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Beilschmiedia alloiophylla

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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 UUID64400c7a633f5039677013
Scientific name Beilschmiedia alloiophylla
Authority (Rusby) Kosterm.
First published in Recueil Trav. Bot. Néerl. 1938, xxxv. 849;.

Description Top

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Synonyms Top

Scientific name Authority First published in
Ocotea alloiophylla Rusby Descr. S. Amer. Pl. : 21 (1920)

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

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-0000561791
Tropicos 17802444
KEW urn:lsid:ipni.org:names:3010840-1
The Plant List kew-2672367
Open Tree Of Life 5699379
NCBI Taxonomy 1345219
IUCN Red List 144052529
IPNI 1010840-1
GBIF 4178492
EOL 5393521

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
N-Methyl Costaricine and Costaricine, Two Potent Butyrylcholinesterase Inhibitors from Alseodaphne pendulifolia Gamb. Husna Hasnan MH, Sivasothy Y, Khaw KY, Nafiah MA, Hazni H, Litaudon M, Wan Ruzali WA, Liew SY, Awang K Int J Mol Sci 27-Jun-2023
PMCID:PMC10341795
doi:10.3390/ijms241310699
PMID:37445877
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
Potential of Naturally Derived Alkaloids as Multi-Targeted Therapeutic Agents for Neurodegenerative Diseases Kong YR, Tay KC, Su YX, Wong CK, Tan WN, Khaw KY Molecules 30-Jan-2021
PMCID:PMC7866829
doi:10.3390/molecules26030728
PMID:33573300
A Decade of Antifungal Leads from Natural Products: 2010–2019 Aldholmi M, Marchand P, Ourliac-Garnier I, Le Pape P, Ganesan A Pharmaceuticals (Basel) 12-Dec-2019
PMCID:PMC6958371
doi:10.3390/ph12040182
PMID:31842280
Anti-Infective and Anti-Cancer Properties of the Annona Species: Their Ethnomedicinal Uses, Alkaloid Diversity, and Pharmacological Activities Nugraha AS, Damayanti YD, Wangchuk P, Keller PA Molecules 03-Dec-2019
PMCID:PMC6930583
doi:10.3390/molecules24234419
PMID:31816948
Physicochemical Characterization and Biological Activities of the Triterpenic Mixture α,β-Amyrenone Ferreira RG, Silva Júnior WF, Veiga Junior VF, Lima ÁA, Lima ES Molecules 16-Feb-2017
PMCID:PMC6155755
doi:10.3390/molecules22020298
PMID:28212341
Endiandric Acid Derivatives and Other Constituents of Plants from the Genera Beilschmiedia and Endiandra (Lauraceae) Ndjakou Lenta B, Chouna JR, Nkeng-Efouet PA, Sewald N Biomolecules 14-May-2015
PMCID:PMC4496702
doi:10.3390/biom5020910
PMID:26117852
Anti-acetylcholinesterase, anti-α-glucosidase, anti-leishmanial and anti-fungal activities of chemical constituents of Beilschmiedia species. Mollataghi A, Coudiere E, Hadi AH, Mukhtar MR, Awang K, Litaudon M, Ata A Fitoterapia 01-Mar-2012
doi:10.1016/J.FITOTE.2011.11.009
PMID:22119096

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
> Alkaloids and derivatives / Aporphines
(6aR)-9-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol 57335897 Click to see CN1CCC2=C3C1CC4=C(C3=CC(=C2)O)C=CC(=C4)OC 281.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
(6aS)-2,3-Dimethoxy-5,6,6a,7-tetrahydro-4H-benzo[de][1,3]benzodioxolo[5,6-g]quinolin-1-ol 57336190 Click to see COC1=C(C(=C2C3=CC4=C(C=C3CC5C2=C1CCN5)OCO4)O)OC 341.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
(R)-Asimilobine 12308663 Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O 267.32 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol 248507 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol 267400 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
Asimilobine 160875 Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O 267.32 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1016/J.FITOTE.2011.11.009

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