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Garcinia griffithii

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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 UUID64401d28d0f30445817634
Scientific name Garcinia griffithii
Authority T.Anderson
First published in Fl. Brit. India 1: 266 (1874)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Malay pokok kandis
Malay kandis

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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No germination or propagation data was added yet.

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-0000694343
Tropicos 100340364
KEW urn:lsid:ipni.org:names:427980-1
The Plant List kew-2816877
Open Tree Of Life 724101
NCBI Taxonomy 180106
IPNI 427980-1
iNaturalist 346369
GBIF 3714442
EOL 5708850
USDA GRIN 71006

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
Recent Advances in Chemistry and Bioactivities of Secondary Metabolites from the Genus Acremonium Qin Y, Lu H, Qi X, Lin M, Gao C, Liu Y, Luo X J Fungi (Basel) 03-Jan-2024
PMCID:PMC10820033
doi:10.3390/jof10010037
PMID:38248947
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
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
A Comprehensive Review of Autophagy and Its Various Roles in Infectious, Non-Infectious, and Lifestyle Diseases: Current Knowledge and Prospects for Disease Prevention, Novel Drug Design, and Therapy Khandia R, Dadar M, Munjal A, Dhama K, Karthik K, Tiwari R, Yatoo MI, Iqbal HM, Singh KP, Joshi SK, Chaicumpa W Cells 03-Jul-2019
PMCID:PMC6678135
doi:10.3390/cells8070674
PMID:31277291
An antiproliferative xanthone of Symphonia pauciflora from the Madagascar rainforest Pan E, Cao S, Brodie PJ, Miller JS, Rakotodrajaona R, Ratovoson F, Birkinshaw C, Andriantsiferana R, Rasamison VE, Kingston DG Nat Prod Commun 01-May-2010
PMCID:PMC2930018
PMID:20521541
Antiplasmodial and other constituents from four Indonesian Garcinia spp. Elfita E, Muharni M, Latief M, Darwati D, Widiyantoro A, Supriyatna S, Bahti HH, Dachriyanus D, Cos P, Maes L, Foubert K, Apers S, Pieters L Phytochemistry 01-May-2009
doi:10.1016/J.PHYTOCHEM.2009.04.024
PMID:19481231
In Tropical Lowland Rain Forests Monocots have Tougher Leaves than Dicots, and Include a New Kind of Tough Leaf Dominy NJ, Grubb PJ, Jackson RV, Lucas PW, Metcalfe DJ, Svenning JC, Turner IM Ann Bot 03-Apr-2008
PMCID:PMC2710255
doi:10.1093/aob/mcn046
PMID:18387969
Xanthones and benzophenones from Garcinia griffithii and Garcinia mangostana. Nguyen LH, Venkatraman G, Sim KY, Harrison LJ Phytochemistry 01-Jul-2005
doi:10.1016/J.PHYTOCHEM.2005.04.032
PMID:16173114
Griffipavixanthone, a novel cytotoxic bixanthone from Garcinia griffithii and G. pavifolia Yuan-Jian Xu, Shu-Geng Cao, Xiao-Hua Wu, Yee-Hing Lai, B.H.K. Tan, J.T. Pereira, S.H. Goh, Ganapathi Venkatraman, Leslie J. Harrison, Keng-Yeow Sim Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(98)02007-3

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(+)-Isoxanthochymol 14282765 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://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
(1S,3S,9S,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 14282764 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://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
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://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
Isogarcinol 11135781 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://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,5S,6R,7S)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-7-[(2Z)-3,7-dimethylocta-2,6-dienyl]-6-methyl-1,5-bis(3-methylbut-2-enyl)-6-(4-methylpent-3-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 102398194 Click to see CC(=CCCC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)C)C 670.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Griselinoside 155589 Click to see COC(=O)C1CC(=O)C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 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 https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
Stigmasterol glucoside 6602508 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 https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(8aS,12aS)-1,3,6,7-tetrahydroxy-9,9,11-trimethyl-8-(3,4,6,8-tetrahydroxy-9-oxoxanthen-1-yl)-8,8a,10,12a-tetrahydroindeno[1,2-a]xanthen-13-one 137705277 Click to see CC1=CC2C(C(C3=C(C(=C4C(=C23)C(=O)C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C7=C6C(=O)C8=C(C=C(C=C8O7)O)O)O)O)C(C1)(C)C 652.60 unknown https://doi.org/10.1016/S0040-4039(98)02007-3
(8S,8Ar,12aR)-1,3,6,7-tetrahydroxy-9,9,11-trimethyl-8-(3,4,6,8-tetrahydroxy-9-oxoxanthen-1-yl)-8,8a,10,12a-tetrahydroindeno[1,2-a]xanthen-13-one 15884596 Click to see CC1=CC2C(C(C3=C(C(=C4C(=C23)C(=O)C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C7=C6C(=O)C8=C(C=C(C=C8O7)O)O)O)O)C(C1)(C)C 652.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
1,3,5,6-Tetrahydroxyxanthone 5479774 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O 260.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
1,6-Dihydroxyxanthone 5493674 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3)O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,5-Dihydroxy-3,6-dimethoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one 44191407 Click to see CC(=CCC1=CC2=C(C(=C1OC)O)OC3=CC(=C(C(=C3C2=O)O)CC=C(C)C)OC)C 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.024
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
5,4'-Dihydroxy-7-methoxy-8-prenylflavanone 11688951 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)OC)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032

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