L-Buthionine-(S,R)-sulfoximine hydrochloride is a cell-permeable, potent, fast acting, orally active and irreversible inhibitor of g-glutamylcysteine synthetase and depletes cellular glutathione levels. The IC 50 value of L-Buthionine-(S,R)-sulfoximine on Appearance:Solid In Vitro:L-Buthionine-(S,R)-sulfoximine (BSO: 50 μM) treatment for 48 hr results in a 95% decrease in ZAZ and M14 melanoma cell line GSH levels, and a 60% decrease in GST enzyme activity. GST-π protein and mRNA levels are significantly reduced in both cell lines. In Vivo:BSO causes an elevated frequency of DNA deletions during mouse development. BSO treatment reduced GSH concentration in mouse fetuses by 55% and 70% at 2 mM and 20 mM BSO doses, respectively, compared to untreated mice. Co-treatment with 2 mM BSO and 20 mM Biological Activity:L-Buthionine-(S,R)-sulfoximine hydrochloride is a cell-permeable, potent, fast acting, orally active and irreversible inhibitor of g-glutamylcysteine synthetase and depletes cellular glutathione levels. The IC 50 value of L-Buthionine-(S,R)-sulfoximine o
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L-Buthionine-(S,R)-sulfoximine hydrochloride
CAS number:unknown molecular formula:C8H19ClN2O3S
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| Chinese alias | L-丁硫氨酸-(S,R)-亚砜亚胺盐酸盐 | ||
| English alias | - | ||
| CAS number | unknown | molecular formula | C8H19ClN2O3S |
| molecular weight | 258.77 g/mol | Exact mass | - |
| PSA | - | logp | - |
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