Amburana cearensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Amburana cearensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fd8e9c98d7674401730
Scientific name Amburana cearensis
Authority (Allemão) A.C.Sm.
First published in Trop. Woods62: 30 (1940)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amburana claudii Schwacke & Taub. H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam.3(3): 387 (1894)
Torresea cearensis Allemão Trab. Comm. Sci. Expl., Bot.2: 17 (1864)

Common names Top

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Language Common/alternative name
Spanish umburana do cheiro
gn trébol
gn yvyra piriri guasu
Japanese アンブラナ・ケアレンシス
Lithuanian paprastasis rievonis
Dutch cumaru-nordestino
Portuguese cumaru-nordestino
Quechua ishpinku
Chinese 巴拉圭豆
Chinese 巴西良木豆

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 North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000182165
UNII M6F7BTP61E
Tropicos 13015576
KEW urn:lsid:ipni.org:names:11101-2
The Plant List ild-28260
Open Tree Of Life 1053008
NCBI Taxonomy 149628
IUCN Red List 32291
IPNI 11101-2
iNaturalist 189204
GBIF 2945821
Freebase /m/02vsx5n
EOL 642758
USDA GRIN 313272
Wikipedia Amburana_cearensis

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
Short-term restoration practices change the bacterial community in degraded soil from the Brazilian semiarid Silva DE, Costa RM, Campos JR, Rocha SM, de Araujo Pereira AP, Melo VM, Oliveira FA, de Alcantara Neto F, Mendes LW, Araujo AS Sci Rep 21-Mar-2024
PMCID:PMC10957980
doi:10.1038/s41598-024-57690-y
PMID:38514851
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Plant parentage influences the type of timber use by traditional peoples of the Brazilian Caatinga Pedrosa KM, Ramos MB, La Torre-Cuadros MD, Lopes SD PLoS One 17-Oct-2023
PMCID:PMC10581497
doi:10.1371/journal.pone.0286434
PMID:37847702
Brazilian Amazon Red Propolis: Leishmanicidal Activity and Chemical Composition of a New Variety of Red Propolis Dutra RP, de Sousa MM Jr, Mignoni MS, de Oliveira KG, Pereira EB, Figueredo AS, da Costa AA, Dias TG, Vasconcelos CC, Silva LA, Reis AS, Lopes AJ Metabolites 21-Sep-2023
PMCID:PMC10535413
doi:10.3390/metabo13091027
PMID:37755307
Amburana cearensis seed extract stimulates astrocyte glutamate homeostatic mechanisms in hippocampal brain slices and protects oligodendrocytes against ischemia Ferreira RS, Ribeiro PR, Silva JH, Hoppe JB, de Almeida MM, de Lima Ferreira BC, Andrade GB, de Souza SB, Ferdandez LG, de Fátima Dias Costa M, Salbego CG, Rivera AD, Longoni A, de Assis AM, Pieropan F, Moreira JC, Costa SL, Butt AM, da Silva VD BMC Complement Med Ther 11-May-2023
PMCID:PMC10173544
doi:10.1186/s12906-023-03959-0
PMID:37170258
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
Plant-Derived Compounds and Extracts as Modulators of Plasmin Activity—A Review Kolodziejczyk-Czepas J, Czepas J Molecules 09-Feb-2023
PMCID:PMC9965408
doi:10.3390/molecules28041677
PMID:36838662
Natural Flavonoid Derivatives Have Pan-Coronavirus Antiviral Activity Mori M, Quaglio D, Calcaterra A, Ghirga F, Sorrentino L, Cammarone S, Fracella M, D’Auria A, Frasca F, Criscuolo E, Clementi N, Mancini N, Botta B, Antonelli G, Pierangeli A, Scagnolari C Microorganisms 25-Jan-2023
PMCID:PMC9960971
doi:10.3390/microorganisms11020314
PMID:36838279
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
Vegetation cover and seasonality as indicators for selection of forage resources by local agro-pastoralists in the Brazilian semiarid region da Cunha SS, Ramos MB, de Almeida HA, Maciel MG, de Souza SM, Pedrosa KM, de Faria Lopes S Sci Rep 07-Sep-2022
PMCID:PMC9452531
doi:10.1038/s41598-022-18282-w
PMID:36071152
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
How Do Taxonomic and Functional Diversity Metrics Change Along an Aridity Gradient in a Tropical Dry Forest? de Oliveira AC, Nunes A, Oliveira MA, Rodrigues RG, Branquinho C Front Plant Sci 07-Jul-2022
PMCID:PMC9302379
doi:10.3389/fpls.2022.923219
PMID:35873975
Assessment of Biodiversity in Food Consumption Studies: A Systematic Review de Medeiros MF, Silva SG, Teixeira CD, Lima SC, Marchioni DM, Jacob MC Front Nutr 14-Jun-2022
PMCID:PMC9237621
doi:10.3389/fnut.2022.832288
PMID:35774537
Amburana cearensis leaf extract protects against cisplatin-induced ovarian damage through regulation of p-PTEN and p-Akt proteins in mice Gouveia BB, Barberino RS, Menezes VG, Monte AP, Silva RL, Palheta Jr RC, Rolim LA, Pereira EC, Oliveira Jr RG, Almeida JR, Matos MH Iran J Basic Med Sci 01-Jun-2022
PMCID:PMC9320200
doi:10.22038/IJBMS.2022.58927.13092
PMID:35949305

