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Daphniphyllum glaucescens

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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 UUID6440378ceda8d415290041
Scientific name Daphniphyllum glaucescens
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 1153 (1827)

Description 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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Name Authority First published in
Daphniphyllum glaucescens var. blumeanum (Baill. ex Müll.Arg.) J.J.Sm. Bijdr. Boomsoort. Java 12: 328 (1910)
Daphniphyllum glaucescens var. glaucescens Unknown
Daphniphyllum glaucescens var. lancifolium (Hook.f.) Rafidah Blumea 53: 444 (2008)

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
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sulawesi

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000937699
Tropicos 10100003
KEW urn:lsid:ipni.org:names:344227-1
The Plant List kew-56364
Open Tree Of Life 787468
NCBI Taxonomy 122833
IPNI 344227-1
GBIF 7311236
USDA GRIN 13288

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
Dual Effects of 3-epi-betulin from Daphniphyllum glaucescens in Suppressing SARS-CoV-2-Induced Inflammation and Inhibiting Virus Entry Yeh YJ, Chao TL, Chang YJ, Chang SY, Lu CH, Chao CH, Su WC, Tseng CP, Lai MM, Cheng JC Int J Mol Sci 01-Dec-2023
PMCID:PMC10707724
doi:10.3390/ijms242317040
PMID:38069363
Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Sep-2022
PMCID:PMC9500622
doi:10.3390/insects13090826
PMID:36135527
Glaulactams A–C, daphniphyllum alkaloids from Daphniphyllum glaucescens Chao CH, Cheng JC, Gonçalves TP, Huang KW, Lin CC, Huang HC, Hwang SY, Wu YC Sci Rep 18-Oct-2018
PMCID:PMC6193994
doi:10.1038/s41598-018-33748-6
PMID:30337630
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
Phytochemicals and Biogenic Metallic Nanoparticles as Anticancer Agents Rao PV, Nallappan D, Madhavi K, Rahman S, Jun Wei L, Gan SH Oxid Med Cell Longev 23-Feb-2016
PMCID:PMC4781993
doi:10.1155/2016/3685671
PMID:27057273
The genus Cladosporium Bensch K, Braun U, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2012
PMCID:PMC3390897
doi:10.3114/sim0003
PMID:22815589
Deep simple epicotyl morphophysiological dormancy in seeds of two Viburnum species, with special reference to shoot growth and development inside the seed Chien CT, Chen SY, Tsai CC, Baskin JM, Baskin CC, Kuo-Huang LL Ann Bot 11-May-2011
PMCID:PMC3119608
doi:10.1093/aob/mcr096
PMID:21562028
Formal Alder-ene reaction of a bicyclo[1.1.0]butane in the synthesis of the tricyclic quaternary ammonium core of daphniglaucins Ueda M, Walczak MA, Wipf P Tetrahedron Lett 01-Jun-2008
PMCID:PMC2575373
doi:10.1016/j.tetlet.2008.07.179
PMID:19129907
Daphniglaucins A and B, Novel Polycyclic Quaternary Alkaloids from Daphniphyllum glaucescens. Jun'ichi Kobayashi, Hiroshi Takatsu, Ya‐Chin Shen, Hiroshi Morita Wiley 30-Jun-2005
doi:10.1002/CHIN.200337171
Daphniglaucins D—H, J, and K, New Alkaloids from Daphniphyllum glaucescens. Hiroshi Takatsu, Hiroshi Morita, Ya‐Ching Shen, Jun'ichi Kobayashi Wiley 13-Nov-2004
doi:10.1002/CHIN.200447185
Daphniglaucins D–H, J, and K, new alkaloids from Daphniphyllum glaucescens Hiroshi Takatsu, Hiroshi Morita, Ya-Ching Shen, Jun'ichi Kobayashi Elsevier BV 21-Jun-2004
doi:10.1016/J.TET.2004.05.078
Daphniglaucin C, a novel tetracyclic alkaloid from Daphniphyllum glaucescens Hiroshi Morita, Hiroshi Takatsu, Ya-Ching Shen, Jun’ichi Kobayashi Elsevier BV 16-Dec-2003
doi:10.1016/J.TETLET.2003.11.116
Daphniglaucins A and B, novel polycyclic quaternary alkaloids from Daphniphyllum glaucescens. Kobayashi J, Takatsu H, Shen YC, Morita H Org Lett 15-May-2003
doi:10.1021/OL034388P
PMID:12735764

