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Jaborosa rotacea

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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
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Details Top

Internal ID UUID6440412772f98166263778
Scientific name Jaborosa rotacea
Authority (Lillo) Hunz. & Barboza
First published in Kurtziana 19: 105. 1987

Description Top

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Synonyms Top

Scientific name Authority First published in
Jaborosa rotacea var. tucumanensis Figueroa Romero, Muruaga & Bulacio Lilloa 40(1): 6 (5-13; figs. 1-5). 2000 [11 May 2000]
Trechonaetes rotacea Lillo Primera Reun. Nac. Soc. Argent. Ci. Nat. 1916: 227. 1919

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001021983
Tropicos 29608868
KEW urn:lsid:ipni.org:names:278977-2
The Plant List tro-29608868
Open Tree Of Life 5784095
NCBI Taxonomy 1608017
IPNI 944787-1
GBIF 7299962

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
Editorial: The Role of Flower Color in Angiosperm Evolution Narbona E, Arista M, Whittall JB, Camargo MG, Shrestha M Front Plant Sci 17-Sep-2021
PMCID:PMC8484755
doi:10.3389/fpls.2021.736998
PMID:34603361
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
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
The role of metals in mammalian olfaction of low molecular weight organosulfur compounds Block E, Batista VS, Matsunami H, Zhuang H, Ahmed L Nat Prod Rep 10-May-2017
PMCID:PMC5542778
doi:10.1039/c7np00016b
PMID:28471462
Phytotoxic withanolides from Jaborosa rotacea. Nicotra VE, Ramacciotti NS, Gil RR, Oberti JC, Feresin GE, Guerrero CA, Baggio RF, Garland MT, Burton G J Nat Prod 01-May-2006
doi:10.1021/NP0600090
PMID:16724841

