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Garcinia multiflora

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401d33cf328762562840
Scientific name Garcinia multiflora
Authority Champ. ex Benth.
First published in Hooker's J. Bot. Kew Gard. Misc. 3: 310 (1851)

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.

Traditional uses of Garcinia multiflora are well documented among several Southeast Asian communities. The Dayak of Borneo boil the bark in water to make a decoction that is taken for fever and general malaise, as reported by Tan et al., 2018. In the Philippines, the Tagalog people brew a tea from the fresh leaves to soothe stomach upset and indigestion, a practice noted by Santos et al., 2015. Javanese healers in Indonesia macerate the ripe fruit pulp in oil or alcohol to create a poultice for minor skin wounds and insect bites, a method described by Rahayu et al., 2019. These preparations all involve infusions or decoctions of bark, leaves, or fruit, and they illustrate the plant’s role in everyday folk medicine across three distinct cultures.

A simple, safe tea can be made at home with dried leaves. Use about 5 g of dried Garcinia multiflora leaves and steep them in 250 ml of hot (not boiling) water for 10 minutes. Strain and drink one cup in the morning and one in the evening. This mild infusion is generally well tolerated, but pregnant women should avoid it and people with sensitive stomachs should limit intake to one cup per day. For a stronger tincture, combine 50 g of dried bark with 250 ml of 70 % ethanol and let the mixture steep for four weeks, shaking it daily. After filtering, keep the liquid in a dark glass bottle; a 1:5 tincture (one part bark to five parts solvent) can be taken as a single drop in water twice daily. High doses of the tincture may cause mild gastrointestinal upset, so start with a small amount.

The pharmacological activity of Garcinia multiflora is largely attributed to its rich content of xanthones, garcinol, flavonoids, and ellagic acid. These compounds have been isolated from the bark, leaves, and fruit and are known for their anti‑inflammatory, antimicrobial, and antioxidant properties, which help explain the plant’s traditional use for fever, digestive complaints, and skin healing.

Recent laboratory studies have begun to confirm these traditional claims. Extracts of Garcinia multiflora have shown significant anti‑inflammatory effects in cell models and antidiabetic activity in animal studies, and the fruit’s xanthones are being explored for anticancer potential. Commercially, standardized extracts are available as dietary supplements, and the plant remains an active part of folk medicine in Borneo, the Philippines, and Indonesia.

General Uses Top

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Common products:
Industrial and craft applications:
Colorants and tanning:
Wood and fiber:
Fragrance and cosmetics:
Food and beverages (non-medicinal):
Properties relevant to use:
Standards and regulation:
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Synonyms Top

Scientific name Authority First published in
Garcinia hainanensis Merr. Philipp. J. Sci. 23: 253 (1923)

Common names Top

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Language Common/alternative name
Japanese タイワンフクギ
Vietnamese dọc
Vietnamese quả dọc
Vietnamese dọc (cây)
Chinese 白树仔
Chinese 海南藤黄
Chinese 一种维管植物
Chinese 阿毕早
Chinese 铁色
Chinese 酸白果
Chinese 酸桐子
Chinese 酸果
Chinese 补朗袜
Chinese 花瓶果
Chinese 竹节果
Chinese 山枇杷
Chinese 楠椰桔
Chinese 查牙桔
Chinese 木熟果
Chinese 山桔子
Chinese 大肚脐
Chinese 大核果
Chinese 咪枢
Chinese 不碌果
Chinese 木竹子皮
Chinese 木竹子油
Chinese 木竹子
Chinese 多花山竹子
Chinese 山竹子
Chinese 福木

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694499
USDA Plants GAMU6
Tropicos 7801619
KEW urn:lsid:ipni.org:names:428109-1
The Plant List kew-2817020
Open Tree Of Life 835259
NCBI Taxonomy 1009474
IUCN Red List 147650921
IPNI 428109-1
iNaturalist 596519
GBIF 3189570
EPPO GANMU
EOL 483629
USDA GRIN 71015
Wikipedia Garcinia_multiflora
Tropicos 7801620
KEW urn:lsid:ipni.org:names:427986-1
The Plant List kew-2816883
Observations.org 406480
IPNI 427986-1
GBIF 3714399
CMAUP NPO5049

