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Garcinia atroviridis

Garcinia atroviridis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64401d1bd103b354388281
Scientific name Garcinia atroviridis
Authority Griff. ex 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
Arabic جندم أصام
Indonesian asam keping
Indonesian asam potong
Indonesian asam gelugur
Indonesian asam gelugor
jv asem gelugur
min asam galugua
Malay pokok asam keping
Malay asam gelugur
Malay pokok asam gelugur
Malay pokok asam gelugor
Malay asam keping
Malay asam gelugor
Thai ส้มแขก
Chinese 酸黄果
Chinese 亞參果
Chinese 亞叁果

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000694142
UNII OPZ446V4C1
Tropicos 100340224
KEW urn:lsid:ipni.org:names:427811-1
The Plant List kew-2816686
Open Tree Of Life 724104
NCBI Taxonomy 180101
IPNI 427811-1
iNaturalist 425637
GBIF 3711121
Freebase /m/05zx779
EOL 5708672
USDA GRIN 429725
Wikipedia Garcinia_atroviridis
CMAUP NPO10332

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
Leaf extract of Garcinia atroviridis promotes anti-heat stress and antioxidant effects in Caenorhabditis elegans Chuaijit S, Punsawad C, Winoto V, Plaingam W, Kongkaew I, Phetcharat A, Ichikawa T, Kubo M, Kawakami F, Tedasen A, Chatatikun M Front Pharmacol 07-Mar-2024
PMCID:PMC10955098
doi:10.3389/fphar.2024.1331627
PMID:38515852
Chlorogenic acid in green bean coffee on body weight: a systematic review and meta-analysis of randomized controlled trials Kanchanasurakit S, Saokaew S, Phisalprapa P, Duangjai A Syst Rev 14-Sep-2023
PMCID:PMC10503105
doi:10.1186/s13643-023-02311-4
PMID:37710316
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Development of Oral In Situ Gelling Liquid Formulations of Garcinia Extract for Treating Obesity Fungfoung K, Praparatana R, Issarachot O, Wiwattanapatapee R Gels 16-Aug-2023
PMCID:PMC10453886
doi:10.3390/gels9080660
PMID:37623115
3D-Printed Polylactic Acid/Lignin Films with Great Mechanical Properties and Tunable Functionalities towards Superior UV-Shielding, Haze, and Antioxidant Properties Ye H, He Y, Li H, You T, Xu F Polymers (Basel) 24-Jun-2023
PMCID:PMC10346654
doi:10.3390/polym15132806
PMID:37447452
Design of Biodegradable Films Using Pecan Nut Cake Extracts for Food Packing Alves JD, Canabarro NI, Boeira CP, Melo PT, Aouada MR, da Rosa CS Foods 26-Mar-2023
PMCID:PMC10093672
doi:10.3390/foods12071405
PMID:37048226
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines Muhamad M, Ab.Rahim N, Wan Omar WA, Nik Mohamed Kamal NN Bioinorg Chem Appl 23-Sep-2022
PMCID:PMC9525761
doi:10.1155/2022/8546079
PMID:36193250
3D Printed gelatin film with Garcinia atroviridis extract Yap KL, Kong I, Abdul Kalam Saleena L, Pui LP J Food Sci Technol 18-Jun-2022
PMCID:PMC9525530
doi:10.1007/s13197-022-05508-y
PMID:36193470
Effect on the Properties of Edible Starch-Based Films by the Incorporation of Additives: A Review Singh GP, Bangar SP, Yang T, Trif M, Kumar V, Kumar D Polymers (Basel) 13-May-2022
PMCID:PMC9147565
doi:10.3390/polym14101987
PMID:35631869
Perceiving SARS-CoV-2 Mpro and PLpro dual inhibitors from pool of recognized antiviral compounds of endophytic microbes: an in silico simulation study Prajapati J, Patel R, Rao P, Saraf M, Rawal R, Goswami D Struct Chem 08-Apr-2022
PMCID:PMC8990578
doi:10.1007/s11224-022-01932-0
PMID:35431517
Neuraminidase Inhibitor of Garcinia atroviridis L. Fruits and Leaves Using Partial Purification and Molecular Characterization Muchtaridi M, Nuwarda RF, Ikram EH, Abdul Rahim AS, Gazzali AM, Wahab HA Molecules 30-Jan-2022
PMCID:PMC8840166
doi:10.3390/molecules27030949
PMID:35164214
Potential roles of Garcinia family as antimetabolic syndrome Kuswandi A, Tarawaan VM, Goenawan H, Muchtaridi M, Lesmana R J Adv Pharm Technol Res 21-Jan-2022
PMCID:PMC8820346
doi:10.4103/japtr.japtr_218_21
PMID:35223433
Silver nanomaterials: synthesis and (electro/photo) catalytic applications Sharma RK, Yadav S, Dutta S, Kale HB, Warkad IR, Zbořil R, Varma RS, Gawande MB Chem Soc Rev 18-Oct-2021
PMCID:PMC8942099
doi:10.1039/d0cs00912a
PMID:34661205
Green Metallic Nanoparticles for Cancer Therapy: Evaluation Models and Cancer Applications Tinajero-Díaz E, Salado-Leza D, Gonzalez C, Martínez Velázquez M, López Z, Bravo-Madrigal J, Knauth P, Flores-Hernández FY, Herrera-Rodríguez SE, Navarro RE, Cabrera-Wrooman A, Krötzsch E, Carvajal ZY, Hernández-Gutiérrez R Pharmaceutics 18-Oct-2021
PMCID:PMC8537602
doi:10.3390/pharmaceutics13101719
PMID:34684012

