Garcinia kola - Unknown
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Internal ID UUID64401d2cc12f3979648834
Scientific name Garcinia kola
Authority Heckel
First published in Bull. Soc. Bot. France 30(Rev. Bibliogr.): 150 (1883)

Description Top

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Synonyms Top

Scientific name Authority First published in
Garcinia akawaensis Spirl. Bull. Jard. Bot. État Bruxelles 29: 323 (1959)
Garcinia bergheana Spirl. Bull. Jard. Bot. État Bruxelles 29: 324 (1959)
Garcinia conrauana Engl. Bot. Jahrb. Syst. 40: 562 (1908)
Garcinia dinklagei Engl. Bot. Jahrb. Syst. 40: 561 (1908)
Garcinia giadidi De Wild. Ann. Mus. Congo Belge, Bot. , sér. 5, 2: 55 (1907)

Common names Top

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Language Common/alternative name
English bitter kola
Fulah mijingooro
French bitter kola
French petit kola
Portuguese orobo
Portuguese orobô
Portuguese orogbo

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694394
UNII YR81TT037U
USDA Plants GAKO
Tropicos 7801582
KEW urn:lsid:ipni.org:names:428024-1
The Plant List kew-2816924
PFAF Garcinia kola
Open Tree Of Life 154999
NCBI Taxonomy 469930
IUCN Red List 34715
IPNI 428024-1
iNaturalist 192553
GBIF 3189563
Freebase /m/02w0fkj
EPPO GANKO
EOL 483626
USDA GRIN 71007
Wikipedia Garcinia_kola
CMAUP NPO19561

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
Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M Heliyon 21-Mar-2024
PMCID:PMC10999872
doi:10.1016/j.heliyon.2024.e28247
PMID:38590891
Plant use and perceptions in the context of sexual health among people of Congolese descent in Belgium Van Damme L, Chatrou L, de la Peña E, Kibungu P, Bolya CS, Van Damme P, Vanhove W, Ceuterick M, De Meyer E J Ethnobiol Ethnomed 19-Feb-2024
PMCID:PMC10877895
doi:10.1186/s13002-024-00662-3
PMID:38373968
Anti-Inflammatory and Immunomodulatory Properties of a Crude Polysaccharide Derived from Green Seaweed Halimeda tuna: Computational and Experimental Evidences Kraiem M, Ben Hamouda S, Eleroui M, Ajala M, Feki A, Dghim A, Boujhoud Z, Bouhamed M, Badraoui R, Pujo JM, Essafi-Benkhadir K, Kallel H, Ben Amara I Mar Drugs 11-Feb-2024
PMCID:PMC10890560
doi:10.3390/md22020085
PMID:38393056
Kolaviron neuroprotective effect against okadaic acid-provoked cognitive impairment Nazari-Serenjeh M, Baluchnejadmojarad T, Hatami-Morassa M, Fahanik-Babaei J, Mehrabi S, Tashakori-Miyanroudi M, Ramazi S, Mohamadi-Zarch SM, Nourabadi D, Roghani M Heliyon 01-Feb-2024
PMCID:PMC10864987
doi:10.1016/j.heliyon.2024.e25564
PMID:38356522
Correction: Maňourová et al. Domestication Potential of Garcinia kola Heckel (Clusiaceae): Searching for Diversity in South Cameroon. Plants 2023, 12, 742 Maňourová A, Chinheya IP, Kalousová M, Ruiz-Chután JA, Okafor UC, Tchoundjeu Z, Tsobeng A, Van Damme P, Lojka B Plants (Basel) 18-Dec-2023
PMCID:PMC10748099
doi:10.3390/plants12244191
PMID:38140521
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Optimized preparation of activated carbon with high porosities based on puck shells (Afrostyrax lepidophyllus) by response surface methodology and physico-chemical characterization Nzetchuen Kouahou G, Fotsop CG, Adoum Amola L, Donlifack Atemkeng C, Kamdem Tamo A, Teikam Kenda G, TIEGAM TAGNE RF, Kamgaing T R Soc Open Sci 06-Dec-2023
PMCID:PMC10698491
doi:10.1098/rsos.230911
PMID:38077221
Artemisia brevifolia Wall. Ex DC Enhances Cefixime Susceptibility by Reforming Antimicrobial Resistance Zafar A, Wasti Y, Majid M, Muntaqua D, Bungau SG, Haq IU Antibiotics (Basel) 20-Oct-2023
PMCID:PMC10604168
doi:10.3390/antibiotics12101553
PMID:37887253
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
An in vivo and in silico evaluation of the hepatoprotective potential of Gynura procumbens: A promising agent for combating hepatotoxicity Tithi TI, Tahsin MR, Anjum J, Zaman TS, Aktar F, Bahar NB, Tasnim S, Sultana A, Jahan I, Afrin SS, Akter T, Sen P, Koly FJ, Reza MS, Chowdhury JA, Kabir S, Chowdhury AA, Amran MS PLoS One 15-Sep-2023
PMCID:PMC10503776
doi:10.1371/journal.pone.0291125
PMID:37713406
Bioactivities of Garcinia kola enzymatic hydrolysates at different enzyme–substrate ratios Salami SA, Osukoya OA, Adewale OB, Odekanyin O, Obafemi TO, Kuku A AMB Express 26-Jul-2023
PMCID:PMC10371964
doi:10.1186/s13568-023-01583-2
PMID:37495834
Prevalence, motivation, and associated factors of medicinal herbs consumption in pregnant women from Eastern Mediterranean Regional Office: a systematic review Bouqoufi A, Lahlou L, Ait El Hadj F, Abdessadek M, Obtel M, Khabbal Y Pharm Biol 14-Jul-2023
PMCID:PMC10351469
doi:10.1080/13880209.2023.2229388
PMID:37452524
Red Quinoa Hydrolysates with Antioxidant Properties Improve Cardiovascular Health in Spontaneously Hypertensive Rats López-Moreno M, Jiménez-Moreno E, Márquez Gallego A, Vera Pasamontes G, Uranga Ocio JA, Garcés-Rimón M, Miguel-Castro M Antioxidants (Basel) 16-Jun-2023
PMCID:PMC10295081
doi:10.3390/antiox12061291
PMID:37372021
Acknowledging the use of botanicals to treat diabetic foot ulcer during the 21st century: A systematic review Narzary I, Swarnakar A, Kalita M, Middha SK, Usha T, Babu D, Mochahary B, Brahma S, Basumatary J, Goyal AK World J Clin Cases 16-Jun-2023
PMCID:PMC10303622
doi:10.12998/wjcc.v11.i17.4035
PMID:37388781

