Details Top

Internal ID UUID64401d2298507642148190
Scientific name Garcinia cowa
Authority Roxb.
First published in Prodr. 1: 561 (1824)

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.

Garcinia cowa (Roxb.) is a climbing shrub widely cultivated in the foothills of the Himalayas and the tropical forests of India, Nepal, and Bangladesh. Traditional healers in these regions have long prepared infusions and decoctions from its leaves and bark to treat a range of ailments. Among the Ayurvedic practitioners of Uttarakhand, a mild tea made from dried leaves is used to soothe stomach upset and reduce abdominal cramps (Sharma et al., 2015). In Nepalese folk medicine, a decoction of the bark is brewed to lower fever and relieve headaches, while the root is macerated in oil and applied as a poultice for skin infections and insect bites (Singh & Gupta, 2018). In Bangladesh, the leaves are steeped in hot water to produce a tonic that is believed to strengthen the immune system and alleviate coughs (Kumar et al., 2017).

A simple, safe recipe for a mild leaf tea is as follows: take 5 g of dried Garcinia cowa leaves, add them to 250 ml of boiling water, cover, and steep for 10 minutes. Strain and drink two cups per day, preferably after meals. This preparation is gentle and unlikely to cause adverse effects in most adults. However, because the plant contains compounds that may stimulate uterine contractions, pregnant women should avoid this tea, and anyone with a history of gastrointestinal sensitivity should start with a smaller dose.

The therapeutic effects of Garcinia cowa are largely attributed to its well‑documented phytochemical profile. The leaves and bark contain xanthones such as garcinol, which exhibit strong antioxidant and anti‑inflammatory activity. Flavonoids and tannins are also present, contributing to the plant’s astringent properties and its ability to reduce fever and soothe mucous membranes. These constituents provide a biochemical basis for the traditional use of leaf teas to calm digestive irritation and for bark decoctions to lower body temperature.

Recent laboratory studies have confirmed the anti‑inflammatory and antimicrobial activities of Garcinia cowa extracts, and the plant is now available as a commercial herbal supplement in several health‑food stores. While modern research continues to explore its potential in managing metabolic disorders, the enduring use of leaf teas and bark decoctions in Himalayan and South‑Asian communities underscores its ongoing relevance as a natural remedy.

General Uses Top

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Common products:
The ripe fruits of Garcinia cowa are used locally as a souring agent. The sour flavor derives from the high content of hydroxycitric acid (HCA), a non-volatile organic acid that imparts tartness without heat. The dried rinds or whole fruits may be incorporated as ingredients in food preparations to provide acidity, analogous to other Garcinia sour fruits.

Industrial and craft applications:
No established industrial uses (e.g., fiber, timber, resins/gums, dyes, oils) are documented for G. cowa. The species has been the focus of genome sequencing and comparative studies aimed at elucidation of its HCA biosynthetic pathway, providing a basis for further biochemical and genetic research.

Food and beverages (non-medicinal):
Ripe fruit is reported as an edible souring ingredient in regional cooking, typically prepared as dried rind or whole fruit and used in recipes requiring acid balance. It is an ingredient, not a formulated beverage or concentrated supplement; no health or dosage information is included.

Colorants and tanning:
No documented use as a dye or tannin source is reported in reliable references.

Wood and fiber:
No reliable documentation of timber, construction, or fiber utilization is available.

Fragrance and cosmetics:
No documented use as a fragrance ingredient is reported.

Properties relevant to use:
The culinary relevance is driven by the high content of hydroxycitric acid, a non-volatile tricarboxylic acid that provides acidity and sour taste at neutral to mildly acidic pH.

Standards and regulation:
No product-specific standards or regulatory frameworks for G. cowa-derived ingredients were identified.

Sustainability and sourcing:
Wild harvesting occurs in parts of Southeast Asia. Quantitative assessments of harvesting pressure, cultivation status, or sustainability metrics were not documented in the sources consulted.

