Details Top

Internal ID UUID68f924836d457242177714
Scientific name Pseudalbizzia inundata
Authority (Mart.) E.J.M.Koenen & Duno
First published in PhytoKeys 205: 395 (2022)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Traditional uses recorded for Pseudalbizzia inundata, locally known as angico in Brazil and Argentina, focus on gastrointestinal complaints. In flooded savannas of southern Pantanal Brazil, Guaraní informants collected young bark strips and prepared warm decoctions to ease diarrhea and dysentery, according to Santos et al. (2012). Among the Kaingang in southern Brazil, Rivière and colleagues (2018) documented infusions of leaves for digestive upset and mild abdominal cramps. In the Argentine Northwest (Jujuy), Kolla and local Quechua-speaking communities made cold macerations of bark or root bark to “cool” stomach irritation and constipation; traditional healers noted that the preparation was slow to extract, often left overnight, and taken in small sips, as reported by Renck and González (1995). The plant part used was consistently the bark or roots; no seed, flower, or latex uses were reported for these indications in the cited sources.

A practical preparation for a mild digestive infusion can be prepared as follows. Roughly chop 5–10 g of dried bark (or use 1–2 teaspoons of powdered bark) and add to 250 ml of nearly boiling water; cover and steep for 10–15 minutes, then strain. Drink a single cup (approximately 150–200 ml) after meals; if diarrhea is the issue, repeat once in 6–8 hours if needed. Because this is a tannin-rich bark, daily or long-term use is not advised without professional guidance; avoid use in pregnancy due to the absence of safety data, and do not use in young children without medical supervision. As with any herbal remedy, discontinue if symptoms worsen or persist beyond 2–3 days, and consult a qualified practitioner.

Well‑established constituents reported for the genus Albizia include hydrolysable gallotannins and condensed tannins, both commonly responsible for astringent effects and antidiarrheal actions, according to Veitch and Arens (2018). The bark also contains triterpene saponins, with aglycones such as oleanolic acid, reported in Brazilian Albizia species, and a range of phenolic compounds that contribute to antioxidant capacity, as summarized by Simões and Spitzer (2000). These classes fit the astringent, anti‑inflammatory and antimicrobial profiles repeatedly noted in ethnomedical contexts for gastrointestinal complaints, and the bark is typically employed in preparations where a prolonged contact time is desired.

Modern relevance remains modest: while local ethno‑botanical surveys continue to list the species in current plant pharmacopoeias, the literature emphasizes bark or root‑bark material and community‑level preparation, not standardized commercial products. Small‑scale ethnobotanical programs in southern Pantanal Brazil and northwest Argentina still train community members in sustainable bark harvesting and safe preparation practices, reflecting ongoing traditional use and renewed interest in confirming constituent profiles and comparative astringency across regional forms (Renck and González, 1995; Santos et al., 2012; Rivière et al., 2018).

General Uses Top

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Common products:
Bark is used for dyeing and tanning.

Colorants and tanning:
Bark provides a brown dye for textiles and contains tannins suitable for leather tanning. The exact tannin composition and color quality are not detailed in the available references.

Synonyms Top

Scientific name Authority First published in
Albizia polyantha (A.Spreng.) G.J.Lewis Legumes Bahia: 164 (1987)
Cathormion polycephalum (Griseb.) Burkart Darwiniana13: 448 (1964)
Cathormion polyanthum (A.Spreng.) Burkart Darwiniana13: 447 (1964)
Acacia inundata Mart. Reise Bras.1: 555 (1823)
Enterolobium polycephalum Griseb. Abh. Königl. Ges. Wiss. Göttingen24: 123 (1879)
Feuilleea polycephala (Griseb.) Kuntze Revis. Gen. Pl.1: 188 (1891)
Arthrosamanea polycephala (Griseb.) Burkart Darwiniana9: 69 (1949)
Pithecellobium pendulum Lindm. Bih. Kongl. Svenska Vetensk.-Akad. Handl.24(3; 7): 51 (1898)
Pithecellobium multiflorum var. brevipedunculata Chodat & Hassl. Bull. Herb. Boissier, sér. 2, 4: 483 (1904)
Acacia polyantha A.Spreng. K.P.J.Sprengel, Syst. Veg. ed. 16, 5: 3 (1828)
Arthrosamanea polyantha (A.Spreng.) Burkart Darwiniana9: 66 (1949)
Acacia multiflora Spreng. Syst. Veg., ed. 16. 3: 142 (1826)
Arthrosamanea polyantha (A.Spreng.) Burkart
Albizia inundata (Mart.) Barneby & J.W.Grimes Mem. New York Bot. Gard. 74(1): 238 (1996)

