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Pseudoprospero firmifolium

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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 UUID644020a59a5a0967765172
Scientific name Pseudoprospero firmifolium
Authority (Baker) Speta
First published in Phyton (Horn) 38: 116 (1998)

Description Top

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Synonyms Top

Scientific name Authority First published in
Scilla firmifolia Baker Refug. Bot. 3(App.): 7 (1870)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pseudoprospero firmifolium subsp. firmifolium (Baker) Speta Unknown
Pseudoprospero firmifolium subsp. natalensis J.C.Manning Bothalia 39: 232 (2009)

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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No germination or propagation data was added yet.

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-0000723079
Tropicos 50277203
KEW urn:lsid:ipni.org:names:1003496-1
The Plant List kew-285054
Open Tree Of Life 101491
NCBI Taxonomy 208145
IPNI 1003496-1
iNaturalist 592577
GBIF 2774040
EOL 1015595

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
A Comprehensive Review on Chemotaxonomic and Phytochemical Aspects of Homoisoflavonoids, as Rare Flavonoid Derivatives Mottaghipisheh J, Stuppner H Int J Mol Sci 08-Mar-2021
PMCID:PMC7962952
doi:10.3390/ijms22052735
PMID:33800482
Antiangiogenic Activity and Cytotoxicity of Triterpenoids and Homoisoflavonoids from Massonia pustulata and Massonia bifolia. Schwikkard SL, Whitmore H, Corson TW, Sishtla K, Langat MK, Carew M, Mulholland DA Planta Med 28-Feb-2018
PMCID:PMC6467464
doi:10.1055/a-0577-5322
PMID:29490386
Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies) Ali SS, Yu Y, Pfosser M, Wetschnig W Ann Bot 27-Oct-2011
PMCID:PMC3241591
doi:10.1093/aob/mcr274
PMID:22039008
Homoisoflavanones from Pseudoprospero firmifolium of the monotypic tribe Pseudoprospereae (Hyacinthaceae: Hyacinthoideae). Koorbanally C, Sewjee S, Mulholland DA, Crouch NR, Dold A Phytochemistry 01-Nov-2007
doi:10.1016/J.PHYTOCHEM.2007.08.005
PMID:17884116

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 / Prenol lipids / Triterpenoids
(3beta,17alpha,23S)-17,23-Epoxy-3,29-dihydroxy-27-norlanost-8-en-24-one 73816064 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
15-Deoxoeucosterol 21632988 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans
(3R)-3-[(3,4-dimethoxyphenyl)methyl]-3,5-dihydroxy-7-methoxy-2H-chromen-4-one 162870442 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=CC(=C3C2=O)O)OC)O)OC 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
(3R)-3-[(3,4-dimethoxyphenyl)methyl]-3,5-dihydroxy-7,8-dimethoxy-2H-chromen-4-one 162870443 Click to see COC1=C(C=C(C=C1)CC2(COC3=C(C2=O)C(=CC(=C3OC)OC)O)O)OC 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
(3S)-3,5-dihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7,8-dimethoxy-2H-chromen-4-one 163082382 Click to see COC1=C(C=C(C=C1)CC2(COC3=C(C2=O)C(=CC(=C3OC)OC)O)O)O 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
(3S)-3,5,6-trihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2H-chromen-4-one 162868893 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=C(C(=C3C2=O)O)O)OC)O)O 362.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
(3S)-3,5,7-trihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-2H-chromen-4-one 162991059 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=CC(=C3C2=O)O)O)O)O 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
3-[(3,4-dimethoxyphenyl)methyl]-3,5-dihydroxy-7-methoxy-2H-chromen-4-one 90942759 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=CC(=C3C2=O)O)OC)O)OC 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
3-[(3,4-dimethoxyphenyl)methyl]-3,5-dihydroxy-7,8-dimethoxy-2H-chromen-4-one 90848764 Click to see COC1=C(C=C(C=C1)CC2(COC3=C(C2=O)C(=CC(=C3OC)OC)O)O)OC 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
3,5-dihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7,8-dimethoxy-2H-chromen-4-one 91220081 Click to see COC1=C(C=C(C=C1)CC2(COC3=C(C2=O)C(=CC(=C3OC)OC)O)O)O 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
3,5,6-trihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2H-chromen-4-one 91083756 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=C(C(=C3C2=O)O)O)OC)O)O 362.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005
3,5,7-trihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-2H-chromen-4-one 91551865 Click to see COC1=C(C=C(C=C1)CC2(COC3=CC(=CC(=C3C2=O)O)O)O)O 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.005

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