Fridericia platyphylla - Unknown
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Internal ID UUID644027390a0e7537034467
Scientific name Fridericia platyphylla
Authority (Cham.) L.G.Lohmann
First published in Ann. Missouri Bot. Gard. 99: 442 (2014)

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Synonyms Top

Scientific name Authority First published in
Bignonia brachypoda var. acutifolia DC. Prodr. 9: 145 (1845)
Bignonia brachypoda var. cuneata DC. Prodr. 9: 145 (1845)
Bignonia brachypoda var. elliptica DC. Prodr. 9: 145 (1845)
Bignonia brachypoda var. firmula DC. Prodr. 9: 146 (1845)
Bignonia brachypoda var. heterophylla DC. Prodr. 9: 145 (1845)
Arrabidaea brachypoda var. acuminata Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. attenuata Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. cuneata Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. firma Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. induta Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. platyphylla Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea brachypoda var. rigida Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Arrabidaea platyphylla var. acuminata Bureau & K.Schum. Fl. Bras. 8(2): 39 (1896)
Arrabidaea platyphylla var. cuneata Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. elliptica Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. firma Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. firmula Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. heterophylla Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. induta Bureau & K.Schum. Fl. Bras. 8(2): 39 (1896)
Arrabidaea platyphylla var. lasiorrhachis Bureau & K.Schum. Fl. Bras. 8(2): 40 (1896)
Arrabidaea platyphylla var. puberula Bureau & K.Schum. Fl. Bras. 8(2): 41 (1896)
Arrabidaea platyphylla var. stricta Bureau & K.Schum. Fl. Bras. 8(2): 41 (1896)
Petastoma simplicifolium Miers Proc. Roy. Hort. Soc. London 3: 194 (1863)
Bignonia brachypoda var. pubescens Sond. Linnaea 22: 559. 1849
Arrabidaea brachypoda Bureau Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1893: 98 (1894)
Bignonia platyphylla Cham. Linnaea 7: 679 (1832)
Bignonia regnelliana Sond. Linnaea 22: 558 (1849)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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 North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Northern South America
      • Guyana
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000778656
Tropicos 100193256
KEW urn:lsid:ipni.org:names:77142054-1
The Plant List kew-317212
Open Tree Of Life 420427
NCBI Taxonomy 353935
IPNI 77142054-1
iNaturalist 854054
GBIF 8235385

