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Visnea mocanera

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffb6282148825222286
Scientific name Visnea mocanera
Authority L.f.
First published in Suppl. Pl. : 251 (1782)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Visnea canariensis Oken Allg. Naturgesch. 3(3): 932 (1841)
Mocanera canariensis J.St.-Hil. Expos. Fam. Nat. ii. 371 (1805).

Common names Top

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Language Common/alternative name
English mocan
Spanish mocán
Esperanto mokano
Finnish mokano
Finnish mokkamarja
Portuguese mocano

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-0000425406
Tropicos 100354997
KEW urn:lsid:ipni.org:names:829744-1
The Plant List kew-2462423
Open Tree Of Life 736466
Observations.org 134492
NCBI Taxonomy 1007890
IUCN Red List 30338
IPNI 829744-1
iNaturalist 182221
GBIF 7793182
Freebase /m/02y__tl
EPPO VSNMO
Elurikkus 621726
USDA GRIN 41810
Wikipedia Visnea_mocanera

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
Some Nanocarrier’s Properties and Chemical Interaction Mechanisms with Flavones Espíndola C Molecules 22-Mar-2023
PMCID:PMC10051830
doi:10.3390/molecules28062864
PMID:36985836
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Time-calibrated phylogenies reveal mediterranean and pre-mediterranean origin of the thermophilous vegetation of the Canary Islands Martín-Hernanz S, Nogales M, Valente L, Fernández-Mazuecos M, Pomeda-Gutiérrez F, Cano E, Marrero P, Olesen JM, Heleno R, Vargas P Ann Bot 03-Jan-2023
PMCID:PMC10147335
doi:10.1093/aob/mcac160
PMID:36594263
The Development of Pharmacophore Models for the Search of New Natural Inhibitors of SARS-CoV-2 Spike RBD–ACE2 Binding Interface Semenov VA, Krivdin LB Molecules 15-Dec-2022
PMCID:PMC9788546
doi:10.3390/molecules27248938
PMID:36558067
A new strategy for osteoarthritis therapy: Inhibition of glycolysis Tan C, Li L, Han J, Xu K, Liu X Front Pharmacol 10-Nov-2022
PMCID:PMC9685317
doi:10.3389/fphar.2022.1057229
PMID:36438808
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Biogeography of Mediterranean Hotspot Biodiversity: Re-Evaluating the 'Tertiary Relict' Hypothesis of Macaronesian Laurel Forests Kondraskov P, Schütz N, Schüßler C, de Sequeira MM, Guerra AS, Caujapé-Castells J, Jaén-Molina R, Marrero-Rodríguez Á, Koch MA, Linder P, Kovar-Eder J, Thiv M PLoS One 14-Jul-2015
PMCID:PMC4501571
doi:10.1371/journal.pone.0132091
PMID:26173113
Phenolic Composition of the “Mocán” (<i>Visnea</i><i>mocanera</i>L.f.) Margarita Hernández-Pérez, Teresa Hernández, Carmen Gómez-Cordovés, Isabel Estrella, Rosa M. Rabanal American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/JF9505335

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/JF9505335
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1021/JF9505335
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1021/JF9505335
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1021/JF9505335
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/JF9505335
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatrienes
1,8,11-Heptadecatriene, (Z,Z)- 5352709 Click to see 234.40 unknown https://doi.org/10.1021/JF9505335
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1S,5R,8R,9S,10R,11S,13R,14S,16S,17R,18S,19S)-10,13-dihydroxy-5-methyl-12-methylidene-3-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-yl] benzoate 101933335 Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7O)OC(=O)C8=CC=CC=C8 447.50 unknown https://doi.org/10.1021/JF9505335
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1021/JF9505335
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown https://doi.org/10.1021/JF9505335
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2-hydroxy-2-methyl-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]propanamide 162854059 Click to see 302.37 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1021/JF9505335
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1021/JF9505335
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1021/JF9505335
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1021/JF9505335
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Chrysanthemin 44256715 Click to see 449.40 unknown https://doi.org/10.1021/JF9505335
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1021/JF9505335
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1021/JF9505335
Malvidin 3-Glucoside 443652 Click to see 493.40 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/JF9505335
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1021/JF9505335
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1021/JF9505335
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1021/JF9505335
> Phenylpropanoids and polyketides / Macrolides and analogues
Avermectin A1b 9940924 Click to see 873.10 unknown https://doi.org/10.1021/JF9505335

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