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
5-[(2R)-2-(hydroxymethyl)-2-methylchromen-6-yl]-3-methoxybenzene-1,2-diol 163046064 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3=CC(=C(C(=C3)OC)O)O)CO 314.30 unknown https://doi.org/10.3987/COM-94-6773
5-[2-(Hydroxymethyl)-2-methylchromen-6-yl]-3-methoxybenzene-1,2-diol 163046063 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3=CC(=C(C(=C3)OC)O)O)CO 314.30 unknown https://doi.org/10.3987/COM-94-6773
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds
2-Hydroxy-6-[2-[4-[3-[2-(4-hydroxyphenyl)ethyl]-5-methoxyphenoxy]phenyl]ethyl]-4-methoxybenzoic acid 162919332 Click to see COC1=CC(=CC(=C1)CCC2=CC=C(C=C2)O)OC3=CC=C(C=C3)CCC4=C(C(=CC(=C4)OC)O)C(=O)O 514.60 unknown https://doi.org/10.3987/COM-97-7854
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
Di-(Z)-feruloylsecoisolariciresinol 24898244 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(2R)-2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-6-[hydroxy(phenyl)methylidene]-2,4-bis(3-methylbut-2-enyl)cyclohex-4-ene-1,3-dione 139031176 Click to see CC(=CCCC(=CCC1(C(=O)C(=C(C(=C(C2=CC=CC=C2)O)C1=O)O)CC=C(C)C)CC=C(C)C)C)C 502.70 unknown https://doi.org/10.3109/13880209509065369
Kolanone 11953940 Click to see CC(=CCCC(=CCC1(C(=O)C(=C(C(=C(C2=CC=CC=C2)O)C1=O)O)CC=C(C)C)CC=C(C)C)C)C 502.70 unknown https://doi.org/10.3109/13880209509065369
> 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/10.3987/COM-92-6291
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(2E,6E,10E)-13-[(2S)-6-hydroxy-2,8-dimethyl-3,4-dihydrochromen-2-yl]-2,6,10-trimethyltrideca-2,6,10-trienal 163195349 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C=O)O 410.60 unknown https://doi.org/10.3987/COM-97-7854
(2S)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]chroman-6-ol 13988400 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/10.3987/COM-97-7854
(c)(1/2)-Tocotrienol pound>>Tocotrienol, delta 53394607 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/10.3987/COM-97-7854
13-(6-Hydroxy-2,8-dimethyl-3,4-dihydrochromen-2-yl)-2,6,10-trimethyltrideca-2,6,10-trienal 85208627 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C=O)O 410.60 unknown https://doi.org/10.3987/COM-97-7854
13-(6-Hydroxy-2,8-dimethyl-3,4-dihydrochromen-2-yl)-2,6,10-trimethyltrideca-2,6,10-trienoic acid 74493487 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C(=O)O)O 426.60 unknown https://doi.org/10.3987/COM-97-7854
CID 133556427 133556427 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C(=O)O)O 426.60 unknown https://doi.org/10.3987/COM-97-7854
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/10.3987/COM-97-7854
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
triptogelin C-1 10459206 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 516.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
11alpha-Methoxyurs-12-ene-3beta,16beta-diol 44235666 Click to see CC1CCC2(C(CC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1C)C)O)C 472.70 unknown via CMAUP database
12,23-Dihydroxy-11alpha-methoxyurs-12-ene-3-one 44235900 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
13beta,28-Epoxy-23-hydroxyursane-3,12-dione 101485480 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(=O)C6(C)CO)C)C)C 470.70 unknown via CMAUP database
13beta,28-Epoxy-3beta-hydroxy-12-oxoursane-23-al 101485479 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(C6(C)C=O)O)C)C)C 470.70 unknown via CMAUP database
3beta,12-Dihydroxy-11alpha-methoxyurs-12-ene-23-al 44235896 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
6beta,12-Dihydroxy-11alpha-methoxy-24-norurs-12-ene-3-one 44235898 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CC(C5C4(CCC(=O)C5C)C)O)C)OC)O)C2C1C)C)C 472.70 unknown via CMAUP database
Microtropioside B 101506966 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)O)C)C 502.60 unknown via CMAUP database
Microtropioside C 101506967 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)OC5C(C(C(C(O5)CO)O)O)O)C)C 664.80 unknown via CMAUP database