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
6-Hydroxymellein 172675 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
Isocoumarin, 3,4-dihydro-6,8-dihydroxy-3-methyl- 439718 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Methyl 2,4-dihydroxy-6-[2-hydroxy-5,6-dimethoxy-3,4-bis(3-methylbut-2-enyl)phenoxy]benzoate 101249096 Click to see CC(=CCC1=C(C(=C(C(=C1O)OC2=CC(=CC(=C2C(=O)OC)O)O)OC)OC)CC=C(C)C)C 472.50 unknown https://doi.org/10.1515/ZNB-2003-0414
> Benzenoids / Naphthalenes / Naphthols and derivatives
8-Methoxynaphthalene-1-ol 10866824 Click to see COC1=CC=CC2=C1C(=CC=C2)O 174.20 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Benzenoids / Tetralins
(4S)-4-hydroxy-8-methoxy-3,4-dihydro-2H-naphthalen-1-one 23651310 Click to see COC1=CC=CC2=C1C(=O)CCC2O 192.21 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
(S)-Isosclerone 10442251 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
Nodulisporone 44423671 Click to see COC1=CC=CC2=C1C(=O)CCC2O 192.21 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Lignans, neolignans and related compounds
(11S,17R,19R)-7,15,17,19-tetrahydroxypentacyclo[10.7.1.02,11.03,8.016,20]icosa-1,3(8),4,6,12(20),13,15-heptaen-9-one 162915103 Click to see C1C(C2=C(C=CC3=C2C(=C4C3CC(=O)C5=C4C=CC=C5O)C1O)O)O 336.30 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
(11S,17R,19R)-7,15,19-trihydroxy-17-methoxypentacyclo[10.7.1.02,11.03,8.016,20]icosa-1,3(8),4,6,12(20),13,15-heptaen-9-one 162870662 Click to see COC1CC(C2=C3C(CC(=O)C4=C3C=CC=C4O)C5=C2C1=C(C=C5)O)O 350.40 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
2-(Acetyloxymethyl)hexa-2,4-dienoic acid 74079204 Click to see CC=CC=C(COC(=O)C)C(=O)O 184.19 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
Xylarenoic acid 23651309 Click to see CC=CC=C(COC(=O)C)C(=O)O 184.19 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
(Z)-docos-14-enoic acid 92033112 Click to see CCCCCCCC=CCCCCCCCCCCCCC(=O)O 338.60 unknown https://doi.org/10.1515/ZNB-2003-0414
Docos-14-enoic acid 54090186 Click to see CCCCCCCC=CCCCCCCCCCCCCC(=O)O 338.60 unknown https://doi.org/10.1515/ZNB-2003-0414
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2S,3R,4E,6E)-4-methoxyocta-4,6-diene-2,3-diol 163195656 Click to see CC=CC=C(C(C(C)O)O)OC 172.22 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
(2S,3R)-4-methoxyocta-4,6-diene-2,3-diol 162945692 Click to see CC=CC=C(C(C(C)O)O)OC 172.22 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones / Ubiquinones
Atrovirinone 9981481 Click to see CC(=CCC1=C(C(=O)C(=C(C1=O)OC)OC2=CC(=CC(=C2C(=O)OC)O)O)CC=C(C)C)C 456.50 unknown https://doi.org/10.1515/ZNB-2003-0414
https://doi.org/10.1021/NP000563O
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
Ergosterol peroxide 5351516 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3E,8aR)-3-benzylidene-2-methyl-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione 163191172 Click to see CN1C(=CC2=CC=CC=C2)C(=O)N3CCCC3C1=O 256.30 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
