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Cecropia glaziovii

Cecropia glaziovii - 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 UUID64400ff9b2c60963098543
Scientific name Cecropia glaziovii
Authority Snethl.
First published in Notizbl. Bot. Gart. Berlin-Dahlem 8: 358 (1923)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cecropia macranthera Warb. ex Glaz. Bull. Soc. Bot. France 59(Mém. 3g): 645, nomen. 1913 [1912 publ. 1913]

Common names Top

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Language Common/alternative name
Portuguese embaúba-vermelha

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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000592227
Tropicos 21300065
KEW urn:lsid:ipni.org:names:292376-2
The Plant List kew-2707034
Open Tree Of Life 6110975
NCBI Taxonomy 1824952
IUCN Red List 191124181
IPNI 292376-2
iNaturalist 83966
GBIF 4013471

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
Anti-Leishmania compounds can be screened using Leishmania spp. expressing red fluorescence (tdTomato) Cruz MG, Santi AM, de Morais-Teixeira E, Caldeira AS, de Siqueira EP, Oliveira E, Alves TM, Murta SM Antimicrob Agents Chemother 08-Dec-2023
PMCID:PMC10777850
doi:10.1128/aac.00509-23
PMID:38063403
Flavonoids with Anti-Herpes Simplex Virus Properties: Deciphering Their Mechanisms in Disrupting the Viral Life Cycle Šudomová M, Hassan ST Viruses 29-Nov-2023
PMCID:PMC10748012
doi:10.3390/v15122340
PMID:38140581
A Critical Appraisal of the Most Recent Investigations on the Hepatoprotective Action of Brazilian Plants Garcia-Manieri JA, Correa VG, Backes E, de Sá-Nakanishi AB, Bracht L, Comar JF, Corrêa RC, Peralta RM, Bracht A Plants (Basel) 12-Dec-2022
PMCID:PMC9785989
doi:10.3390/plants11243481
PMID:36559593
Green Hydrogel Synthesis: Emphasis on Proteomics and Polymer Particle-Protein Interaction Chafran L, Carfagno A, Altalhi A, Bishop B Polymers (Basel) 06-Nov-2022
PMCID:PMC9656617
doi:10.3390/polym14214755
PMID:36365747
Multiple Roles of Chitosan in Mucosal Drug Delivery: An Updated Review Mura P, Maestrelli F, Cirri M, Mennini N Mar Drugs 20-May-2022
PMCID:PMC9146108
doi:10.3390/md20050335
PMID:35621986
Procyanidin C1 from Viola odorata L. inhibits Na+,K+-ATPase Heger T, Zatloukal M, Kubala M, Strnad M, Gruz J Sci Rep 29-Apr-2022
PMCID:PMC9055044
doi:10.1038/s41598-022-11086-y
PMID:35487935
Flavonoids Target Human Herpesviruses That Infect the Nervous System: Mechanisms of Action and Therapeutic Insights Šudomová M, Berchová-Bímová K, Mazurakova A, Šamec D, Kubatka P, Hassan ST Viruses 13-Mar-2022
PMCID:PMC8949561
doi:10.3390/v14030592
PMID:35336999
Climate change threatens native potential agroforestry plant species in Brazil Lima VP, de Lima RA, Joner F, Siddique I, Raes N, ter Steege H Sci Rep 10-Feb-2022
PMCID:PMC8831634
doi:10.1038/s41598-022-06234-3
PMID:35145191
Paving New Roads Towards Biodiversity-Based Drug Development in Brazil: Lessons from the Past and Future Perspectives Braga FC Rev Bras Farmacogn 17-Sep-2021
PMCID:PMC8447804
doi:10.1007/s43450-021-00181-2
PMID:34548709
pH-Responsive Nanocomposite Based Hydrogels for the Controlled Delivery of Ticagrelor; In Vitro and In Vivo Approaches Shahid N, Erum A, Zaman M, Tulain UR, Shoaib QU, Majeed A, Rasool MF, Imran I, Alshehri S, Noorani B, Alqahtani F Int J Nanomedicine 16-Sep-2021
PMCID:PMC8455181
doi:10.2147/IJN.S330186
PMID:34556985
An Updated Overview of the Emerging Role of Patch and Film-Based Buccal Delivery Systems Jacob S, Nair AB, Boddu SH, Gorain B, Sreeharsha N, Shah J Pharmaceutics 05-Aug-2021
PMCID:PMC8399227
doi:10.3390/pharmaceutics13081206
PMID:34452167
Green Synthesized Chitosan/Chitosan Nanoforms/Nanocomposites for Drug Delivery Applications Sivanesan I, Gopal J, Muthu M, Shin J, Mari S, Oh J Polymers (Basel) 09-Jul-2021
PMCID:PMC8309384
doi:10.3390/polym13142256
PMID:34301013
Insights into Terminal Sterilization Processes of Nanoparticles for Biomedical Applications Bernal-Chávez SA, Del Prado-Audelo ML, Caballero-Florán IH, Giraldo-Gomez DM, Figueroa-Gonzalez G, Reyes-Hernandez OD, González-Del Carmen M, González-Torres M, Cortés H, Leyva-Gómez G Molecules 03-Apr-2021
PMCID:PMC8038324
doi:10.3390/molecules26072068
PMID:33916823
The dear enemy effect drives conspecific aggressiveness in an Azteca-Cecropia system Zorzal G, Camarota F, Dias M, Vidal DM, Lima E, Fregonezi A, Campos RI Sci Rep 17-Mar-2021
PMCID:PMC7970830
doi:10.1038/s41598-021-85070-3
PMID:33731789
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYMED.2008.02.006

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