S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE
![S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE Structure](https://image.chemsrc.com/caspic/454/35446-36-7.png)
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE structure
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Common Name | S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE | ||
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| CAS Number | 35446-36-7 | Molecular Weight | 270.37100 | |
| Density | 1.363 g/cm3 | Boiling Point | 459.8ºC at 760 mmHg | |
| Molecular Formula | C11H14N2O2S2 | Melting Point | 191-193ºC | |
| MSDS | USA | Flash Point | 231.9ºC | |
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Phenylalkyl isothiocyanate-cysteine conjugates as glutathione S-transferase stimulating agents.
J. Med. Chem. 35 , 185, (1992) To develop analogues of phenylalkyl isothiocyanate with less toxicity and better biological activity, two water-soluble phenylalkyl isothiocyanate-cysteine conjugates, S-[N-benzyl(thiocarbamoyl)]-L-cysteine (1) and S-[N-(3-phenylpropyl)(thiocarbamoyl)]-L-cyst... |
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The metabolism of benzyl isothiocyanate and its cysteine conjugate in guinea-pigs and rabbits.
Xenobiotica 12(9) , 535-42, (1982) 1. Following oral administration of benzyl isothiocyanate or its cysteine conjugate the major metabolite isolated from urine of guinea-pigs and rabbits was a cyclic mercaptopyruvate conjugate, 4-hydroxy-4-carboxy-3-benzylthiazolidin-2-thione. 2. Renal excreti... |
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