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 / Yuzurimine-type alkaloids
methyl (1R,2R,3R,5R,6S,10S,16R,17R)-2-(hydroxymethyl)-6-methyl-20-oxo-8-azahexacyclo[11.5.1.11,5.02,10.03,8.016,19]icos-13(19)-ene-17-carboxylate 162932529 Click to see CC1CN2CC3CCC4=C5C(CC4)C(CC56C3(C2CC1C6=O)CO)C(=O)OC 385.50 unknown https://doi.org/10.1016/J.TET.2004.05.078
methyl 13-(hydroxymethyl)-2-methoxy-17-methyl-1-azoniaheptacyclo[10.6.1.13,6.01,14.02,16.03,13.09,20]icos-9(20)-ene-5-carboxylate 85315193 Click to see CC1C[N+]23CC4CCC5=C6C(CC5)C(CC67C4(C2CC1C73OC)CO)C(=O)OC 400.50 unknown https://doi.org/10.1002/CHIN.200337171
Methyl 2-(hydroxymethyl)-6-methyl-20-oxo-8-azahexacyclo[11.5.1.11,5.02,10.03,8.016,19]icos-13(19)-ene-17-carboxylate 162932528 Click to see CC1CN2CC3CCC4=C5C(CC4)C(CC56C3(C2CC1C6=O)CO)C(=O)OC 385.50 unknown https://doi.org/10.1016/J.TET.2004.05.078
> Organoheterocyclic compounds / Azaspirodecane derivatives
methyl (1R,3R,4R,10S,14S,15R,18R,19R)-18-(acetyloxymethyl)-19-hydroxy-14-methyl-12-azahexacyclo[10.6.1.11,4.010,18.015,19.07,20]icos-7(20)-ene-3-carboxylate 21580233 Click to see CC1CN2CC3CCC4=C5C(CC4)C(CC56C3(CCC1C62O)COC(=O)C)C(=O)OC 429.50 unknown https://doi.org/10.1016/J.TET.2004.05.078
Methyl 18-(acetyloxymethyl)-14-methyl-12-azahexacyclo[10.6.1.11,4.010,18.015,19.07,20]icos-7(20)-ene-3-carboxylate 12312639 Click to see CC1CN2CC3CCC4=C5C(CC4)C(CC56C2C1CCC63COC(=O)C)C(=O)OC 413.50 unknown https://doi.org/10.1002/CHIN.200447185
Methyl 18-(acetyloxymethyl)-19-hydroxy-14-methyl-12-azahexacyclo[10.6.1.11,4.010,18.015,19.07,20]icos-7(20)-ene-3-carboxylate 72787095 Click to see CC1CN2CC3CCC4=C5C(CC4)C(CC56C3(CCC1C62O)COC(=O)C)C(=O)OC 429.50 unknown https://doi.org/10.1016/J.TET.2004.05.078
> Organoheterocyclic compounds / Indoles and derivatives
methyl 3-[(1R,6R,10R,13R,14S,17S)-16-formyl-10-(hydroxymethyl)-14-methyl-9-oxo-16-azatetracyclo[8.7.0.02,6.013,17]heptadec-2-en-1-yl]propanoate 10001236 Click to see CC1CN(C2C1CCC3(C2(C4=CCCC4CCC3=O)CCC(=O)OC)CO)C=O 403.50 unknown https://doi.org/10.1016/J.TETLET.2003.11.116
Methyl 3-[16-formyl-10-(hydroxymethyl)-14-methyl-9-oxo-16-azatetracyclo[8.7.0.02,6.013,17]heptadec-2-en-1-yl]propanoate 85088458 Click to see CC1CN(C2C1CCC3(C2(C4=CCCC4CCC3=O)CCC(=O)OC)CO)C=O 403.50 unknown https://doi.org/10.1016/J.TETLET.2003.11.116
> Organoheterocyclic compounds / Indolizidines
(1R,7R,10R,11R,15S,18R,23R)-11-methyl-5-oxa-13-azahexacyclo[11.9.1.01,7.07,15.010,23.018,22]tricos-21-en-4-one 163009004 Click to see CC1CN2CC3CCC4CCC=C4C56C2C1CCC35COC(=O)CC6 341.50 unknown https://doi.org/10.1021/OL034388P
(1R,7R,10R,11S,15S,18R,23S)-11-methyl-5-oxa-13-azahexacyclo[11.9.1.01,7.07,15.010,23.018,22]tricos-21-en-4-one 101727336 Click to see CC1CN2CC3CCC4CCC=C4C56C2C1CCC35COC(=O)CC6 341.50 unknown https://doi.org/10.1002/CHIN.200337171
11-Methyl-5-oxa-13-azahexacyclo[11.9.1.01,7.07,15.010,23.018,22]tricos-21-en-4-one 12309032 Click to see CC1CN2CC3CCC4CCC=C4C56C2C1CCC35COC(=O)CC6 341.50 unknown https://doi.org/10.1021/OL034388P

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