Garcinia macrophylla - Unknown
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Internal ID UUID64401d2fa428c621566227
Scientific name Garcinia macrophylla
Authority Mart.
First published in Flora 24(2 Beibl.): 35 (1841)

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Synonyms Top

Scientific name Authority First published in
Rheedia macrophylla (Mart.) Planch. & Triana Ann. Sci. Nat., Bot. , sér. 4, 14: 309 (1860)
Rheedia macrophylla var. benthamiana Vesque Monogr. Phan. 8: 500 (1893)
Garcinia megaphylla Verdc. Kew Bull. 31(2): 262. 1976 [11 Aug 1976]
Rheedia sagotiana Engl. Fl. Bras. 12(1): 460 (1888)
Rheedia macrantha Standl. & Steyerm. Publ. Field Mus. Nat. Hist., Bot. Ser. 23: 65. 1944

Common names Top

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Language Common/alternative name
Persian چاریچولا

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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Guatemala
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694438
Tropicos 7800805
INPN 765647
KEW urn:lsid:ipni.org:names:428065-1
The Plant List kew-2816965
Open Tree Of Life 307408
NCBI Taxonomy 469955
IUCN Red List 147302480
IPNI 428065-1
iNaturalist 291399
GBIF 3713878
Freebase /m/0zdsp3s
EOL 5708831
USDA GRIN 71010
Wikipedia Garcinia_macrophylla
CMAUP NPO11962

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
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
A taxonomic revision of Garcinia section Xanthochymus (Clusiaceae) in Thailand Ngernsaengsaruay C, Chanton P, Chaiprasongsuk M, Leksungnoen N PeerJ 20-Dec-2023
PMCID:PMC10748532
doi:10.7717/peerj.16572
PMID:38144192
Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics Roy N, Das R, Paira R, Paira P RSC Adv 25-Jul-2023
PMCID:PMC10369265
doi:10.1039/d3ra02003g
PMID:37501776
Type 2 Diabetes (T2DM) and Parkinson’s Disease (PD): a Mechanistic Approach Sabari SS, Balasubramani K, Iyer M, Sureshbabu HW, Venkatesan D, Gopalakrishnan AV, Narayanaswamy A, Senthil Kumar N, Vellingiri B Mol Neurobiol 28-Apr-2023
PMCID:PMC10144908
doi:10.1007/s12035-023-03359-y
PMID:37118323
Antibacterial effects of natural compounds on biofilm formation of Streptococcus mutans Kamarehei F, Mehdiabadi M, Naderi F Clin Exp Dent Res 25-Oct-2022
PMCID:PMC9760147
doi:10.1002/cre2.673
PMID:36281582
Phytochemical Profile, Preliminary Toxicity, and Antioxidant Capacity of the Essential Oils of Myrciaria floribunda (H. West ex Willd.) O. Berg. and Myrcia sylvatica (G. Mey) DC. (Myrtaceae) de Moraes ÂA, Ferreira OO, da Costa LS, Almeida LQ, Varela EL, Cascaes MM, de Jesus Pereira Franco C, Percário S, do Nascimento LD, de Oliveira MS, Andrade EH Antioxidants (Basel) 21-Oct-2022
PMCID:PMC9658195
doi:10.3390/antiox11102076
PMID:36290799
Flavonols and Flavones as Potential anti-Inflammatory, Antioxidant, and Antibacterial Compounds Chagas MD, Behrens MD, Moragas-Tellis CJ, Penedo GX, Silva AR, Gonçalves-de-Albuquerque CF Oxid Med Cell Longev 06-Sep-2022
PMCID:PMC9470311
doi:10.1155/2022/9966750
PMID:36111166
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Alleviation of Herbicide Toxicity in Solanum lycopersicum L.—An Antioxidant Stimulation Approach Ibrahim RI, Alkhudairi UA, Alhusayni SA Plants (Basel) 30-Aug-2022
PMCID:PMC9459734
doi:10.3390/plants11172261
PMID:36079642
Natural Products Inhibitors of Monoamine Oxidases—Potential New Drug Leads for Neuroprotection, Neurological Disorders, and Neuroblastoma Chaurasiya ND, Leon F, Muhammad I, Tekwani BL Molecules 04-Jul-2022
PMCID:PMC9268457
doi:10.3390/molecules27134297
PMID:35807542
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Fruitful exchanges: social networks and food resources amidst change Schramski S, Barbosa de Lima AC Agric Food Secur 16-Feb-2022
PMCID:PMC8853342
doi:10.1186/s40066-021-00342-5
PMID:35194513
20th IUPAB International Congress, 45th SBBf Congress and 50th Annual Meeting of SBBq: Poster Abstracts N/A Biophys Rev 28-Oct-2021
PMCID:PMC8551951
doi:10.1007/s12551-021-00845-2
Molecular mechanisms of inhibiting glucosyltransferases for biofilm formation in Streptococcus mutans Zhang Q, Ma Q, Wang Y, Wu H, Zou J Int J Oral Sci 30-Sep-2021
PMCID:PMC8481554
doi:10.1038/s41368-021-00137-1
PMID:34588414
Anticancer Properties and Mechanism of Action of Oblongifolin C, Guttiferone K and Related Polyprenylated Acylphloroglucinols Bailly C, Vergoten G Nat Prod Bioprospect 29-Sep-2021
PMCID:PMC8479269
doi:10.1007/s13659-021-00320-1
PMID:34586597

