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Pleurothyrium cinereum

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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 UUID6440475ba6a76575080807
Scientific name Pleurothyrium cinereum
Authority van der Werff
First published in Ann. Missouri Bot. Gard. 80: 61 (1993)

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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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

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Database ID/link to page
World Flora Online wfo-0001071439
Tropicos 17804657
KEW urn:lsid:ipni.org:names:303653-2
The Plant List tro-17804657
Open Tree Of Life 360220
Observations.org 459180
NCBI Taxonomy 128689
IUCN Red List 181582332
IPNI 303653-2
GBIF 5685828
EOL 5402117
Elurikkus 570497

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
Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M Heliyon 07-Dec-2022
PMCID:PMC9801090
doi:10.1016/j.heliyon.2022.e12013
PMID:36590503
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Coagulation System Activation for Targeting of COVID-19: Insights into Anticoagulants, Vaccine-Loaded Nanoparticles, and Hypercoagulability in COVID-19 Vaccines Abdel-Bakky MS, Amin E, Ewees MG, Mahmoud NI, Mohammed HA, Altowayan WM, Abdellatif AA Viruses 24-Jan-2022
PMCID:PMC8876839
doi:10.3390/v14020228
PMID:35215822
Antioxidant and Anti-Inflammatory Activities of Kigelia africana (Lam.) Benth. Nabatanzi A, Nkadimeng SM, Lall N, Kabasa JD, McGaw LJ Evid Based Complement Alternat Med 17-Jun-2020
PMCID:PMC7317318
doi:10.1155/2020/4352084
PMID:32655661
Dataset of permanent plots of trees with dbh >10cm in Mashpi rainforest biodiversity reserve, a remnant of the Chocó forest in Northern Ecuador Toasa G, Morochz C, Oleas NH Data Brief 12-Jun-2020
PMCID:PMC7327807
doi:10.1016/j.dib.2020.105845
PMID:32637474
Antinociceptive Effect of Hinokinin and Kaurenoic Acid Isolated from Aristolochia odoratissima L. Montiel-Ruiz RM, Córdova-de la Cruz M, González-Cortázar M, Zamilpa A, Gómez-Rivera A, López-Rodríguez R, Lobato-García CE, Blé-González EA Molecules 24-Mar-2020
PMCID:PMC7145305
doi:10.3390/molecules25061454
PMID:32213823
Chemical Structures of Lignans and Neolignans Isolated from Lauraceae Li Y, Xie S, Ying J, Wei W, Gao K Molecules 30-Nov-2018
PMCID:PMC6321345
doi:10.3390/molecules23123164
PMID:30513687
Natural Products for Antithrombosis Chen C, Yang FQ, Zhang Q, Wang FQ, Hu YJ, Xia ZN Evid Based Complement Alternat Med 17-May-2015
PMCID:PMC4449941
doi:10.1155/2015/876426
PMID:26075003
Macrophyllin-type bicyclo[3.2.1]octanoid neolignans from the leaves of Pleurothyrium cinereum. Coy ED, Cuca LE, Sefkow M J Nat Prod 01-Jul-2009
doi:10.1021/NP9000569
PMID:19548690

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,5R,9S,10R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 137705706 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP9000569
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP9000569
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP9000569
> Organoheterocyclic compounds / Benzodioxoles
(1R,5R,6R,7S)-8-hydroxy-1,5-dimethoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 101485482 Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
(1R,5S,6R,7R,8R)-8-hydroxy-5-methoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 162918072 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C(=C3)OC)OCO4 372.40 unknown https://doi.org/10.1021/NP9000569
(1R,5S,6R,7S)-1,5-dimethoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-dione 162853505 Click to see CC1C(C2(C(=O)C(=CC1(C2=O)OC)CC=C)OC)C3=CC4=C(C(=C3)OC)OCO4 400.40 unknown https://doi.org/10.1021/NP9000569
(1S,4R,5R,6S,7R)-4-hydroxy-1,5-dimethoxy-6-(7-methoxy-1,3-benzodioxol-5-yl)-7-methyl-3-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one 162917421 Click to see CC1C(C2(C(C(=CC1(C2=O)OC)CC=C)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
(1S,5R,6R,7R)-8-hydroxy-5-methoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 101485481 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C(=C3)OC)OCO4 372.40 unknown https://doi.org/10.1021/NP9000569
(1S,5S,6R,7S,8S)-8-hydroxy-1,5-dimethoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 162963476 Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
1,5-Dimethoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-dione 56661398 Click to see CC1C(C2(C(=O)C(=CC1(C2=O)OC)CC=C)OC)C3=CC4=C(C(=C3)OC)OCO4 400.40 unknown https://doi.org/10.1021/NP9000569
4-Hydroxy-1,5-dimethoxy-6-(7-methoxy-1,3-benzodioxol-5-yl)-7-methyl-3-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one 74959117 Click to see CC1C(C2(C(C(=CC1(C2=O)OC)CC=C)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
8-Hydroxy-1,5-dimethoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 56674808 Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
8-Hydroxy-5-methoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 56657485 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C(=C3)OC)OCO4 372.40 unknown https://doi.org/10.1021/NP9000569
Cinerin A 45487088 Click to see CC1C(C2(C(=O)C(=CC1(C2=O)OC)CC=C)OC)C3=CC4=C(C(=C3)OC)OCO4 400.40 unknown https://doi.org/10.1021/NP9000569
Cinerin B 45487095 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C(=C3)OC)OCO4 372.40 unknown https://doi.org/10.1021/NP9000569
Cinerin C 44232714 Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569
Cinerin D 45273291 Click to see CC1C(C2(C(C(=CC1(C2=O)OC)CC=C)O)OC)C3=CC4=C(C(=C3)OC)OCO4 402.40 unknown https://doi.org/10.1021/NP9000569

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