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Mesembryanthemum ladismithiense

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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 UUID6440828497451825791745
Scientific name Mesembryanthemum ladismithiense
Authority Klak
First published in in Taxon 56: 752. 2007.

Description Top

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Synonyms Top

Scientific name Authority First published in
Sceletium strictum L.Bolus in S. African Gard. 17: 399. 1927.

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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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-0000507613
KEW urn:lsid:ipni.org:names:77083441-1
The Plant List kew-2604939
Open Tree Of Life 614032
NCBI Taxonomy 246242
IPNI 77083441-1
iNaturalist 589845
GBIF 3703623

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
Skeletons in the closet? Using a bibliometric lens to visualise phytochemical and pharmacological activities linked to Sceletium, a mood enhancer Reddy K, Stafford GI, Makunga NP Front Plant Sci 21-Mar-2024
PMCID:PMC10991851
doi:10.3389/fpls.2024.1268101
PMID:38576783
Mass Spectrometry Metabolomics and Feature-Based Molecular Networking Reveals Population-Specific Chemistry in Some Species of the Sceletium Genus Reddy K, Stander MA, Stafford GI, Makunga NP Front Nutr 29-Mar-2022
PMCID:PMC9001948
doi:10.3389/fnut.2022.819753
PMID:35425789
Total synthesis of natural products using hypervalent iodine reagents Maertens G, L'Homme C, Canesi S Front Chem 05-Jan-2015
PMCID:PMC4283662
doi:10.3389/fchem.2014.00115
PMID:25601909
Sceletium alkaloids. IV. Biosynthesis of mesembrine and related alkaloids. Amino acid precursors P. W. Jeffs, W. C. Archie, Richard L. Hawks, D. S. Farrier American Chemical Society (ACS) 19-Mar-2005
doi:10.1021/JA00744A032
A new enantioselective route to the Sceletium alkaloids via a cyclopentanone–cyclohexenone transformation Masato Hayashi, Tomohiro Unno, Michiyasu Takahashi, Kunio Ogasawara Elsevier BV 26-Mar-2003
doi:10.1016/S0040-4039(02)00033-3

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
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
3a-(3,4-Dimethoxyphenyl)-1-methyl-2,3,4,5,7,7a-hexahydroindol-6-one 499683 Click to see CN1CCC2(C1CC(=O)CC2)C3=CC(=C(C=C3)OC)OC 289.40 unknown https://doi.org/10.1021/JA00744A032
CID 46898090 46898090 Click to see CN1CCC2(C1CC(C=C2)O)C3=CC(=C(C=C3)OC)OC 289.40 unknown https://doi.org/10.1021/JA00744A032
Mesembrenol 139262238 Click to see CN1CCC2(C1CC(C=C2)O)C3=CC(=C(C=C3)OC)OC 289.40 unknown https://doi.org/10.1021/JA00744A032
Mesembrine 394162 Click to see CN1CCC2(C1CC(=O)CC2)C3=CC(=C(C=C3)OC)OC 289.40 unknown https://doi.org/10.1016/S0040-4039(02)00033-3
https://doi.org/10.1021/JA00744A032
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Tortuosamine 101324747 Click to see CNCCC1(CCC2=C(C1)C=CC=N2)C3=CC(=C(C=C3)OC)OC 326.40 unknown https://doi.org/10.1016/S0040-4039(02)00033-3

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Contributors Top

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Collections Top

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