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Vismia guianensis

Vismia guianensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Vismia guianensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Vismia guianensis - 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 UUID643ffb0dad3c1656608931
Scientific name Vismia guianensis
Authority (Aubl.) Pers.
First published in Syn. Pl. 2: 86 (1807)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vismia sieberiana Klotzsch Reis. Br.-Guiana 3: 999 (1849)
Vismia acuminata (Lam.) Pers. Syn. Pl. 2: 86 (1806)
Vismia caparosa Kunth Nov. Gen. Sp. 5: 182 (1822)
Vismia guianensis var. acuminata (Lam.) M.E.Berg Bol. Mus. Paraense "Emilio Goeldi," N.S., Bot. 40: 7 (1971)
Caopia acuminata (Lam.) Kuntze Revis. Gen. Pl. 1: 59 (1891)
Caopia guianensis (Aubl.) A.Lyons Pl. Nam. , ed. 2: 94 (1907)
Hypericum acuminatum Lam. Encycl. 4: 150 (1797)
Hypericum cuspidatum Willd. ex Spreng. Syst. Veg. 3: 351 (1826)
Hypericum eugeniifolium Willd. ex Spreng. Syst. Veg. 3: 350 (1826)
Hypericum guianense Aubl. Hist. Pl. Guiane 2: 784 (1775)
Caopia reichardtiana Kuntze Revis. Gen. Pl. 1: 59 (1891)
Vismia latifolia var. acuminata (Lam.) Sagot Ann. Sci. Nat., Bot. , sér. 6, 11: 163 (1881)
Vismia acuminata var. caparosa (Kunth) Choisy Prodr. 1: 543 (1824)
Vismia baccifera var. angustifolia Reichardt Fl. Bras. 12(1): 204 (1878)
Vismia cearensis Huber Bull. Herb. Boissier , sér. 2, 1: 313 (1901)
Vismia guaramirangae Huber Bull. Herb. Boissier , sér. 2, 1: 313 (1901)
Vismia reichardtiana (Kuntze) Ewan Contr. U.S. Natl. Herb. 35: 348 (1962)
Vismia guianensis var. glabrata Choisy Prodr. [A. P. de Candolle] 1: 542. 1824 [mid Jan 1824]

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Honduras
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000422374
Tropicos 7801342
INPN 733044
KEW urn:lsid:ipni.org:names:30051774-2
The Plant List kew-2457881
Open Tree Of Life 273714
NCBI Taxonomy 999598
IUCN Red List 179298101
IPNI 30051774-2
iNaturalist 83760
GBIF 7330275
EPPO VMIGU
EOL 5708510

