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Blandfordia punicea

Blandfordia punicea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440255457473518765017
Scientific name Blandfordia punicea
Authority Sweet
First published in Hort. Brit. , ed. 2: 517 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aletris punicea Labill. Nov. Holl. Pl. 1: 85 (1805)
Blandfordia backhousii Lindl. Edwards's Bot. Reg. 31: t. 18 (1845)
Blandfordia grandiflora var. backhousei Hook.f. Fl. Tasman. 2: 49 (1858)
Blandfordia grandiflora var. marginata (Herb.) Hook.f. Fl. Tasman. 2: 49 (1858)
Blandfordia marginata Herb. Edwards's Bot. Reg. 28: t. 84 (1842)

Common names Top

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Language Common/alternative name
English tasmanian christmas bell
German weihnachtsglocke
Chinese 香水花科

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000761606
KEW urn:lsid:ipni.org:names:531919-1
The Plant List kew-300605
Open Tree Of Life 628349
NCBI Taxonomy 49702
IPNI 531919-1
iNaturalist 85482
GBIF 5305360
Freebase /m/02q4t9r
EPPO BNFPU
EOL 1086242
USDA GRIN 454887
Wikipedia Blandfordia_punicea

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)!
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Title Authors Publication Released IDs
A Universal Probe Set for Targeted Sequencing of 353 Nuclear Genes from Any Flowering Plant Designed Using k-Medoids Clustering Johnson MG, Pokorny L, Dodsworth S, Botigué LR, Cowan RS, Devault A, Eiserhardt WL, Epitawalage N, Forest F, Kim JT, Leebens-Mack JH, Leitch IJ, Maurin O, Soltis DE, Soltis PS, Wong GK, Baker WJ, Wickett NJ Syst Biol 10-Dec-2018
PMCID:PMC6568016
doi:10.1093/sysbio/syy086
PMID:30535394
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457
First Nuclear DNA C‐values for 28 Angiosperm Genera HANSON L, BROWN RL, BOYD A, JOHNSON MA, BENNETT MD Ann Bot 01-Jan-2003
PMCID:PMC4240350
doi:10.1093/aob/mcg005
PMID:12495917
Punisterone [(20<i>R</i>,24<i>S</i>)-25-Deoxy-11α,20,24-trihydroxyecdysone]:  A New Phytoecdysteroid from <i>Blandfordia punicea</i> Satyajit D. Sarker, Laurence N. Dinan, Jean-Pierre Girault, René Lafont, Peter G. Waterman American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960377B

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(14S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-17-[(3R)-2,3,5-trihydroxy-6-methylheptan-2-yl]-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 70679503 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,5-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 5320955 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 4254739 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1021/NP960377B
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,5-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 71436499 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 271604 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1021/NP960377B
24-epi-Pterosterone 11027254 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown https://doi.org/10.1021/NP960377B
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
CID 11799446 11799446 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
Ponasterone C 15249992 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
Pterosterone 441836 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown https://doi.org/10.1021/NP960377B
Turkesterone 14376672 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1021/NP960377B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
2,3,14,22,25-Pentahydroxycholest-7-en-6-one 4233007 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown https://doi.org/10.1021/NP960377B
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown https://doi.org/10.1021/NP960377B
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
Atpenin A5 54676868 Click to see CC(CC(C)C(=O)C1=C(C(=C(NC1=O)OC)OC)O)C(CCl)Cl 366.20 unknown https://doi.org/10.1021/NP960377B

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