Genomes (via NCBI) Top

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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
Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis da Costa CS, Marques EM, do Nascimento JR, Lima VA, Santos-Oliveira R, Figueredo AS, de Jesus CM, de Souza Nunes GC, Brandão CM, de Jesus ET, Sa MC, Tanaka AA, Braga G, Santos AC, de Lima RB, Silva LA, Alencar LM, da Rocha CQ, Gonçalves RS Pharmaceutics 08-Feb-2024
PMCID:PMC10891960
doi:10.3390/pharmaceutics16020252
PMID:38399306
From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 14-Oct-2023
PMCID:PMC10609244
doi:10.3390/molecules28207089
PMID:37894567
In vitro activity and mechanism of cell death induction of cyanomethyl vinyl ethers derivatives against Trypanosoma cruzi Bethencourt-Estrella CJ, Delgado-Hernández S, López-Arencibia A, San Nicolás-Hernández D, Tejedor D, García-Tellado F, Lorenzo-Morales J, Piñero JE Int J Parasitol Drugs Drug Resist 31-May-2023
PMCID:PMC10276036
doi:10.1016/j.ijpddr.2023.05.001
PMID:37311268
Flavonoid brachydin B decreases viability, proliferation, and migration in human metastatic prostate (DU145) cells grown in 2D and 3D culture models Serpeloni JM, Ribeiro DL, Weiss GF, de Oliveira LC, Fujiike AY, Nunes HL, da Rocha CQ, Guembarovski RL, Cólus IM Toxicol Res (Camb) 01-Apr-2023
PMCID:PMC10141769
doi:10.1093/toxres/tfad019
PMID:37125333
Therapeutic Potential of Luteolin on Cancer Çetinkaya M, Baran Y Vaccines (Basel) 27-Feb-2023
PMCID:PMC10057337
doi:10.3390/vaccines11030554
PMID:36992138
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294
The Major Facilitator Superfamily and Antimicrobial Resistance Efflux Pumps of the ESKAPEE Pathogen Staphylococcus aureus Stephen J, Salam F, Lekshmi M, Kumar SH, Varela MF Antibiotics (Basel) 07-Feb-2023
PMCID:PMC9952236
doi:10.3390/antibiotics12020343
PMID:36830254
Antibacterial potential of chalcones and its derivatives against Staphylococcus aureus da Silva L, Donato IA, Gonçalves CA, Scherf JR, dos Santos HS, Mori E, Coutinho HD, da Cunha FA 3 Biotech 01-Dec-2022
PMCID:PMC9712905
doi:10.1007/s13205-022-03398-7
PMID:36466769
The Current State of Knowledge in Biological Properties of Cirsimaritin Benali T, Jaouadi I, Ghchime R, El Omari N, Harboul K, Hammani K, Rebezov M, Shariati MA, Mubarak MS, Simal-Gandara J, Zengin G, Park MN, Kim B, Mahmud S, Lee LH, Bouyahya A Antioxidants (Basel) 19-Sep-2022
PMCID:PMC9495358
doi:10.3390/antiox11091842
PMID:36139916
A Review of the Phytochemistry and Pharmacological Properties of the Genus Arrabidaea do Nascimento JR, de Jesus Alves Miranda A, Vieira FC, Rodrigues CD, Vasconcelos LN, Filho JL, Lopes AC, Tangerina MM, Vilegas W, da Rocha CQ Pharmaceuticals (Basel) 25-May-2022
PMCID:PMC9227117
doi:10.3390/ph15060658
PMID:35745577
The Antitumoral/Antimetastatic Action of the Flavonoid Brachydin A in Metastatic Prostate Tumor Spheroids In Vitro Is Mediated by (Parthanatos) PARP-Related Cell Death Ribeiro DL, Tuttis K, de Oliveira LC, Serpeloni JM, Gomes IN, Lengert AV, da Rocha CQ, Reis RM, Cólus IM, Antunes LM Pharmaceutics 29-Apr-2022
PMCID:PMC9147598
doi:10.3390/pharmaceutics14050963
PMID:35631550
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
Antiproliferative Activity of Two Unusual Dimeric Flavonoids, Brachydin E and Brachydin F, Isolated from Fridericia platyphylla (Cham.) L.G.Lohmann: In Vitro and Molecular Docking Evaluation de Lima CA, Cubero MC, Franco YE, Rodrigues CD, do Nascimento JR, Vendramini-Costa DB, Sciani JM, da Rocha CQ, Longato GB Biomed Res Int 11-Feb-2022
PMCID:PMC8856817
doi:10.1155/2022/3319203
PMID:35187163
Chalcone Scaffolds, Bioprecursors of Flavonoids: Chemistry, Bioactivities, and Pharmacokinetics Rudrapal M, Khan J, Dukhyil AA, Alarousy RM, Attah EI, Sharma T, Khairnar SJ, Bendale AR Molecules 26-Nov-2021
PMCID:PMC8659147
doi:10.3390/molecules26237177
PMID:34885754
Aglycone flavonoid brachydin A shows selective cytotoxicity and antitumoral activity in human metastatic prostate (DU145) cancer cells de Oliveira LC, Nunes HL, Ribeiro DL, do Nascimento JR, da Rocha CQ, de Syllos Cólus IM, Serpeloni JM Cytotechnology 29-Sep-2021
PMCID:PMC8554999
doi:10.1007/s10616-021-00495-y
PMID:34776627

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/BF00985673
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00985673
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(6S,6aR,7S,12aR)-1,8-dimethoxy-6-phenyl-7-[(E)-2-phenylethenyl]-6,6a,7,12a-tetrahydrochromeno[3,2-c]chromene-3,10-diol 90682495 Click to see COC1=CC(=CC2=C1C(C3C(OC4=C(C3O2)C(=CC(=C4)O)OC)C5=CC=CC=C5)C=CC6=CC=CC=C6)O 508.60 unknown https://doi.org/10.1021/NP401060J
(6S,6aR,7S,12aR)-1,8-dimethoxy-7-[(E)-2-(4-methoxyphenyl)ethenyl]-6-phenyl-6,6a,7,12a-tetrahydrochromeno[3,2-c]chromene-3,10-diol 90682494 Click to see COC1=CC=C(C=C1)C=CC2C3C(OC4=C(C3OC5=C2C(=CC(=C5)O)OC)C(=CC(=C4)O)OC)C6=CC=CC=C6 538.60 unknown https://doi.org/10.1021/NP401060J
(6S,6aR,7S,12aR)-7-[(E)-2-(4-hydroxyphenyl)ethenyl]-1,8-dimethoxy-6-phenyl-6,6a,7,12a-tetrahydrochromeno[3,2-c]chromene-3,10-diol 90682493 Click to see COC1=CC(=CC2=C1C(C3C(OC4=C(C3O2)C(=CC(=C4)O)OC)C5=CC=CC=C5)C=CC6=CC=C(C=C6)O)O 524.60 unknown https://doi.org/10.1021/NP401060J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/S0305-1978(01)00149-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4'-Dihydroxy-5,6,7-trimethoxyflavone 9967964 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)OC)OC 344.30 unknown https://doi.org/10.1016/S0305-1978(01)00149-1
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1016/S0305-1978(01)00149-1
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0305-1978(01)00149-1

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