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Garcinia dioica

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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 UUID64401d2500982290231426
Scientific name Garcinia dioica
Authority Blume
First published in Verh. Batav. Genootsch. Kunst. ix. 170 (1823).

Description Top

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Synonyms Top

Scientific name Authority First published in
Garcinia cladostigma Pierre Fl. Forest. Cochinch. 5: 30 (1883)
Garcinia trechostigna Pierre Fl. Forest. Cochinch. 5: 31 (1883)
Rhinostigma parvifolium Miq. Fl. Ned. Ind., Eerste Bijv. : 495 (1861)

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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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694280
Tropicos 100340323
KEW urn:lsid:ipni.org:names:427923-1
The Plant List kew-2816817
Open Tree Of Life 6099688
IPNI 427925-1
GBIF 3714815
USDA GRIN 71001

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)!
Title Authors Publication Released IDs
Three New Xanthones from the Bark of Garcinia dioica. Munekazu IINUMA, Hideki TOSA, Toshiyuki TANAKA, Soedarsono RISWAN Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.44.232
Antibacterial activity of xanthones from guttiferaeous plants against methicillin-resistant Staphylococcus aureus. Iinuma M, Tosa H, Tanaka T, Asai F, Kobayashi Y, Shimano R, Miyauchi K J Pharm Pharmacol 01-Aug-1996
doi:10.1111/J.2042-7158.1996.TB03988.X
PMID:8887739

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,7-Trihydroxy-2,4-diisoprenylxanthone 10643491 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)CC=C(C)C)O)C 380.40 unknown https://doi.org/10.1248/CPB.44.232
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 5748685 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 410.50 unknown https://doi.org/10.1248/CPB.44.232
1-[(2Z)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 6450342 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 410.50 unknown https://doi.org/10.1248/CPB.44.232
https://doi.org/10.1111/J.2042-7158.1996.TB03988.X
1-[(E)-5-[(2S)-3,3-dimethyloxiran-2-yl]-3-methylpent-2-enyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 163186449 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CCC4C(O4)(C)C 426.50 unknown https://doi.org/10.1248/CPB.44.232
1,3,6-Trihydroxy-8-(6,7-epoxy-3,7-dimethyl-2-octenyl)-7-methoxyxanthone 85260025 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CCC4C(O4)(C)C 426.50 unknown https://doi.org/10.1248/CPB.44.232
3,6,8-Trihydroxy-1-(7-hydroxy-3,7-dimethylocta-2,5-dienyl)-2-methoxyxanthen-9-one 85190793 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CC=CC(C)(C)O 426.50 unknown https://doi.org/10.1248/CPB.44.232
3,6,8-trihydroxy-1-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienyl]-2-methoxyxanthen-9-one 10574428 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CC=CC(C)(C)O 426.50 unknown https://doi.org/10.1248/CPB.44.232
Rubraxanthone 9953366 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 410.50 unknown https://doi.org/10.1248/CPB.44.232
https://doi.org/10.1111/J.2042-7158.1996.TB03988.X

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