Develop or use appropriate analytical methods to quantify and characterize the reactivity of the thiol surrogates. Techniques such as NMR, mass spectrometry, and chromatography can be valuable in this analysis.
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1-[3',5'-bis(trifluoromethyl)phenyl]-2,5-dihydropyrrole-2,5-dione
Doxycycline hydrochloride
6-{(E)-(3R,7R)-7-[(2S,3S,5S)-5-Ethyl-5-((2R,5R,6S)-5-ethyl-5-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-3-methyl-tetrahydro-furan-2-yl]-3,5-dimethyl-6-oxo-non-4-enyl}-2-hydroxy-3-methyl-benzoic acid benzyl ester
(S)-β-(N-phenylacetylamino)-β-(4-fluorophenyl)propionic acid
(R)-2-acetoxy-1-t-butoxycarbonylamido-3-pentene
benzyl 2-[N2-BOC-N1-[N-2-(trimethylsilyl)ethylsulfonyl-D-Ser(N-FMOC-Gly-Sar-L-Me-Val(β-OH))]-hydrazinol-3-(tert-butyldimethylsilyloxy)-4-(1,3-dioxan-2-yl)]-(2S,3S)-butanoate