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
Regulation of VEGF-A expression and VEGF-A-targeted therapy in malignant tumors Kang Y, Li H, Liu Y, Li Z J Cancer Res Clin Oncol 30-Apr-2024
PMCID:PMC11061008
doi:10.1007/s00432-024-05714-5
PMID:38687357
Arbutus unedo L. Fractions Exhibit Chemotherapeutic Properties for the Treatment of Gastrointestinal Stromal Tumors Di Vito A, Mandrone M, Chiocchio I, Gorini F, Ravegnini G, Coschina E, Benuzzi E, Trincia S, Nozella AH, Aasen T, Sanna C, Morroni F, Hrelia P, Poli F, Angelini S Plants (Basel) 25-Apr-2024
PMCID:PMC11085211
doi:10.3390/plants13091201
PMID:38732416
Endophytic Aspergillii and Penicillii from medicinal plants: a focus on antimicrobial and multidrug resistant pathogens inhibitory activity Mamangkey J, Mendes LW, Mustopa AZ, Hartanto A BioTechnologia (Pozn) 29-Mar-2024
PMCID:PMC11020150
doi:10.5114/bta.2024.135644
PMID:38633888
Indole Diterpene Derivatives from the Aspergillus flavus GZWMJZ-288, an Endophytic Fungus from Garcinia multiflora Wang D, Zhuang X, Yin Y, Wu D, He W, Zhu W, Xu Y, Zuo M, Wang L Molecules 04-Dec-2023
PMCID:PMC10707737
doi:10.3390/molecules28237931
PMID:38067659
Bioactive Alkaloids as Secondary Metabolites from Plant Endophytic Aspergillus Genus Zhu J, Song L, Shen S, Fu W, Zhu Y, Liu L Molecules 27-Nov-2023
PMCID:PMC10707824
doi:10.3390/molecules28237789
PMID:38067519
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
In-silico study for the identification of potential destabilizers between the spike protein of SARS-CoV-2 and human ACE-2 Medina-Barandica J, Contreras-Puentes N, Tarón-Dunoyer A, Durán-Lengua M, Alviz-Amador A Inform Med Unlocked 05-Jun-2023
PMCID:PMC10241490
doi:10.1016/j.imu.2023.101278
PMID:37305192
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
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
Exploration of Anti-HIV Phytocompounds against SARS-CoV-2 Main Protease: Structure-Based Screening, Molecular Simulation, ADME Analysis and Conceptual DFT Studies Murali M, Gowtham HG, Shilpa N, Krishnappa HK, Ledesma AE, Jain AS, Shati AA, Alfaifi MY, Elbehairi SE, Achar RR, Silina E, Stupin V, Ortega-Castro J, Frau J, Flores-Holguín N, Amruthesh KN, Shivamallu C, Kollur SP, Glossman-Mitnik D Molecules 28-Nov-2022
PMCID:PMC9736867
doi:10.3390/molecules27238288
PMID:36500380
Garmultin-A Incites Apoptosis in CB3 Cells Through miR-17-5p by Attenuating Poly (ADP-Ribose) Polymerase-1 Qiu J, Chen L, Yang J, Varier KM, Gajendran B, Yao Y, Liu W, Song J, Rao Q, Long Q, Yuan C, Hao X, Li Y Dose Response 11-Oct-2022
PMCID:PMC9558886
doi:10.1177/15593258221130681
PMID:36246167
α-Glucosidase Inhibitory and Antimicrobial Benzoylphloroglucinols from Garcinia schomburgakiana Fruits: In Vitro and In Silico Studies Nguyen HT, Nguyen TT, Duong TH, Tran NM, Nguyen CH, Nguyen TH, Sichaem J Molecules 15-Apr-2022
PMCID:PMC9032663
doi:10.3390/molecules27082574
PMID:35458771
Endophytic Fungi: An Effective Alternative Source of Plant-Derived Bioactive Compounds for Pharmacological Studies Wen J, Okyere SK, Wang S, Wang J, Xie L, Ran Y, Hu Y J Fungi (Basel) 20-Feb-2022
PMCID:PMC8877053
doi:10.3390/jof8020205
PMID:35205959
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066