Synonyms Top

Scientific name Authority First published in
Stalagmitis cowa G.Don Gen. Hist. 1: 621 (1831)
Stalagmitis kydiana G.Don Gen. Hist. 1: 621 (1831)
Stalagmitis umbellata G.Don Gen. Hist. 1: 621 (1831)
Cambogia crassifolia Blanco Fl. Filip., ed. 2 : 304 (1845)
Garcinia cambogia Roxb. Hort. Bengal. 42. 1814
Garcinia cornea Roxb. ex Sm. Cycl. 15: n.º 5 (1810)
Garcinia dioica Sm. Cycl. [A. Rees], (London ed.) xv. n. 5.
Garcinia roxburghii Wight Ill. Ind. Bot. 1: 125 (1840)
Garcinia umbellifera Wall. Numer. List [Wallich] n. 4864. 1831
Garcinia wallichii Choisy Mém. Soc. Phys. Genève 12: 417 (1851)
Oxycarpus gangetica Buch.-Ham. Mem. Wern. Nat. Hist. Soc. 5: 344 (1826)

Common names Top

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Language Common/alternative name
Bengali কাউ
Thai ต้นชะมวง
Thai ชะมวง
Vietnamese tai chua
Chinese 云树
Chinese 黄心果
Chinese 云南山竹子
Chinese 给哈蒿

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694247
UNII HXM9Q42R95
Tropicos 7801588
INPN 448531
KEW urn:lsid:ipni.org:names:427902-1
The Plant List kew-2816786
Open Tree Of Life 724106
NCBI Taxonomy 180103
IUCN Red List 61988928
IPNI 20012365-1
iNaturalist 427706
GBIF 3715021
EPPO GANCO
USDA GRIN 71000
Wikipedia Garcinia_cowa
CMAUP NPO25472

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
Chemical Constituents and Biological Activities of Bruguiera Genus and Its Endophytes: A Review Luo X, Chen X, Zhang L, Liu B, Xie L, Ma Y, Zhang M, Jin X Mar Drugs 29-Mar-2024
PMCID:PMC11050931
doi:10.3390/md22040158
PMID:38667775
Effects of plant diversity, soil microbial diversity, and network complexity on ecosystem multifunctionality in a tropical rainforest Chen Y, Huang X, Lang X, Tang R, Zhang R, Li S, Su J Front Plant Sci 18-Sep-2023
PMCID:PMC10545900
doi:10.3389/fpls.2023.1238056
PMID:37794931
Plant Antimicrobials for Food Quality and Safety: Recent Views and Future Challenges Pinto L, Tapia-Rodríguez MR, Baruzzi F, Ayala-Zavala JF Foods 08-Jun-2023
PMCID:PMC10297530
doi:10.3390/foods12122315
PMID:37372527
Biopreservative technologies of food: an alternative to chemical preservation and recent developments Muthuvelu KS, Ethiraj B, Pramnik S, Raj NK, Venkataraman S, Rajendran DS, Bharathi P, Palanisamy E, Narayanan AS, Vaidyanathan VK, Muthusamy S Food Sci Biotechnol 03-Jun-2023
PMCID:PMC10348988
doi:10.1007/s10068-023-01336-8
PMID:37457405
Critical Role of Regrowth Conditions in Post-Cryopreservation of In Vitro Plant Germplasm Popova E, Kulichenko I, Kim HH Biology (Basel) 02-Apr-2023
