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Eriolarynx lorentzii

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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 UUID6440411dd3580605139908
Scientific name Eriolarynx lorentzii
Authority (Dammer) Hunz.
First published in Kurtziana 28(1): 66. 2000..

Description Top

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Synonyms Top

Scientific name Authority First published in
Acnistus lorentzii Dammer Repert. Spec. Nov. Regni Veg. 15: 393. 1919
Dunalia lorentzii (Dammer) Sleumer Lilloa 23: 135. 1950
Vassobia lorentzii (Dammer) Hunz. Kurtziana 10: 24. 1977

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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-0001021576
Tropicos 50216494
KEW urn:lsid:ipni.org:names:1016239-1
The Plant List kew-2796916
Open Tree Of Life 315007
NCBI Taxonomy 304107
IUCN Red List 207885005
IPNI 1016239-1
GBIF 3797279

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
Anti-proliferative withanolides from the Solanaceae: a structure-activity study Zhang H, Samadi AK, Cohen MS, Timmermann BN Pure Appl Chem 15-Apr-2012
PMCID:PMC3789375
doi:10.1351/PAC-CON-11-10-08
PMID:24098060
Withanolides from Vassobia lorentzii. Misico RI, Gil RR, Oberti JC, Veleiro AS, Burton G J Nat Prod 01-Oct-2000
doi:10.1021/NP000022Z
PMID:11076546

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 / Steroid lactones / Withanolides and derivatives
(1S,2S,5S,6R,8R,9R,12S,13R,17S,18R,20R)-6-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-8,17-dihydroxy-6,13-dimethyl-7,19-dioxahexacyclo[10.9.0.02,9.05,9.013,18.018,20]henicos-15-en-14-one 21606678 Click to see CC1=C(C(=O)OC(C1)C2(C3CCC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C(O2)O)C)C 484.60 unknown https://doi.org/10.1021/NP000022Z
(1S,2S,5S,6R,8S,9R,12S,13R,17S,18R,20R)-6-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-8,17-dihydroxy-6,13-dimethyl-7,19-dioxahexacyclo[10.9.0.02,9.05,9.013,18.018,20]henicos-15-en-14-one 21606679 Click to see CC1=C(C(=O)OC(C1)C2(C3CCC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C(O2)O)C)C 484.60 unknown https://doi.org/10.1021/NP000022Z
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6-hydroxy-16-(hydroxymethyl)-2-methyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 73800274 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)CO)O)C 486.60 unknown https://doi.org/10.1021/NP000022Z
18-hydroxywithanolide D 21606687 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)CO)O)C 486.60 unknown https://doi.org/10.1021/NP000022Z
6-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-8,17-dihydroxy-6,13-dimethyl-7,19-dioxahexacyclo[10.9.0.02,9.05,9.013,18.018,20]henicos-15-en-14-one 73800270 Click to see CC1=C(C(=O)OC(C1)C2(C3CCC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C(O2)O)C)C 484.60 unknown https://doi.org/10.1021/NP000022Z

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