Albizia inundata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID643fdb2cc4136515987208
Scientific name Albizia inundata
Authority (Mart.) Barneby & J.W.Grimes
First published in Mem. New York Bot. Gard.74(1): 238 (1996)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Albizia polyantha (A.Spreng.) G.J.Lewis Legumes Bahia: 164 (1987)
Acacia polyantha A.Spreng.
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)

Common names Top

Add a new one! Suggest a correction!

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

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000194386
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

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
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
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
The “Hidden Diversity” of Medicinal Plants in Northeastern Brazil: Diagnosis and Prospects for Conservation and Biological Prospecting Cavalcanti DR, Albuquerque UP Evid Based Complement Alternat Med 20-Oct-2013
PMCID:PMC3817947
doi:10.1155/2013/102714
PMID:24228056
Cytotoxic oleanane-type saponins from Albizia inundata. Zhang H, Samadi AK, Rao KV, Cohen MS, Timmermann BN J Nat Prod 25-Mar-2011
PMCID:PMC3090140
doi:10.1021/NP100702P
PMID:21314099
Cytotoxic Oleanane-type Saponins from Albizia inundata Zhang H, Samadi AK, Rao KV, Cohen MS, Timmermann BN J Nat Prod 11-Feb-2011
PMCID:PMC3090140
doi:10.1021/np100702p
PMID:21314099

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
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 CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)O)O)C)C)C)COC7C(C(C(CO7)O)O)O)O)O 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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 781.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
10-[6-[[4,5-Dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-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 76152479 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
3-O-[alpha-L-arabinopyranosyl-(1->6)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl oleanolic acid 10795385 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)COC7C(C(C(CO7)O)O)O)O)O 792.00 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 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/
3-O-[alpha-L-arabinopyranosyl(1->6)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl echinocystic acid 14217288 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)O)O)C)C)C)COC7C(C(C(CO7)O)O)O)O)O 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 CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C(=O)O)C 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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 781.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
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 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/
Pitheduloside B 54582302 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Pitheduloside C 54581283 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 883.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090140/
Pitheduloside K 21582615 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C(=O)O)C 1061.20 unknown via CMAUP database
> 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 C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(4-Hydroxyphenyl)-3-[[2-O-(4-O-acetyl-alpha-L-rhamnopyranosyl)-6-O-alpha-L-rhamnopyranosyl-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-4H-1-benzopyran-4-one 10700439 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)OC6C(C(C(C(O6)C)OC(=O)C)O)O)O)O)O)O)O 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 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown via CMAUP database
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 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
S-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 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.