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Phyllanthus meghalayensis

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID64405eea5549b992544754
Scientific name Phyllanthus meghalayensis
Authority Chakrab. & N.P.Balakr.
First published in J. Econ. Taxon. Bot. 33(3): 714. 2009 [20 Nov 2009]

Description Top

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Synonyms Top

Scientific name Authority First published in
Glochidion acuminatum Müll.Arg. Linnaea 32: 68 (1863)
Glochidion bicolor Hayata J. Coll. Sci. Imp. Univ. Tokyo 20(3): 18 (1904)
Glochidion hayatae Croizat & H.Hara J. Jap. Bot. 16: 316 (1940)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Phyllanthus meghalayensis var. siamensis (Airy Shaw) Chakrab. & N.P.Balakr. J. Econ. Taxon. Bot. 33(3): 714. 2009 [20 Nov 2009]

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-0001333082
KEW urn:lsid:ipni.org:names:77119597-1
Open Tree Of Life 3949
NCBI Taxonomy 271518
IUCN Red List 135812889
IPNI 77119597-1
GBIF 7388829

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
Trait matching in a multi‐species geographic mosaic of leafflower plants, brood pollinators, and cheaters Hao K, Liu T, Hembry DH, Luo S Ecol Evol 04-Jul-2023
PMCID:PMC10318581
doi:10.1002/ece3.10228
PMID:37408629
Diversity and species-specificity of brood pollination of leafflower trees (Phyllanthaceae: Glochidion) by leafflower moths (Lepidoptera: Epicephala) in tropical Southeast Asia (Cambodia) Chheang P, Hembry DH, Yao G, Luo SX Plant Divers 16-Jul-2021
PMCID:PMC9043405
doi:10.1016/j.pld.2021.07.001
PMID:35505992
Chemical Diversity of Plant Cyanogenic Glycosides: An Overview of Reported Natural Products Yulvianti M, Zidorn C Molecules 30-Jan-2021
PMCID:PMC7866531
doi:10.3390/molecules26030719
PMID:33573160
Understanding intraspecific variation of floral scent in light of evolutionary ecology Delle-Vedove R, Schatz B, Dufay M Ann Bot 30-Jun-2017
PMCID:PMC5737645
doi:10.1093/aob/mcx055
PMID:28873948
A Novel, Enigmatic Basal Leafflower Moth Lineage Pollinating a Derived Leafflower Host Illustrates the Dynamics of Host Shifts, Partner Replacement, and Apparent Coadaptation in Intimate Mutualisms Luo SX, Yao G, Wang Z, Zhang D, Hembry DH Am Nat 12-Jan-2017
PMCID:PMC6103454
doi:10.1086/690623
PMID:28350503
Isolation and characterization of 11 microsatellite markers for Glochidion acuminatum (Phyllanthaceae) Mochizuki K, Nagano AJ, Kudoh H, Kawakita A Appl Plant Sci 05-Sep-2014
PMCID:PMC4162668
doi:10.3732/apps.1400045
PMID:25225630
A Novel Dimeric Butenolide, Glochidiolide, from the Leaves of Glochidion Acuminatum MUELL. Hideaki OTSUKA, Kaori KOTANI, Masahiko BANDO, Masaru KIDO, Yoshio TAKEDA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.1180
Glochidiolide, isoglochidiolide, acuminaminoside, and glochidacuminosides A-D from the leaves of Glochidion acuminatum MUELL. Otsuka H, Takeda Y, Hirata E, Shinzato T, Bando M Chem Pharm Bull (Tokyo) 01-May-2004
doi:10.1248/CPB.52.591
PMID:15133212

