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Jaborosa laciniata

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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 UUID644041266a2dc184840257
Scientific name Jaborosa laciniata
Authority (Miers) Hunz. & Barboza
First published in Kurtziana 19: 102. 1987

Description Top

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Synonyms Top

Scientific name Authority First published in
Trechonaetes bridgesii Dunal Prodr. [A. P. de Candolle] 13(1): 468. 1852 [10 May 1852]
Trechonaetes laciniata Miers London J. Bot. 4: 350 (-351). 1845

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile North

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001021968
Tropicos 29605116
KEW urn:lsid:ipni.org:names:816013-1
The Plant List tro-29605116
Open Tree Of Life 5784098
NCBI Taxonomy 1608009
IPNI 278974-2
GBIF 3801935

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
Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms Dembitsky VM Molecules 20-Jul-2023
PMCID:PMC10384810
doi:10.3390/molecules28145549
PMID:37513423
Floral Scent Evolution in the Genus Jaborosa (Solanaceae): Influence of Ecological and Environmental Factors Moré M, Soteras F, Ibañez AC, Dötterl S, Cocucci AA, Raguso RA Plants (Basel) 23-Jul-2021
PMCID:PMC8398055
doi:10.3390/plants10081512
PMID:34451557
Summer Diet of Horses (Equus ferus caballus Linn.), Guanacos (Lama guanicoe Müller), and European Brown Hares (Lepus europaeus Pallas) in the High Andean Range of the Coquimbo Region, Chile Castellaro G, Orellana CL, Escanilla JP Animals (Basel) 03-May-2021
PMCID:PMC8147654
doi:10.3390/ani11051313
PMID:34063638
Flower Diversification Across “Pollinator Climates”: Sensory Aspects of Corolla Color Evolution in the Florally Diverse South American Genus Jaborosa (Solanaceae) Moré M, Ibañez AC, Drewniak ME, Cocucci AA, Raguso RA Front Plant Sci 07-Dec-2020
PMCID:PMC7750315
doi:10.3389/fpls.2020.601975
PMID:33365042
Withanolides from Jaborosa caulescens var. bipinnatifida Zhang H, Cao CM, Gallagher RJ, Day VW, Montenegro G, Timmermann BN Phytochemistry 05-Dec-2013
PMCID:PMC3947017
doi:10.1016/j.phytochem.2013.11.005
PMID:24314746
Withanolides from Jaborosa laciniata. Cirigliano AM, Veleiro AS, Misico RI, Tettamanzi MC, Oberti JC, Burton G J Nat Prod 01-Oct-2007
doi:10.1021/NP070197+
PMID:17883258
Trechonolide A, a new withanolide type from Trechonaetes laciniata David Lavie, Roberto Bessalle, Mauricio J. Pestchanker, Hugo E. Gottlieb, Felix Frolow, Oscar S. Giordano Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82290-6
Jaborosalactone L, a withanolide from Jaborosa leucotricha David Lavie, Hugo E. Gottlieb, Mauricio J. Pestchanker, Oscar S. Giordano Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81259-5

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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,4R,5R,10R,11S,13S,15R,16R,17R,20S)-15-[(2S)-3,4-dimethyl-5-oxo-2H-furan-2-yl]-4,5,17-trihydroxy-13-methoxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162913040 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)O)C5C2(C1(CC5)O)C)OC)C6C(=C(C(=O)O6)C)C 516.60 unknown https://doi.org/10.1021/NP070197+
(1S,2S,4R,6S,11R,12S,14S,16R,17R,18R,21S)-16-[(2R)-3,4-dimethyl-5-oxo-2H-furan-2-yl]-14,18-dihydroxy-11,17,21-trimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 162916597 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)O)C7C(=C(C(=O)O7)C)C 484.60 unknown https://doi.org/10.1016/S0031-9422(00)82290-6
https://doi.org/10.1016/S0031-9422(00)81259-5
(1S,2S,4R,6S,11R,12S,14S,16R,17R,18R,21S)-16-[(2R)-3,4-dimethyl-5-oxo-2H-furan-2-yl]-18-hydroxy-14-methoxy-11,17,21-trimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 163018046 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)OC)C7C(=C(C(=O)O7)C)C 498.60 unknown https://doi.org/10.1016/S0031-9422(00)82290-6
https://doi.org/10.1016/S0031-9422(00)81259-5
16-(3,4-dimethyl-5-oxo-2H-furan-2-yl)-18-hydroxy-14-methoxy-11,17,21-trimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 163018044 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)OC)C7C(=C(C(=O)O7)C)C 498.60 unknown https://doi.org/10.1016/S0031-9422(00)82290-6
https://doi.org/10.1016/S0031-9422(00)81259-5
4-(3,4-Dimethyl-5-oxo-2,5-dihydro-2-furanyl)-2a,5a-dihydroxy-3,6b,12c-trimethyl-1,2,2a,3,4,5a,6,6a,6b,11a,12,12a,12b,12c-tetradecahydrocyclopenta[de]oxireno[2',3':4,4a]naphtho[2,1-g]chromen-7(10H)-one 632998 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)O)C7C(=C(C(=O)O7)C)C 484.60 unknown https://doi.org/10.1016/S0031-9422(00)82290-6
https://doi.org/10.1016/S0031-9422(00)81259-5
Ergosta-2,24-dien-26-oic acid, 12,22-epoxy-5,6,12,17,23-pentahydroxy-1-oxo-, gamma-lactone, (5alpha,6beta,12alpha,17alpha,22R,23S)- 101712267 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)O)C5C2(C1(CC5)O)C)O)C6C(=C(C(=O)O6)C)C 502.60 unknown https://doi.org/10.1021/NP070197+
trechonolide A 46878357 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)O)C7C(=C(C(=O)O7)C)C 484.60 unknown https://doi.org/10.1016/S0031-9422(00)82290-6
https://doi.org/10.1021/NP070197+

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