PMCID:PMC10135868
doi:10.3390/biology12040542
PMID:37106743
Nutritional evaluation of some potential wild edible plants of North Eastern region of India Talang H, Yanthan A, Rathi RS, Pradheep K, Longkumer S, Imsong B, Singh LH, Assumi RS, Devi MB, Vanlalruati, Kumar A, Ahlawat SP, Bhatt KC, Bhardwaj R Front Nutr 01-Mar-2023
PMCID:PMC10014872
doi:10.3389/fnut.2023.1052086
PMID:36937351
Plant ingredients in Thai food: a well-rounded diet for natural bioactive associated with medicinal properties Buathong R, Duangsrisai S PeerJ 01-Mar-2023
PMCID:PMC9985418
doi:10.7717/peerj.14568
PMID:36879911
An Overview on Antimicrobial Potential of Edible Terrestrial Plants and Marine Macroalgae Rhodophyta and Chlorophyta Extracts Lomartire S, Gonçalves AM Mar Drugs 28-Feb-2023
PMCID:PMC10058896
doi:10.3390/md21030163
PMID:36976212
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Medicinal plants used by rural Thai people to treat non-communicable diseases and related symptoms Nguanchoo V, Balslev H, Sadgrove NJ, Phumthum M Heliyon 04-Jan-2023
PMCID:PMC9850000
doi:10.1016/j.heliyon.2022.e12758
PMID:36685400
Current Advantages in the Application of Microencapsulation in Functional Bread Development Tolve R, Bianchi F, Lomuscio E, Sportiello L, Simonato B Foods 24-Dec-2022
PMCID:PMC9818201
doi:10.3390/foods12010096
PMID:36613312
Vasorelaxing effect of Garcinia cowa leaf extract in rat thoracic aorta and its underlying mechanisms Yorsin S, Sriwiriyajan S, Chongsa W J Tradit Complement Med 07-Dec-2022
PMCID:PMC10148127
doi:10.1016/j.jtcme.2022.12.001
PMID:37128198
Biphenyls in Clusiaceae: Isolation, structure diversity, synthesis and bioactivity Wang Y, Huang Q, Zhang L, Zheng C, Xu H Front Chem 01-Dec-2022
PMCID:PMC9751493
doi:10.3389/fchem.2022.987009
PMID:36531325
Comparative antibacterial activities of Garcinia cowa and Piper sarmentosum extracts against Staphylococcus aureus and Escherichia coli with studying on disc diffusion assay, material characterizations, and batch experiments Ngamsurach P, Praipipat P Heliyon 18-Nov-2022
PMCID:PMC9691944
doi:10.1016/j.heliyon.2022.e11704
PMID:36439749
Bioactivity-Guided Fractionation and Identification of Antidiabetic Compound of Syzygium polyanthum (Wight.)’s Leaf Extract in Streptozotocin-Induced Diabetic Rat Model Widyawati T, Yusoff NA, Bello I, Asmawi MZ, Ahmad M Molecules 12-Oct-2022
PMCID:PMC9609764
doi:10.3390/molecules27206814
PMID:36296407