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
(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/NP0600090
(1S,2S,4R,5R,10S,11S,13S,16R,17R,20S)-5-chloro-16-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-4,13,17-trihydroxy-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162970133 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC(C5(C4(C(=O)C=CC5)C)Cl)O)C6C3(C2(CC6)O)C)O)C 521.00 unknown https://doi.org/10.1021/NP0600090
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/NP0600090
5-Chloro-16-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-4,13,17-trihydroxy-10,20-dimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 73024668 Click to see CC1=C(C(=O)OC(C1)C2COC3(CC4C(CC(C5(C4(C(=O)C=CC5)C)Cl)O)C6C3(C2(CC6)O)C)O)C 521.00 unknown https://doi.org/10.1021/NP0600090
9,10,16-Trihydroxy-4,17,20,21,24-pentamethyl-23-oxahexacyclo[11.10.1.01,19.03,12.04,9.016,24]tetracosa-6,20-diene-5,18,22-trione 73016991 Click to see CC1C(=O)C2C(=C(C(=O)OC23CC4C(CC(C5(C4(C(=O)C=CC5)C)O)O)C6C3(C1(CC6)O)C)C)C 484.60 unknown https://doi.org/10.1021/NP0600090
Jaborosalactone 31 44583789 Click to see CC1C(=O)C2C(=C(C(=O)OC23CC4C(CC(C5(C4(C(=O)C=CC5)C)O)O)C6C3(C1(CC6)O)C)C)C 484.60 unknown https://doi.org/10.1021/NP0600090
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2S,4R,5R,10R,11S,13S,15S,16R,17R,20S)-15-[(2S)-3,4-dimethyl-5-oxo-2H-furan-2-yl]-4,5,13,17-tetrahydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 163009294 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/NP0600090
(1S,2S,4R,5R,10R,11S,13S,15S,16S,17R,20S)-4,5,13,17-tetrahydroxy-4',5',10,16,20-pentamethylspiro[14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-ene-15,2'-3H-pyran]-6',9-dione 162961434 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 502.60 unknown https://doi.org/10.1021/NP0600090
(1S,2S,4R,6S,11R,12S,14S,16S,17R,18R,21S)-16-[(2S)-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 162916596 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/10.1021/NP0600090
(1S,2S,4S,5S,10R,11S,13S,15S,16R,17R,20S)-4-chloro-15-[(2S)-3,4-dimethyl-5-oxo-2H-furan-2-yl]-5,13,17-trihydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 162909045 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)Cl)C5C2(C1(CC5)O)C)O)C6C(=C(C(=O)O6)C)C 521.00 unknown https://doi.org/10.1021/NP0600090
(1S,3R,4R,7R,8S,11R,12R,15S,16S,18R,19R,24R,25S,27S)-1,7,12,18,19-pentahydroxy-7,8,24,27-tetramethyl-2,5,9-trioxaheptacyclo[13.11.1.03,11.04,8.012,27.016,25.019,24]heptacos-21-ene-6,23-dione 162864795 Click to see CC12C3CCC1(C4COC5(C(C4OC2(CC6C3CC(C7(C6(C(=O)C=CC7)C)O)O)O)OC(=O)C5(C)O)C)O 534.60 unknown https://doi.org/10.1021/NP0600090
(1S,3R,4S,7R,8R,11R,12R,15S,16S,18R,20S,25R,26S,28S)-1,7,12-trihydroxy-7,8,25,28-tetramethyl-2,5,9,19-tetraoxaoctacyclo[13.12.1.03,11.04,8.012,28.016,26.018,20.020,25]octacos-22-ene-6,24-dione 162922163 Click to see CC12C3CCC1(C4COC5(C(C4OC2(CC6C3CC7C8(C6(C(=O)C=CC8)C)O7)O)OC(=O)C5(C)O)C)O 516.60 unknown https://doi.org/10.1021/NP0600090
1,7,12-Trihydroxy-7,8,25,28-tetramethyl-2,5,9,19-tetraoxaoctacyclo[13.12.1.03,11.04,8.012,28.016,26.018,20.020,25]octacos-22-ene-6,24-dione 72997625 Click to see CC12C3CCC1(C4COC5(C(C4OC2(CC6C3CC7C8(C6(C(=O)C=CC8)C)O7)O)OC(=O)C5(C)O)C)O 516.60 unknown https://doi.org/10.1021/NP0600090
1,7,12,18,19-Pentahydroxy-7,8,24,27-tetramethyl-2,5,9-trioxaheptacyclo[13.11.1.03,11.04,8.012,27.016,25.019,24]heptacos-21-ene-6,23-dione 73029581 Click to see CC12C3CCC1(C4COC5(C(C4OC2(CC6C3CC(C7(C6(C(=O)C=CC7)C)O)O)O)OC(=O)C5(C)O)C)O 534.60 unknown https://doi.org/10.1021/NP0600090
14',18'-dihydroxy-4,5,11',17',21'-pentamethylspiro[3H-pyran-2,16'-5,15-dioxahexacyclo[12.6.1.02,12.04,6.06,11.018,21]henicos-8-ene]-6,10'-dione 73026918 Click to see CC1C2(CCC3C2(C(CC4C3CC5C6(C4(C(=O)C=CC6)C)O5)(OC17CC(=C(C(=O)O7)C)C)O)C)O 484.60 unknown https://doi.org/10.1021/NP0600090
15-(3,4-dimethyl-5-oxo-2H-furan-2-yl)-4,5,13,17-tetrahydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 73000092 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/NP0600090
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/10.1021/NP0600090
4-chloro-15-(3,4-dimethyl-5-oxo-2H-furan-2-yl)-5,13,17-trihydroxy-10,16,20-trimethyl-14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-en-9-one 73070469 Click to see CC1C(OC2(CC3C(CC(C4(C3(C(=O)C=CC4)C)O)Cl)C5C2(C1(CC5)O)C)O)C6C(=C(C(=O)O6)C)C 521.00 unknown https://doi.org/10.1021/NP0600090
4-chloro-5,13,17-trihydroxy-4',5',10,16,20-pentamethylspiro[14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-ene-15,2'-3H-pyran]-6',9-dione 73061289 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)O)Cl)(OC16CC(=C(C(=O)O6)C)C)O)C)O 521.00 unknown https://doi.org/10.1021/NP0600090
4,13,17-trihydroxy-4',5',10,16,20-pentamethylspiro[14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icosa-5,7-diene-15,2'-3H-pyran]-6',9-dione 73039061 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5=CC=CC(=O)C45C)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 484.60 unknown https://doi.org/10.1021/NP0600090
4,5,13,17-tetrahydroxy-4',5',10,16,20-pentamethylspiro[14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-ene-15,2'-3H-pyran]-6',9-dione 73017083 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 502.60 unknown https://doi.org/10.1021/NP0600090
5-chloro-4,13,17-trihydroxy-4',5',10,16,20-pentamethylspiro[14-oxapentacyclo[11.6.1.02,11.05,10.017,20]icos-7-ene-15,2'-3H-pyran]-6',9-dione 72984424 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)Cl)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 521.00 unknown https://doi.org/10.1021/NP0600090
Jaborosalactone 28 44583790 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)Cl)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 521.00 unknown https://doi.org/10.1021/NP0600090
Jaborosalactone 29 44583786 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5(C4(C(=O)C=CC5)C)O)Cl)(OC16CC(=C(C(=O)O6)C)C)O)C)O 521.00 unknown https://doi.org/10.1021/NP0600090
Jaborosalactone 30 44583787 Click to see CC1C2(CCC3C2(C(CC4C3CC(C5=CC=CC(=O)C45C)O)(OC16CC(=C(C(=O)O6)C)C)O)C)O 484.60 unknown https://doi.org/10.1021/NP0600090
Jaborosalactone 46 46888758 Click to see CC1C2(CCC3C2(C(CC4C3CC5C6(C4(C(=O)C=CC6)C)O5)(OC17CC(=C(C(=O)O7)C)C)O)C)O 484.60 unknown https://doi.org/10.1021/NP0600090

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