Daphnandra apatela - Unknown
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Internal ID UUID64400558645cd968811807
Scientific name Daphnandra apatela
Authority Schodde
First published in Fl. Australia 2: 455 (2007)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000506967
Tropicos 100320539
KEW urn:lsid:ipni.org:names:77081981-1
The Plant List kew-2604139
Open Tree Of Life 5919635
NCBI Taxonomy 1842751
IUCN Red List 192227401
IPNI 77081981-1
iNaturalist 543981
GBIF 3782685
Freebase /m/0b6lxns
EOL 5402942
Wikipedia Daphnandra_apatela

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Genomics of the critically endangered monotypic genus Sinopora: the plastome of S. hongkongensis (Lauraceae) Carrion AD, Hinsinger DD, Strijk JS Mitochondrial DNA B Resour 07-Jan-2020
PMCID:PMC7748805
doi:10.1080/23802359.2019.1703590
PMID:33366565
Structure elucidation of antiproliferative bisbenzylisoquinoline alkaloids from Anisocycla grandidieri from the Madagascar dry forest Liu Y, Harinantenaina L, Brodie PJ, Slebodnick C, Callmander MW, Rakotondrajaona R, Rakotobe E, Rasamison VE, TenDyke K, Shen Y, Kingston DG Magn Reson Chem 10-Jun-2013
PMCID:PMC3747959
doi:10.1002/mrc.3976
PMID:23754698
Alkaloids of Daphnandra apatela IRC Bick, S Sotheeswaran CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9782077

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
(+)-1,2-Dehydrotelobine 10415402 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)OC)OC 560.60 unknown https://doi.org/10.1071/CH9782077
(+)-Cocsoline 3085062 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1071/CH9782077
(8R,21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene 93473840 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)OC)OC 562.70 unknown https://doi.org/10.1071/CH9782077
13,27-Dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene 85136688 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)OC)OC 560.60 unknown https://doi.org/10.1071/CH9782077
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaen-13-ol 21579623 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)OC 546.60 unknown https://doi.org/10.1071/CH9782077
Apateline 15560531 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1071/CH9782077
Dehydroapateline 44559250 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)OC 546.60 unknown https://doi.org/10.1071/CH9782077
Trigilletine 301935 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)OC)OC 562.70 unknown https://doi.org/10.1071/CH9782077

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