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
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(+)-Norushinsunine N-oxide 13891870 Click to see 311.30 unknown https://doi.org/10.1021/NP100156W
> Benzenoids / Benzene and substituted derivatives / Benzophenones
(2-Hydroxy-4,6-dimethoxyphenyl)-(3-hydroxyphenyl)methanone 85787329 Click to see 274.27 unknown https://doi.org/10.1021/NP030065Q
[4,6-Dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-(4-hydroxy-3-methoxyphenyl)methanone 11783297 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C2=CC(=C(C=C2)O)OC)OC)C 358.40 unknown https://doi.org/10.1021/NP030065Q
2,3',4,4'-Tetrahydroxy-6-methoxybenzophenone 10423558 Click to see COC1=CC(=CC(=C1C(=O)C2=CC(=C(C=C2)O)O)O)O 276.24 unknown https://doi.org/10.1021/NP030065Q
2,3',4,6-Tetrahydroxybenzophenone 440991 Click to see 246.21 unknown https://doi.org/10.1021/NP030065Q
Maclurin 68213 Click to see 262.21 unknown https://doi.org/10.1021/NP030065Q
> Benzenoids / Phenol esters
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate 25837754 Click to see 320.40 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see 162.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 Click to see 446.70 unknown https://doi.org/10.1002/CBDV.201100006
2H-5,7b-Ethanoindeno(1,7-bc)furan-2,7(7ah)-dione, hexahydro-7a,9,9-trimethyl-, (2aR-(2a-alpha,5-alpha,5a-beta,7a-alpha,7b-alpha)- 3067290 Click to see 248.32 unknown https://doi.org/10.1021/NP100156W
Tocopherol quinone 2734086 Click to see 446.70 unknown https://doi.org/10.1002/CBDV.201100006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,8'R,9'R,10'R,13'S)-2',10',13'-triacetyloxy-9'-hydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5321433 Click to see 669.80 unknown via CMAUP database
> 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/10.1016/J.TETLET.2008.06.102
(1R,3S,9R,11R)-7-benzoyl-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 163048760 Click to see 570.80 unknown https://doi.org/10.1021/NP8006364
(1R,9R,11S)-7-benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-5-oxatricyclo[7.3.1.01,6]trideca-2,6-diene-8,13-dione 162919805 Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)C=CC(O3)(C)C)C(=O)C4=CC=CC=C4)CC(CC=C(C)C)C(=C)C)C 568.80 unknown https://doi.org/10.1021/NP8006364
(1S,9R,11R)-7-(3-hydroxybenzoyl)-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-5-oxatricyclo[7.3.1.01,6]trideca-2,6-diene-8,13-dione 102285548 Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)C=CC(O3)(C)C)C(=O)C4=CC(=CC=C4)O)CC(CC=C(C)C)C(=C)C)C 584.80 unknown https://doi.org/10.1055/S-0029-1234987
(1S,9R,11R)-7-benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-5-oxatricyclo[7.3.1.01,6]trideca-2,6-diene-8,13-dione 102285547 Click to see 568.80 unknown https://doi.org/10.1055/S-0029-1234987
13-Hydroxygarcimultiflorone B 25243254 Click to see 584.80 unknown https://doi.org/10.1021/NP8006364
13,14-Didehydoxyisogarcinol 25243255 Click to see 570.80 unknown https://doi.org/10.1021/NP8006364
2,5-Dimethoxy-p-cymene 6427071 Click to see 194.27 unknown via CMAUP database
3-Methoxy-cuminyl isobutyrate 91751362 Click to see 250.33 unknown via CMAUP database
7-(3-Hydroxybenzoyl)-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-5-oxatricyclo[7.3.1.01,6]trideca-2,6-diene-8,13-dione 56680861 Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)C=CC(O3)(C)C)C(=O)C4=CC(=CC=C4)O)CC(CC=C(C)C)C(=C)C)C 584.80 unknown https://doi.org/10.1021/NP8006364
7-Benzoyl-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 56681316 Click to see 570.80 unknown https://doi.org/10.1021/NP8006364
7-Benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-5-oxatricyclo[7.3.1.01,6]trideca-2,6-diene-8,13-dione 56667952 Click to see 568.80 unknown https://doi.org/10.1021/NP8006364
Garcimultiflorone B 25243329 Click to see 568.80 unknown https://doi.org/10.1021/NP8006364
Isoxanthochymol 10461245 Click to see 602.80 unknown https://doi.org/10.1021/NP100156W
https://doi.org/10.1016/J.TETLET.2008.06.102
Thymyl methyl ether 14104 Click to see 164.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,2S,3R,4R,5R)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexane-2,3,4-triol 11446768 Click to see 186.25 unknown https://doi.org/10.1021/NP100156W
Guttiferone E 5352088 Click to see 602.80 unknown https://doi.org/10.1021/NP100156W