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,5R,7R,8S)-3-(3,4-Dihydroxybenzoyl)-4-hydroxy-8-methyl-1,5,7-tris(3-methyl-2-butenyl)-8-(4-methyl-3-pentenyl)bicyclo[3.3.1]non-3-ene-2,9-dione 139071568 Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC=C(C)C)CC=C(C)C)C)C 602.80 unknown https://doi.org/10.1055/S-2003-43204
Guttiferone A 5352090 Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC=C(C)C)CC=C(C)C)C)C 602.80 unknown https://doi.org/10.1055/S-2003-43204
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,5R,6S,7R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,5,6-tris(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 132598259 Click to see CC(=CCCC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C1CC=C(C)C)(C2=O)CC=C(C)C)CC=C(C)C)C)C 642.90 unknown https://doi.org/10.1055/S-2003-43204
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown via CMAUP database
Selina-4(15),7(11)-dien-8-one 13986100 Click to see CC(=C1CC2C(=C)CCCC2(CC1=O)C)C 218.33 unknown via CMAUP database
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C)(C)C)O 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2003-43204
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(4S,9R)-15,16-dihydroxy-4,5,5,9,10,10-hexamethyl-3,8,13-trioxapentacyclo[10.8.0.02,6.07,11.014,19]icosa-1(12),2(6),7(11),14(19),15,17-hexaen-20-one 163010608 Click to see CC1C(C2=C(O1)C3=C(C4=C2OC(C4(C)C)C)OC5=C(C3=O)C=CC(=C5O)O)(C)C 396.40 unknown https://doi.org/10.1002/CHIN.198120320
15,16-Dihydroxy-4,5,5,9,10,10-hexamethyl-3,8,13-trioxapentacyclo[10.8.0.02,6.07,11.014,19]icosa-1(12),2(6),7(11),14(19),15,17-hexaen-20-one 71440418 Click to see CC1C(C2=C(O1)C3=C(C4=C2OC(C4(C)C)C)OC5=C(C3=O)C=CC(=C5O)O)(C)C 396.40 unknown https://doi.org/10.1002/CHIN.198120320
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(R)-gamma-Decalactone 183870 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown via CMAUP database
(S)-gamma-Octanolactone 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
2(3H)-Furanone, dihydro-5-octyl-, (5R)- 10888889 Click to see CCCCCCCCC1CCC(=O)O1 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol 6428573 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)OC(=O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O 664.60 unknown via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-afzelechin 73353883 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-ent-epiafzelechin 5317051 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Geranin A 5317050 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Mahuannin A 5317052 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Talbotaflavone 5315272 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/10.1021/NP50036A033
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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