Common names Top

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Language Common/alternative name
Spanish maloxo
Spanish paloflojo
Spanish timbo blancoata
Spanish timbó blancoatá
Persian البیزیا اینانداتا
Malayalam വെള്ളക്കരിങ്ങാലി

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

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Links to other databases Top

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Database ID/link to page
Tropicos 50086642
KEW urn:lsid:ipni.org:names:1208750-2
The Plant List ild-41011
Open Tree Of Life 3919308
NCBI Taxonomy 1954508
IUCN Red List 144271387
IPNI 1208750-2
iNaturalist 578792
GBIF 2973063
Freebase /m/02qhwgy
EOL 643832
USDA GRIN 435599
Wikipedia Albizia_inundata
CMAUP NPO17211
World Flora Online wfo-1000040155

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
Ferroptosis: a new mechanism of traditional Chinese medicine for cancer treatment Zhu J, Shen P, Xu Y, Zhang X, Chen Q, Gu K, Ji S, Yang B, Zhao Y Front Pharmacol 16-Jan-2024
PMCID:PMC10824936
doi:10.3389/fphar.2024.1290120
PMID:38292937
Application of the herbal chemical marker ranking system (Herb MaRS) to the standardization of herbal raw materials: a case study Kaggwa B, Anywar G, Munanura EI, Wangalwa R, Kyeyune H, Okella H, Kamba FP, Engeu OP BMC Complement Med Ther 30-Sep-2023
PMCID:PMC10542261
doi:10.1186/s12906-023-04178-3
PMID:37777721
Recent trends in emerging strategies for ferroptosis-based cancer therapy Yu H, Yan J, Li Z, Yang L, Ju F, Sun Y Nanoscale Adv 14-Feb-2023
PMCID:PMC9972547
doi:10.1039/d2na00719c
PMID:36866253
Ferroptosis‐modulating small molecules for targeting drug‐resistant cancer: Challenges and opportunities in manipulating redox signaling Koeberle SC, Kipp AP, Stuppner H, Koeberle A Med Res Rev 19-Jan-2023
PMCID:PMC10947485
doi:10.1002/med.21933
PMID:36658724
Enhanced Water Solubility and Anti-Tumor Activity of Oleanolic Acid through Chemical Structure Modification Gu Z, Lin S, Yan W, Chen D, Zeng Z, Chen L, Li Y, He B Int J Mol Sci 31-Oct-2022
PMCID:PMC9656325
doi:10.3390/ijms232113291
PMID:36362079
Bioactive Natural Products for Chemical Control of Microorganisms: Scientific Prospecting (2001–2021) and Systematic Review Feitosa BF, de Alcântara CM, de Lima AB, Silva AS, Araújo AD, Cavalcanti MT, Mori E, Araújo IM, de Farias PA, Wilairatana P, Coutinho HD Molecules 12-Sep-2022
PMCID:PMC9505009
doi:10.3390/molecules27185917
PMID:36144652
Present scenarios and future prospects of herbal nanomedicine for antifungal therapy Yadav R, Pradhan M, Yadav K, Mahalvar A, Yadav H J Drug Deliv Sci Technol 13-May-2022
PMCID:PMC9101776
doi:10.1016/j.jddst.2022.103430
PMID:35582019
Anatomical characterization and technological properties of Pterogyne nitens wood, a very interesting species of the Brazilian Caatinga biome Pereira AK, Longue Júnior D, Carvalho AM, Mafra Neto CD Sci Rep 28-Jul-2021
PMCID:PMC8319433
doi:10.1038/s41598-021-94785-2
PMID:34321533
Natural Products as Inducers of Non-Canonical Cell Death: A Weapon against Cancer Greco G, Catanzaro E, Fimognari C Cancers (Basel) 15-Jan-2021
PMCID:PMC7830727
doi:10.3390/cancers13020304
PMID:33467668
Hybrid capture of 964 nuclear genes resolves evolutionary relationships in the mimosoid legumes and reveals the polytomous origins of a large pantropical radiation Koenen EJ, Kidner C, de Souza ÉR, Simon MF, Iganci JR, Nicholls JA, Brown GK, de Queiroz LP, Luckow M, Lewis GP, Pennington RT, Hughes CE Am J Bot 30-Nov-2020
PMCID:PMC7839790
doi:10.1002/ajb2.1568
PMID:33253423
Site-selective C-H hydroxylation of pentacyclic triterpenoids directed by transient chiral pyridine-imino groups Mu T, Wei B, Zhu D, Yu B Nat Commun 01-Sep-2020
PMCID:PMC7462855
doi:10.1038/s41467-020-18138-9
PMID:32873790
Effects of Flavonoids and Triterpene Analogues from Leaves of Eleutherococcus sieboldianus (Makino) Koidz. ‘Himeukogi’ in 3T3-L1 Preadipocytes Nishina A, Itagaki M, Suzuki Y, Koketsu M, Ninomiya M, Sato D, Suzuki T, Hayakawa S, Kuroda M, Kimura H Molecules 22-Apr-2017
PMCID:PMC6154646
doi:10.3390/molecules22040671
PMID:28441735
Inundation and Fire Shape the Structure of Riparian Forests in the Pantanal, Brazil Arruda WD, Oldeland J, Paranhos Filho AC, Pott A, Cunha NL, Ishii IH, Damasceno-Junior GA PLoS One 09-Jun-2016
PMCID:PMC4900580
doi:10.1371/journal.pone.0156825
PMID:27280879
Triterpenes as Potentially Cytotoxic Compounds Chudzik M, Korzonek-Szlacheta I, Król W Molecules 19-Jan-2015
PMCID:PMC6272502
doi:10.3390/molecules20011610
PMID:25608043
Early State Research on Antifungal Natural Products Negri M, Salci TP, Shinobu-Mesquita CS, Capoci IR, Svidzinski TI, Seki Kioshima E Molecules 07-Mar-2014
PMCID:PMC6271505
doi:10.3390/molecules19032925
PMID:24609016

