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Inga umbellifera

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd73b241e8459966392
Scientific name Inga umbellifera
Authority (Vahl) DC.

Ethnobotanical Use Top

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General Uses 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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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 North
      • Brazil Northeast
      • Brazil West-central
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000173674
Tropicos 13021409
INPN 733878
KEW urn:lsid:ipni.org:names:1035636-2
The Plant List ild-19816
Open Tree Of Life 19672
NCBI Taxonomy 486089
IUCN Red List 129739050
IPNI 1035636-2
GBIF 5358027
EOL 639894
USDA GRIN 436432

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
Toxicity of meta-Tyrosine Tyminski M, Ciacka K, Staszek P, Gniazdowska A, Krasuska U Plants (Basel) 17-Dec-2021
PMCID:PMC8707607
doi:10.3390/plants10122800
PMID:34961269
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
Small Neotropical primates promote the natural regeneration of anthropogenically disturbed areas Heymann EW, Culot L, Knogge C, Smith AC, Tirado Herrera ER, Müller B, Stojan-Dolar M, Lledo Ferrer Y, Kubisch P, Kupsch D, Slana D, Koopmann ML, Ziegenhagen B, Bialozyt R, Mengel C, Hambuckers J, Heer K Sci Rep 25-Jul-2019
PMCID:PMC6658533
doi:10.1038/s41598-019-46683-x
PMID:31346187
Tracking of Host Defenses and Phylogeny During the Radiation of Neotropical Inga-Feeding Sawflies (Hymenoptera; Argidae) Endara MJ, Nicholls JA, Coley PD, Forrister DL, Younkin GC, Dexter KG, Kidner CA, Pennington RT, Stone GN, Kursar TA Front Plant Sci 23-Aug-2018
PMCID:PMC6116116
doi:10.3389/fpls.2018.01237
PMID:30190723
Current Challenges in Plant Eco-Metabolomics Peters K, Worrich A, Weinhold A, Alka O, Balcke G, Birkemeyer C, Bruelheide H, Calf OW, Dietz S, Dührkop K, Gaquerel E, Heinig U, Kücklich M, Macel M, Müller C, Poeschl Y, Pohnert G, Ristok C, Rodríguez VM, Ruttkies C, Schuman M, Schweiger R, Shahaf N, Steinbeck C, Tortosa M, Treutler H, Ueberschaar N, Velasco P, Weiß BM, Widdig A, Neumann S, van Dam NM Int J Mol Sci 06-May-2018
PMCID:PMC5983679
doi:10.3390/ijms19051385
PMID:29734799
High herbivore pressure favors constitutive over induced defense Bixenmann RJ, Coley PD, Weinhold A, Kursar TA Ecol Evol 29-Jul-2016
PMCID:PMC5016630
doi:10.1002/ece3.2208
PMID:27648224
Quantitative and qualitative shifts in defensive metabolites define chemical defense investment during leaf development in Inga, a genus of tropical trees Wiggins NL, Forrister DL, Endara M, Coley PD, Kursar TA Ecol Evol 08-Jan-2016
PMCID:PMC4729263
doi:10.1002/ece3.1896
PMID:26843932
Using targeted enrichment of nuclear genes to increase phylogenetic resolution in the neotropical rain forest genus Inga (Leguminosae: Mimosoideae) Nicholls JA, Pennington RT, Koenen EJ, Hughes CE, Hearn J, Bunnefeld L, Dexter KG, Stone GN, Kidner CA Front Plant Sci 17-Sep-2015
PMCID:PMC4584976
doi:10.3389/fpls.2015.00710
PMID:26442024
Macroecological and macroevolutionary patterns of leaf herbivory across vascular plants Turcotte MM, Davies TJ, Thomsen CJ, Johnson MT Proc Biol Sci 22-Jul-2014
PMCID:PMC4071545
doi:10.1098/rspb.2014.0555
PMID:24870043
Corrigendum to “Cinnamoyl glucosides of catechin and dimeric procyanidins from young leaves of Inga umbellifera (Fabaceae)” [Phytochemistry 65 (2004) 351–358] John Lokvam, Phyllis D. Coley, Thomas A. Kursar Elsevier BV 12-May-2004
doi:10.1016/J.PHYTOCHEM.2004.03.023

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R,4S,5S,6R)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 21589947 Click to see 1032.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[(2R,3S,4S,5R,6R)-6-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 21589948 Click to see 1032.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[(2S,3S,4S,5R,6S)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 163187474 Click to see 1032.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[2-[[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-phenylprop-2-enoate 73808233 Click to see 1032.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[6-[[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-phenylprop-2-enoate 73808234 Click to see 1032.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5S,6R)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 21589944 Click to see 582.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[(2R,3S,4S,5R,6R)-6-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4-dihydroxy-5-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 21589946 Click to see 712.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[(2R,3S,4S,5R,6R)-6-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 21589943 Click to see 582.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[(2S,3R,4R,5S,6S)-6-[[(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 163194143 Click to see 582.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[2-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-phenylprop-2-enoate 73808231 Click to see 582.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[6-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4-dihydroxy-5-(3-phenylprop-2-enoyloxy)oxan-2-yl]methyl 3-phenylprop-2-enoate 73808232 Click to see 712.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023
[6-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-phenylprop-2-enoate 73808230 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=CC=C5)O)O)O 582.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.023

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