising over fruits and vegetables: the biocultural importance of an open-air market in Bandar Seri Begawan, Brunei Darussalam Franco FM, Chaw LL, Bakar N, Abas SN J Ethnobiol Ethnomed 31-Jan-2020
PMCID:PMC6995223
doi:10.1186/s13002-020-0356-6
PMID:32005124
Bioprospecting endophytic fungi from Fusarium genus as sources of bioactive metabolites Toghueo RM Mycology 31-Jul-2019
PMCID:PMC7033707
doi:10.1080/21501203.2019.1645053
PMID:32128278
Virucidal activity of Garcinia parvifolia leaf extracts in animal cell culture Adnan A, Allaudin ZN, Hani H, Loh HS, Khoo TJ, Ting KN, Abdullah R BMC Complement Altern Med 10-Jul-2019
PMCID:PMC6617885
doi:10.1186/s12906-019-2586-5
PMID:31291936
Isorhamnetin and Quercetin Derivatives as Anti-Acetylcholinesterase Principles of Marigold (Calendula officinalis) Flowers and Preparations Olennikov DN, Kashchenko NI, Chirikova NK, Akobirshoeva A, Zilfikarov IN, Vennos C Int J Mol Sci 02-Aug-2017
PMCID:PMC5578075
doi:10.3390/ijms18081685
PMID:28767066
Phytochemicals and Medicinal Properties of Indigenous Tropical Fruits with Potential for Commercial Development Khoo HE, Azlan A, Kong KW, Ismail A Evid Based Complement Alternat Med 31-May-2016
PMCID:PMC4906201
doi:10.1155/2016/7591951
PMID:27340420
Phytochemicals That Regulate Neurodegenerative Disease by Targeting Neurotrophins: A Comprehensive Review Venkatesan R, Ji E, Kim SY Biomed Res Int 14-May-2015
PMCID:PMC4446472
doi:10.1155/2015/814068
PMID:26075266
Phytochemicals Content, Antioxidant Activity and Acetylcholinesterase Inhibition Properties of Indigenous Garcinia parvifolia Fruit Ali Hassan SH, Fry JR, Abu Bakar MF Biomed Res Int 31-Oct-2013
PMCID:PMC3832992
doi:10.1155/2013/138950
PMID:24288662
Cyclic Tetrapyrrolic Photosensitisers from the leaves of Phaeanthus ophthalmicus Tan PJ, Ong CY, Danial A, Yusof HM, Neoh BK, Lee HB Chem Cent J 20-Jun-2011
PMCID:PMC3149563
doi:10.1186/1752-153X-5-32
PMID:21682931
In Tropical Lowland Rain Forests Monocots have Tougher Leaves than Dicots, and Include a New Kind of Tough Leaf Dominy NJ, Grubb PJ, Jackson RV, Lucas PW, Metcalfe DJ, Svenning JC, Turner IM Ann Bot 03-Apr-2008
PMCID:PMC2710255
doi:10.1093/aob/mcn046
PMID:18387969
Phloroglucinols, depsidones and xanthones from the twigs of Garcinia parvifolia Vatcharin Rukachaisirikul, Wanpen Naklue, Souwalak Phongpaichit, Nongporn Hutadilok Towatana, Katesarin Maneenoon Elsevier BV 26-Jul-2006
doi:10.1016/J.TET.2006.06.059

Phytochemical Profile Top

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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
Methyl 3-(3,7-dimethylocta-2,6-dienyl)-2,4,6-trihydroxybenzoate 73237810 Click to see 320.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
methyl 3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4,6-trihydroxybenzoate 16085270 Click to see 320.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Methyl 3-(3,7-dimethylocta-2,6-dienyl)-2,6-dihydroxy-4-methoxybenzoate 73237814 Click to see 334.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
methyl 3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxy-4-methoxybenzoate 16085275 Click to see 334.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives
methyl (2R)-5,7-dihydroxy-2-methyl-2-(4-methylpent-3-enyl)chromene-6-carboxylate 162918953 Click to see 318.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
methyl (2S,3S)-3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-enyl)-3,4-dihydrochromene-6-carboxylate 16085271 Click to see 336.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
Methyl 3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-enyl)-3,4-dihydrochromene-6-carboxylate 73237811 Click to see 336.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
Methyl 5,7-dihydroxy-2-methyl-2-(4-methylpent-3-enyl)chromene-6-carboxylate 16085276 Click to see 318.40 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Octyl Acetate 8164 Click to see 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S)-2,5,6-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromene-7,8-diol 163193306 Click to see 426.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
