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Platymiscium floribundum

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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 UUID643fd76165cec014789590
Scientific name Platymiscium floribundum
Authority Vogel
First published in Linnaea11: 199 (1837)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Platymiscium floribundum var. floribundum Vogel Unknown
Platymiscium floribundum var. latifolium (Benth.) Benth. C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1B): 273 (1862)
Platymiscium floribundum var. nitens (Vogel) Klitg. Kew Bull.54: 971 (1999 publ. 2000)
Platymiscium floribundum var. obtusifolium (Harms) Klitg. Kew Bull.54: 971 (1999 publ. 2000)

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 Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000174222
Tropicos 13032011
KEW urn:lsid:ipni.org:names:515226-1
The Plant List ild-20338
Open Tree Of Life 786349
NCBI Taxonomy 500185
IUCN Red List 124099142
IPNI 515226-1
iNaturalist 461655
GBIF 2944754
EOL 638627
USDA GRIN 437021
CMAUP NPO24543

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
Heterologous biosynthesis of medicarpin using engineered Saccharomyces cerevisiae Lu C, Du R, Fu H, Zhang J, Zhao M, Wei Y, Lin W Synth Syst Biotechnol 23-Nov-2023
PMCID:PMC10711132
doi:10.1016/j.synbio.2023.11.003
PMID:38090379
In vitro and in vivo evaluation of antibacterial and anti-biofilm properties of five ethnomedicinal plants against oral bacteria by TEM Fathi F, Sadrnia M, Arjomandzadegan M, Mohajerani HR Avicenna J Phytomed 01-Mar-2021
PMCID:PMC8051319
PMID:33907676
Antitumor Potential of the Isoflavonoids (+)- and (−)-2,3,9-Trimethoxypterocarpan: Mechanism-of-Action Studies Farias K, da Costa RF, Meira AS, Diniz-Filho J, Bezerra EM, Freire VN, Guest P, Nikahd M, Ma X, Gardiner MG, Banwell MG, de Oliveira MD, de Moraes MO, do Ó Pessoa C ACS Med Chem Lett 20-May-2020
PMCID:PMC7294723
doi:10.1021/acsmedchemlett.0c00097
PMID:32551011
Protective effect of Platymiscium floribundum Vog. in tree extract on periodontitis inflammation in rats Freire JM, Chaves HV, Teixeira AH, de Sousa LH, Pinto IR, Costa JJ, de Sousa NA, Pereira KM, Girão VC, Ferreira VC, dos Santos JE, Lima MA, Pimenta AT, Montenegro RD, de Moraes ME, Pinto VD, Filho GC, Bezerra MM PLoS One 04-Nov-2019
PMCID:PMC6827912
doi:10.1371/journal.pone.0223800
PMID:31682614
Overview of the Structure–Function Relationships of Mannose-Specific Lectins from Plants, Algae and Fungi Barre A, Bourne Y, Van Damme EJ, Rougé P Int J Mol Sci 10-Jan-2019
PMCID:PMC6359319
doi:10.3390/ijms20020254
PMID:30634645
Natural products as new antimitotic compounds for anticancer drug development Paier CR, Maranhão SS, Carneiro TR, Lima LM, Rocha DD, da Silva Santos R, de Farias KM, de Moraes-Filho MO, Pessoa C Clinics (Sao Paulo) 27-Nov-2018
PMCID:PMC6256996
doi:10.6061/clinics/2018/e813s
PMID:30540125
Anticancer Properties of Graviola (Annona muricata): A Comprehensive Mechanistic Review Rady I, Bloch MB, Chamcheu RC, Banang Mbeumi S, Anwar MR, Mohamed H, Babatunde AS, Kuiate JR, Noubissi FK, El Sayed KA, Whitfield GK, Chamcheu JC Oxid Med Cell Longev 30-Jul-2018
PMCID:PMC6091294
doi:10.1155/2018/1826170
PMID:30151067
The Role of the MAPK Signaling, Topoisomerase and Dietary Bioactives in Controlling Cancer Incidence Selim KA, Abdelrasoul H, Aboelmagd M, Tawila AM Diseases 26-Apr-2017
PMCID:PMC5547980
doi:10.3390/diseases5020013
PMID:28933366
Different susceptibilities of Leishmania spp. promastigotes to the Annona muricata acetogenins annonacinone and corossolone, and the Platymiscium floribundum coumarin scoparone Vila-Nova NS, de Morais SM, Falcão MJ, Alcantara TT, Ferreira PA, Cavalcanti ES, Vieira IG, Campello CC, Wilson M Exp Parasitol 08-Dec-2012
PMCID:PMC5426951
doi:10.1016/j.exppara.2012.11.025
PMID:23232251
Identity and relationships of the Arboreal Caatinga among other floristic units of seasonally dry tropical forests (SDTFs) of north-eastern and Central Brazil Santos RM, Oliveira-Filho AT, Eisenlohr PV, Queiroz LP, Cardoso DB, Rodal MJ Ecol Evol 01-Feb-2012
PMCID:PMC3298952
doi:10.1002/ece3.91
PMID:22423333
Chemical Composition and Botanical Origin of Red Propolis, a New Type of Brazilian Propolis Silva BB, Rosalen PL, Cury JA, Ikegaki M, Souza VC, Esteves A, Alencar SM Evid Based Complement Alternat Med 07-Jul-2007
PMCID:PMC2529384
doi:10.1093/ecam/nem059
PMID:18830449
Induction of apoptosis by pterocarpans from Platymiscium floribundum in HL-60 human leukemia cells. Militão GC, Dantas IN, Pessoa C, Falcão MJ, Silveira ER, Lima MA, Curi R, Lima T, Moraes MO, Costa-Lotufo LV Life Sci 11-Apr-2006
doi:10.1016/J.LFS.2005.09.044
PMID:16316665
Antimitotic properties of pterocarpans isolated from Platymiscium floribundum on sea urchin eggs. Militão GC, Jimenez PC, Wilke DV, Pessoa C, Falcão MJ, Sousa Lima MA, Silveira ER, de Moraes MO, Costa-Lotufo LV Planta Med 01-Jul-2005
doi:10.1055/S-2005-871277
PMID:16041657
Cytotoxic flavonoids from Platymiscium floribundum. Falcão MJ, Pouliquem YB, Lima MA, Gramosa NV, Costa-Lotufo LV, Militão GC, Pessoa C, de Moraes MO, Silveira ER J Nat Prod 01-Mar-2005
doi:10.1021/NP049854D
PMID:15787450

