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Cadia purpurea

Cadia purpurea - 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 UUID643fdeaa243d3755462859
Scientific name Cadia purpurea
Authority (G.Piccioli) Aiton
First published in Hort. Kew.3: 492 (1789)

Description Top

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Synonyms Top

Scientific name Authority First published in
Spaendoncea tamarindifolia Desf. Ann. Bot. (Usteri)9: 18 (1796)
Cadia arabica J.F.Gmel. Syst. Nat. ed. 13[bis]: 667 (1791)
Cadia pendula J.St.-Hil. Expos. Fam. Nat.2: 206 (1805)
Cadia varia L'Hér. Mag. Encycl.5: 29 (1795)
Panciatica purpurea G.Piccioli Hort. Panciat.: 9 (1783)

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

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-0000212052
Tropicos 13049078
KEW urn:lsid:ipni.org:names:482606-1
The Plant List ild-7130
Open Tree Of Life 434075
NCBI Taxonomy 53844
IUCN Red List 144277213
IPNI 482605-1
iNaturalist 581603
GBIF 2968353
EOL 702833
USDA GRIN 8275

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
Indigenous knowledge on the practice of milk container fumigation and its effect on microbial safety of milk among pastoral communities in west Guji zone, southern Ethiopia Lemma H, Asefa L, Gemechu T, Demissie F, Loka B, Dhengesu D, Kumela G, Karbana G, Daba C Heliyon 10-Feb-2024
PMCID:PMC10878909
doi:10.1016/j.heliyon.2024.e25877
PMID:38384507
Use of wild edible and nutraceutical plants in Raya-Azebo District of Tigray Region, northern Ethiopia Giday M, Teklehaymanot T Trop Med Health 24-Oct-2023
PMCID:PMC10594744
doi:10.1186/s41182-023-00550-8
PMID:37872596
Antioxidant Potential of Ethiopian Medicinal Plants and Their Phytochemicals: A Review of Pharmacological Evaluation Nigussie G, Siyadatpanah A, Norouzi R, Debebe E, Alemayehu M, Dekebo A Evid Based Complement Alternat Med 12-Oct-2023
PMCID:PMC10586904
doi:10.1155/2023/1901529
PMID:37868204
Cheminformatics-Based Study Identifies Potential Ebola VP40 Inhibitors Broni E, Ashley C, Adams J, Manu H, Aikins E, Okom M, Miller WA III, Wilson MD, Kwofie SK Int J Mol Sci 27-Mar-2023
PMCID:PMC10094735
doi:10.3390/ijms24076298
PMID:37047270
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Advances in Research on the Regulation of Floral Development by CYC-like Genes Chai Y, Liu H, Chen W, Guo C, Chen H, Cheng X, Chen D, Luo C, Zhou X, Huang C Curr Issues Mol Biol 02-Mar-2023
PMCID:PMC10047570
doi:10.3390/cimb45030131
PMID:36975501
Soil organic carbon, total nitrogen stocks and CO2 emissions in top- and subsoils with contrasting management regimes in semi-arid environments Okolo CC, Gebresamuel G, Zenebe A, Haile M, Orji JE, Okebalama CB, Eze CE, Eze E, Eze PN Sci Rep 20-Jan-2023
PMCID:PMC9860075
doi:10.1038/s41598-023-28276-x
PMID:36670181
Community composition and phyto-diversity assessment of ganda roba and ganda shabbo sites in Damota natural vegetation, eastern Ethiopia Hussein A Heliyon 20-Oct-2022
PMCID:PMC9634035
doi:10.1016/j.heliyon.2022.e11163
PMID:36339994
In Vitro Antibacterial and Antioxidant Activities and Molecular Docking Analysis of Phytochemicals from Cadia purpurea Roots Kiros T, Eswaramoorthy R, Melaku Y, Dekebo A J Trop Med 24-Feb-2022
PMCID:PMC8894027
doi:10.1155/2022/4190166
PMID:35251187
Flower, seed, and fruit development in three Tunisian species of Polygonum: Implications for their taxonomy and evolution of distyly in Polygonaceae Mahmoudi M, Boughalleb F, Pellegrino G, Abdellaoui R, Nasri N PLoS One 10-Jan-2020
PMCID:PMC6953800
doi:10.1371/journal.pone.0227099
PMID:31923204
Ecosystem Service Values Changes in Response to Land-Use/Land-Cover Dynamics in Dry Afromontane Forest in Northern Ethiopia Solomon N, Segnon AC, Birhane E Int J Environ Res Public Health 22-Nov-2019
PMCID:PMC6926997
doi:10.3390/ijerph16234653
PMID:31766672
The effects of land cover change on carbon stock dynamics in a dry Afromontane forest in northern Ethiopia Solomon N, Pabi O, Annang T, Asante IK, Birhane E Carbon Balance Manag 06-Sep-2018
PMCID:PMC6127076
doi:10.1186/s13021-018-0103-7
PMID:30191432
Human-Forest interfaces in Hugumburda-Gratkhassu National Forest Priority Area, North-eastern Ethiopia Kidane L, Nemomissa S, Bekele T J Ethnobiol Ethnomed 23-Feb-2018
PMCID:PMC5824611
doi:10.1186/s13002-018-0218-7
PMID:29471862
Evolutionary response to the Qinghai-Tibetan Plateau uplift: phylogeny and biogeography of Ammopiptanthus and tribe Thermopsideae (Fabaceae) Shi W, Liu PL, Duan L, Pan BR, Su ZH PeerJ 31-Jul-2017
PMCID:PMC5541923
doi:10.7717/peerj.3607
PMID:28785518
Potential of Traditional Knowledge of Plants in the Management of Arthropods in Livestock Industry with Focus on (Acari) Ticks Wanzala W Evid Based Complement Alternat Med 17-Jul-2017
PMCID:PMC5536150
doi:10.1155/2017/8647919
PMID:28798806

