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Polhillia involucrata

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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 UUID643fd9a6cf71f547393686
Scientific name Polhillia involucrata
Authority (Thunb.) B.-E.van Wyk & A.L.Schutte
First published in Kew Bull.44: 420 (1989)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psoralea involucrata Thunb. Prodr. Pl. Cap.: 136 (1800)
Melolobium involucratum (Thunb.) C.H.Stirt. S. African J. Bot.52: 355 (1986)
Argyrolobium involucratum (Thunb.) Harv. W.H.Harvey & auct. suc. (eds.), Fl. Cap.2: 75 (1862)

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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

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-0000186629
The Plant List ild-33111
IPNI 947032-1
GBIF 2951619
EOL 695199
Open Tree Of Life 398900

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
The major alkaloids of the genus Melolobium B-E. van Wyk, G.H. Verdoorn, Linda Burger, R. Greinwald Elsevier BV 20-Jul-2016
doi:10.1016/S0254-6299(16)31308-4
The major alkaloids of the genus Polhillia B-E. van Wyk, G.H. Verdoorn, R. Greinwald Elsevier BV 20-Jul-2016
doi:10.1016/S0254-6299(16)31309-6

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 / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,4S,9R,10S)-4-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163061089 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O 264.36 unknown https://doi.org/10.1016/S0254-6299(16)31309-6
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 51018075 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/S0254-6299(16)31309-6
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 163185252 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/S0254-6299(16)31309-6
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0254-6299(16)31308-4
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0254-6299(16)31308-4
> Organoheterocyclic compounds / Indolizidines
(1R,9R,10R)-7,14-diazatetracyclo[7.6.1.02,7.010,14]hexadeca-2,4-dien-6-one 6352153 Click to see C1CC2C3CC(CN2C1)C4=CC=CC(=O)N4C3 230.31 unknown https://doi.org/10.1016/S0254-6299(16)31309-6

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