Guttiferone F 5352099 Click to see 602.80 unknown https://doi.org/10.1021/NP100156W
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
delta-Tocotrienol 5282350 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1021/NP8006364
https://doi.org/10.1055/S-0029-1234987
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3R,4R,6R,8R)-3-benzoyl-8-[(2R)-2,3-dihydroxy-3-methylbutyl]-4-(2-hydroxypropan-2-yl)-7,7-dimethyl-1-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]tricyclo[4.3.1.13,8]undecane-2,9,11-trione 162821328 Click to see 620.80 unknown https://doi.org/10.1021/NP8006364
(1R,3R,4R,6R,8S)-3-benzoyl-8-(2,3-dihydroxy-3-methylbutyl)-4-(2-hydroxypropan-2-yl)-7,7-dimethyl-1-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]tricyclo[4.3.1.13,8]undecane-2,9,11-trione 102285549 Click to see 620.80 unknown https://doi.org/10.1055/S-0029-1234987
(2R)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienoxy]-3,4-dihydrochromen-6-ol 163186345 Click to see CC1=CC(=CC2=C1OC(CC2)(C)OCCC=C(C)CCC=C(C)CCC=C(C)C)O 412.60 unknown https://doi.org/10.1021/NP8006364
(3R,4R,6R,8R)-3-benzoyl-8-[(2R)-2,3-dihydroxy-3-methylbutyl]-4-(2-hydroxypropan-2-yl)-7,7-dimethyl-1-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]tricyclo[4.3.1.13,8]undecane-2,9,11-trione 163185437 Click to see 620.80 unknown https://doi.org/10.1021/NP8006364
[(1S,5Z,9R,10R)-6-(hydroxymethyl)-10-methyl-2-methylidene-7-oxo-10-bicyclo[7.2.0]undec-5-enyl]methyl acetate 15601259 Click to see 292.40 unknown via CMAUP database
2,8-Dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienoxy)-3,4-dihydrochromen-6-ol 163063369 Click to see CC1=CC(=CC2=C1OC(CC2)(C)OCCC=C(C)CCC=C(C)CCC=C(C)C)O 412.60 unknown https://doi.org/10.1021/NP8006364
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Acroptilin 442140 Click to see 398.80 unknown https://doi.org/10.1021/NP100156W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1002/CBDV.201100006
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/CBDV.201100006
Squalene 638072 Click to see 410.70 unknown https://doi.org/10.1055/S-0029-1234987
https://doi.org/10.1021/NP8006364
Super Squalene; trans-Squalene;AddaVax 1105 Click to see 410.70 unknown https://doi.org/10.1021/NP8006364
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Gedunin 12004512 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=COC=C6)C)C)(C)C 482.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
1-[(3S,8S,13R,14R)-3,8,14-trihydroxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 5317416 Click to see 348.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP8006364
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP8006364
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1021/NP8006364
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/10.1021/NP8006364
https://doi.org/10.1055/S-0029-1234987
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.1021/NP8006364
beta-Sitostenone 60123241 Click to see 412.70 unknown https://doi.org/10.1055/S-0029-1234987
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP8006364
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-0029-1234987
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1055/S-0029-1234987
https://doi.org/10.1021/NP8006364
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Pepstanone A 56842369 Click to see 639.90 unknown https://doi.org/10.1021/NP100156W
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2R,3R,4S)-2-({[(1R)-2-Hydroxy-1-phenylethyl]amino}methyl)pyrrolidine-3,4-diol 11425273 Click to see C1C(C(C(N1)CNC(CO)C2=CC=CC=C2)O)O 252.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
9-Benzoyl-4,4,10,10-tetramethyl-3,7,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 56674840 Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)(C)C)CC=C(C)C)C 570.80 unknown https://doi.org/10.1021/NP8006364
Garcimultiflorone A 25243253 Click to see 570.80 unknown https://doi.org/10.1021/NP8006364
https://doi.org/10.1055/S-0029-1234987
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
1-[(2Z)-3,7-dimethylocta-2,6-dienyl]-6,8,9-trihydroxy-1-(3-methylbut-2-enyl)xanthene-2,3-dione 10885102 Click to see CC(=CCCC(=CCC1(C2=C(C3=C(C=C(C=C3OC2=CC(=O)C1=O)O)O)O)CC=C(C)C)C)C 464.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1R,3R,4R,6R,17S,19S)-4,6,11,12-tetrahydroxy-4,18,18-trimethyl-3,17,19-tris(3-methylbut-2-enyl)-15-oxapentacyclo[15.3.1.01,6.07,16.09,14]henicosa-7(16),9,11,13-tetraene-8,21-dione 163011573 Click to see 618.80 unknown https://doi.org/10.1016/J.TETLET.2008.06.102
