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Glochidion sphaerogynum

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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 UUID64403d042d8d4431389304
Scientific name Glochidion sphaerogynum
Authority (Müll.Arg.) Kurz
First published in Forest Fl. Burma ii. 346. 1877

Description Top

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Synonyms Top

Scientific name Authority First published in
Glochidion fagifolium (Müll.Arg.) Hook.f. Fl. Brit. India 5(14): 312–313 1887

Common names Top

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Language Common/alternative name
Chinese 水油甘
Chinese 圆果算盘子
Chinese 山柑算盘子
Chinese 算盘子叶
Chinese 山柑树
Chinese 栗叶算盘子

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000973575
Tropicos 50057065
KEW urn:lsid:ipni.org:names:349642-1
The Plant List kew-90763
Open Tree Of Life 457252
NCBI Taxonomy 544978
IPNI 349641-1
GBIF 3080312
EOL 1143133
CMAUP NPO15319

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
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Antioxidant activity and antidiabetic activities of Northern Thai indigenous edible plant extracts and their phytochemical constituents Dedvisitsakul P, Watla-iad K Heliyon 23-Sep-2022
PMCID:PMC9519484
doi:10.1016/j.heliyon.2022.e10740
PMID:36185148
Glochidion littorale Leaf Extract Exhibits Neuroprotective Effects in Caenorhabditis elegans via DAF-16 Activation Bagoudou AF, Zheng Y, Nakabayashi M, Rawdkuen S, Park HY, Vattem DA, Sato K, Nakamura S, Katayama S Molecules 28-Jun-2021
PMCID:PMC8271589
doi:10.3390/molecules26133958
PMID:34203560
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Multiple Coexisting Species and the First Known Case of a Cheater in Epicephala (Gracillariidae) Associated with a Species of Glochidion (Phyllanthaceae) in Tropical Asia Wang Z, Yang X, Zhang Z, Shi F, Li H J Insect Sci 25-Aug-2020
PMCID:PMC7447135
doi:10.1093/jisesa/ieaa081
PMID:32841344
Anti-Infectious Plants of the Thai Karen: A Meta-Analysis Phumthum M, Balslev H Antibiotics (Basel) 02-Jun-2020
PMCID:PMC7345792
doi:10.3390/antibiotics9060298
PMID:32498413
Medicinal plants from swidden fallows and sacred forest of the Karen and the Lawa in Thailand Junsongduang A, Balslev H, Inta A, Jampeetong A, Wangpakapattanawong P J Ethnobiol Ethnomed 24-Jun-2013
PMCID:PMC3702467
doi:10.1186/1746-4269-9-44
PMID:23800255
Cytotoxic activity of lupane-type triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum two of which induce apoptosis. Puapairoj P, Naengchomnong W, Kijjoa A, Pinto MM, Pedro M, Nascimento MS, Silva AM, Herz W Planta Med 01-Mar-2005
doi:10.1055/S-2005-837818
PMID:15770539

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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Roseoside 9930064 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11R,11aR,11bS,13aS,13bR)-11-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 44559215 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol 44559213 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
1beta-Hydroxylup-20(29)-en-3-one 14167334 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1055/S-2005-837818
20(29)-Lupene-3,23-diol 21672675 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C 442.70 unknown https://doi.org/10.1055/S-2005-837818
3-Epiglochidiol 13969552 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1055/S-2005-837818
Glochidiol 13969554 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1055/S-2005-837818
Glochidonol 14167335 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1055/S-2005-837818
Lup-20(29)-Ene-3bate,23-Diol 14167263 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C 442.70 unknown https://doi.org/10.1055/S-2005-837818
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2005-837818
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2005-837818
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(3-hydroxy-5-methoxy-4-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 11723266 Click to see CC1=C(C=C(C=C1OC)OC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown via CMAUP database
[2,6-dihydroxy-3-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone 10393178 Click to see CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(C(C(C(O3)CO)O)O)O)O)C(=O)C4=CC=CC=C4)O 568.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azepines
3-chloro-4-hydroxy-7-(2-hydroxy-2-methylpropyl)-1H-azepine-2,5-dione 54749583 Click to see CC(C)(CC1=CC(=O)C(=C(C(=O)N1)Cl)O)O 245.66 unknown via CMAUP database
4-hydroxy-7-(2-hydroxy-2-methylpropyl)-1H-azepine-2,5-dione 54749584 Click to see CC(C)(CC1=CC(=O)C(=CC(=O)N1)O)O 211.21 unknown via CMAUP database
Pestalactam C 54749585 Click to see CC(=CC1=CC(=O)C(=C(C(=O)N1)Cl)O)C 227.64 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
(2S,3S,4S,5R,6S)-6-[6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 11798847 Click to see C1=CC(=C(C(=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Myricetin 3-O-glucuronide 5487413 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 5316590 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 10961589 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=C(C(=C3C2=O)O)O)O)O)C4=CC=C(C=C4)O)O)O)O 464.40 unknown via CMAUP database
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6''-O-(3,4,5-Trihydroxybenzoyl)quercimeritrin 100968215 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database

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