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
Seasonal dynamics of Amblyomma cajennense (Fabricius, 1787) sensu stricto in a degraded area of the Amazon biome, with notes on Rickettsia amblyommatis infection de Araújo FE, Martins TF, Ramos CC, Nogueira RM, Faccini JL, Tavares MA, de Lima NJ, de Almeida Júnior EB, de Sousa-Paula LC, Dantas-Torres F, da Silva Krawczak F, Costa-Junior LM, Labruna MB, Dall′Agnol LT, Luz HR Parasit Vectors 27-Oct-2023
PMCID:PMC10612284
doi:10.1186/s13071-023-05978-9
PMID:37891604
French Guiana honeys from the Amazon biome: First description of volatile fraction and antioxidant capacity Jiang W, Paolini J, Bereau D, Battesti MJ, Yang Y, Jean-Marie É, Costa J, Robinson JC Heliyon 22-Jul-2023
PMCID:PMC10404971
doi:10.1016/j.heliyon.2023.e18526
PMID:37554807
Symbiont Identity Impacts the Microbiome and Volatilome of a Model Cnidarian-Dinoflagellate Symbiosis Wuerz M, Lawson CA, Oakley CA, Possell M, Wilkinson SP, Grossman AR, Weis VM, Suggett DJ, Davy SK Biology (Basel) 17-Jul-2023
PMCID:PMC10376011
doi:10.3390/biology12071014
PMID:37508443
Antimicrobial and Anti-Infective Activity of Natural Products—Gaining Knowledge from Novel Studies Fernandes ES, da Silva Figueiredo IF, Monteiro CR, Monteiro-Neto V Antibiotics (Basel) 15-Jun-2023
PMCID:PMC10295247
doi:10.3390/antibiotics12061051
PMID:37370369
Pestalotioid Species Associated with Medicinal Plants in Southwest China and Thailand Sun YR, Jayawardena RS, Sun JE, Wang Y Microbiol Spectr 10-Jan-2023
PMCID:PMC9927317
doi:10.1128/spectrum.03987-22
PMID:36625649
Prenylated Benzophenones from Vismia Guianensis Reduced Nematode Growth and Chemotaxis Gerald C, Howard RK, Adesina R, Hamer S, Christian OE J Nematol 08-Jan-2023
PMCID:PMC9871599
doi:10.2478/jofnem-2022-0054
PMID:36742267
The Anti-Virulence Effect of Vismia guianensis against Candida albicans and Candida glabrata Motta EP, Farias JR, da Costa AA, da Silva AF, Oliveira Lopes AJ, Cartágenes MD, Nicolete R, Abreu AG, Fernandes ES, Nascimento FR, da Rocha CQ, Monteiro CA, Guerra RN Antibiotics (Basel) 16-Dec-2022
PMCID:PMC9774440
doi:10.3390/antibiotics11121834
PMID:36551490
The uppermost monoterpenes improving Cinnamomum camphora thermotolerance by serving signaling functions Xu C, Wang B, Luo Q, Ma Y, Zheng T, Wang Y, Cai Y, Zuo Z Front Plant Sci 15-Dec-2022
PMCID:PMC9800025
doi:10.3389/fpls.2022.1072931
PMID:36589079
Host‐tree selection by the ant garden‐initiating arboreal ponerine Neoponera goeldii Dejean A, Rossi V, Azémar F, Compin A, Petitclerc F, Talaga S, Corbara B Ecology 25-Sep-2022
PMCID:PMC10078305
doi:10.1002/ecy.3843
PMID:36156795
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Fungal Species from Rhododendron sp.: Discosia rhododendricola sp.nov, Neopestalotiopsis rhododendricola sp.nov and Diaporthe nobilis as a New Host Record. Chaiwan N, Jeewon R, Pem D, Jayawardena RS, Nazurally N, Mapook A, Promputtha I, Hyde KD J Fungi (Basel) 26-Aug-2022
PMCID:PMC9504118
doi:10.3390/jof8090907
PMID:36135632
Neopestalotiopsis siciliana sp. nov. and N. rosae Causing Stem Lesion and Dieback on Avocado Plants in Italy Fiorenza A, Gusella G, Aiello D, Polizzi G, Voglmayr H J Fungi (Basel) 25-May-2022
PMCID:PMC9225166
doi:10.3390/jof8060562
PMID:35736045
Taste and chemical composition as drives for utilitarian redundancy and equivalence: a case study in local medical systems in Northeastern Brazil Reinaldo RC, Santoro FR, Albuquerque UP, de Medeiros PM J Ethnobiol Ethnomed 25-Jan-2022
PMCID:PMC8787910
doi:10.1186/s13002-022-00503-1
PMID:35078497
Morphology, Phylogeny, and Pathogenicity of Pestalotioid Species on Camellia oleifera in China Li L, Yang Q, Li H J Fungi (Basel) 15-Dec-2021
PMCID:PMC8705482
doi:10.3390/jof7121080
PMID:34947061
Neopestalotiopsis Species Associated with Flower Diseases of Macadamia integrifolia in Australia Prasannath K, Shivas RG, Galea VJ, Akinsanmi OA J Fungi (Basel) 17-Sep-2021
PMCID:PMC8471233
doi:10.3390/jof7090771
PMID:34575809