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
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
(6R)-6-[(1R,3R,8R,9aS)-8-hydroxy-1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]piperidin-2-one 162999045 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)O)CO 282.38 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
[(2R,7R,9R,9aS)-9-(hydroxymethyl)-7-[(2R)-6-oxopiperidin-2-yl]-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] 1H-pyrrole-2-carboxylate 163188467 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)OC(=O)C4=CC=CN4)CO 375.50 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
[(2R,7R,9R,9aS)-9-(hydroxymethyl)-7-[(2R)-6-oxopiperidin-2-yl]-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] 2-phenylacetate 162927582 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)OC(=O)CC4=CC=CC=C4)CO 400.50 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
[9-(hydroxymethyl)-7-(6-oxopiperidin-2-yl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] 1H-pyrrole-2-carboxylate 73801189 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)OC(=O)C4=CC=CN4)CO 375.50 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
[9-(hydroxymethyl)-7-(6-oxopiperidin-2-yl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-2-yl] 2-phenylacetate 162927581 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)OC(=O)CC4=CC=CC=C4)CO 400.50 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
Cadiamine 442944 Click to see C1CC(NC(=O)C1)C2CC(C3CC(CCN3C2)O)CO 282.38 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(-)-Sparteine 3966 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1055/S-0028-1097842
(14-Oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl) 2-phenylacetate 162992256 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)OC(=O)CC5=CC=CC=C5 382.50 unknown https://doi.org/10.1055/S-0028-1097842
(16-hydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl) 1H-pyrrole-2-carboxylate 162886311 Click to see C1CC2C3CC(C4CC(CCN4C3)OC(=O)C5=CC=CN5)C(N2C(=O)C1)O 373.40 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
(1R,2S,8S,9S,10R,12R)-8,12-dihydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 162956359 Click to see C1CC2C3CC(C4CC(CCN4C3)O)C(N2C(=O)C1)O 280.36 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
(1S,2R,9S,10S,12S)-12-ethoxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 162952601 Click to see CCOC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 292.40 unknown https://doi.org/10.1055/S-0028-1097843
(1S,2S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 12310674 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
(1S,2S,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 1492637 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1055/S-0028-1097842
[(1R,2S,4R,9S,10R,16S)-16-hydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] 1H-pyrrole-2-carboxylate 163185552 Click to see C1CC2C3CC(C4CC(CCN4C3)OC(=O)C5=CC=CN5)C(N2C(=O)C1)O 373.40 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
[(1S,2S,4S,9S,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] 2-phenylacetate 162992257 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)OC(=O)CC5=CC=CC=C5 382.50 unknown https://doi.org/10.1055/S-0028-1097842
12-Ethoxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 53463265 Click to see CCOC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 292.40 unknown https://doi.org/10.1055/S-0028-1097843
13-Hydroxylupanine 250873 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1055/S-0028-1097600
https://doi.org/10.1016/S0040-4039(00)93815-2
8,12-Dihydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 162956357 Click to see C1CC2C3CC(C4CC(CCN4C3)O)C(N2C(=O)C1)O 280.36 unknown https://doi.org/10.1016/S0040-4039(00)93815-2
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1055/S-0028-1097842
Hydroxylupanine 73404 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1055/S-0028-1097600
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1055/S-0028-1097842
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097842
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097842

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