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Ampelozizyphus amazonicus

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 UUID644008e58d869609191771
Scientific name Ampelozizyphus amazonicus
Authority Ducke
First published in Arq. Inst. Biol. Veg. 2: 158 (1935)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English ampelozizipheae
Spanish ampelozizipheae
German ampelozizipheae
Chinese 亚马孙蔓枣

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
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000531791
Tropicos 27500364
INPN 734686
KEW urn:lsid:ipni.org:names:11511-2
The Plant List kew-2634618
Open Tree Of Life 140513
NCBI Taxonomy 106660
IUCN Red List 179280128
IPNI 11511-2
GBIF 3877225
EOL 5536004

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
Myrtucommulones and Related Acylphloroglucinols from Myrtaceae as a Promising Source of Multitarget SARS-CoV-2 Cycle Inhibitors Mendonça SC, Gomes BA, Campos MF, da Fonseca TS, Esteves ME, Andriolo BV, Cheohen CF, Constant LE, da Silva Costa S, Calil PT, Tucci AR, de Oliveira TK, Rosa AD, Ferreira VN, Lima JN, Miranda MD, da Costa LJ, da Silva ML, Scotti MT, Allonso D, Leitão GG, Leitão SG Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054083
doi:10.3390/ph17040436
PMID:38675398
Natural products as a source of Coronavirus entry inhibitors Szabó D, Crowe A, Mamotte C, Strappe P Front Cell Infect Microbiol 21-Feb-2024
PMCID:PMC10915212
doi:10.3389/fcimb.2024.1353971
PMID:38449827
Antiviral, Cytoprotective, and Anti-Inflammatory Effect of Ampelozizyphus amazonicus Ducke Ethanolic Wood Extract on Chikungunya Virus Infection Rocha DC, Sisnande T, Gavino-Leopoldino D, Guimarães-Andrade IP, Cruz FF, Assunção-Miranda I, Mendonça SC, Leitão GG, Simas RC, Mohana-Borges R, Leitão SG, Allonso D Viruses 09-Nov-2023
PMCID:PMC10674702
doi:10.3390/v15112232
PMID:38005909
Anti-SARS-CoV-2 Activity of Ampelozizyphus amazonicus (Saracura-Mirá): Focus on the Modulation of the Spike-ACE2 Interaction by Chemically Characterized Bark Extracts by LC-DAD-APCI-MS/MS Campos MF, Mendonça SC, Peñaloza EM, de Oliveira BA, Rosa AS, Leitão GG, Tucci AR, Ferreira VN, Oliveira TK, Miranda MD, Allonso D, Leitão SG Molecules 01-Apr-2023
PMCID:PMC10095690
doi:10.3390/molecules28073159
PMID:37049921
Ancient Rhamnaceae flowers impute an origin for flowering plants exceeding 250-million-years ago He T, Lamont BB iScience 18-Jun-2022
PMCID:PMC9254029
doi:10.1016/j.isci.2022.104642
PMID:35800761
Potential of Triterpenic Natural Compound Betulinic Acid for Neglected Tropical Diseases New Treatments Rocha V, Quadros H, Meira C, Silva L, Carvalho D, Hodel K, Moreira D, Soares M Biomedicines 01-Apr-2022
PMCID:PMC9027248
doi:10.3390/biomedicines10040831
PMID:35453582
Saracura-Mirá, a Proposed Brazilian Amazonian Adaptogen from Ampelozizyphus amazonicus Leitão SG, Leitão GG, de Oliveira DR Plants (Basel) 12-Jan-2022
PMCID:PMC8781190
doi:10.3390/plants11020191
PMID:35050079
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
COVID-19 Prophylaxis Efforts Based on Natural Antiviral Plant Extracts and Their Compounds Sytar O, Brestic M, Hajihashemi S, Skalicky M, Kubeš J, Lamilla-Tamayo L, Ibrahimova U, Ibadullayeva S, Landi M Molecules 30-Jan-2021
PMCID:PMC7866841
doi:10.3390/molecules26030727
PMID:33573318
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Towards a dynamic list of Amazonian tree species ter Steege H, Mota de Oliveira S, Pitman NC, Sabatier D, Antonelli A, Guevara Andino JE, Aymard GA, Salomão RP Sci Rep 05-Mar-2019
PMCID:PMC6401171
doi:10.1038/s41598-019-40101-y
PMID:30837572
Molecular Farming in Artemisia annua, a Promising Approach to Improve Anti-malarial Drug Production Pulice G, Pelaz S, Matías-Hernández L Front Plant Sci 18-Mar-2016
PMCID:PMC4796020
doi:10.3389/fpls.2016.00329
PMID:27047510
Evaluation of Antiplasmodial activity of extracts and constituents from Ampelozizyphus amazonicus do Carmo DF, Amaral AC, Machado M, Lopes D, Echevarria A, Rosário VE, Silva JR Pharmacogn Mag 01-Oct-2015
PMCID:PMC4653334
doi:10.4103/0973-1296.166071
PMID:26664012
Biologic Activity and Biotechnological Development of Natural Products Carvalho JC, Perazzo FF, Machado L, Bereau D Biomed Res Int 24-Dec-2013
PMCID:PMC3884605
doi:10.1155/2013/971745
PMID:24455743
Amazonian Plant Natural Products: Perspectives for Discovery of New Antimalarial Drug Leads Pohlit AM, Lima RB, Frausin G, Silva LF, Lopes SC, Moraes CB, Cravo P, Lacerda MV, Siqueira AM, Freitas-Junior LH, Costa FT Molecules 02-Aug-2013
PMCID:PMC6270278
doi:10.3390/molecules18089219
PMID:23917112

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,7S,10R,11R,14R,15S,16R,17R,19R,22R)-2,6,6,10,16-pentamethyl-17-(3-methyl-2-methylidenebutyl)-18,20-dioxahexacyclo[17.2.1.01,14.02,11.05,10.015,19]docosane-7,16,22-triol 163041555 Click to see CC(C)C(=C)CC1C(C2C3CCC4C5(CCC(C(C5CCC4(C36COC2(C6O)O1)C)(C)C)O)C)(C)O 502.70 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,5a-dicarboxylic acid 20056137 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/0031-9422(91)83076-W
(1S,2R,5S,7S,10R,11R,14R,15S,16S,18S,20S)-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosane-7,16-diol 162963946 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
[(1R,2R,5S,7S,10R,11R,14R,15S,16R,17R,19R,22R)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-16-hydroxy-2,6,6,10,16-pentamethyl-17-(3-methyl-2-methylidenebutyl)-18,20-dioxahexacyclo[17.2.1.01,14.02,11.05,10.015,19]docosan-22-yl] acetate 162971255 Click to see 853.00 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
[7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-16-hydroxy-2,6,6,10,16-pentamethyl-17-(3-methyl-2-methylidenebutyl)-18,20-dioxahexacyclo[17.2.1.01,14.02,11.05,10.015,19]docosan-22-yl] acetate 162971254 Click to see 853.00 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
2,6,6,10,16-Pentamethyl-17-(3-methyl-2-methylidenebutyl)-18,20-dioxahexacyclo[17.2.1.01,14.02,11.05,10.015,19]docosane-7,16,22-triol 163041554 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
2,6,6,10,16-Pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosane-7,16-diol 18360876 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)O)C)(C)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)90728-3
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(91)83076-W
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(91)83076-W
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)83076-W

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