71 to 80 of 121 Results
Adessi, Tonino G.; Riveira, Martín J.; De La Horra, Camila; Centurión, Enzo F. G., 2024, "1D and 2D Nuclear Magnetic Resonance spectra raw data for the compounds huajiaosimuline and related synthetic and natural pyranoquinolones.", https://doi.org/10.57715/UNR/BVWFGK, RDA UNR, V1
Introduction In the context of natural product synthesis, spectroscopic information has been collected for six compounds of the pyranoquinolone alkaloid type. These include Huajiaosimuline and Simulansine, alkaloids isolated from the species Zanthoxylum simulans, and four synthet... |
RAR Archive - 23.1 MB -
MD5: dde60c753b1a7ebc52a84b32271cf5ef
Inside this file can be found the raw data of all NMR experiments performed for the compound “Huajiaosimuline”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR experiment, COSY;... |
RAR Archive - 23.1 MB -
MD5: 674efbd13ab9965e18ddf46108719b88
Inside this file can be found the raw data of all NMR experiments performed for the compound “Epoxyzanthosimuline”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR experiment, CO... |
RAR Archive - 21.3 MB -
MD5: 41421e760a4ee4a4c6ab427936dcf35c
Inside this file can be found the raw data of all NMR experiments performed for the compound “Simulansine”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR experiment, COSY; NMR_... |
RAR Archive - 23.3 MB -
MD5: 88f0c03eb4aba5e973bb26c862e63d4d
Inside this file can be found the raw data of all NMR experiments performed for the compound “Diol side product”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR experiment, COSY... |
RAR Archive - 22.2 MB -
MD5: 5e104ee65e2031c1b79c22a110f15ff9
Inside this file can be found the raw data of all NMR experiments performed for the compound “Diol monoacetate side product”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR expe... |
RAR Archive - 24.4 MB -
MD5: 1f7a78cfe037029edef2f0a7c71a6e47
Inside this file can be found the raw data of all NMR experiments performed for the compound “Diol monotriflate side product”, organized in folders with the following codes: NMR_1D_1H for the 1H NMR experiment; NMR_1D_13C for the 13C NMR experiment; NMR_2D_COSY for the 2D NMR exp... |
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TIFF Image - 154.9 KB -
MD5: 5b24f6bcd2a0873a17eba017bc3f6a0a
Inside this image file can be observed the chemical structures of six compounds alkaloid type pyranoquinolone, studied in this dataset: Huajiaosimuline; Epoxyzantosimuline; Simulansine; Diol Side Product; Diol Side Product monoacetate; and Diol Side Product monotriflate. |
Plain Text - 8.2 KB -
MD5: 7667ad684378b4e4f05e79108d51d903
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Bortolotti, Ana; Almada, Juan Cruz; Porrini, Lucía; Albanesi, Daniela; Miguel, Virginia; Cybulski, Larisa, 2024, "Experimental evidence of a new mechanism of activation of bacterial histidine kinases", https://doi.org/10.57715/UNR/MPA7NB, RDA UNR, V1, UNF:6:MyNjHceGjMJ3qmUD9nYL3Q== [fileUNF]
This data set shows a new mechanism of activation of histidine kinases that participate in signal transduction in bacteria. Experimental evidence was obtained after sequence homology analysis, generation of variant kinases, and their biochemical and structural studies. The techni... |
