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Garcinia lateriflora

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64401d2dc436d385210290
Scientific name Garcinia lateriflora
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 214 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Garcinia javanica Blume Bijdr. Fl. Ned. Ind. : 215 (1825)

Common names Top

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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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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-tropical
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Philippines
      • Sulawesi

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000694411
USDA Plants GALA15
Tropicos 100340406
KEW urn:lsid:ipni.org:names:428037-1
The Plant List kew-2816940
Open Tree Of Life 154997
NCBI Taxonomy 469931
IPNI 428037-1
GBIF 3189557
EPPO GANLA
EOL 483627
USDA GRIN 311276
CMAUP NPO27881

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
A review on computational approaches that support the researches on traditional Chinese medicines (TCM) against COVID-19 Ruchawapol C, Fu WW, Xu HX Phytomedicine 06-Jul-2022
PMCID:PMC9259013
doi:10.1016/j.phymed.2022.154324
PMID:35841663
Natural biflavones are potent inhibitors against SARS-CoV-2 papain-like protease Li L, Ma L, Hu Y, Li X, Yu M, Shang H, Zou Z Phytochemistry 12-Oct-2021
PMCID:PMC8506144
doi:10.1016/j.phytochem.2021.112984
PMID:34757253
Lipoxygenase Inhibition by Plant Extracts Lončarić M, Strelec I, Moslavac T, Šubarić D, Pavić V, Molnar M Biomolecules 25-Jan-2021
PMCID:PMC7911790
doi:10.3390/biom11020152
PMID:33503885
Natural product scaffolds as inspiration for the design and synthesis of 20S human proteasome inhibitors Hubbell GE, Tepe JJ RSC Chem Biol 16-Sep-2020
PMCID:PMC8009326
doi:10.1039/d0cb00111b
PMID:33791679
Light and nutrient limitations for tree growth on young versus old soils in a Bornean tropical montane forest Aiba SI, Kitayama K J Plant Res 07-Aug-2020
PMCID:PMC7429538
doi:10.1007/s10265-020-01217-9
PMID:32767161
Potential Anticancer Agents Characterized from Selected Tropical Plants Ren Y, Carcache de Blanco EJ, Fuchs JR, Soejarto DD, Burdette JE, Swanson SM, Kinghorn AD J Nat Prod 04-Mar-2019
PMCID:PMC6441492
doi:10.1021/acs.jnatprod.9b00018
PMID:30830783
Constructing Molecular Complexity and Diversity: Total Synthesis of Natural Products of Biological and Medicinal Importance Nicolaou KC, Hale CR, Nilewski C, Ioannidou HA Chem Soc Rev 28-Jun-2012
PMCID:PMC3426871
doi:10.1039/c2cs35116a
PMID:22743704
The Relevance of Higher Plants in Lead Compound Discovery Programs Kinghorn AD, Pan L, Fletcher JN, Chai H J Nat Prod 08-Jun-2011
PMCID:PMC3158731
doi:10.1021/np200391c
PMID:21650152
Absolute Configuration of (−)-Gambogic Acid, an Antitumor Agent Ren Y, Yuan C, Chai HB, Ding Y, Li XC, Ferreira D, Kinghorn AD J Nat Prod 10-Nov-2010
PMCID:PMC3052414
doi:10.1021/np100422z
PMID:21067206
Proteasome-inhibitory and cytotoxic constituents of Garcinia lateriflora: absolute configuration of caged xanthones Ren Y, Lantvit DD, Carcache de Blanco EJ, Kardono LB, Riswan S, Chai H, Cottrell CE, Farnsworth NR, Swanson SM, Ding Y, Li XC, Marais JP, Ferreira D, Kinghorn AD Tetrahedron 17-Jul-2010
PMCID:PMC2923493
doi:10.1016/j.tet.2010.05.010
PMID:20730041
The use of non-wood forest products by migrants in a new settlement: experiences of a Visayan community in Palawan, Philippines Lacuna-Richman C J Ethnobiol Ethnomed 07-Sep-2006
PMCID:PMC1586005
doi:10.1186/1746-4269-2-36
PMID:16959026
Cytotoxic prenylxanthones from Garcinia bracteata. Thoison O, Fahy J, Dumontet V, Chiaroni A, Riche C, Tri MV, Sévenet T J Nat Prod 01-Apr-2000
doi:10.1021/NP9903088
PMID:10785410

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Dotriacontanol 96117 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 466.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Acetylursolic acid 619164 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
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 via CMAUP database
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1S,2S,7S,16S,18R)-11-methoxy-6,6,7,20,20-pentamethyl-18-(3-methylbut-2-enyl)-3,8,19-trioxahexacyclo[14.4.1.02,14.02,18.04,12.05,9]henicosa-4,9,11,14-tetraene-13,17-dione 101027047 Click to see CC1C(C2=C3C(=C(C=C2O1)OC)C(=O)C4=CC5CC6C4(O3)C(C5=O)(OC6(C)C)CC=C(C)C)(C)C 478.60 unknown https://doi.org/10.1021/NP9903088
(E)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 46867195 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C 562.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(E)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-5-[(2R)-2-hydroxy-3-methylbut-3-enyl]-17,17-dimethyl-7-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 163194382 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC(C(=C)C)O)O)C 578.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
4-[6,8-Dihydroxy-5-(2-hydroxy-3-methylbut-3-enyl)-17,17-dimethyl-7-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 73657200 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC(C(=C)C)O)O)C 578.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
Bractatin 44583731 Click to see CC(=CCC12C(=O)C3CC(C14C(=C3)C(=O)C5=C(O4)C(=C(C=C5O)O)C(C)(C)C=C)C(O2)(C)C)C 464.50 unknown https://doi.org/10.1021/NP9903088
Gaudichaudic acid 73008062 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C 562.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(3R,4S)-3,4,7,9,12-pentahydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-b]xanthen-6-one 46866949 Click to see CC1(C(C(C2=C(O1)C(=C3C(=C2)C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)C 360.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(E)-4-[(1S,2S,17S,19R)-12-hydroxy-5-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8,8,21,21-tetramethyl-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 163189073 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)O 576.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(Z)-4-[(1S,2S,15R,16R,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid 46867070 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 592.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 54580250 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(Z)-4-[(1S,2S,9R,17S,19R)-9,12-dihydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,11,15-tetraen-19-yl]-2-methylbut-2-enoic acid 163190381 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)CC(C(O2)(C)C)O)C 578.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(Z)-4-[(2S,15R,16R,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid 101514984 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 592.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
3,4,7,9,12-Pentahydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-b]xanthen-6-one 75236797 Click to see CC1(C(C(C2=C(O1)C(=C3C(=C2)C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)C 360.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
4-[12-Hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid 75236845 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 592.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
4-[12-Hydroxy-5-(2-hydroxy-3-methylbut-3-enyl)-8,8,21,21-tetramethyl-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 73657202 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)O 576.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
4-[9,12-Dihydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,11,15-tetraen-19-yl]-2-methylbut-2-enoic acid 75236897 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)CC(C(O2)(C)C)O)C 578.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
CID 550587 550587 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(+)-Volkensiflavone 23844069 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
(2R)-6-[(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 101514983 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC(=C(C=C5)O)O)O)C6=CC=C(C=C6)O 558.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162962625 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC(=C(C=C5)O)O)O)C6=CC=C(C=C6)O 558.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
Morelloflavone 5319895 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
Rhusflavanone 466314 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC=C(C=C5)O)O)C6=CC=C(C=C6)O 542.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
Rhusflavone 12114300 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC=C(C=C5)O)O)C6=CC=C(C=C6)O 542.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923493/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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