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Daphnandra dielsii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644015b45dbb2614076229
Scientific name Daphnandra dielsii
Authority Perkins
First published in Pflanzenr. , IV, 101: 46 (1901)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000637425
Tropicos 100320540
KEW urn:lsid:ipni.org:names:581857-1
The Plant List kew-2756797
Open Tree Of Life 6025121
IPNI 97970-3
GBIF 3782645

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)!
Title Authors Publication Released IDs
ChemInform Abstract: Alkaloids of Daphnandra dielsii. Part 4. Chemical and Spectroscopic Evidence for the Structure of Daphnine A. S. HOWARD, J. HARLEY‐MASON, J. BALDAS, I. R. C. BICK Wiley 03-Sep-2010
doi:10.1002/CHIN.199349265
Alkaloids of Daphnandra dielsii. I. Tertiary Bases. Isolation and Structural Determination of Dielsine CD Critchett, HRW Dharmaratne, S Sotheeswaran, AM Galal, PL Schiff, IRC Bick CSIRO Publishing 03-Sep-2010
doi:10.1071/CH9892043
Alkaloids of Daphnandra dielsii. II. Daphnine. Isolation and Characterization AS Howard, J Harleymason, IRC Bick CSIRO Publishing 03-Sep-2010
doi:10.1071/CH9901129
Nortenuipine-2'b-N-oxide, a New Bisbenzylisoquinoline Alkaloid from Daphnandra dielsii Paul L. Schiff, Jr., Ahmed M. Galal, Colin D. Critchett, I. Ralph C. Bick, Subramaniam Sotheeswaran, Cong-yuan Gao, Fu-tyan Lin, Francis K. Duah, Emil W. Fu, Lan K. Wong The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-89-4957

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
> Lignans, neolignans and related compounds
(-)-Nortenuipine 284740 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=CC(=CC6=C5OCO6)CC7C8=C(O3)C(=C(C=C8CCN7C)OC)O)OC 622.70 unknown https://doi.org/10.3987/COM-89-4957
https://doi.org/10.1071/CH9892043
(-)-Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown https://doi.org/10.1071/CH9892043
https://doi.org/10.3987/COM-89-4957
(12S,20S,31R)-18-methoxy-13,30-dimethyl-2,5,7,22,39-pentaoxa-13,30-diazanonacyclo[31.2.2.13,10.112,16.120,24.123,27.04,8.026,31.020,40]hentetraconta-1(35),3(41),4(8),9,16(40),17,23,25,27(38),33,36-undecaen-19-one 54602142 Click to see 620.70 unknown https://doi.org/10.1071/CH9892043
https://doi.org/10.3987/COM-89-4957
(3S,22R)-16,27-dimethoxy-4,21-dimethyl-12,29,37-trioxa-4,21-diazaoctacyclo[28.2.2.17,11.110,14.114,18.124,28.03,8.022,36]octatriaconta-1(33),7(38),8,10,16,18(36),24(35),25,27,30(34),31-undecaen-15-one 102152736 Click to see 606.70 unknown https://doi.org/10.1071/CH9892043
https://doi.org/10.3987/COM-89-4957
6,6'-Dimethoxy-2,2'-dimethyloxyacanthan-7,12'-diol 122728 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)O)OC 594.70 unknown https://doi.org/10.3987/COM-89-4957
Aromoline 362574 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)O)OC 594.70 unknown https://doi.org/10.3987/COM-89-4957
Oxyacanthan, 6,6',7,12'-tetramethoxy-2,2'-dimethyl-, (1'alpha)- 21587580 Click to see 622.70 unknown https://doi.org/10.1071/CH9892043
Oxyacanthine 442333 Click to see 608.70 unknown https://doi.org/10.3987/COM-89-4957
Repanduline 494545 Click to see 620.70 unknown https://doi.org/10.3987/COM-89-4957
https://doi.org/10.1071/CH9892043
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
4-methyl-1H-indeno[1,2-b]pyridine-2,5-dione 457731 Click to see CC1=CC(=O)NC2=C1C(=O)C3=CC=CC=C32 211.22 unknown https://doi.org/10.1071/CH9892043
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(25E)-32,39-dimethoxy-9,27-dimethyl-2,15,17,20-tetraoxa-27-aza-9-azoniaoctacyclo[24.6.2.23,6.221,24.112,19.05,10.014,18.030,34]nonatriaconta-1(32),3(39),4,6(38),9,12,14(18),19(37),21,23,25,28,30,33,35-pentadecaen-4-olate 152772198 Click to see 616.70 unknown https://doi.org/10.1071/CH9901129
32,39-Dimethoxy-9,27-dimethyl-2,15,17,20-tetraoxa-9,27-diazaoctacyclo[24.6.2.23,6.221,24.112,19.05,10.014,18.030,34]nonatriaconta-1(32),3(39),5(10),6(38),12,14(18),19(37),21,23,25,28,30,33,35-tetradecaen-4-one 163194681 Click to see CN1CCC2=CC(=C3C(=O)C2=C1CC4=CC5=C(C(=C4)OC6=CC=C(C=C6)C=C7C8=CC(=C(C=C8C=CN7C)OC)O3)OCO5)OC 616.70 unknown https://doi.org/10.1071/CH9901129
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1002/CHIN.199349265
https://doi.org/10.1071/CH9901129

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