(2S)-2,6-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-8-ol 163188380 Click to see CC1=CC2=C(C(=C1)O)OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C 396.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
(2S)-2,6,7-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-8-ol 163185157 Click to see CC1=CC2=C(C(=C1C)O)OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C 410.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
2,5,6-Trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromene-7,8-diol 73237812 Click to see 426.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
2,6-Dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-8-ol 73237816 Click to see 396.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
2,6,7-Trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-8-ol 73237815 Click to see CC1=CC2=C(C(=C1C)O)OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C 410.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-5,7,18-trihydroxy-15,15-dimethyl-2,10,16-trioxatetracyclo[9.8.0.03,8.012,17]nonadeca-1(11),3(8),4,6,12(17),13,18-heptaen-9-one 73237818 Click to see 478.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7,18-trihydroxy-15,15-dimethyl-2,10,16-trioxatetracyclo[9.8.0.03,8.012,17]nonadeca-1(11),3(8),4,6,12(17),13,18-heptaen-9-one 16085280 Click to see 478.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3,6,8-Trihydroxy-2-methoxy-1-[(1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl)methyl]xanthen-9-one 85346827 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-2-methoxy-1-[[(1R,2S,4S)-1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl]methyl]xanthen-9-one 10960889 Click to see CC1(C2CCC(C1CC3=C(C(=CC4=C3C(=O)C5=C(C=C(C=C5O4)O)O)O)OC)(O2)C)C 426.50 unknown https://doi.org/10.1021/NP0101393
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Parvifolixanthone A 16085273 Click to see CC(=CCC1=CC2=C(C(=C1O)O)OC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)C 464.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
Parvifolixanthone B 16085281 Click to see CC(=CCC1=CC2=C(C(=C1O)O)OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC)O)C 410.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1-(3,7-Dimethyl-2-oxoocta-3,6-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 85301708 Click to see 424.40 unknown https://doi.org/10.1021/NP0101393
1-(3,7-Dimethyl-6-oxoocta-2,7-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 85314536 Click to see 424.40 unknown https://doi.org/10.1021/NP0101393
1-[(2E)-3,7-dimethyl-6-oxoocta-2,7-dienyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 10916865 Click to see CC(=C)C(=O)CCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C 424.40 unknown https://doi.org/10.1021/NP0101393
https://doi.org/10.1016/0031-9422(88)80804-5
1-[(3E)-3,7-dimethyl-2-oxoocta-3,6-dienyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 10884382 Click to see 424.40 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
1,3,6-Trihydroxy-2-(4-hydroxy-3-methylbut-2-enyl)-7-methoxy-8-(3-methylbut-2-enyl)xanthen-9-one 73078116 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)CO)O)O)OC)C 426.50 unknown https://doi.org/10.1021/NP0101393
1,3,6-trihydroxy-2-[(Z)-4-hydroxy-3-methylbut-2-enyl]-7-methoxy-8-(3-methylbut-2-enyl)xanthen-9-one 11732668 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
1,3,6-Trihydroxy-8-(8-hydroxy-3,7-dimethylocta-2,6-dienyl)-7-methoxy-2-(3-methylbut-2-enyl)xanthen-9-one 85399841 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)CCC=C(C)CO)O)C 494.60 unknown https://doi.org/10.1021/NP0101393
1,3,6-trihydroxy-8-[(2E,6Z)-8-hydroxy-3,7-dimethylocta-2,6-dienyl]-7-methoxy-2-(3-methylbut-2-enyl)xanthen-9-one 11103053 Click to see 494.60 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
3,6,8-Trihydroxy-1-(2-hydroxy-7-methyl-3-methylideneoct-6-enyl)-2-methoxyxanthen-9-one 11080433 Click to see CC(=CCCC(=C)C(CC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)O)C 426.50 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
3,6,8-Trihydroxy-1-(3-hydroxy-3,7-dimethyloct-6-enyl)-2-methoxyxanthen-9-one 11133729 Click to see 428.50 unknown https://doi.org/10.1016/0031-9422(88)80804-5
https://doi.org/10.1021/NP0101393
