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

Description Top

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Garcinia parvifolia, also known as Kundong or Brunei cherry, is a tropical evergreen tree found in Borneo, Peninsular Malaysia, Sulawesi, and Sumatra. It can grow up to 33 meters in height and is commonly found at elevations of 600-800 meters in humid environments. The tree is used by humans for its bark, wood, leaves, and fruit. It is propagated through seeds and can produce fruit in just 4 years. The bark is used to produce resin, while the wood is used for furniture and carving. The leaves are eaten as a vegetable and the tree is also used as a rootstock for mangosteen. The fruit of the kundong tree can be eaten raw or cooked and has a sour taste with a sweet white pulp. It is often used to add a sour flavor to dishes like curry. The fruit resembles a purple mangosteen and is about the size of a cherry, which is why it is also known as Brunei cherry or red mangosteen.

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
su ceuri
Chinese 野山竹

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

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 CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)C(=O)OC)O)C)C 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 CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)C(=O)OC)O)C)C 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 CC(=CCCC(=CCC1=C(C=C(C(=C1O)C(=O)OC)O)OC)C)C 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 CC(=CCCC(=CCC1=C(C=C(C(=C1O)C(=O)OC)O)OC)C)C 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 CC(=CCCC1(C=CC2=C(O1)C=C(C(=C2O)C(=O)OC)O)C)C 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 CC(=CCCC1(C(CC2=C(O1)C=C(C(=C2O)C(=O)OC)O)O)C)C 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 CC(=CCCC1(C(CC2=C(O1)C=C(C(=C2O)C(=O)OC)O)O)C)C 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 CC(=CCCC1(C=CC2=C(O1)C=C(C(=C2O)C(=O)OC)O)C)C 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 CCCCCCCCOC(=O)C 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 CC1=C(C(=C(C2=C1CCC(O2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O)O)C 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 CC1=C(C(=C(C2=C1CCC(O2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O)O)C 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 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
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 CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C4=C(C(=C3)O)OC(C=C4)(C)C)OC2=O)O)C)C 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 CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C4=C(C(=C3)O)OC(C=C4)(C)C)OC2=O)O)C)C 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 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/10.1016/0031-9422(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 CC(=CCC=C(C)C(=O)CC1=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
1-(3,7-Dimethyl-6-oxoocta-2,7-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 85314536 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
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 CC(=CCC=C(C)C(=O)CC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C 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 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/10.1016/0031-9422(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 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/10.1016/0031-9422(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 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/10.1016/0031-9422(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 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,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 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)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-2-methoxyxanthen-9-one 10884418 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/10.1016/0031-9422(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 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/10.1021/NP0101393
3,6,8-trihydroxy-1-[(2S)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]-2-methoxyxanthen-9-one 162989745 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/10.1021/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 CC(=CCCC(=C)C(=O)CC1=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
3,6,8-Trihydroxy-2-methoxy-1-(7-methyl-3-methylidene-2-oxooct-7-enyl)xanthen-9-one 163106095 Click to see CC(=C)CCCC(=C)C(=O)CC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC 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 CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)C)C 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 CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)C)C 478.60 unknown https://doi.org/10.1016/J.TET.2006.06.059
Rubraxanthone 9953366 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 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 COC1=C2C=CC(=O)OC2=C3C=COC3=C1 216.19 unknown via CMAUP database
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 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
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 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
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 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 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
2,3,7,9-Tetrahydroxy-4,8-bis(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 10501818 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3)O)O)CC=C(C)C)OC2=O)O)C 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 CC(=CCC1=C(C(=C2C(=C1O)C(=O)OC3=C(O2)C=C(C(=C3CC=C(C)C)O)O)CC=C(C)C)O)C 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 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
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 CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3)O)O)CC=C(C)C)OC2=O)O)C)C 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 CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3)O)O)CC=C(C)C)OC2=O)O)C)C 480.50 unknown https://doi.org/10.1021/NP000141E

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