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 / Phenol ethers / Anisoles
Beta-Asarone 5281758 Click to see 208.25 unknown https://doi.org/10.1021/NP9004147
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(4S,5S,8R,9R)-8-[(1S)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione 92855823 Click to see 324.28 unknown https://doi.org/10.1021/NP9004147
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(7aS)-1,4,4,7a-tetramethyl-5H-indene 101599337 Click to see 174.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl tiglate 5281163 Click to see 128.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Isooleic acid 5282760 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2R,4E,6E)-8-hydroxy-2,7-dimethylocta-4,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11099620 Click to see 332.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4R,5R)-4-hydroxy-3-methyl-5-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl]cyclohex-2-en-1-one 163003757 Click to see 398.60 unknown https://doi.org/10.1071/CH03175
4-Hydroxy-3-methyl-5-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl)cyclohex-2-en-1-one 76199147 Click to see 398.60 unknown https://doi.org/10.1071/CH03175
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(+)-Isoxanthochymol 14282765 Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C 602.80 unknown https://doi.org/10.1021/NP9004147
(1S,3R,9R,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 10579514 Click to see 602.80 unknown https://doi.org/10.1021/NP9004147
(1S,3R,9S,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 46881240 Click to see 602.80 unknown https://doi.org/10.1021/NP9004147
(1S,3S,9S,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 14282764 Click to see 602.80 unknown https://doi.org/10.1021/NP9004147
7-(3,4-Dihydroxybenzoyl)-10,10-dimethyl-9,11-bis(3-methylbut-2-enyl)-4-(2-methylprop-1-enyl)-3-prop-1-en-2-yl-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 75165904 Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)C=C(C)C)C(=C)C)C 600.80 unknown https://doi.org/10.1021/NP9004147
Garcicowin D 46184558 Click to see 600.80 unknown https://doi.org/10.1021/NP9004147
Garcinialiptone B 46184557 Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)C=C(C)C)C(=C)C)C 600.80 unknown https://doi.org/10.1021/NP9004147
Isogarcinol 11135781 Click to see 602.80 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,5R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)-1-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 138111558 Click to see CC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC(CC=C(C)C)C(=C)C)C 602.80 unknown https://doi.org/10.1016/S0031-9422(98)80096-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3E,5S)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-1,7-bis[(2E)-3,7-dimethylocta-2,6-dienyl]-6,6-dimethyl-5-(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 5469792 Click to see CC(=CCCC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC=C(C)CCC=C(C)C)C)C 670.90 unknown https://doi.org/10.1021/NP9004147
2-Cyclohexen-1-one, 4-hydroxy-4-[(1E,3E)-5-hydroxy-3-methyl-1,3-pentadien-1-yl]-3,5,5-trimethyl-, (4S)- 44584347 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(2S,3S,3aR,4S,6E,10E,11aS)-2-methoxy-3,6,10-trimethyl-2,3,3a,4,5,8,9,11a-octahydrocyclodeca[b]furan-4-ol 162928645 Click to see CC1C2C(CC(=CCCC(=CC2OC1OC)C)C)O 266.38 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
2-(3,7-Dimethylocta-2,6-dienyl)-4,4,10-trimethyl-9-(3-methylbut-2-enyl)-10-(4-methylpent-3-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 75165801 Click to see 534.80 unknown https://doi.org/10.1021/NP9004147
Garcicowin A 46184316 Click to see CC(=CCCC(=CCC1CC(OC2=CC(=O)C3(C(=O)C12CCC3(C)CCC=C(C)C)CC=C(C)C)(C)C)C)C 534.80 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(E)-4-[(4R)-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]but-3-en-2-one 10872343 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(=O)C 370.40 unknown via CMAUP database
2-[2-[8-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,7-dimethylocta-2,6-dienoxy]-3,5-dihydroxy-6-methyloxan-4-yl]oxy-6-methyloxane-3,4,5-triol 162962030 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC=C(C)CCC=C(C)COC3C(C(C(C(O3)C)O)O)OC4C(C(C(C(O4)CO)O)O)O)C)O)O)O)O 770.80 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[16-Acetyloxy-2,6,14,17-tetramethyl-3,11-dioxo-14-(5-oxooxolane-3-carbonyl)-10-oxatetracyclo[7.7.1.02,7.013,17]heptadecan-4-yl] acetate 162983623 Click to see CC1CC(C(=O)C2(C1CC3C4(C2C(CC(C4CC(=O)O3)(C)C(=O)C5CC(=O)OC5)OC(=O)C)C)C)OC(=O)C 546.60 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S,3aR,6Z,9R,10E,11aS)-9-hydroxy-6-(hydroxymethyl)-3,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one 163011021 Click to see CC1C2CCC(=CCC(C(=CC2OC1=O)C)O)CO 266.33 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1S,2R,4S,5R,8R,10S,13R,14R,17S,18R,20S)-10-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 162899635 Click to see 1223.30 unknown https://doi.org/10.1021/NP9004147
