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Vismia baccifera

Vismia baccifera - 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 UUID643ffb0dbbbc2632142655
Scientific name Vismia baccifera
Authority (L.) Planch. & Triana
First published in Ann. Sci. Nat., Bot. , sér. 4, 18: 300 (1862)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vismia guttifera Pers. Syn. Pl. 2: 86 (1806)
Caopia baccifera (L.) Kuntze Revis. Gen. Pl. 1: 59 (1891)
Hypericum bacciferum L. Mant. Pl. 2: 277 (1771)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Vismia baccifera subsp. baccifera Unknown
Vismia baccifera subsp. dealbata (Kunth) Ewan Contr. U.S. Natl. Herb. 35: 334 (1962)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000422382
Tropicos 7800775
INPN 735415
KEW urn:lsid:ipni.org:names:434100-1
The Plant List kew-2457893
Open Tree Of Life 949350
NCBI Taxonomy 198795
IUCN Red List 136783476
IPNI 434100-1
iNaturalist 153264
GBIF 7330329
EOL 5708497
Wikipedia Vismia_baccifera

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
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
The Triprenylated Anthranoid Ferruginin A, a Promising Scaffold for the Development of Novel Antibiotics against Gram-Positive Bacteria Casciaro B, Ghirga F, Cappiello F, Vergine V, Loffredo MR, Cammarone S, Puglisi E, Tortora C, Quaglio D, Mori M, Botta B, Mangoni ML Antibiotics (Basel) 11-Jan-2022
PMCID:PMC8773144
doi:10.3390/antibiotics11010084
PMID:35052961
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Bioactive Compounds as Potential Agents for Sexually Transmitted Diseases Management: A Review to Explore Molecular Mechanisms of Action Sharifi-Rad J, Quispe C, Rahavian A, Pereira Carneiro JN, Rocha JE, Alves Borges Leal AL, Bezerra Morais Braga MF, Melo Coutinho HD, Ansari Djafari A, Alarcón-Zapata P, Martorell M, Antika G, Tumer TB, Cruz-Martins N, Helon P, Paprocka P, Koch W, Docea AO, Calina D Front Pharmacol 24-Aug-2021
PMCID:PMC8421529
doi:10.3389/fphar.2021.674682
PMID:34504422
The potential of plant systems to break the HIV‐TB link Habibi P, Daniell H, Soccol CR, Grossi‐de‐Sa MF Plant Biotechnol J 18-Jul-2019
PMCID:PMC6737023
doi:10.1111/pbi.13110
PMID:30908823
Unraveling the in vitro antitumor activity of Vismia baccifera against HepG2: role of hydrogen peroxide Trepiana J, Ruiz-Larrea MB, Ruiz-Sanz JI Heliyon 29-Jun-2018
PMCID:PMC6039853
doi:10.1016/j.heliyon.2018.e00675
PMID:30003166
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Bioactive Constituents of Anatolian Salvia Species Gülaçtı Topçu, Rümeysa Yücer, Halil Şenol Springer International Publishing 19-Mar-2018
doi:10.1007/978-3-319-73900-7_2
Long-Term Vegetation Dynamics in a Megadiverse Hotspot: The Ice-Age Record of a Pre-montane Forest of Central Ecuador Montoya E, Keen HF, Luzuriaga CX, Gosling WD Front Plant Sci 20-Feb-2018
PMCID:PMC5826276
doi:10.3389/fpls.2018.00196
PMID:29515609
Plants in our combating strategies against Mycobacterium tuberculosis: progress made and obstacles met Gupta VK, Kumar MM, Bisht D, Kaushik A Pharm Biol 07-Apr-2017
PMCID:PMC6130758
doi:10.1080/13880209.2017.1309440
PMID:28385088
Neighbourhood structure and light availability influence the variations in plant design of shrubs in two cloud forests of different successional status Guzmán Q JA, Cordero RA Ann Bot 30-May-2016
PMCID:PMC4934397
doi:10.1093/aob/mcw078
PMID:27245635
Antimycobacterial and HIV-1 Reverse Transcriptase Activity of Julianaceae and Clusiaceae Plant Species from Mexico Gómez-Cansino R, Espitia-Pinzón CI, Campos-Lara MG, Guzmán-Gutiérrez SL, Segura-Salinas E, Echeverría-Valencia G, Torras-Claveria L, Cuevas-Figueroa XM, Reyes-Chilpa R Evid Based Complement Alternat Med 23-Apr-2015
PMCID:PMC4423034
doi:10.1155/2015/183036
PMID:25983849
Piper and Vismia Species from Colombian Amazonia Differentially Affect Cell Proliferation of Hepatocarcinoma Cells Lizcano LJ, Siles M, Trepiana J, Hernández ML, Navarro R, Ruiz-Larrea MB, Ruiz-Sanz JI Nutrients 30-Dec-2014
PMCID:PMC4303832
doi:10.3390/nu7010179
PMID:25558904
Review of Apanteles sensu stricto (Hymenoptera, Braconidae, Microgastrinae) from Area de Conservación Guanacaste, northwestern Costa Rica, with keys to all described species from Mesoamerica Fernández-Triana JL, Whitfield JB, Rodriguez JJ, Smith MA, Janzen DH, Hallwachs WD, Hajibabaei M, Burns JM, Solis MA, Brown J, Cardinal S, Goulet H, Hebert PD Zookeys 24-Feb-2014
PMCID:PMC3950464
doi:10.3897/zookeys.383.6418
PMID:24624021
Succession of Ephemeral Secondary Forests and Their Limited Role for the Conservation of Floristic Diversity in a Human-Modified Tropical Landscape van Breugel M, Hall JS, Craven D, Bailon M, Hernandez A, Abbene M, van Breugel P PLoS One 11-Dec-2013
PMCID:PMC3859589
doi:10.1371/journal.pone.0082433
PMID:24349283