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 / Saccharolipids
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(4S)-4-hydroxycyclohexen-1-yl]acetyl]oxyoxan-2-yl]methyl 2-[(4S)-4-hydroxycyclohexen-1-yl]acetate 21577091 Click to see C1CC(=CCC1O)CC(=O)OCC2C(C(C(C(O2)OC(=O)CC3=CCC(CC3)O)O)O)O 456.50 unknown https://doi.org/10.1248/CPB.52.591
[3,4,5-Trihydroxy-6-[2-(4-hydroxycyclohexen-1-yl)acetyl]oxyoxan-2-yl]methyl 2-(4-hydroxycyclohexen-1-yl)acetate 73802903 Click to see C1CC(=CCC1O)CC(=O)OCC2C(C(C(C(O2)OC(=O)CC3=CCC(CC3)O)O)O)O 456.50 unknown https://doi.org/10.1248/CPB.52.591
2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[2-[(4S)-4-hydroxycyclohexen-1-yl]acetyl]oxymethyl]oxan-2-yl]oxyphenyl]acetic acid 21577090 Click to see C1CC(=CCC1O)CC(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CC(=O)O)O)O)O 452.50 unknown https://doi.org/10.1248/CPB.52.591
2-[2-[3,4,5-Trihydroxy-6-[[2-(4-hydroxycyclohexen-1-yl)acetyl]oxymethyl]oxan-2-yl]oxyphenyl]acetic acid 73802902 Click to see C1CC(=CCC1O)CC(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CC(=O)O)O)O)O 452.50 unknown https://doi.org/10.1248/CPB.52.591
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
[(2R,3R,4S,5S,6R)-2-[(S)-cyano-(4-hydroxyphenyl)methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 21577092 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 463.40 unknown https://doi.org/10.1248/CPB.52.591
[2-[Cyano-(4-hydroxyphenyl)methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 73802904 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 463.40 unknown https://doi.org/10.1248/CPB.52.591
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-(2-Amino-1-benzofuran-3-yl)-2-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 73802901 Click to see C1=CC=C(C(=C1)CC(=O)C2=C(OC3=CC=CC=C32)N)OC4C(C(C(C(O4)CO)O)O)O 429.40 unknown https://doi.org/10.1248/CPB.52.591
2-(beta-D-Glucopyranosyloxy)benzeneacetic acid 10979933 Click to see C1=CC=C(C(=C1)CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 314.29 unknown https://doi.org/10.1248/CPB.52.591
2-Hydroxyphenylacetic acid O-b-D-glucoside 76503563 Click to see C1=CC=C(C(=C1)CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 314.29 unknown https://doi.org/10.1248/CPB.52.591
Acuminaminoside 21577089 Click to see C1=CC=C(C(=C1)CC(=O)C2=C(OC3=CC=CC=C32)N)OC4C(C(C(C(O4)CO)O)O)O 429.40 unknown https://doi.org/10.1248/CPB.52.591
> Organoheterocyclic compounds / Benzofurans
(3a,7'a(2'H,6H)-Bibenzofuran)-2,2'(3H)-dione, 6',7,7',7a-tetrahydro-6,6'-dihydroxy-, (3aS,6S,6'S,7aS,7'aR)- 154162 Click to see C1C(C=CC2(C1OC(=O)C2)C34CC(C=CC3=CC(=O)O4)O)O 304.29 unknown https://doi.org/10.1248/CPB.52.591
https://doi.org/10.1248/CPB.46.1180
6-Hydroxy-7a-(6-hydroxy-2-oxo-3,6,7,7a-tetrahydro-1-benzofuran-3a-yl)-6,7-dihydro-1-benzofuran-2-one 73802900 Click to see C1C(C=CC2(C1OC(=O)C2)C34CC(C=CC3=CC(=O)O4)O)O 304.29 unknown https://doi.org/10.1248/CPB.52.591
https://doi.org/10.1248/CPB.46.1180
Isoglochidiolide 21577088 Click to see C1C(C=CC2(C1OC(=O)C2)C34CC(C=CC3=CC(=O)O4)O)O 304.29 unknown https://doi.org/10.1248/CPB.52.591

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