(1S,2S,4S,5R,6S,9S,10R,11R,14R,15S,18S,23R)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10-(hydroxymethyl)-6,10,14,15,21,21-hexamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 45270111 Click to see 780.90 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(E)-N-[(3S,4R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-4-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide 11154961 Click to see CC=C(C)C(=O)NC1CCC2(C3CCC4(C(C3CC=C2C1O)CCC4C(C)N(C)C)C)C 442.70 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Card-20(22)-enolide, 2,3-((6,10-dihydroxy-9-methyl-8-oxa-1-thia-4-azaspiro(4.5)dec-3-ene-6,7-diyl)bis(oxy))-14-hydroxy-, (2-alpha(7S,9R),3-beta,5-alpha)- 78169140 Click to see 589.70 unknown https://doi.org/10.1021/NP9004147
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate 162964060 Click to see 841.00 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
https://doi.org/10.1021/JF800416J
> 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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Acetylgliotoxin G 139584851 Click to see 432.60 unknown https://doi.org/10.1021/NP9004147
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
Aspereline H 139588514 Click to see 979.20 unknown https://doi.org/10.1021/NP9004147
> 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/S0031-9422(00)86224-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(2R,3R)-2-Hydroxycitric acid 5,2-lactone 101406944 Click to see C1C(=O)OC(C1(C(=O)O)O)C(=O)O 190.11 unknown https://doi.org/10.1016/S0031-9422(00)86224-X
1,2,3-Propanetricarboxylic acid, 1,2-dihydroxy- 123908 Click to see 208.12 unknown https://doi.org/10.1016/S0021-9673(98)00054-5
alpha-Hydroxycitric acid 57473313 Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)OO 208.12 unknown https://doi.org/10.1016/S0021-9673(98)00054-5
Hydroxycitric acid lactone, (-)-(P) 9859390 Click to see C1C(=O)OC(C1(C(=O)O)O)C(=O)O 190.11 unknown https://doi.org/10.1016/S0031-9422(00)86224-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(7aS)-2,4,5,7aalpha-Tetrahydro-1alpha,4,4,7aalpha-tetramethyl-1H-inden-2alpha-ol 101609001 Click to see CC1C(C=C2C1(C=CCC2(C)C)C)O 192.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see 457.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-2-[4-[(2S,11R)-11-hydroxy-4-oxo-1,5,9-triazacyclotridec-2-yl]phenoxy]-6-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 44605335 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3CC(=O)NCCCNCC(CCN3)O)OC4C(C(C(C(O4)COC(=O)C5=CC=CC=C5)O)O)O)O)O 719.80 unknown https://doi.org/10.1021/NP9004147
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(1R,6S,8R)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.01,6]undec-4-ene 21636591 Click to see 208.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(3S)-3-ethoxynonane 101915605 Click to see 172.31 unknown via CMAUP database
Heptane, 1-ethoxy- 519677 Click to see 144.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
2-Hydroxy-3,4,7-trimethoxydibenzofuran 10355969 Click to see 274.27 unknown via CMAUP database
2,8-Dihydroxy-3,4,7-trimethoxydibenzofuran 441782 Click to see COC1=C(C=C2C3=CC(=C(C(=C3OC2=C1)OC)OC)O)O 290.27 unknown via CMAUP database
Epsilon-Cotonefuran 10334385 Click to see 290.27 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1R,13R,15R,16S)-6,7-dihydroxy-16-methyl-1,13,15-tris(3-methylbut-2-enyl)-16-(4-methylpent-3-enyl)-3-oxatetracyclo[11.3.1.02,11.04,9]heptadeca-2(11),4,6,8-tetraene-10,12,17-trione 102164368 Click to see 600.80 unknown https://doi.org/10.1016/J.TET.2009.11.034
https://doi.org/10.1021/JF800416J
1,3,5-Trihydroxy-6-methoxyxanthone 5479775 Click to see 274.22 unknown https://doi.org/10.1248/CPB.54.126
1,5,6-Trihydroxy-3,7-dimethoxyxanthone 5479778 Click to see COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)OC)O)O)O 304.25 unknown https://doi.org/10.1248/CPB.54.126
1,6-Dihydroxyxanthone 5493674 Click to see 228.20 unknown https://doi.org/10.1139/V09-123
13-(3,7-Dimethylocta-2,6-dienyl)-6,7-dihydroxy-16,16-dimethyl-1,15-bis(3-methylbut-2-enyl)-3-oxatetracyclo[11.3.1.02,11.04,9]heptadeca-2(11),4,6,8-tetraene-10,12,17-trione 162887367 Click to see CC(=CCCC(=CCC12CC(C(C(C1=O)(C3=C(C2=O)C(=O)C4=CC(=C(C=C4O3)O)O)CC=C(C)C)(C)C)CC=C(C)C)C)C 600.80 unknown https://doi.org/10.1016/J.TET.2009.11.034
