T o develop analogues of phenylalkyl isothiocyanate with less toxicity and better biological activity, two water-soluble phenylalkyl isothiocyanate-cysteine conjugates, S-[N-benzyl (thiocarbamoyl)]-cysteine (1) and S-[N-(bphenyl-propyl)(thiocarbamoyl)]-cysteine (2), were synthesized. The induction of increased activity of the detoxifying enzyme glutathione S- transferase by the conjugates and their parent compounds was determined and compared ...
![S-[N-(3-苯丙基)氨基硫羰基]-L-半胱氨酸结构式](https://image.chemsrc.com/caspic/366/137915-13-0.png)