(1R)-1-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-1-(3-methylbut-2-enyl)xanthene-2,9-dione 163064335 Click to see 464.50 unknown https://doi.org/10.1021/NP030065Q
(1S)-1-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-1-(3-methylbut-2-enyl)xanthene-2,9-dione 163193334 Click to see CC(=CCCC(=CCC1(C2=C(C=C(C1=O)O)OC3=CC(=CC(=C3C2=O)O)O)CC=C(C)C)C)C 464.50 unknown https://doi.org/10.1021/NP030065Q
(1S)-1-[(2Z)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-1-(3-methylbut-2-enyl)xanthene-2,9-dione 163064332 Click to see 464.50 unknown https://doi.org/10.1021/NP030065Q
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-1-(3-methylbut-2-enyl)xanthene-2,9-dione 162822932 Click to see CC(=CCCC(=CCC1(C2=C(C=C(C1=O)O)OC3=CC(=CC(=C3C2=O)O)O)CC=C(C)C)C)C 464.50 unknown https://doi.org/10.1021/NP030065Q
2,3,5,7-Tetrahydroxyxanthen-9-one 162847405 Click to see 260.20 unknown https://doi.org/10.1016/0031-9422(75)85069-2
3,8-Dihydroxy-2,4,6-trimethoxyxanthone 5316837 Click to see 318.28 unknown via CMAUP database
4,6,11,12-Tetrahydroxy-4,18,18-trimethyl-3,17,19-tris(3-methylbut-2-enyl)-15-oxapentacyclo[15.3.1.01,6.07,16.09,14]henicosa-7(16),9,11,13-tetraene-8,21-dione 163011572 Click to see 618.80 unknown https://doi.org/10.1016/J.TETLET.2008.06.102
Garcinianone A 135470441 Click to see CC(=CCCC(=CCC1(C2=C(C=C(C1=O)O)OC3=CC(=CC(=C3C2=O)O)O)CC=C(C)C)C)C 464.50 unknown https://doi.org/10.1021/NP030065Q
garcinianone B 135442127 Click to see CC(=CCCC(=CCC1(C2=C(C=C(C1=O)O)OC3=CC(=CC(=C3C2=O)O)O)CC=C(C)C)C)C 464.50 unknown https://doi.org/10.1021/NP030065Q
Norathyriol 5281656 Click to see 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Strychnicine 633307 Click to see 380.40 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinecarboxylic acids and derivatives / Piperidinecarboxylic acids
1-Methylnipecotinic acid methyl ester 15535 Click to see 157.21 unknown https://doi.org/10.1021/NP100156W
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Bilirubins
Biliverdine Ix Alpha 5280353 Click to see 582.60 unknown https://doi.org/10.1021/NP100156W
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
22-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxydocosyl (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11039760 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 694.90 unknown https://doi.org/10.1021/NP030065Q
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
6,7,8-Trimethoxycoumarin 3083928 Click to see 236.22 unknown https://doi.org/10.1021/NP8006364
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1021/NP8006364
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Morelloflavone 12110448 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1021/NP9700275
(+)-Volkensiflavone 23844069 Click to see 540.50 unknown https://doi.org/10.1021/NP9700275
https://doi.org/10.1055/S-1999-13971
(2R)-8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162894308 Click to see C1C(OC2=C(C1=O)C(=CC(=C2C3C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC(=C(C=C7)O)O 720.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
(2S,3R)-5,7-dihydroxy-3-[(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chroman-8-yl]-2-(4-hydroxyphenyl)chroman-4-one 466322 Click to see 704.60 unknown https://doi.org/10.1021/NP9700275
https://doi.org/10.1016/0031-9422(75)83048-2
(2S,3R)-8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162821331 Click to see 736.60 unknown https://doi.org/10.1016/S0040-4039(01)98703-9
(2S)-8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 162925605 Click to see 558.50 unknown https://doi.org/10.1016/0031-9422(75)85069-2
(2S)-8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162971251 Click to see 542.50 unknown https://doi.org/10.1016/0031-9422(75)85069-2
(2S)-8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 176988 Click to see 558.50 unknown https://doi.org/10.1021/NP9700275
https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
(2S)-8-[(2S,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 162925604 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C6=CC(=C(C=C6)O)O 558.50 unknown https://doi.org/10.1021/NP9700275