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
> Benzenoids / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methoxy-7-methyl-3-[(E)-3-methylbut-1-enyl]-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methoxy-6-methyl-2-[(E)-3-methylbut-1-enyl]-10H-anthracen-9-one 163079573 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2C4C5=CC(=C(C(=C5C(=O)C6=C4C=C(C=C6O)C)O)C=CC(C)C)OC)OC)C=CC(C)C)O 674.80 unknown https://doi.org/10.1021/NP020566W
(3R)-3,8,9-trihydroxy-6-methoxy-3-methyl-7-[(E)-3-methylbut-1-enyl]-2,4-dihydroanthracen-1-one 162926208 Click to see CC(C)C=CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O 356.40 unknown https://doi.org/10.1021/NP020566W
(3S)-3,8,9-trihydroxy-6-methoxy-3-methyl-7-[(E)-3-methylbut-1-enyl]-2,4-dihydroanthracen-1-one 163193514 Click to see CC(C)C=CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O 356.40 unknown https://doi.org/10.1021/NP020566W
1,6,8-trihydroxy-3-methyl-2,4,7-tris(3-methylbut-2-enyl)-10H-anthracen-9-one 162909884 Click to see CC1=C(C2=C(C(=C1CC=C(C)C)O)C(=O)C3=C(C(=C(C=C3C2)O)CC=C(C)C)O)CC=C(C)C 460.60 unknown https://doi.org/10.1016/0040-4020(79)87031-3
10-[4,5-dihydroxy-2-methoxy-7-methyl-3-(3-methylbut-1-enyl)-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-1-enyl)-10H-anthracen-9-one 73321763 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2C4C5=CC(=C(C(=C5C(=O)C6=C4C=C(C=C6O)C)O)C=CC(C)C)OC)OC)C=CC(C)C)O 674.80 unknown https://doi.org/10.1021/NP020566W
10-[4,5-dihydroxy-2-methoxy-7-methyl-3-[(E)-3-methylbut-1-enyl]-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methoxy-6-methyl-2-[(E)-3-methylbut-1-enyl]-10H-anthracen-9-one 21577158 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2C4C5=CC(=C(C(=C5C(=O)C6=C4C=C(C=C6O)C)O)C=CC(C)C)OC)OC)C=CC(C)C)O 674.80 unknown https://doi.org/10.1007/978-3-319-73900-7_2
3,8,9-Trihydroxy-6-methoxy-3-methyl-7-(3-methylbut-1-enyl)-2,4-dihydroanthracen-1-one 85087686 Click to see CC(C)C=CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O 356.40 unknown https://doi.org/10.1021/NP020566W
Deacetylvismione A 9998380 Click to see CC(C)C=CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O 356.40 unknown https://doi.org/10.1007/978-3-319-73900-7_2
deacetylvismione H 13940837 Click to see CC(=CCOC1=CC(=C2C(=C1)C=C3CC(CC(=O)C3=C2O)(C)O)O)C 342.40 unknown https://doi.org/10.1007/978-3-319-73900-7_2
Vismione A 5458776 Click to see CC(C)C=CC1=C(C2=C(C3=C(CC(CC3=O)(C)OC(=O)C)C=C2C=C1OC)O)O 398.40 unknown https://doi.org/10.1021/NP50047A031
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-1-enyl)anthracene-9,10-dione 628167 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C=CC(C)C)O 352.40 unknown https://doi.org/10.1016/0031-9422(81)84067-8
1,8-Dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-2-enyl)anthracene-9,10-dione 11783130 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)CC=C(C)C)O 352.40 unknown https://doi.org/10.1021/NP020566W
Vismiaquinone 5378723 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C=CC(C)C)O 352.40 unknown https://doi.org/10.1007/978-3-319-73900-7_2
https://doi.org/10.1021/NP020566W
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-trans-Carveol 443178 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/0040-4020(79)87031-3
> Organoheterocyclic compounds / Naphthopyrans
(9R)-9,12-dihydroxy-5-methoxy-2,2,9-trimethyl-8,10-dihydronaphtho[6,7-h]chromen-11-one 154497676 Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C 354.40 unknown https://doi.org/10.1021/NP020566W
Vismione B 10247551 Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C 354.40 unknown https://doi.org/10.1021/NP020566W
https://doi.org/10.1021/NP50047A031
https://doi.org/10.1007/978-3-319-73900-7_2
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
[3-Chloro-10a-(3,7-dimethylocta-2,6-dienyl)-8-hydroxy-2,2,4a-trimethyl-5,6,10-trioxo-3,4-dihydrobenzo[g]chromen-9-ylidene]-iminoazanium 163185986 Click to see CC(=CCCC(=CCC12C(=O)C3=C(C(=O)C=C(C3=[N+]=N)O)C(=O)C1(CC(C(O2)(C)C)Cl)C)C)C 488.00 unknown https://doi.org/10.1016/0040-4020(79)87031-3

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