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,3R)-2-azaniumyl-3-hydroxybutanoate 6971019 Click to see CC(C(C(=O)[O-])[NH3+])O 119.12 unknown via CMAUP database
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(2S)-4-amino-2-ammonio-4-oxobutanoate 6992089 Click to see C(C(C(=O)[O-])[NH3+])C(=O)N 132.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-(7-Hydroxy-6-methoxy-4-oxochromen-3-yl)-5-methoxycyclohexa-2,5-diene-1,4-dione 101757825 Click to see COC1=CC(=O)C(=CC1=O)C2=COC3=CC(=C(C=C3C2=O)OC)O 328.27 unknown https://doi.org/10.1021/NP049854D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1021/NP049854D
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1021/NP049854D
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1016/J.LFS.2005.09.044
https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
(6aS,11aS)-2,3,9-trimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 71182772 Click to see COC1=CC2=C(C=C1)C3COC4=CC(=C(C=C4C3O2)OC)OC 314.30 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
https://doi.org/10.1016/J.LFS.2005.09.044
(6aS,11aS)-3-methoxy-2-(3-methylbut-2-en-1-yl)-6H-[1]benzofuro[3,2-c][1]benzopyran-6a,9(11aH)-diol 92470518 Click to see CC(=CCC1=CC2=C(C=C1OC)OCC3(C2OC4=C3C=CC(=C4)O)O)C 354.40 unknown via CMAUP database
(6aS,11aS)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,4-diol 102184129 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)O 286.28 unknown https://doi.org/10.1016/J.LFS.2005.09.044
https://doi.org/10.1055/S-2005-871277
https://doi.org/10.1021/NP049854D
2,3,9-Trimethoxypterocarpan 11151159 Click to see COC1=CC2=C(C=C1)C3COC4=CC(=C(C=C4C3O2)OC)OC 314.30 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
https://doi.org/10.1016/J.LFS.2005.09.044
3,9-Dimethoxypterocarpan 454892 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1016/J.LFS.2005.09.044
https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
4-Hydroxy-2,3,9-trimethoxypterocarpan 12218867 Click to see COC1=CC2=C(C=C1)C3COC4=C(C(=C(C=C4C3O2)OC)OC)O 330.30 unknown https://doi.org/10.1021/NP049854D
4-Hydroxymedicarpin 11536537 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)O 286.28 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1016/J.LFS.2005.09.044
https://doi.org/10.1055/S-2005-871277
6H-Benzofuro(3,2-c)(1)benzopyran, 6a,11a-dihydro-3,9-dimethoxy-, (6aR,11aR)-rel- 364159 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
https://doi.org/10.1016/J.LFS.2005.09.044
6H-Benzofuro[3,2-c][1]benzopyran-3,10-diol, 6a,11a-dihydro-9-methoxy-, (6aS,11aS)- 44446857 Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1055/S-2005-871277
https://doi.org/10.1016/J.LFS.2005.09.044
https://doi.org/10.1021/NP049854D
Glyceollin 162807 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4(C3OC5=C4C=CC(=C5)O)O)C 338.40 unknown via CMAUP database
Glyceollin Ii 181883 Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4(C3OC5=C4C=CC(=C5)O)O)C 338.40 unknown via CMAUP database
Glyceollin Iii 11954193 Click to see CC(=C)C1CC2=CC3=C(C=C2O1)OCC4(C3OC5=C4C=CC(=C5)O)O 338.40 unknown via CMAUP database
Homopterocarpin 101795 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1021/NP049854D
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/NP049854D
Vesticarpan 44257448 Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1021/NP049854D
https://doi.org/10.1055/S-2005-871277
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-[3-(2-Hydroxy-4-methoxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxy-6-methoxy-3-(4-methoxyphenyl)chromen-4-one 11169313 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4=C(C=C5C(=C4)OC=C(C5=O)C6=C(C=C(C=C6)OC)O)OC 594.60 unknown https://doi.org/10.1021/NP049854D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP049854D
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP049854D

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