Microtropioside D 101506968 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(COC5C(C(C(C(O5)CO)O)O)O)O)C)C 664.80 unknown via CMAUP database
Microtropioside E 101506969 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
Microtropioside F 101506970 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
Microtropin A 102448004 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin B 102448005 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin C 102448006 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin D 102448007 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OCC=C(CO)C#N)O)O)O)O 405.40 unknown via CMAUP database
Microtropin E 102448008 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C)O)O)O)O 352.38 unknown via CMAUP database
Microtropin F 102448009 Click to see CCC(COC1C(C(C(C(O1)COC(=O)C(CC)(C(C)O)O)O)O)O)O 382.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.3109/13880209509065369
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-en-6-ol 162820419 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)O)C)C 438.70 unknown https://doi.org/10.3109/13880209509065369
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.3109/13880209509065369
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
28-Hydroxy-2,3-secooleana-12-ene 2,3-dioic acid 3-methyl ester 44235899 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)OC)C)C2C1)C)CO)C 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 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 / Hexacarboxylic acids and derivatives
[(1S,2R,4S,5R,6S,7R,8S,9R,12R)-4,5,12-triacetyloxy-7,8-dibenzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-6-yl]methyl benzoate 24898243 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 756.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2R,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14414924 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 574.60 unknown via CMAUP database
15-Acetoxyorbiculin G 24898039 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6 698.80 unknown via CMAUP database
1alpha,2alpha-Diacetoxy-6beta,9beta,15-tribenzoyloxy-beta-dihydroagarofuran 16109789 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 698.80 unknown via CMAUP database
Mutangin 44419602 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 636.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Ethyl vanillin 8467 Click to see CCOC1=C(C=CC(=C1)C=O)O 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Phenylbenzofurans
5-(1-Benzofuran-5-yl)-3-methoxybenzene-1,2-diol 11780117 Click to see COC1=CC(=CC(=C1O)O)C2=CC3=C(C=C2)OC=C3 256.25 unknown https://doi.org/10.3987/COM-93-6667
https://doi.org/10.3987/COM-94-6773
5-(4-Hydroxy-3,5-dimethoxyphenyl)-1-benzofuran-4-ol 85693147 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C3=C(C=C2)OC=C3)O 286.28 unknown https://doi.org/10.3987/COM-92-6291
https://doi.org/10.3987/COM-93-6667
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2-Hydroxy-1-methoxy-xanthen-9-one 10399460 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1080/10575639908041215
2-Hydroxyxanthone 74708 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C=CC(=C3)O 212.20 unknown https://doi.org/10.1080/10575639908041215
3-Hydroxy-4-methoxyxanthen-9-one 5464639 Click to see COC1=C(C=CC2=C1OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1080/10575639908041215
4-Hydroxyxanthone 611428 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O 212.20 unknown https://doi.org/10.1080/10575639908041215
> Organoheterocyclic compounds / Naphthopyrans
Microtropioside A 101506965 Click to see CC1(C2CCC34COCC(C(O3)(CCC4C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C 500.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
1-Methyl-2-pyrrolidinone 13387 Click to see CN1CCCC1=O 99.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Brevetoxins and derivatives
