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Internal ID UUID64404d7f6c852619035768
Scientific name Sohnreyia excelsa
Authority K.Krause
First published in Notizbl. Königl. Bot. Gart. Berlin 6: 148 (1914)

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Synonyms Top

Scientific name Authority First published in
Spathelia excelsa (K.Krause) R.S.Cowan & Brizicky Mem. New York Bot. Gard. 10(2): 64 (1960)

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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 West-central
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001132728
Tropicos 28100260
KEW urn:lsid:ipni.org:names:238191-2
NCBI Taxonomy 2821074
IPNI 238191-2
iNaturalist 1119635
GBIF 3837800
Wikipedia Sohnreyia_excelsa

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
Isolation of arginase inhibitors from the bioactivity-guided fractionation of Byrsonima coccolobifolia leaves and stems. de Sousa LR, Ramalho SD, Burger MC, Nebo L, Fernandes JB, da Silva MF, Iemma MR, Corrêa CJ, de Souza DH, Lima MI, Vieira PC J Nat Prod 28-Feb-2014
doi:10.1021/NP400717M
PMID:24521209
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights Appelhans MS, Smets E, Razafimandimbison SG, Haevermans T, van Marle EJ, Couloux A, Rabarison H, Randrianarivelojosia M, Keßler PJ Ann Bot 01-Jun-2011
PMCID:PMC3101142
doi:10.1093/aob/mcr076
PMID:21610209
Alkaloids from Spathelia excelsa: their chemosystematic significance. Lima Mda P, Rosas LV, da Silva MF, Ferreira AG, Fernandes JB, Vieira PC Phytochemistry 01-Jul-2005
doi:10.1016/J.PHYTOCHEM.2005.05.019
PMID:16002107

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 / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroquinolines
2-(10-hydroxy-10-methyldodecyl)-3-methoxy-3H-quinolin-4-one 86066329 Click to see CCC(C)(CCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-(11-hydroxy-11-methyldodecyl)-3-methoxy-3H-quinolin-4-one 86066332 Click to see CC(C)(CCCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-(12-hydroxytridecyl)-3-methoxy-3H-quinolin-4-one 86066494 Click to see CC(CCCCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
3-methoxy-2-(12-oxotridecyl)-3H-quinolin-4-one 86066327 Click to see CC(=O)CCCCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1OC 371.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
6-hydroxy-2-(3-hydroxy-3-methylbutyl)-3H-quinolin-4-one 129716298 Click to see CC(C)(CCC1=NC2=C(C=C(C=C2)O)C(=O)C1)O 247.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
7-hydroxy-2-(3-hydroxy-3-methylbutyl)-3H-quinolin-4-one 129716385 Click to see CC(C)(CCC1=NC2=C(C=CC(=C2)O)C(=O)C1)O 247.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroxyquinolines
6-hydroxy-2-(3-hydroxy-3-methylbutyl)-1H-quinolin-4-one 91528975 Click to see CC(C)(CCC1=CC(=O)C2=C(N1)C=CC(=C2)O)O 247.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
2-(10-hydroxy-10-methyldodecyl)-3-methoxy-1H-quinolin-4-one 90848757 Click to see CCC(C)(CCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-(11-hydroxy-11-methyldodecyl)-3-methoxy-1H-quinolin-4-one 91527455 Click to see CC(C)(CCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-(12-hydroxytridecyl)-3-methoxy-1H-quinolin-4-one 91595096 Click to see CC(CCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-[(10R)-10-hydroxy-10-methyldodecyl]-3-methoxy-1H-quinolin-4-one 162962489 Click to see CCC(C)(CCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
2-[(12S)-12-hydroxytridecyl]-3-methoxy-1H-quinolin-4-one 163190335 Click to see CC(CCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 373.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
3-methoxy-2-(12-oxotridecyl)-1H-quinolin-4-one 90872051 Click to see CC(=O)CCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC 371.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
7-hydroxy-2-(3-hydroxy-3-methylbutyl)-1H-quinolin-4-one 91466094 Click to see CC(C)(CCC1=CC(=O)C2=C(N1)C=C(C=C2)O)O 247.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP400717M
https://doi.org/10.1016/J.PHYTOCHEM.2005.05.019

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