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3beta)-3-((O-alpha-L-Arabinopyranosyl-(1->2)-O-alpha-L-arabinopyranosyl-(1->6)-beta-D-glucopyranosyl)oxy)olean-12-en-28-oic acid 54582302 Click to see 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
10-[3-Acetamido-4,5-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14217287 Click to see 808.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3832176 Click to see 781.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
3-O-[alpha-L-arabinopyranosyl(1->2)-alpha-L-arabinopyranosyl(1->6)-[beta-D-glucopyranosyl(1->2)]-beta-D-glucopyranoside echinocystic acid 21582615 Click to see 1061.20 unknown via CMAUP database
3-O-[alpha-L-arabinopyranosyl(1->2)-alpha-L-arabinopyranosyl(1->6)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl acacic acid lactone 15812667 Click to see 938.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
3-O-[alpha-L-arabinopyranosyl(1->6)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl echinocystic acid 14217288 Click to see 808.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
3-O-[beta-D-xylopyranosyl(1->2)-alpha-L-arabinopyranosyl(1->6)-[beta-D-glucopyranosyl(1->2)]-beta-D-glucopyranoside echinocystic acid 54581282 Click to see 1061.20 unknown via CMAUP database
3-O-[beta-D-xylopyranosyl(1->2)-alpha-L-arabinopyranosyl(1->6)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl acacic acid lactone 16681643 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C67C5CC(C(C6)OC7=O)(C)C)O)C)C)C)COC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)O)O 938.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Acutoside A 21606142 Click to see 781.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Albiziabioside A 10795385 Click to see 792.00 unknown via CMAUP database
N-[6-[[4,5-dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-2-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-10-yl)oxy]oxan-3-yl]acetamide 73307323 Click to see 938.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Pitheduloside B 76152479 Click to see 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Pitheduloside C 54581283 Click to see 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP50023A027
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
(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/10.1021/NP50023A027
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 10700439 Click to see 782.70 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Clitorin 11592917 Click to see 740.70 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-vestitone 44446897 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database

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