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D,L-Buthionine-(S,R)-sulfoximine hydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
D,L-Buthionine-(S,R)-sulfoximine hydrochloride图片
规格:98%
分子量:258.77

D,L-Buthionine-(S,R)-sulfoximine hydrochloride (Buthionine sulfoximine hydrochloride) 是谷氨酰半胱氨酸合成酶生物合成的有效抑制剂。
货号:ajcx13834
CAS:N/A
分子式:C8H19ClN2O3S
分子量:258.77
溶解度:H2O: ≥ 140 mg/mL (541.02 mM); DMSO: ≥ 125 mg/mL (483.05 mM); Ethanol: 25 mg/mL (96.61 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

D,L-Buthionine-(S,R)-sulfoximine hydrochloride (Buthionine sulfoximine hydrochloride) is a potent inhibitor of glutamylcysteine synthetase biosynthesis. Glutamylcysteine synthetase[1]

Buthionine sulfoximine is an analogs of methionine sulfoximine and inhibits gamma-glutamylcysteine synthetase about 20 times more effectively than prothionine sulfoximine and at least 100 times more effectively than methionine sulfoximine[1].

Treatment of mice bearing HT1080 and HT1080/DR4 xenografts with a continuous i.v infusion of nontoxic doses of D,L-Buthionine-(S,R)-sulfoximine (300 and 600 mg/kg/day) produce a 60% reduction of GSH plasma levels and greater than 95 % reduction in GSH tumor levels in both parental and multidrug-resistant tumors[2].

[1]. Griffith OW, et al. Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine). J Biol Chem. 1979 Aug 25;254(16):7558-60. [2]. Vanhoefer U, et al. d,l-buthionine-(S,R)-sulfoximine potentiates in vivo the therapeutic efficacy of doxorubicin against multidrug resistance protein-expressing tumors. Clin Cancer Res. 1996 Dec;2(12):1961-8.

 
 
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