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Plocama pendula

Plocama pendula - 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 UUID643fe85dda148667877207
Scientific name Plocama pendula
Authority Aiton
First published in Hort. Kew. 1: 292 (1789)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bartlingia scoparia Rchb. Flora 7: 241 (1824)

Common names Top

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Language Common/alternative name
Spanish balo

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000278960
Tropicos 100245137
KEW urn:lsid:ipni.org:names:760838-1
The Plant List kew-161420
Open Tree Of Life 589085
Observations.org 138096
NCBI Taxonomy 58388
IUCN Red List 104191669
IPNI 760838-1
iNaturalist 627397
GBIF 2904111
EPPO PCMPE
EOL 1097262
Elurikkus 328993
USDA GRIN 28873
Wikipedia Plocama_pendula

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
Effects of endozoochory and diploendozoochory by captive wild mammals on Juniperus deppeana seeds Rubalcava‐Castillo FA, Valdivia‐Flores AG, Luna‐Ruíz JD, Íñiguez‐Dávalos LI, Martínez‐Calderón VM, Meraz Jiménez AD, Sosa‐Ramírez J Ecol Evol 04-Jul-2023
PMCID:PMC10319472
doi:10.1002/ece3.10262
PMID:37408625
Hyphoderma paramacaronesicum sp. nov. (Meruliaceae, Polyporales, Basidiomycota), a cryptic lineage to H. macaronesicum Martín MP, Zhang LF, Fernández-López J, Dueñas M, Rodríguez-Armas JL, Beltrán-Tejera E, Telleria MT Fungal Syst Evol 08-Aug-2018
PMCID:PMC7225581
doi:10.3114/fuse.2018.02.05
PMID:32467888
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Contrasting Selective Pressures on Seed Traits of Two Congeneric Species by Their Main Native Guilds of Dispersers on Islands Nogales M, González-Castro A, Marrero P, Bonnaud E, Traveset A PLoS One 07-May-2013
PMCID:PMC3646774
doi:10.1371/journal.pone.0063266
PMID:23667598
Dihydroanthracenones and hydronaphthalenones from the roots of Plocama pendula Braulio M. Fraga, Nayra Quintana, Carmen E. Díaz Elsevier BV 30-Dec-2011
doi:10.1016/J.PHYTOL.2011.12.010
Impact of Alien Plant Invaders on Pollination Networks in Two Archipelagos Padrón B, Traveset A, Biedenweg T, Díaz D, Nogales M, Olesen JM PLoS One 17-Jul-2009
PMCID:PMC2707600
doi:10.1371/journal.pone.0006275
PMID:19609437
Anthraquinones from natural and transformed roots of Plocama pendula. Fraga BM, Quintana N, Díaz CE Chem Biodivers 01-Feb-2009
doi:10.1002/CBDV.200800047
PMID:19235160
Nuclear DNA Amounts in Macaronesian Angiosperms SUDA J, KYNCL T, FREIOVÁ R Ann Bot 01-Jul-2003
PMCID:PMC4243629
doi:10.1093/aob/mcg104
PMID:12824074

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 / Anthracenes
(2R)-5,9-dihydroxy-2-methyl-3,4-dihydro-2H-anthracen-1-one 162961142 Click to see CC1CCC2=CC3=C(C=CC=C3O)C(=C2C1=O)O 242.27 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.010
(2R)-6,9-dihydroxy-5-methoxy-2-methyl-3,4-dihydro-2H-anthracen-1-one 162866477 Click to see CC1CCC2=CC3=C(C=CC(=C3OC)O)C(=C2C1=O)O 272.29 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.010
(4aR,9aS,10R)-10-hydroxy-2-methyl-4,4a,9a,10-tetrahydro-1H-anthracen-9-one 101064501 Click to see CC1=CCC2C(C1)C(=O)C3=CC=CC=C3C2O 228.29 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.010
10-hydroxy-2-methyl-4,4a,9a,10-tetrahydro-1H-anthracen-9-one 162971410 Click to see CC1=CCC2C(C1)C(=O)C3=CC=CC=C3C2O 228.29 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.010
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
1-Methoxy-3-hydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid methyl ester 11141475 Click to see COC1=C2C(=CC(=C1C(=O)OC)O)C(=O)C3=CC=CC=C3C2=O 312.27 unknown https://doi.org/10.1002/CBDV.200800047
Ethyl 1,3-dihydroxy-9,10-dioxoanthracene-2-carboxylate 10041193 Click to see CCOC(=O)C1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 312.27 unknown https://doi.org/10.1002/CBDV.200800047
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.1002/CBDV.200800047
1-Hydroxy-3-methoxy-2-methylanthracene-9,10-dione 10611938 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)OC 268.26 unknown https://doi.org/10.1002/CBDV.200800047
1-Hydroxy-5-methoxy-2-methylanthracene-9,10-dione 13970503 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC=C3OC)O 268.26 unknown https://doi.org/10.1002/CBDV.200800047
1,5-Dihydroxy-2-methylanthracene-9,10-dione 182449 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC=C3O)O 254.24 unknown https://doi.org/10.1002/CBDV.200800047
1,5-Dimethoxy-2-methylanthracene-9,10-dione 85919892 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC=C3OC)OC 282.29 unknown https://doi.org/10.1002/CBDV.200800047
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1002/CBDV.200800047
Digiferruginol 32209 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)CO)O 254.24 unknown https://doi.org/10.1002/CBDV.200800047
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1-Methoxy-3-hydroxy-2-ethoxymethylanthraquinone 5070780 Click to see CCOCC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 312.30 unknown https://doi.org/10.1002/CBDV.200800047
1-Methoxy-3-hydroxy-9,10-anthracenedione 620298 Click to see COC1=CC(=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1002/CBDV.200800047
1,3-Dimethoxy-2-hydroxy-9,10-anthraquinone 15118825 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3C2=O)OC)O 284.26 unknown https://doi.org/10.1002/CBDV.200800047
1,6-Dihydroxy-3,5,7-trimethoxy-2-methylanthracene-9,10-dione 162989511 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C(=C3C2=O)OC)O)OC)OC 344.30 unknown https://doi.org/10.1002/CBDV.200800047
1,6-Dihydroxy-5-methoxy-2-methylanthracene-9,10-dione 482558 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3OC)O)O 284.26 unknown https://doi.org/10.1002/CBDV.200800047
2-(Methoxymethyl)-1,3-dihydroxyanthraquinone 149782 Click to see COCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 284.26 unknown https://doi.org/10.1002/CBDV.200800047
2-Hydroxy-1,3,7-trimethoxy-6-methylanthracene-9,10-dione 163080913 Click to see CC1=CC2=C(C=C1OC)C(=O)C3=C(C(=C(C=C3C2=O)OC)O)OC 328.30 unknown https://doi.org/10.1002/CBDV.200800047
3-Hydroxy-1,2-dimethoxyanthracene-9,10-dione 57509304 Click to see COC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 284.26 unknown https://doi.org/10.1002/CBDV.200800047
9,10-Anthracenedione, 3-hydroxy-1-methoxy-2-(methoxymethyl)- 5319467 Click to see COCC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 298.29 unknown https://doi.org/10.1002/CBDV.200800047
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1002/CBDV.200800047
Lucidin ethyl ether 28578 Click to see CCOCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 298.29 unknown https://doi.org/10.1002/CBDV.200800047
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1002/CBDV.200800047
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown https://doi.org/10.1002/CBDV.200800047

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