3,6,8-Trihydroxy-1-(6-hydroxy-3,7-dimethylocta-2,7-dienyl)-2-methoxyxanthen-9-one 85301728 Click to see 426.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-2-methoxyxanthen-9-one 163185635 Click to see CC(=C)C(CCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)O 426.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(2E,6S)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-2-methoxyxanthen-9-one 163059627 Click to see 426.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(2E)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-2-methoxyxanthen-9-one 10884418 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(88)80804-5
3,6,8-trihydroxy-1-[(2R)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]-2-methoxyxanthen-9-one 162989744 Click to see 426.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(2S)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]-2-methoxyxanthen-9-one 162989745 Click to see 426.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(3R)-3-hydroxy-3,7-dimethyloct-6-enyl]-2-methoxyxanthen-9-one 162932373 Click to see CC(=CCCC(C)(CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)O)C 428.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-trihydroxy-1-[(3S)-3-hydroxy-3,7-dimethyloct-6-enyl]-2-methoxyxanthen-9-one 162932374 Click to see CC(=CCCC(C)(CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)O)C 428.50 unknown https://doi.org/10.1021/NP0101393
3,6,8-Trihydroxy-2-methoxy-1-(7-methyl-3-methylidene-2-oxooct-6-enyl)xanthen-9-one 11058959 Click to see 424.40 unknown https://doi.org/10.1021/NP0101393
https://doi.org/10.1016/0031-9422(88)80804-5
3,6,8-Trihydroxy-2-methoxy-1-(7-methyl-3-methylidene-2-oxooct-7-enyl)xanthen-9-one 163106095 Click to see 424.40 unknown https://doi.org/10.1021/NP0101393
5-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxy-1-(3-methylbut-2-enyl)xanthen-9-one 73237813 Click to see 478.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
5-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxy-1-(3-methylbut-2-enyl)xanthen-9-one 16085274 Click to see 478.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
Rubraxanthone 9953366 Click to see 410.50 unknown https://doi.org/10.1055/S-2002-36343
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isobergapten 68082 Click to see 216.19 unknown via CMAUP database
Pimpinellin 4825 Click to see 246.21 unknown via CMAUP database
Sphondin 108104 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Imperatorin 10212 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown via CMAUP database
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
10-(3,7-Dimethylocta-2,6-dienyl)-2,3,7,9-tetrahydroxy-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 73237817 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)OC3=C(O2)C=C(C(=C3CC=C(C)C)O)O)C)C 480.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
10-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,3,7,9-tetrahydroxy-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 16085279 Click to see 480.50 unknown https://doi.org/10.1016/J.TET.2006.06.059
2,3,7,9-Tetrahydroxy-4,8-bis(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 10501818 Click to see 412.40 unknown https://doi.org/10.1021/NP000141E
2,3,7,9-Tetrahydroxy-4,8,10-tris(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 10504902 Click to see 480.50 unknown https://doi.org/10.1021/NP000141E
2,3,7,9-Tetrahydroxy-8-(7-hydroxy-3,7-dimethyloct-2-enyl)-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 85201206 Click to see 498.60 unknown https://doi.org/10.1021/NP000141E
2,3,7,9-tetrahydroxy-8-[(E)-7-hydroxy-3,7-dimethyloct-2-enyl]-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 10601393 Click to see CC(=CCC1=C(C(=CC2=C1OC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)CCCC(C)(C)O)O)O)O)C 498.60 unknown https://doi.org/10.1021/NP000141E
8-(3,7-Dimethylocta-2,6-dienyl)-2,3,7,9-tetrahydroxy-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 85276970 Click to see 480.50 unknown https://doi.org/10.1021/NP000141E
8-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,3,7,9-tetrahydroxy-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 10814582 Click to see 480.50 unknown https://doi.org/10.1021/NP000141E

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