Suggestions(5)
Exact(2)
The chemical structures of both compounds are shown in Fig. 1.
The TGA spectra for both compounds are shown in Fig. 9a, b, respectively.
Similar(58)
As both compounds were shown to bind to PPARγ, the substitution of the TZD moiety may be beneficial from a drug design perspective.
Both compounds were shown to be present in plant extracts at concentrations in the picomole range per mg of dry weight.
Both compounds were shown to inhibit both melanin synthesis and methicillin-resistant Staphylococcus aureus (MRSA) growth.
Results of the antimalarial screening for both extracts and compounds are shown in Table 3.
The structures of these two compounds are shown below.
The structures of these compounds are shown in Table 8.
The synthesized trisubstituted triazine compounds are shown in Table 3.
The top 5 hit compounds are shown as red dots.
The characteristics of other compounds are shown in Table 6.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com