2-[[(24Z,49Z)-41-Hydroxy-4,8,10,46-tetramethyl-14-oxo-2,7,13,17,21,28,34,38,43,47-decaoxadecacyclo[25.24.0.03,22.06,20.08,18.012,16.029,48.033,46.035,44.037,42]henpentaconta-24,49-dien-39-yl]methyl]prop-2-enal 6437089 Click to see CC1CC2C(CC(=O)O2)OC3CC4C(CC(C5C(O4)CC=CCC6C(O5)CC=CC7C(O6)CCCC8C(O7)(CC9C(O8)CC2C(O9)C(CC(O2)CC(=C)C=O)O)C)C)OC3(C1)C 867.10 unknown https://doi.org/10.3987/COM-97-7854
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-8-[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 11685475 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC=C(C=C6)O)O)O 558.50 unknown https://doi.org/10.1248/CPB.53.1034
https://doi.org/10.1055/S-0029-1186081
(2R)-8-[(2S,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 124385005 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/10.3987/COM-98-S(H)40
(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 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/10.3987/COM-98-S(H)40
(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/10.3987/COM-98-S(H)40
[3,8'-Bi-4H-1-benzopyran]-4,4'-dione, 2,2',3,3'-tetrahydro-3',5,5',7,7'-pentahydroxy-2,2'-bis(4-hydroxyphenyl)-, (2S,2'R,3R,3'R)- 5317534 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC=C(C=C6)O)O)O 558.50 unknown https://doi.org/10.1055/S-0029-1186081
https://doi.org/10.3987/COM-97-7854
https://doi.org/10.1248/CPB.53.1034
2-(3,4-Dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 3512641 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O)O 590.50 unknown https://doi.org/10.1021/JF205175B
3'',3''',4',5,5'',7,7''-Heptahydroxy-4'''-methoxy-3,8''-biflavanone 3512640 Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)C4C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)O 588.50 unknown https://doi.org/10.1016/S0278-6915(00)00039-9
8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one 15280449 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=C(C5=O)O)C6=CC=C(C=C6)O)O)O)O 556.50 unknown https://doi.org/10.3987/COM-98-S(H)40
https://doi.org/10.3987/COM-97-7854
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10007880 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=C(C5=O)O)C6=CC=C(C=C6)O)O)O)O 556.50 unknown https://doi.org/10.3987/COM-98-S(H)40
https://doi.org/10.3987/COM-95-7157
https://doi.org/10.3987/COM-97-7854
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 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/10.3987/COM-98-S(H)40
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chroman-3-yl]-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chroman-4-one 501506 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O 574.50 unknown https://doi.org/10.3987/COM-97-7854
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1021/NP50023A026
https://doi.org/10.3987/COM-98-S(H)40
Dihydromorelloflavone 11467081 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/10.3987/COM-98-S(H)40
Garcinia biflavonoid 2 161259 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O 574.50 unknown https://doi.org/10.3987/COM-97-7854
Garcinianin 44575314 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=C(C5=O)O)C6=CC=C(C=C6)O)O)O)O 556.50 unknown https://doi.org/10.3987/COM-98-S(H)40
https://doi.org/10.3987/COM-97-7854
https://doi.org/10.3987/COM-95-7157
Kolaflavanone 155169 Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)C4C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)O 588.50 unknown https://doi.org/10.1016/S0278-6915(00)00039-9
https://doi.org/10.1007/BF02007729
https://doi.org/10.1111/J.2042-7158.1990.TB05412.X
https://doi.org/10.1021/NP50023A026
https://doi.org/10.1016/0021-9673(94)87067-5
https://doi.org/10.1016/J.LFS.2008.11.012
https://doi.org/10.1089/JMF.2008.0138
https://doi.org/10.21236/ADA406859
Manniflavanone 198549 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O)O 590.50 unknown https://doi.org/10.1021/JF205175B
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50023A026
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1021/NP50023A026
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown via CMAUP database

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