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Pleodendron costaricense

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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 UUID643ff84408e3a914644791
Scientific name Pleodendron costaricense
Authority N.Zamora, Hammel & Aguilar
First published in Lankesteriana 5: 211 (2005)

Description Top

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Synonyms Top

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Common names Top

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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

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-0000398713
Tropicos 50291053
KEW urn:lsid:ipni.org:names:60440984-2
The Plant List kew-2415475
Open Tree Of Life 1016777
NCBI Taxonomy 549616
IUCN Red List 136055038
IPNI 60440984-2
iNaturalist 430193
GBIF 3877821
EOL 5035526

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
Biological activity of the essential oils from Cinnamodendron dinisii and Siparuna guianensis Andrade MA, Cardoso MD, Gomes MD, de Azeredo CM, Batista LR, Soares MJ, Rodrigues LM, Figueiredo AC Braz J Microbiol 01-Mar-2015
PMCID:PMC4512063
doi:10.1590/S1517-838246120130683
PMID:26221107
Chemical Composition and Antioxidant Activity of Essential Oils from Cinnamodendron dinisii Schwacke and Siparuna guianensis Aublet Andrade MA, Cardoso MD, de Andrade J, Silva LF, Teixeira ML, Resende JM, Figueiredo AC, Barroso JG Antioxidants (Basel) 26-Nov-2013
PMCID:PMC4665518
doi:10.3390/antiox2040384
PMID:26784471
Phytochemistry and antifungal properties of the newly discovered tree Pleodendron costaricense. Treyvaud Amiguet V, Petit P, Ta CA, Nuñez R, Sánchez-Vindas P, Alvarez LP, Smith ML, Arnason JT, Durst T J Nat Prod 01-Jul-2006
doi:10.1021/NP0504863
PMID:16872133

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 / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/NP0504863
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/NP0504863
(1S,4S,5S)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hex-2-ene 12444328 Click to see CC1C=CC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1021/NP0504863
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/NP0504863
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(2S)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]chroman-6-ol 13988400 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1021/NP0504863
(c)(1/2)-Tocotrienol pound>>Tocotrienol, delta 53394607 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1021/NP0504863
delta-Tocotrienol 5282350 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1021/NP0504863
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP0504863
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1S,7R,8aS)-1,8a-dimethyl-7-propan-2-yl-7,8-dihydro-1H-naphthalene-2,6-dione 11844355 Click to see CC1C(=O)C=CC2=CC(=O)C(CC12C)C(C)C 232.32 unknown https://doi.org/10.1021/NP0504863
1,8a-dimethyl-7-propan-2-yl-7,8-dihydro-1H-naphthalene-2,6-dione 73123482 Click to see CC1C(=O)C=CC2=CC(=O)C(CC12C)C(C)C 232.32 unknown https://doi.org/10.1021/NP0504863
> 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/10.1021/NP0504863
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/10.1021/NP0504863
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/10.1021/NP0504863
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(5-acetyloxy-7,8-diformyl-8-hydroxy-4,4,8a-trimethyl-2,3,4a,5-tetrahydro-1H-naphthalen-1-yl) acetate 73123481 Click to see CC(=O)OC1CCC(C2C1(C(C(=CC2OC(=O)C)C=O)(C=O)O)C)(C)C 366.40 unknown https://doi.org/10.1021/NP0504863
Parritadial 11844354 Click to see CC(=O)OC1CCC(C2C1(C(C(=CC2OC(=O)C)C=O)(C=O)O)C)(C)C 366.40 unknown https://doi.org/10.1021/NP0504863
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1S,4R,4aS,8R,8aR)-4,8-diacetyloxy-2-formyl-1-hydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1-carboxylic acid 163103544 Click to see CC(=O)OC1CCC(C2C1(C(C(=CC2OC(=O)C)C=O)(C(=O)O)O)C)(C)C 382.40 unknown https://doi.org/10.1021/NP0504863
> Organic oxygen compounds / Organic oxides
Tadeonal 72503 Click to see CC1(CCCC2(C1CC=C(C2C=O)C=O)C)C 234.33 unknown https://doi.org/10.1021/NP0504863
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,4S,4aS,8aS)-4-hydroxy-5,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 163059235 Click to see CC1(CCCC2(C1C(C=C(C2C=O)C=O)O)C)C 250.33 unknown https://doi.org/10.1021/NP0504863
4-Hydroxy-5,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 163059234 Click to see CC1(CCCC2(C1C(C=C(C2C=O)C=O)O)C)C 250.33 unknown https://doi.org/10.1021/NP0504863
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,4R,4aS,8aS)-1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 14313008 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1021/NP0504863
[(1S,4S,4aS,8aS)-3,4-diformyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate 12303259 Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O 308.40 unknown https://doi.org/10.1021/NP0504863
1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 3504627 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1021/NP0504863
Cinnamodial 442354 Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O 308.40 unknown https://doi.org/10.1021/NP0504863
Cinnamodial B812927K060 321973 Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O 308.40 unknown https://doi.org/10.1021/NP0504863
Mukaadial 159088 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1021/NP0504863
> Organoheterocyclic compounds / Naphthofurans
[(5S,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-3-oxo-1,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] acetate 44583865 Click to see CC(=O)OC1C=C2C(=O)OCC2(C3(C1C(CCC3)(C)C)C)O 308.40 unknown https://doi.org/10.1021/NP0504863
Cinnamosmolide 12303262 Click to see CC(=O)OC1C=C2C(=O)OCC2(C3(C1C(CCC3)(C)C)C)O 308.40 unknown https://doi.org/10.1021/NP0504863
Cinnamosmolide B812927K029 99943 Click to see CC(=O)OC1C=C2C(=O)OCC2(C3(C1C(CCC3)(C)C)C)O 308.40 unknown https://doi.org/10.1021/NP0504863

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