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Alangium longiflorum

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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 UUID64403779c6b78002583051
Scientific name Alangium longiflorum
Authority Merr.
First published in Philipp. J. Sci., C 7: 319 (1912)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alangium longifolium Merr. Philipp. J. Sci., C 7: 319 (1912)
Alangium octopetalum Vidal Revis. Pl. Vasc. Filip. 146. 1886 (1886)

Common names Top

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Language Common/alternative name
Arabic علنج طويل الأزهار

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Alangium longiflorum var. brachyanthum (Merr.) W.J.de Wilde & Duyfjes Thai Forest Bull., Bot. 44: 82 (2016)
Alangium longiflorum var. longiflorum Unknown

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
  • Asia-tropical
    • Malesia
      • Borneo
      • Malaya
      • Maluku
      • Philippines
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000937302
Tropicos 100143023
KEW urn:lsid:ipni.org:names:271417-1
The Plant List kew-5598
Open Tree Of Life 299292
NCBI Taxonomy 616982
IUCN Red List 37769
IPNI 271417-1
iNaturalist 189106
GBIF 3701872
Freebase /m/02x7rgr
EOL 6874583
USDA GRIN 2109
Wikipedia Alangium_longiflorum

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
Virus-like particles (VLPs): A promising platform for combating against Newcastle disease virus Taghizadeh MS, Niazi A, Afsharifar A Vaccine X 14-Jan-2024
PMCID:PMC10811427
doi:10.1016/j.jvacx.2024.100440
PMID:38283623
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Modelling studies reveal the importance of the C-terminal inter motif loop of NSP1 as a promising target site for drug discovery and screening of potential phytochemicals to combat SARS-CoV-2 Prabhu D, Rajamanikandan S, Sureshan M, Jeyakanthan J, Saraboji K J Mol Graph Model 19-Apr-2021
PMCID:PMC8053965
doi:10.1016/j.jmgm.2021.107920
PMID:33933885
Alangium longiflorum Merr. Leaf Extract Induces Apoptosis in A549 Lung Cancer Cells with Minimal NFκB Transcriptional Activation Marquez CM, Garcia JG, Antonio JG, Jacinto SD, Velarde MC Asian Pac J Cancer Prev 01-Aug-2020
PMCID:PMC7771936
doi:10.31557/APJCP.2020.21.8.2453
PMID:32856878
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
Antiproliferative Alkaloids from Alangium longiflorum, an Endangered Tropical Plant Species Takeuchi M, Saito Y, Goto M, Miyake K, Newman DJ, O’Keefe BR, Lee KH, Nakagawa-Goto K J Nat Prod 14-Aug-2018
PMCID:PMC6421842
doi:10.1021/acs.jnatprod.8b00411
PMID:30106296
Separation and SAR study of HIF-1alpha inhibitory tubulosines from Alangium cf. longiflorum. Klausmeyer P, McCloud TG, Uranchimeg B, Melillo G, Scudiero DA, Cardellina JH 2nd, Shoemaker RH Planta Med 01-Feb-2008
doi:10.1055/S-2008-1034315
PMID:18302092
Cytotoxic Alangium alkaloids from Alangium longiflorum. Sakurai N, Nakagawa-Goto K, Ito J, Sakurai Y, Nakanishi Y, Bastow KF, Cragg G, Lee KH Phytochemistry 01-May-2006
doi:10.1016/J.PHYTOCHEM.2006.01.009
PMID:16530796

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
> Alkaloids and derivatives / Emetine alkaloids
(2S,3R,11bS)-3-ethyl-2-[[(1S)-6-hydroxy-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-9-methoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-10-ol 163193442 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)O)OC)O)OC 452.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
10-Demethylcephaeline 185699 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)O)OC)O)OC 452.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
3-ethyl-2-[(6-hydroxy-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-9-methoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-10-ol 53463261 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)O)OC)O)OC 452.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Cephaeline 442195 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)O)OC)OC)OC 466.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Desmethylemetine 2665 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)O)OC)OC)OC 466.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Emetine 10219 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)OC)OC)OC)OC 480.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Isoemetine, tetradehydro- 9426 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=CC(=C(C=C5CCN4)OC)OC)OC)OC 480.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
> Alkaloids and derivatives / Harmala alkaloids
(1'beta)-10,11-Dimethoxytubulosan-8'-ol 165327 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=C(CCN4)C6=C(N5)C=CC(=C6)O)OC)OC 475.60 unknown https://doi.org/10.1055/S-2008-1034315
Tubulosine 72341 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC4C5=C(CCN4)C6=C(N5)C=CC(=C6)O)OC)OC 475.60 unknown https://doi.org/10.1055/S-2008-1034315
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(4S)-4beta-[(S)-1,2,3,4-Tetrahydro-6,7-dimethoxyisoquinoline-1-ylmethyl]-5beta-vinyl-6alpha-(beta-D-glucopyranosyloxy)-5,6-dihydro-4H-pyran-3-carboxylic acid 101718133 Click to see COC1=C(C=C2C(NCCC2=C1)CC3C(C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC 537.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
4-[(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-3-ethenyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 163056293 Click to see COC1=C(C=C2C(NCCC2=C1)CC3C(C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC 537.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,15S,16S,17S)-16-ethenyl-4-hydroxy-5-methoxy-15-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 162920619 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
(1R,15S,16S,17S)-16-ethenyl-4,5-dihydroxy-15-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 162942687 Click to see C=CC1C2CC3C4=CC(=C(C=C4CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O)O 491.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
16-Ethenyl-4-hydroxy-5-methoxy-15-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 5089480 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
16-Ethenyl-4,5-dihydroxy-15-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 4491372 Click to see C=CC1C2CC3C4=CC(=C(C=C4CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O)O 491.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Alangiside 442161 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
Demethylalangiside 443418 Click to see C=CC1C2CC3C4=CC(=C(C=C4CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O)O 491.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
> Organoheterocyclic compounds / Quinolizidines
2-(3-ethyl-10-hydroxy-9-methoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl)acetaldehyde 162854155 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC=O)O)OC 303.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009
2-[(2R,3R,11bS)-3-ethyl-10-hydroxy-9-methoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl]acetaldehyde 101718137 Click to see CCC1CN2CCC3=CC(=C(C=C3C2CC1CC=O)O)OC 303.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.01.009

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