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Bredemeyera floribunda

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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 UUID64400dcdaf588082278912
Scientific name Bredemeyera floribunda
Authority Willd.
First published in Neue Schriften Ges. Naturf. Freunde Berlin 3: 412 (1801)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bredemeyera floribunda f. elliptica Chodat Bull. Herb. Boissier , sér. 2, 3: 57 (1902)
Bredemeyera floribunda var. puberula Kuntze Revis. Gen. Pl. 3(2): 9 (1898)
Bredemeyera floribunda f. subvestita Chodat Bull. Herb. Boissier , sér. 2, 3: 57 (1902)
Bredemeyera lhotzkyana Klotzsch Naturw. Reise Mossambique 6(1): 117 (1861)
Catocoma floribunda Benth. J. Bot. (Hooker) 4: 102 (1841)
Comesperma floribundum A.St.-Hil. Ann. Soc. Roy. Sci. Orléans 9: 56 (1828)

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 South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Venezuelan Antilles
    • Northern South America
      • Guyana
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000572095
Tropicos 25900106
KEW urn:lsid:ipni.org:names:690122-1
The Plant List kew-2683195
Open Tree Of Life 597627
NCBI Taxonomy 174503
IUCN Red List 179279185
IPNI 690122-1
iNaturalist 705291
GBIF 7293394
EPPO BDMFL
EOL 5496298

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
Plant-Derived Toxin Inhibitors as Potential Candidates to Complement Antivenom Treatment in Snakebite Envenomations Adrião AA, dos Santos AO, de Lima EJ, Maciel JB, Paz WH, da Silva FM, Pucca MB, Moura-da-Silva AM, Monteiro WM, Sartim MA, Koolen HH Front Immunol 09-May-2022
PMCID:PMC9126284
doi:10.3389/fimmu.2022.842576
PMID:35615352
An Appraisal of Antidotes’ Effectiveness: Evidence of the Use of Phyto-Antidotes and Biotechnological Advancements Aruwa CE, Mukaila YO, Ajao AA, Sabiu S Molecules 26-Mar-2020
PMCID:PMC7181008
doi:10.3390/molecules25071516
PMID:32225103
Data on ICP OES and emulsion stability of Bredemeyera floribunda root extract: Medicinal plant used by the Brazilian rural population to treat snakebites Tschinkel PF, de Pádua Melo ES, Dutra ZM, de Lima NV, Arakaki DG, Rosa RH, Gonçalves DA, de Souza ID, Guimarães RD, Bogo D, do Nascimento VA Data Brief 23-Apr-2019
PMCID:PMC6503127
doi:10.1016/j.dib.2019.103940
PMID:31080856
Anti-ophidian activity of Bredemeyera floribunda Willd. (Polygalaceae) root extract on the local effects induced by Bothrops jararacussu venom Alves NT, Ximenes RM, Jorge RJ, Silveira JA, Santos JV, Rodrigues FA, Costa PH, Xavier FA Jr, Evangelista JS, Havt A, Soares VC, Toyama MH, Oliveira AN, Araújo RM, Alves RS, Monteiro HS Braz J Med Biol Res 03-Dec-2018
PMCID:PMC6293447
doi:10.1590/1414-431X20187581
PMID:30517287
A Review on Venom Enzymes Neutralizing Ability of Secondary Metabolites from Medicinal Plants Singh P, Yasir M, Hazarika R, Sugunan S, Shrivastava R J Pharmacopuncture 30-Sep-2017
PMCID:PMC5633669
doi:10.3831/KPI.2017.20.020
PMID:30087793
Do Herbal Medicines Have Potential for Managing Snake Bite Envenomation? Gupta YK, Peshin SS Toxicol Int 01-May-2012
PMCID:PMC3388772
doi:10.4103/0971-6580.97194
PMID:22778503
Über Triterpene, VI. Über die Sapogenine von <i>Bredemeyera floribunda</i> Willd Rudolf Tschesche, Achintya Kumar Sen Gupta Wiley 03-Jun-2007
doi:10.1002/CBER.19600930832
Pentaoxygenated xanthones from Bredemeyera floribunda Edilberto R. Silveira, Maria JoséC. Falcão, Alisio Menezes, David G.I. Kingston, Thomas E. Glass Elsevier BV 26-Jul-2002
doi:10.1016/0031-9422(95)00103-E
A new triterpenoid saponin, bredemeyeroside B. from the roots of Bredemeyera floribunda. Daros Mdo D, Matos FJ, Parente JP Planta Med 01-Dec-1996
doi:10.1055/S-2006-957962
PMID:9000884

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 / Terpene glycosides / Diterpene glycosides
(2S,3S,4R,4aS,6aS,8aR,12aR,13S,14aS,14bS)-13-(chloromethyl)-3-hydroxy-4,6a,11,11,14b-pentamethyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 162844742 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)CCl)C(=O)O)C 699.30 unknown https://doi.org/10.1002/CBER.19600930832
13-(chloromethyl)-3-hydroxy-4,6a,11,11,14b-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 162844741 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)CCl)C(=O)O)C 699.30 unknown https://doi.org/10.1002/CBER.19600930832
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4S,4aR,6aR,6bR,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6S)-4-[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162941197 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC4C(C(C(CO4)O)O)O)OC5C(C(CO5)(CO)O)O)O)OC(=O)C67CCC(CC6C8=CCC9C(C8(CC7)CO)(CCC1C9(CC(C(C1(C)C(=O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C)C)(C)C)C)O)O)O)O 1383.50 unknown https://doi.org/10.1055/S-2006-957962
8a-[3-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162941196 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC4C(C(C(CO4)O)O)O)OC5C(C(CO5)(CO)O)O)O)OC(=O)C67CCC(CC6C8=CCC9C(C8(CC7)CO)(CCC1C9(CC(C(C1(C)C(=O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C)C)(C)C)C)O)O)O)O 1383.50 unknown https://doi.org/10.1055/S-2006-957962
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids
13-(chloromethyl)-2,3-dihydroxy-4,6a,11,11,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 200662 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)CCl)C(=O)O)C 537.10 unknown https://doi.org/10.1002/CBER.19600930832
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids / 12-alpha-hydroxysteroids
(2S,3R,4S,4aS,6aR,8aS,12aR,13S,14aR,14bR)-13-(chloromethyl)-2,3-dihydroxy-4,6a,11,11,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 163076882 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)CCl)C(=O)O)C 537.10 unknown https://doi.org/10.1002/CBER.19600930832
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3S,4R,4aS,6aS,8aR,12aR,13S,14aS,14bS)-13-(chloromethyl)-2-hydroxy-4,6a,11,11,14b-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 162896531 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)CCl)C(=O)O)C 699.30 unknown https://doi.org/10.1002/CBER.19600930832
13-(chloromethyl)-2-hydroxy-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 162896530 Click to see CC1(CCC2(CCC3=C(C2C1)C(CC4C3(CCC5C4(CC(C(C5(C)C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)CCl)C(=O)O)C 699.30 unknown https://doi.org/10.1002/CBER.19600930832
> 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/10.1016/0031-9422(95)00103-E
1,7-Dihydroxy-3,4,8-trimethoxyxanthone 76317201 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C3=C(O2)C=CC(=C3OC)O)OC 318.28 unknown https://doi.org/10.1016/0031-9422(95)00103-E
2,6,8-Trihydroxy-1,5-dimethoxyxanthen-9-one 101929533 Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)OC)O 304.25 unknown https://doi.org/10.1016/0031-9422(95)00103-E
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1055/S-2006-957962

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