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1002/PTR.1139
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1590/S0103-50532010000900022
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones / Ubiquinones
2,3-Dimethoxy-5-(7-methoxy-4-oxochromen-3-yl)cyclohexa-2,5-diene-1,4-dione 162956306 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC(=O)C(=C(C3=O)OC)OC 342.30 unknown https://doi.org/10.1590/S0103-50532011000200025
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(3,4-dihydroxybenzoyl)oxymethyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4-dihydroxybenzoate 162955188 Click to see C1=CC(=CC=C1COC(=O)C2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C=C4)O)O)O)O)O 558.50 unknown https://doi.org/10.1590/S0103-50532010000900022
[(2R,3S,4S,5R,6S)-6-[4-[(3,4-dihydroxybenzoyl)oxymethyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162918643 Click to see C1=CC(=CC=C1COC(=O)C2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 574.50 unknown https://doi.org/10.1590/S0103-50532010000900022
[4-[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]methyl 3,4-dihydroxybenzoate 162987804 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)COC(=O)C3=CC(=C(C=C3)O)O)O)O)O 464.40 unknown https://doi.org/10.1590/S0103-50532010000900022
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 3,4-dihydroxybenzoate 13917001 Click to see C1=CC(=CC=C1COC(=O)C2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1590/S0103-50532010000900022
https://doi.org/10.1016/S0031-9422(98)00497-X
https://doi.org/10.1055/S-2008-1074501
Amburoside A 10409977 Click to see C1=CC(=CC=C1COC(=O)C2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(98)00497-X
https://doi.org/10.1590/S0103-50532010000900022
https://doi.org/10.1055/S-2008-1074501
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(3,4,5-Trimethoxyphenyl)-2-propenal 36798 Click to see COC1=CC(=CC(=C1OC)OC)C=CC=O 222.24 unknown https://doi.org/10.1590/S0103-50532011000200025
3,4,5-Trimethoxycinnamaldehyde 5839209 Click to see COC1=CC(=CC(=C1OC)OC)C=CC=O 222.24 unknown https://doi.org/10.1590/S0103-50532011000200025
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2-Hydroxycinnamic acid, (2E)- 637540 Click to see C1=CC=C(C(=C1)C=CC(=O)O)O 164.16 unknown https://doi.org/10.1590/S0103-50532010000900022
ortho-Hydroxycinnamic acid 11968 Click to see C1=CC=C(C(=C1)C=CC(=O)O)O 164.16 unknown https://doi.org/10.1590/S0103-50532010000900022
> Phenylpropanoids and polyketides / Coumarins and derivatives
(2-Oxochromen-6-yl) 3,4-dihydroxybenzoate 162916908 Click to see C1=CC(=C(C=C1C(=O)OC2=CC3=C(C=C2)OC(=O)C=C3)O)O 298.25 unknown https://doi.org/10.1590/S0103-50532010000900022
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1590/S0103-50532010000900022
https://doi.org/10.1016/S0944-7113(97)80071-2
https://doi.org/10.1016/S0031-9422(98)00497-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxycoumarin 99477 Click to see C1=CC2=C(C=CC(=O)O2)C=C1O 162.14 unknown https://doi.org/10.1590/S0103-50532010000900022
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1002/PTR.1139
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown https://doi.org/10.1016/S0944-7113(97)80071-2
https://doi.org/10.1002/PTR.1139
https://doi.org/10.1590/S0103-50532010000900022
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
3-(3-Hydroxy-4-methoxyphenyl)-6,7-dimethoxychromen-4-one 163082857 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC)O 328.30 unknown https://doi.org/10.1590/S0103-50532011000200025
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7-hydroxy-4H-chromen-4-one 5748605 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC 298.29 unknown https://doi.org/10.1590/S0103-50532011000200025
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1590/S0103-50532010000900022
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one 638205 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)OC)OC 342.30 unknown https://doi.org/10.1590/S0103-50532011000200025
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-one 118586 Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1590/S0103-50532011000200025
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/10.1590/S0103-50532011000200025
Homobutein 6438092 Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1590/S0103-50532011000200025
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/10.1590/S0103-50532011000200025
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 4-hydroxy-3-methoxybenzoate 10478156 Click to see COC1=C(C=CC(=C1)C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(98)00497-X
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 4-hydroxy-3-methoxybenzoate 85154042 Click to see COC1=C(C=CC(=C1)C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(98)00497-X

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