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opencc-by-4.0May 2024View details →

Merging Flow Synthesis and Enzymatic Maturation to Expand the Chemical Space of Lasso Peptides

LC-MS, UHPLC, and LC-IM-MS data of the corresponding publication

opencc-by-4.0Nov 2017View details →

Supporting Data for "Synthesis and electrokinetics of cationic spherical nanoparticles in salt-free non-polar media" (Chemical Science, doi:10.1039/c7sc03334f)

TEM micrographs of diblock copolymer micelles (magnification given in file name). Small-angle X-ray (SAXS) and small-angle neutron scattering (SANS) data (Q [1/Å], I(Q) [SAXS - arbitrary, SANS - 1/cm], error I(Q) [same units]).

opencc-by-4.0May 2024View details →

In situ synthesis within micron-sized soft chemical reactors created via programmable aerosol chemistry

Dataset of microscope images to accompany our manuscript. Images are arranged in folder based on experiment number and each folder contains a file describing the images individually.

opencc-by-4.0Mar 2023View details →

Supporting data for 'Chemically Reduced Graphene Oxide based Aerogels (rGOAs) - insight on the surface and textural functionalities dependent on handling the synthesis factors'

Experimental data for the 'Chemically Reduced Graphene Oxide based Aerogels (rGOAs) - insight on the surface and textural functionalities dependent on handling the synthesis factors' manuscript/publication. Package contains following data: 1. File with description of the experimental conditions for rGOAs synthesis, format: .pdf, number of files: 1  2. Data of Boehm titration for graphene oxide used for synthesis of rGOAs, format: .txt, number of files: 12 3. Fourier-transform infrared spectra of rGOA samples and GO used for synthesis, format: .csv, number of files: 16 4. Raw chromatograms of test probes for rGOA samples, format .txt, number of files: 15 folder with 11 files in each

zenodo36/100

Raw Data of the plots presented in the article entitled "Minute-Made, High-Efficiency Nanostructured Bi2Te3 via High-Throughput Green Solution Chemical Synthesis"

This is the collection of raw data for the graphical items presented in the article with given details.  This research has received funding from the Swedish Energy Agency (43521-1) and in part by Swedish Research Agency Council (VR, 2018-03462) and the European Union’s Horizon 2020 research and innovation program under the grant agreement No 863222.

opencc-by-4.0Aug 2021View details →

dryad36/100

Synthesis of photoresponsive liquid crystal elastomers: A general chemical approach

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publicMay 2025View details →

opencc-by-4.0Jun 2021View details →

Chemically Homogeneous Evolution: A rapid population synthesis approach

This contains the data behind the paper <a href="https://doi.org/10.1093/mnras/stab1291">Chemically Homogeneous Evolution: A rapid population synthesis approach</a> See<a href="https://github.com/TeamCOMPAS/COMPAS"> https://github.com/TeamCOMPAS/COMPAS</a> for code information and instructions on parsing the data. Both files are zipped HDF5 files (~7GB & ~15GB when unzipped). COMPAS_Output.h5 was used for the majority of the paper COMPAS_Output_SampledZ.h5 was used to produce fig 14 (as noted in section 4.4.5 of the paper)

Fig. 10 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity

Fig. 10. Inhibitory activity tests of gravitropic bending and elongation for benzocarbocyclic analogues 2 (50 μM, unless otherwise noted). Data for gravitropic bending (left) and elongation (right) represent mean ± SD. Asterisk indicates statistically significant differences between treatments and controls at p <0.05 (Dunnett's test, n = 7).

Fig. 11 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity

Fig. 11. Inhibitory activity tests of gravitropic bending and elongation for benzoheterocyclic analogues. Dose–response relationship study for (a) 3a, (b) 3b, (c) 3c, and (d) 3d are shown. Data for gravitropic bending and elongation represent the mean ±SD. Asterisk indicates statistically significant differences between treatments and controls at p <0.05 (Dunnett's test, n = 7).

Fig. 12 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity

Fig. 12. Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. Asterisk indicates statistically significant differences between treatments and controls at p <0.05 (Dunnett's test, n = 7).

Fig. 8 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity

Fig. 8. Inhibitory activity test for gravitropic bending. Gravitropic vectors before (g1) and after (g2) reorientation are indicated. Length (L, cm) of the root and the angle (θ, degree) of the curvature after reorientation were measured. This figure is representative of a control experiment where no treatment with chemicals was performed.

Fig. 28 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 28. The desulfation reaction catalyzed by sulfatase and used for derivatization in glucosinolate analysis.

Fig. 26 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 26. Mixed reaction catalyzed by "nitrilase" enzymes in crucifers. (A) The strict functional definition of nitrilase activity (E.C. 3.5.5.1). (B) A side reaction catalyzed by crucifer nitrilases to variable degree, probably caused by premature termination of the reaction after the first round of addition of water (Jandhyala et al., 2005), functionally defined as nitrile hydratase activity (E.C. 4.2.1.84).

Fig. 24 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 24. Examples of glucosinolate-derived indole phytoalexins and biosynthetic connections. Asterisks indicate a selected example of a labeling study of the brassinin biosynthesis (Pedras and Yaya, 2013). Question marks above some arrows signify steps that are demonstrated in vivo but for which specific enzymes are not yet known. MYR, myrosinase.

Fig. 25 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 25. Examples of crucifer non-indole phytoalexins derived from phenethyl isothiocyanate (Pedras and To, 2018). Question marks above some arrows signify steps that are demonstrated in vivo but for which specific enzymes are not yet known. MYR, myrosinase.

Fig. 22 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 22. Diverse products of allyl glucosinolate (GSL) depending on presence or absence of specifier proteins. The asterisks over the GSL, the isothiocyanate and the thiocyanate summarize the results of labeling studies (Benn, 1977; Rossiter et al., 2007) as previously detailed (Agerbirk and Olsen, 2012). All GSLs can form isothiocyanates, although some may be unstable, and nitriles. Only aliphatic GSLs with a terminal unsaturation can form epithionitriles. Only allyl GSL and two other GSLs (formally able to form a resonance-stabilized cation) can form organic thiocyanates. Some specifier proteins have other activities than those they are named from, as indicated in brackets. MYR, myrosinase; ESP, epithiospecifier protein; NSP, nitrile specifier protein; TFP, thiocyanate-forming protein.

Fig. 23 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 23. Participation of glutathione and a glutathione-S-transferase in forming a GSL-derived amine as a product of glucosinolate metabolism in intact cells, important for plant immunity. Question marks above some arrows signify steps that are demonstrated in vivo but for which specific enzymes are not yet known. Reactions are unbalanced. Amine and acid products are illustrated as the corresponding ammonium and carboxylate ions, as they would mainly exist at physiological pH. MYR, myrosinase.

Fig. 21 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 21. Selected examples of glucosinolate analogs synthesized for studying the interaction of natural glucosinolates with myrosinase.

Fig. 20 in Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants

Fig. 20. Synthesis of a glucosinolate epitope coupled to bovine serum albumin (BSA), intended for elicitation of an immune response.