The synthesized analog can now be used for photoaffinity labeling experiments. This involves exposing the compound to UV light, which activates the photoreactive group, allowing it to form covalent bonds with nearby proteins or biomolecules. This process is commonly used to identify protein targets or binding sites for the modified compound.
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1-{4-[3-(tert-butyldimethylsilyloxy)propyl]phenyl}-2,2,2-trifluoroethanone O-tosyl oxime
C64H99N19O15*3FH
Phosphonic acid, [6-(3-azidophenyl)-2-oxohexyl]-, dimethyl ester
D-Valine, N-[N-[(3-acetylphenyl)acetyl]-S-[(4-methoxyphenyl)methyl]-L-cysteinyl]-, diphenylmethyl ester
4-AMINO-3 5-DIIODO-L-PHENYLALANINE
L-3,6-di-O-benzyl-4,5-di-O-(dibenzyl phosphoryl)-myo-inositol
octanedioic acid [4-(3-amino-phenyl)-thiazol-2-yl]-amide methyl ester