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
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/10.1007/BF01280287
> Benzenoids / Anthracenes / Anthraquinones
Madagascine 378693 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)C 338.40 unknown https://doi.org/10.1021/NP990226J
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1021/NP990226J
> Benzenoids / Benzene and substituted derivatives / Benzophenones
[(2R)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-phenylmethanone 163020679 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
[(2R)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-phenylmethanone 162981619 Click to see CC(=CCC1=C2C(=C(C(=C1O)C(=O)C3=CC=CC=C3)O)CC(O2)C(C)(C)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
[(2S)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-phenylmethanone 637876 Click to see CC(=CCC1=C2C(=C(C(=C1O)C(=O)C3=CC=CC=C3)O)CC(O2)C(C)(C)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
[(2S)-6-hydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-phenylmethanone 163067404 Click to see CC(=CCC1=C2C(=CC(=C1O)C(=O)C3=CC=CC=C3)CC(O2)C(C)(C)O)C 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
[4,6-Dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-phenylmethanone 102370901 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
[4,6-Dihydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-phenylmethanone 22297869 Click to see CC(=CCC1=C2C(=C(C(=C1O)C(=O)C3=CC=CC=C3)O)CC(O2)C(C)(C)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
phenyl-[(3R)-3,5,7-trihydroxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-8-yl]methanone 163080630 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(C(O2)(C)C)O)C(=O)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
Phenyl-[3,5,7-trihydroxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-8-yl]methanone 102370900 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(C(O2)(C)C)O)C(=O)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP990226J
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP990226J
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP990226J
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP990226J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives / Tanshinlactones and derivatives
(13R)-3-hydroxy-13-(2-hydroxypropan-2-yl)-5-methoxy-9-methyl-12,17-dioxatetracyclo[8.7.0.02,7.011,15]heptadeca-1(10),2,4,6,8,11(15)-hexaen-16-one 162874637 Click to see CC1=CC2=CC(=CC(=C2C3=C1C4=C(CC(O4)C(C)(C)O)C(=O)O3)O)OC 356.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
3-Hydroxy-13-(2-hydroxypropan-2-yl)-5-methoxy-9-methyl-12,17-dioxatetracyclo[8.7.0.02,7.011,15]heptadeca-1(10),2,4,6,8,11(15)-hexaen-16-one 102370902 Click to see CC1=CC2=CC(=CC(=C2C3=C1C4=C(CC(O4)C(C)(C)O)C(=O)O3)O)OC 356.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP990226J
https://doi.org/10.1016/S0031-9422(00)81583-6
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81583-6
https://doi.org/10.1021/NP990226J
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Vismiaguianin A 5324262 Click to see CC1=CC2=CC(=CC(=C2C3=C1C4=C(C=CC(O4)(C)C)C(=O)O3)O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(4R)-6-benzoyl-5,7-dihydroxy-8-(3-methylbut-2-enyl)-4-phenyl-3,4-dihydrochromen-2-one 163034504 Click to see CC(=CCC1=C(C(=C(C2=C1OC(=O)CC2C3=CC=CC=C3)O)C(=O)C4=CC=CC=C4)O)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
(4R)-8-benzoyl-5,7-dihydroxy-6-(3-methylbut-2-enyl)-4-phenyl-3,4-dihydrochromen-2-one 163053024 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)C3=CC=CC=C3)OC(=O)CC2C4=CC=CC=C4)O)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
6-Benzoyl-5,7-dihydroxy-8-(3-methylbut-2-enyl)-4-phenyl-3,4-dihydrochromen-2-one 10094089 Click to see CC(=CCC1=C(C(=C(C2=C1OC(=O)CC2C3=CC=CC=C3)O)C(=O)C4=CC=CC=C4)O)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)00208-9
8-Benzoyl-5,7-dihydroxy-6-(3-methylbut-2-enyl)-4-phenyl-3,4-dihydrochromen-2-one 10071240 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)C3=CC=CC=C3)OC(=O)CC2C4=CC=CC=C4)O)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)00208-9

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