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Jaborosa caulescens

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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 UUID644041263106f153547765
Scientific name Jaborosa caulescens
Authority Gillies & Hook.
First published in Bot. Misc. 1: 347. 1830

Description Top

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Synonyms Top

Scientific name Authority First published in
Dorystigma caulescens Miers London J. Bot. 4: 348. 1845
Jaborosa bipinnatifida (Dunal) F.Meigen Bot. Jahrb. Syst. 17: 270. 1893; 18: 454. 1894
Jaborosa caulescens var. bipinnatifidum Reiche Anales Univ. Chile 124: 750. 1909
Lonchestigma bipinnatifidum (Dunal) Phil. Fl. Atacam. 42. 1860
Lonchestigma caulescens var. bipinnatifidum Dunal Prodr. [A. P. de Candolle] 13(1): 477. 1852 [10 May 1852]
Trechonaetes bipinnatifida Phil. Anales Mus. Nac., Santiago de Chile 1891: 67.

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-0001021956
Tropicos 29600758
KEW urn:lsid:ipni.org:names:816006-1
Open Tree Of Life 5745717
NCBI Taxonomy 1608004
IPNI 816006-1
GBIF 7299981
CMAUP NPO2027

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
Antiproliferative withanolides from several Solanaceous species Zhang H, Cao CM, Gallagher RJ, Timmermann BN Nat Prod Res 28-May-2014
PMCID:PMC4177291
doi:10.1080/14786419.2014.919286
PMID:24871278
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
New Withanolides from Two Varieties of Jaborosa Caulescens Viviana Nicotra, Roberto Gil, Juan Oberti, Gerardo Burton MDPI AG 27-Nov-2008
doi:10.3390/50300514
Withanolides with phytotoxic activity from Jaborosa caulescens var. caulescens and J. caulescens var. bipinnatifida 1. Nicotra VE, Gil RR, Oberti JC, Burton G J Nat Prod 01-May-2007
doi:10.1021/NP070030G
PMID:17428092

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 / Terpene lactones
(1S,2S,4R,6S,11R,12S,14S,17S,18R,21S)-17-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-14,18-dihydroxy-11,21-dimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 162935300 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)O)C 484.60 unknown https://doi.org/10.3390/50300514
(1S,2S,4R,6S,11R,12S,14S,17S,18R,21S)-17-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-18-hydroxy-14-methoxy-11,21-dimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 162951726 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)OC)C 498.60 unknown https://doi.org/10.3390/50300514
12-O-methyljaborosalactone 38 16681116 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)OC)C 498.60 unknown https://doi.org/10.1021/NP070030G
17-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-14,18-dihydroxy-11,21-dimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 73306511 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)O)C 484.60 unknown https://doi.org/10.1021/NP070030G
https://doi.org/10.3390/50300514
17-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-14,18-dihydroxy-11,21-dimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicosan-10-one 73306512 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)CCC6)C)O5)C7C3(C2(CC7)O)C)O)C 486.60 unknown https://doi.org/10.1021/NP070030G
17-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-18-hydroxy-14-methoxy-11,21-dimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 73306993 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)OC)C 498.60 unknown https://doi.org/10.3390/50300514
https://doi.org/10.1021/NP070030G
Jaborosalactone 16680130 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)C=CC6)C)O5)C7C3(C2(CC7)O)C)O)C 484.60 unknown https://doi.org/10.1021/NP070030G
Jaborosalactone 39 16680131 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC5C6(C4(C(=O)CCC6)C)O5)C7C3(C2(CC7)O)C)O)C 486.60 unknown https://doi.org/10.1021/NP070030G
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,2R,4R,10R,11S,13R,16S,17S,20S)-4,13,17-trihydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icosa-5,7-dien-9-one 163005051 Click to see CC1=C(C(=O)OC(C1)(C2COC3(CC4C(CC(C5=CC=CC(=O)C45C)O)C6C3(C2(CC6)O)C)O)O)C 500.60 unknown https://doi.org/10.1021/NP070030G
(1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162897849 Click to see CC1=C(C(=O)OC(C1)(C2COC3(CC4C(CC(C5(C4(C(=O)C=CC5)C)O)O)C6C3(C2(CC6)O)C)O)O)C 518.60 unknown https://doi.org/10.1021/NP070030G
4,13,17-trihydroxy-16-(2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl)-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icosa-5,7-dien-9-one 163005050 Click to see CC1=C(C(=O)OC(C1)(C2COC3(CC4C(CC(C5=CC=CC(=O)C45C)O)C6C3(C2(CC6)O)C)O)O)C 500.60 unknown https://doi.org/10.1021/NP070030G
4,5,13,17-tetrahydroxy-16-(2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl)-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162897848 Click to see CC1=C(C(=O)OC(C1)(C2COC3(CC4C(CC(C5(C4(C(=O)C=CC5)C)O)O)C6C3(C2(CC6)O)C)O)O)C 518.60 unknown https://doi.org/10.1021/NP070030G
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2S,4R,5R,10R,11S,13R,15R,16R,17S,20S)-4,5,13,17-tetrahydroxy-15-[(2S)-2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl]-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162856519 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)O)C5C2(C1(CC5)O)C)O)C6(C(=C(C(=O)O6)C)C)O 518.60 unknown https://doi.org/10.1021/NP070030G
(1S,2S,4R,6S,11R,12S,14R,16S,17R,18S,21S)-14,18-dihydroxy-16-[(2R)-2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl]-11,17,21-trimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 162902950 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)O)C7(C(=C(C(=O)O7)C)C)O 500.60 unknown https://doi.org/10.1021/NP070030G
12-O-ethyljaborosalactone 42 16681115 Click to see CCOC12CC3C(CC(C4(C3(C(=O)C=CC4)C)Cl)O)C5C1(C(CC5)(C(C(O2)C6C(=C(C(=O)O6)C)C)C)O)C 549.10 unknown https://doi.org/10.1021/NP070030G
14,18-Dihydroxy-16-(2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl)-11,17,21-trimethyl-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-en-10-one 162902949 Click to see CC1C(OC2(CC3C(CC4C5(C3(C(=O)C=CC5)C)O4)C6C2(C1(CC6)O)C)O)C7(C(=C(C(=O)O7)C)C)O 500.60 unknown https://doi.org/10.1021/NP070030G
4,5,13,17-Tetrahydroxy-15-(2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl)-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162856518 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)O)C5C2(C1(CC5)O)C)O)C6(C(=C(C(=O)O6)C)C)O 518.60 unknown https://doi.org/10.1021/NP070030G
5-chloro-15-(3,4-dimethyl-5-oxo-2H-furan-2-yl)-13-ethoxy-4,17-dihydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 73306992 Click to see CCOC12CC3C(CC(C4(C3(C(=O)C=CC4)C)Cl)O)C5C1(C(CC5)(C(C(O2)C6C(=C(C(=O)O6)C)C)C)O)C 549.10 unknown https://doi.org/10.1021/NP070030G
5-chloro-15-(3,4-dimethyl-5-oxo-2H-furan-2-yl)-4,13,17-trihydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 73307010 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)Cl)O)C5C2(C1(CC5)O)C)O)C6C(=C(C(=O)O6)C)C 521.00 unknown https://doi.org/10.1021/NP070030G
Jaborosalactone 42 16681155 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)Cl)O)C5C2(C1(CC5)O)C)O)C6C(=C(C(=O)O6)C)C 521.00 unknown https://doi.org/10.1021/NP070030G
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database

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