6,7-Dihydroxy-16-methyl-1,13,15-tris(3-methylbut-2-enyl)-16-(4-methylpent-3-enyl)-3-oxatetracyclo[11.3.1.02,11.04,9]heptadeca-2(11),4,6,8-tetraene-10,12,17-trione 45360195 Click to see CC(=CCCC1(C(CC2(C(=O)C3=C(C1(C2=O)CC=C(C)C)OC4=CC(=C(C=C4C3=O)O)O)CC=C(C)C)CC=C(C)C)C)C 600.80 unknown https://doi.org/10.1016/J.TET.2009.11.034
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1248/CPB.54.126
Norathyriol 5281656 Click to see 260.20 unknown https://doi.org/10.1248/CPB.54.126
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(3R)-5,9,11-trihydroxy-3-methyl-10-(3-methylbut-2-enyl)-3-(4-methylpent-3-enyl)pyrano[3,2-a]xanthen-12-one 163044517 Click to see 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
(3S)-5,9,11-trihydroxy-3-methyl-10-(3-methylbut-2-enyl)-3-(4-methylpent-3-enyl)pyrano[3,2-a]xanthen-12-one 163044518 Click to see CC(=CCCC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)O)C)C 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
1,3,6-Trihydroxy-7-methoxy-2-(3,7-dimethyl-2,6-octadienyl)xanthone 85128675 Click to see 410.50 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-957370
https://doi.org/10.1055/S-2006-959502
1,6-Dihydroxy-3,5-dimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one 101741107 Click to see 356.40 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5-trihydroxyxanthen-9-one 5495932 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C 380.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
5,11-Dihydroxy-9-methoxy-3,3-dimethyl-10-(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one 118735083 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C4=C3CCC(O4)(C)C)O)OC)C 410.50 unknown via CMAUP database
5,11-Dihydroxy-9-methoxy-3,3-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-a]xanthen-12-one 11704200 Click to see 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
6-(3,7-Dihydroxy-3,7-dimethyloctyl)-1,3,5-trihydroxy-2-(4-hydroxy-3-methylbut-2-enyl)-7-methoxyxanthen-9-one 75082430 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C=C3C2=O)OC)CCC(C)(CCCC(C)(C)O)O)O)O)CO 530.60 unknown https://doi.org/10.1139/V09-123
6-[(3R)-3,7-dihydroxy-3,7-dimethyloctyl]-1,3,5-trihydroxy-2-[(E)-4-hydroxy-3-methylbut-2-enyl]-7-methoxyxanthen-9-one 163189293 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C=C3C2=O)OC)CCC(C)(CCCC(C)(C)O)O)O)O)CO 530.60 unknown https://doi.org/10.1139/V09-123
Cowagarcinone B 5316764 Click to see 356.40 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
Cowagarcinone D 101741108 Click to see CC(=CCCC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)O)C)C 462.50 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
Cowaxanthone 10386850 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C=C3C2=O)OC)O)O)C)C 410.50 unknown https://doi.org/10.1055/S-2006-957370
https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-959502
https://doi.org/10.1002/CHIN.200544225
Mangostinone 6478778 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C 380.40 unknown https://doi.org/10.1002/CHIN.200544225
Nigrolineaxanthone E 21576570 Click to see 410.50 unknown https://doi.org/10.1071/CH03175
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Dulxanthone A 10759703 Click to see 342.30 unknown https://doi.org/10.1248/CPB.54.126
nigrolineaxanthone T 11559542 Click to see CC(C)(CCC1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)OC)O 360.40 unknown https://doi.org/10.1248/CPB.54.126
Nigrolineaxanthone V 11553272 Click to see 408.40 unknown https://doi.org/10.1248/CPB.54.126
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7,8-dimethoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 163048406 Click to see 440.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
[4-[8-(3,7-Dimethylocta-2,6-dienyl)-1,3,6-trihydroxy-7-methoxy-9-oxoxanthen-2-yl]-2-methylbut-2-enyl] acetate 72954940 Click to see 536.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
1-(3,7-Dimethylocta-2,6-dienyl)-2,3,6,8-tetrahydroxy-7-(3-methylbut-2-enyl)xanthen-9-one 72992075 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)O)C)C 464.50 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-959502
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxy-4,7-bis(3-methylbut-2-enyl)xanthen-9-one 72981455 Click to see CC(=CCCC(=CCC1=C2C(=C(C(=C1OC)O)CC=C(C)C)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C 546.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one 73086794 Click to see 478.60 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1016/J.PHYTOCHEM.2005.06.025
https://doi.org/10.1055/S-2006-957370
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
https://doi.org/10.1055/S-2006-959502
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 5748685 Click to see 410.50 unknown https://doi.org/10.1071/CH03175
https://doi.org/10.1016/0031-9422(77)80129-5
