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Polygala cyparissias

Polygala cyparissias - 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 UUID64404b3936df8762657970
Scientific name Polygala cyparissias
Authority A.St.-Hil.
First published in Ann. Soc. Roy. Sci. Orléans 9: 47 (1828)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polygala corisoides A.St.-Hil. & Moq. Ann. Soc. Roy. Sci. Orléans 9: 47. 1828 [17 Nov 1828]
Polygala cyparissias var. corisoides Chodat Mém. Soc. Phys. Genève 31, pt. 2, no. 2: 296. 1893

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Uruguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001100126
Tropicos 25900236
KEW urn:lsid:ipni.org:names:691332-1
The Plant List tro-25900236
Open Tree Of Life 762194
NCBI Taxonomy 690779
IPNI 691332-1
GBIF 7293516

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
Flavonoids-Rich Plant Extracts Against Helicobacter pylori Infection as Prevention to Gastric Cancer Ivyna de Araújo Rêgo R, Guedes Silvestre GF, Ferreira de Melo D, Albino SL, Pimentel MM, Silva Costa Cruz SB, Silva Wurzba SD, Rodrigues WF, Goulart de Lima Damasceno BP, Cançado Castellano LR Front Pharmacol 31-Aug-2022
PMCID:PMC9470917
doi:10.3389/fphar.2022.951125
PMID:36120379
Plants against Helicobacter pylori to combat resistance: An ethnopharmacological review Baker DA Biotechnol Rep (Amst) 21-May-2020
PMCID:PMC7248673
doi:10.1016/j.btre.2020.e00470
PMID:32477900
Evaluation of Biological Activity of Polygala Boliviensis in Experimental Models Carneiro da Rocha JL, Araujo de Tripodi Calumby RF, da Silva DF, Neves Brandão H, Flora Villarreal C, de Lima FO Iran J Pharm Res 01-Mar-2019
PMCID:PMC6706750
doi:10.22037/ijpr.2019.1100655
PMID:31531062
Astragalin: A Bioactive Phytochemical with Potential Therapeutic Activities Riaz A, Rasul A, Hussain G, Zahoor MK, Jabeen F, Subhani Z, Younis T, Ali M, Sarfraz I, Selamoglu Z Adv Pharmacol Sci 02-May-2018
PMCID:PMC5954929
doi:10.1155/2018/9794625
PMID:29853868
Exploring the Links between Ethnobotany, Local Therapeutic Practices, and Protected Areas in Santa Catarina Coastline, Brazil Zank S, Hanazaki N Evid Based Complement Alternat Med 17-Nov-2011
PMCID:PMC3235720
doi:10.1155/2012/563570
PMID:22203874
Antifungal activity of five species of Polygala Johann S, Mendes BG, Missau FC, de Resende MA, Pizzolatti MG Braz J Microbiol 01-Sep-2011
PMCID:PMC3768791
doi:10.1590/S1517-838220110003000027
PMID:24031724
Three xanthones from Polygala cyparissias Tânia R. Pinheiro, Valdir Cechinel Filho, Adair R.S. Santos, João B. Calixto, Franco Delle Monache, Moacir G. Pizzolatti, Rosendo A. Yunes Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00051-X
In vitro effect of the extract and the 1,7-dihydroxy-2,3-dimethoxy xanthone from Polygala cyparissias on the contractions induced by inflammatory mediators and ovalbumin in normal and actively sensitised trachea from guinea pig. El Sayah M, Cechinel-Filho V, Pinheiro TR, Yunes RA, Calixto JB Inflamm Res 01-Apr-1999
doi:10.1007/S000110050449
PMID:10344473

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 / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
Sterol 1107 Click to see C1CC2CCC3C4CCC(CC4CCC3C2C1)O 248.40 Unspecified https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10420973/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 137706369 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 521229 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 Unspecified, unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10420973/
https://doi.org/10.1016/S0031-9422(98)00051-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6-Trihydroxy-2,7-dimethoxyxanthen-9-one 5320291 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
1,3,7-Trihydroxy-2-methoxyxanthone 12133315 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O 274.22 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
1,7-Dihydroxy-2,3-dimethoxyxanthone 10039726 Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)OC 288.25 unknown https://doi.org/10.1007/S000110050449
https://doi.org/10.1016/S0031-9422(98)00051-X
1,7-Dihydroxy-2,3-methylenedioxyxanthone 5316803 Click to see C1OC2=C(O1)C(=C3C(=C2)OC4=C(C3=O)C=C(C=C4)O)O 272.21 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
2,7-Dimethoxy-1,3,6,8-tetrahydroxyxanthone 15380735 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)O)O 320.25 unknown https://doi.org/10.1016/S0031-9422(98)00051-X
Isogentisin 5281640 Click to see COC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(98)00051-X

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