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Aniba hostmanniana

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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 UUID6440097549f6e854635329
Scientific name Aniba hostmanniana
Authority (Nees) Mez
First published in Jahrb. Königl. Bot. Gart. Berlin 5: 67 (1889)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aniba gigantifolia O.C.Schmidt Notizbl. Bot. Gart. Berlin-Dahlem 10: 225 (1928)
Aniba pittieri O.C.Schmidt Repert. Spec. Nov. Regni Veg. 31: 168 (1933)
Aydendron hostmannianum Nees Linnaea 21: 499 (1848)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Central America
      • 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-0000536845
Tropicos 17800128
INPN 733485
KEW urn:lsid:ipni.org:names:13841-2
The Plant List kew-2639703
Open Tree Of Life 679883
NCBI Taxonomy 597271
IUCN Red List 143817324
IPNI 13841-2
GBIF 4181158

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
Detection and Quantification of Botanical Impurities in Commercial Oregano (Origanum vulgare) Using Metabarcoding and Digital PCR Lievens A, Paracchini V, Garlant L, Pietretti D, Maquet A, Ulberth F Foods 09-Aug-2023
PMCID:PMC10453138
doi:10.3390/foods12162998
PMID:37627997
Ecological quality of a forest in a state of succession based on structural parameters: A case study in an evergreen Amazonian-Andean forest, Ecuador García-Quintana Y, Arteaga-Crespo Y, Torres-Navarrete B, Robles-Morillo M, Bravo-Medina C, Sarmiento-Rosero A Heliyon 30-Jul-2020
PMCID:PMC7394865
doi:10.1016/j.heliyon.2020.e04592
PMID:32775736
Chemical analysis of Brasilimeria Stach, 1949 (Hexapoda, Collembola, Neanuridae) hemolymphatic secretion, and description of a new species Zeppelini D, Queiroz GC, Lopes NP, Mendonça-Junior FJ PLoS One 21-Feb-2019
PMCID:PMC6383892
doi:10.1371/journal.pone.0212451
PMID:30789930
Long-Term Vegetation Dynamics in a Megadiverse Hotspot: The Ice-Age Record of a Pre-montane Forest of Central Ecuador Montoya E, Keen HF, Luzuriaga CX, Gosling WD Front Plant Sci 20-Feb-2018
PMCID:PMC5826276
doi:10.3389/fpls.2018.00196
PMID:29515609
6-Phenylethyl-5,6-dihydro-2-pyrones From Aniba gigantifolia N.C. Franca, Otto Richard Gottlieb, A.M.Puentes Suarez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)85045-9
Constituents of Aniba hostmanniana O.R. Gottlieb, A.I. da Rocha Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(72)85063-5

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
> Benzenoids / Phenol ethers / Anisoles
gamma-Asarone 636750 Click to see COC1=CC(=C(C=C1CC=C)OC)OC 208.25 unknown https://doi.org/10.1016/0031-9422(72)85063-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
(E)-N-[2-(4-methoxyphenyl)ethyl]-3-(3,4,5-trimethoxyphenyl)prop-2-enamide 7958303 Click to see COC1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC 371.40 unknown https://doi.org/10.1016/0031-9422(72)85063-5
N-[2-(4-Methoxyphenyl)ethyl]-3-(3,4,5-trimethoxyphenyl)-2-propenamide 72087178 Click to see COC1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC 371.40 unknown https://doi.org/10.1016/0031-9422(72)85063-5
> Phenylpropanoids and polyketides / Kavalactones
(+/-)-Dihydromethysticin 229852 Click to see COC1=CC(=O)OC(C1)CCC2=CC3=C(C=C2)OCO3 276.28 unknown https://doi.org/10.1016/0031-9422(73)85045-9
(2R)-4-methoxy-2-[2-(4-methoxyphenyl)ethyl]-2,3-dihydropyran-6-one 162892216 Click to see COC1=CC(=O)OC(C1)CCC2=CC=C(C=C2)OC 262.30 unknown https://doi.org/10.1016/0031-9422(73)85045-9
(6S)-5,6-Dihydro-4-methoxy-6-[2-(4-methoxyphenyl)ethyl]-2H-pyran-2-one 25008953 Click to see COC1=CC(=O)OC(C1)CCC2=CC=C(C=C2)OC 262.30 unknown https://doi.org/10.1016/0031-9422(73)85045-9
11,12-Dimethoxydihydrokawain 592220 Click to see COC1=CC(=O)OC(C1)CCC2=CC(=C(C=C2)OC)OC 292.33 unknown https://doi.org/10.1016/0031-9422(73)85045-9
2H-Pyran-2-one, 6-[2-(3,4-dimethoxyphenyl)ethyl]-5,6-dihydro-4-methoxy-, (S)- 22217085 Click to see COC1=CC(=O)OC(C1)CCC2=CC(=C(C=C2)OC)OC 292.33 unknown https://doi.org/10.1016/0031-9422(73)85045-9
4-methoxy-6-(2-phenylethyl)-5,6-dihydro-2H-pyran-2-one 98356 Click to see COC1=CC(=O)OC(C1)CCC2=CC=CC=C2 232.27 unknown https://doi.org/10.1016/0031-9422(73)85045-9
5,6-Dihydro-4-methoxy-6-[2-(4-methoxyphenyl)ethyl]-2H-pyran-2-one 10084050 Click to see COC1=CC(=O)OC(C1)CCC2=CC=C(C=C2)OC 262.30 unknown https://doi.org/10.1016/0031-9422(73)85045-9
Dihydrokawain 10220256 Click to see COC1=CC(=O)OC(C1)CCC2=CC=CC=C2 232.27 unknown https://doi.org/10.1016/0031-9422(73)85045-9
Dihydromethysticin 88308 Click to see COC1=CC(=O)OC(C1)CCC2=CC3=C(C=C2)OCO3 276.28 unknown https://doi.org/10.1016/0031-9422(73)85045-9
Dihydromethysticin, (R)- 10107480 Click to see COC1=CC(=O)OC(C1)CCC2=CC3=C(C=C2)OCO3 276.28 unknown https://doi.org/10.1016/0031-9422(73)85045-9

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