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-7-(4-hydroxy-3-methylbut-2-enyl)-2-methoxyxanthen-9-one 85154683 Click to see 494.60 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-957370
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
https://doi.org/10.1055/S-2006-959502
1-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxy-4,7-bis(3-methylbut-2-enyl)xanthen-9-one 11489665 Click to see 546.70 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
1-[(2Z)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 6450342 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/10.1071/CH03175
https://doi.org/10.1016/0031-9422(77)80129-5
1,3,6-trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9-oxoxanthene-4-carbaldehyde 11626309 Click to see 438.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
1,7-Dihydroxy-3,6-dimethoxy-2,8-diprenylxanthone 14777483 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)O)CC=C(C)C)OC)C 424.50 unknown https://doi.org/10.3987/COM-11-12163
11Alpha-Mangostanin 46880204 Click to see 426.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
3,6-Dimethylmangostin 231412 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC=C(C)C)OC)C 438.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
5,9-Dihydroxy-8-methoxy-2,2-dimethyl-7,10-bis(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 11503863 Click to see CC(=CCC1=C2C(=C(C(=C1OC)O)CC=C(C)C)OC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)C 476.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
7-(3,7-Dimethylocta-2,6-dienyl)-5,9-dihydroxy-8-methoxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one 78385721 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C)C 476.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
7-O-Methylgarcinone 10435205 Click to see 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.1055/S-2006-957370
https://doi.org/10.1016/S0031-9422(97)00125-8
Beta-Mangostin 5495925 Click to see 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-957370
CID 101671063 101671063 Click to see 494.60 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.1055/S-2006-957370
Cowagarcinone E 11421303 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)COC(=O)C)O)O)OC)C)C 536.60 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
Cowanin 11754819 Click to see 478.60 unknown https://doi.org/10.1055/S-2006-957370
https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1055/S-2006-959502
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.1002/CHIN.200544225
Cowanol 10480887 Click to see 494.60 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
https://doi.org/10.1055/S-2006-957370
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
https://doi.org/10.1055/S-2006-959502
Cowaxanthone B 11316212 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=CC(=C(C(=C3C2=O)CC=C(C)C)OC)OC)O)C 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
Fuscaxanthone A 5324264 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C)C 476.60 unknown https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
Mangostanin 5495929 Click to see 408.40 unknown via CMAUP database
Mangostin 5281650 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C 410.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.02.027
Norcowanin 11518330 Click to see 464.50 unknown https://doi.org/10.3987/COM-11-12163
https://doi.org/10.1002/CHIN.200544225
https://doi.org/10.1055/S-2006-959502
Rubraxanthone 9953366 Click to see 410.50 unknown https://doi.org/10.1071/CH03175
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
O-Demethylforbexanthone 45269778 Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC(=CC(=C4C3=O)O)O)C 326.30 unknown https://doi.org/10.1248/CPB.54.126
Rheediaxanthone A 102060338 Click to see 392.40 unknown https://doi.org/10.1016/S0031-9422(98)80096-4
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Marmelolactone B 101282733 Click to see CC1CC(OC1=O)C=CC(=C)C 166.22 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,9R)-2,2,9-trimethyl-8,12-dioxatricyclo[7.2.1.01,6]dodec-5-ene 21636592 Click to see 208.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Marmelo oxide A 14379832 Click to see 152.23 unknown via CMAUP database
Marmelo oxide B 14379831 Click to see 152.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Marcellomycin 107861 Click to see 845.90 unknown https://doi.org/10.1021/NP9004147
> Phenylpropanoids and polyketides / Depsides and depsidones
2,7,9-Trihydroxy-3-methoxy-4-(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one 101782918 Click to see 358.30 unknown https://doi.org/10.3987/COM-11-12163
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
5,4'-Dihydroxy-7-methoxy-8-prenylflavanone 11688951 Click to see 354.40 unknown https://doi.org/10.1021/JF800416J

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