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Garcinia portoricensis

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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 UUID64401d39133e2974349174
Scientific name Garcinia portoricensis
Authority (Urb.) Alain
First published in Phytologia 61: 353 (1986)

Description Top

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Synonyms Top

Scientific name Authority First published in
Marialva elliptica A.Stahl Estud. Fl. Puerto-Rico 2: 126 (1884)
Clusia acuminata Spreng. Syst. Veg. 2: 599 (1825)
Quapoya acuminata Walp. Repert. Bot. Syst. 1: 393 (1842)
Rheedia portoricensis Urb. Symb. Antill. (Urban). 1(2): 368. 1899 [10 Apr 1899]

Common names Top

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Language Common/alternative name
English palo de cruz

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694585
USDA Plants GAPO2
Tropicos 50328385
KEW urn:lsid:ipni.org:names:943478-1
The Plant List kew-2817105
Open Tree Of Life 373226
NCBI Taxonomy 198788
IPNI 943478-1
iNaturalist 431542
GBIF 3189559
EOL 487548
USDA GRIN 449454

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)!
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Title Authors Publication Released IDs
A new xanthone from the bark extract of Rheedia acuminata and antiplasmodial activity of its major compounds. Marti G, Eparvier V, Litaudon M, Grellier P, Guéritte F Molecules 14-Oct-2010
PMCID:PMC6259415
doi:10.3390/MOLECULES15107106
PMID:20948498
Chemical Investigation of the Genus Rheedia, V. Biflavonoids and Xanthochymol B. Botta, M. Marquina Mac-Quhae, G. Delle Monache, F. Delle Monache, J. F. De Mello American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50036A033
Absolute configuration, conformation, and chiral properties of flavanone-(3→8″)-flavone biflavonoids from Rheedia acuminata Xing-Cong Li, Alpana S Joshi, Bo Tan, Hala N ElSohly, Larry A Walker, Jordan K Zjawiony, Daneel Ferreira Elsevier BV 13-May-2003
doi:10.1016/S0040-4020(02)01096-7

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
7-Epi-Isogarcinol 25242772 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259415/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,5S,7R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)-1-[(2R)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]bicyclo[3.3.1]nonane-2,4,9-trione 101688705 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(CCC(=C)C)C(=C)C)C 602.80 unknown https://doi.org/10.1021/NP50036A033
Xanthochymol 5281574 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(CCC(=C)C)C(=C)C)C 602.80 unknown https://doi.org/10.1021/NP50036A033
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
7-(3,7-Dimethylocta-2,6-dienyl)-1,5,6-trihydroxy-3-methoxyxanthen-9-one 90918464 Click to see CC(=CCCC(=CCC1=CC2=C(C(=C1O)O)OC3=CC(=CC(=C3C2=O)O)OC)C)C 410.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259415/
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[8-[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl] hydrogen sulfate 12110449 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)OS(=O)(=O)O)O 636.50 unknown https://doi.org/10.1016/S0040-4020(02)01096-7
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://doi.org/10.1016/S0040-4020(02)01096-7

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