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Strychnos pseudoquina

Strychnos pseudoquina - 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 UUID644054660e197666025730
Scientific name Strychnos pseudoquina
Authority A.St.-Hil.
First published in Mém. Mus. Hist. Nat. 9: 340 (1822)

Description Top

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Synonyms Top

Scientific name Authority First published in
Strychnos pseudochina Benth. J. Proc. Linn. Soc., Bot. 1: 104 (1856)
Geniostoma febrifugum Spreng. Syst. Veg. 1: 588 (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
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001229072
Tropicos 50059195
KEW urn:lsid:ipni.org:names:547425-1
The Plant List tro-50059195
Open Tree Of Life 651464
NCBI Taxonomy 1040919
IPNI 547425-1
GBIF 7289399

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
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Plant-Derived Epi-Nutraceuticals as Potential Broad-Spectrum Anti-Viral Agents Gabbianelli R, Shahar E, de Simone G, Rucci C, Bordoni L, Feliziani G, Zhao F, Ferrati M, Maggi F, Spinozzi E, Mahajna J Nutrients 08-Nov-2023
PMCID:PMC10675658
doi:10.3390/nu15224719
PMID:38004113
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
A First Look at the Inhibitory Potential of Urospatha sagittifolia (Araceae) Ethanolic Extract for Bothrops atrox Snakebite Envenomation Vera-Palacios AL, Sacoto-Torres JD, Hernández-Altamirano JA, Moreno A, Peñuela-Mora MC, Salazar-Valenzuela D, Mogollón NG, Almeida JR Toxins (Basel) 17-Jul-2022
PMCID:PMC9315696
doi:10.3390/toxins14070496
PMID:35878234
Tryptophan and Biogenic Amines in the Differentiation and Quality of Honey Borges CV, Nunes A, Costa VE, Orsi RD, Basilio LS, Monteiro GC, Maraschin M, Lima GP Int J Tryptophan Res 26-May-2022
PMCID:PMC9152190
doi:10.1177/11786469221102098
PMID:35656455
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Traditional Knowledge to Contemporary Medication in the Treatment of Infectious Disease Dengue: A Review Dhiman M, Sharma L, Dadhich A, Dhawan P, Sharma MM Front Pharmacol 14-Mar-2022
PMCID:PMC8963989
doi:10.3389/fphar.2022.750494
PMID:35359838
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
Limited Treatment Options for Diabetic Wounds: Barriers to Clinical Translation Despite Therapeutic Success in Murine Models Barakat M, DiPietro LA, Chen L Adv Wound Care (New Rochelle) 17-Jun-2021
PMCID:PMC8236303
doi:10.1089/wound.2020.1254
PMID:33050829
Green Approach: ‘‘A Forwarding Step for Curing Leishmaniasis—A Neglected Tropical Disease’’ Sharma L, Dhiman M, Singh A, Sharma MM Front Mol Biosci 28-May-2021
PMCID:PMC8193676
doi:10.3389/fmolb.2021.655584
PMID:34124148
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
Medicinal Plants and Herbal Products From Brazil: How Can We Improve Quality? Palhares RM, Baratto LC, Scopel M, Mügge FL, Brandão MG Front Pharmacol 27-Jan-2021
PMCID:PMC7873041
doi:10.3389/fphar.2020.606623
PMID:33584281
Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules Mohan S, Elhassan Taha MM, Makeen HA, Alhazmi HA, Al Bratty M, Sultana S, Ahsan W, Najmi A, Khalid A Molecules 22-Oct-2020
PMCID:PMC7659943
doi:10.3390/molecules25214878
PMID:33105694
Plants Metabolites: Possibility of Natural Therapeutics Against the COVID-19 Pandemic Bhuiyan FR, Howlader S, Raihan T, Hasan M Front Med (Lausanne) 07-Aug-2020
PMCID:PMC7427128
doi:10.3389/fmed.2020.00444
PMID:32850918

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
> Alkaloids and derivatives / Strychnos alkaloids
(1S,9S,10E,11S,12E,17R)-12-ethylidene-10-(hydroxymethylidene)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-17-ol 11771312 Click to see CC=C1CN2CCC34C2(CC1C(=CO)C3NC5=CC=CC=C45)O 310.40 unknown https://doi.org/10.1248/CPB.53.881
11-Methoxydiaboline 13994712 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C=C(C=C6)OC 382.50 unknown https://doi.org/10.1021/NP50036A007
12-Ethylidene-10-(hydroxymethylidene)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-17-ol 73023471 Click to see CC=C1CN2CCC34C2(CC1C(=CO)C3NC5=CC=CC=C45)O 310.40 unknown https://doi.org/10.1248/CPB.53.881
Diaboline 12312946 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=CC=CC=C61 352.40 unknown https://doi.org/10.1021/NP50036A007
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1021/NP50036A007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.53.881
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1002/CHIN.200603190
https://doi.org/10.1248/CPB.53.881
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1248/CPB.53.881
https://doi.org/10.1002/CHIN.200603190
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1248/CPB.53.881
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Strychnobiflavone 5491475 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2C3=C(C=CC(=C3O)O)C4=C(C(=O)C5=C(C=C(C=C5O4)O)O)OC)O)O)C6=CC(=C(C=C6)O)O 630.50 unknown https://doi.org/10.1021/NP50036A007

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