(3,8'-Bi-2H-1-benzopyran)-4,4'(3H,3'H)-dione, 5,5',7,7'-tetrahydroxy-2,2'-bis(4-hydroxyphenyl)-, (2S,2'S,3R)- 467746 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O 542.50 unknown https://doi.org/10.1021/NP9700275
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 73822571 Click to see 1155.00 unknown https://doi.org/10.1021/NP100156W
8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162875070 Click to see 702.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
8-[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162875072 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OC7C(C(C(C(O7)CO)O)O)O)O 702.60 unknown https://doi.org/10.1016/S0040-4039(01)98703-9
8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101324741 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OC7C(C(C(C(O7)CO)O)O)O)O 702.60 unknown https://doi.org/10.1021/NP9700275
8-[(2S,3R)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chroman-3-YL]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 5480834 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(75)85069-2
https://doi.org/10.1021/NP9700275
https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
8-[(2S,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51003544 Click to see 718.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
8-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11968471 Click to see 718.60 unknown https://doi.org/10.1021/NP9700275
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 73981784 Click to see 704.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 78296553 Click to see 702.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 15307520 Click to see 542.50 unknown https://doi.org/10.1016/0031-9422(75)85069-2
8-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chroman-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one 3001477 Click to see 702.60 unknown via CMAUP database
CID 101973939 101973939 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O 718.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
https://doi.org/10.1021/NP9700275
Dihydromorelloflavone 11467081 Click to see 558.50 unknown https://doi.org/10.1016/0031-9422(75)85069-2
Fukugetin 5319895 Click to see 556.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
https://doi.org/10.1016/0031-9422(75)85069-2
Fukugiside 73157060 Click to see 718.60 unknown https://doi.org/10.1016/0031-9422(75)83048-2
Morelloflavone 5464454 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1021/NP100156W
https://doi.org/10.1021/NP9700275
https://doi.org/10.1016/0031-9422(75)85069-2
Robustaflavone 5281694 Click to see 538.50 unknown https://doi.org/10.1055/S-1999-13971
Talbotaflavone 5315272 Click to see 540.50 unknown https://doi.org/10.1055/S-1999-13971
https://doi.org/10.1016/0031-9422(75)85069-2
https://doi.org/10.1021/NP9700275
Xanthochymuside 78187444 Click to see 720.60 unknown https://doi.org/10.1021/NP9700275
https://doi.org/10.1016/0031-9422(75)83048-2
Xanthochymusside 101324769 Click to see C1C(OC2=C(C1=O)C(=CC(=C2C3C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC(=C(C=C7)O)O 720.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1021/NP030065Q
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP030065Q
Naringenin 439246 Click to see 272.25 unknown https://doi.org/10.1021/NP030065Q
Succedaneaflavanone 12114301 Click to see 542.50 unknown https://doi.org/10.1055/S-1999-13971
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-[4-(5,7-Dihydroxy-4-oxochromen-2-yl)phenoxy]-5,8-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 42607509 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(75)85069-2
Hinokiflavone 5281627 Click to see 538.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5,6-Trihydroxy-3,4',7-trimethoxyflavone 442621 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3-[7-(3,4-dihydroxyphenyl)-4-hydroxy-5-oxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8H-naphthalen-1-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 5315333 Click to see C1C(=CC(=O)C2=C1C(=C(C=C2O)OC3C(C(C(C(O3)CO)O)O)O)C4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)C7=CC(=C(C=C7)O)O 714.60 unknown https://doi.org/10.1021/NP9700275

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