(3E,8aS)-3-benzylidenehexahydropyrrolo[1,2-a]pyrazine-1,4-dione 11874102 Click to see C1CC2C(=O)NC(=CC3=CC=CC=C3)C(=O)N2C1 242.27 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
(8aR)-3-benzylidene-2-methyl-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione 162870663 Click to see CN1C(=CC2=CC=CC=C2)C(=O)N3CCCC3C1=O 256.30 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
3-Benzylidene-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione 617929 Click to see C1CC2C(=O)NC(=CC3=CC=CC=C3)C(=O)N2C1 242.27 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
Variolaric acid 12444681 Click to see CC1=CC(=CC2=C1C(=O)OC3=C(O2)C(=C4C(=C3)COC4=O)O)O 314.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Atroviridin 11267348 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)O)OC4=C(C3=O)C=C(C=C4)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(98)80095-2
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
3,4-Dihydro-8-hydroxy-3,5-dimethylisocoumarin 10330203 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C 192.21 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
5-Methylmellein 14807789 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C 192.21 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Organoheterocyclic compounds / Lactones / Delta valerolactones
4-Hydroxy-6-methyloxan-2-one 241025 Click to see CC1CC(CC(=O)O1)O 130.14 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
4alpha-Hydroxy-6beta-methyltetrahydro-2H-pyran-2-one 5324869 Click to see CC1CC(CC(=O)O1)O 130.14 unknown https://doi.org/10.1111/J.1574-695X.2007.00331.X
> Phenylpropanoids and polyketides / Depsides and depsidones
alpha-Alectoronic acid 15558610 Click to see CCCCCC(=O)CC1=C2C(=CC(=C1)O)OC3=C(C=C(C(=C3CC(=O)CCCCC)C(=O)O)O)OC2=O 512.50 unknown via CMAUP database
Atranorin 68066 Click to see CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2)C)C(=O)OC)O)C)O)C=O)O 374.30 unknown via CMAUP database
Atrovirisidone 10342405 Click to see CC(=CCC1=C(C2=C(C(=C1O)OC)OC3=CC(=CC(=C3C(=O)O2)O)O)CC=C(C)C)C 426.50 unknown https://doi.org/10.1515/ZNB-2003-0414
https://doi.org/10.1021/NP000563O
Lecanoric acid 99613 Click to see CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)O)O)O)O 318.28 unknown via CMAUP database
Parellin 16109864 Click to see CC1=CC(=C(C2=C1C(=O)OC3=C(C(=C(C(=C3O2)C)Cl)OC)C)C=O)O 362.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
CID 101973939 101973939 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)OC7C(C(C(C(O7)CO)O)O)O)O 718.60 unknown https://doi.org/10.1515/ZNB-2003-0414
Fukugetin 5464454 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/10.1515/ZNB-2003-0414
Fukugiside 73157060 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)OC7C(C(C(C(O7)CO)O)O)O)O 718.60 unknown https://doi.org/10.1515/ZNB-2003-0414
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/10.1515/ZNB-2003-0414

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