丁硫氨酸-亚砜亚胺 T5371
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
100 mg | 83730-53-4 | ¥828.00 | 询底价 |
25 mg | 83730-53-4 | ¥343.00 | 询底价 |
50 mg | 83730-53-4 | ¥497.00 | 询底价 |
Product Introduction
Bioactivity
英文名: L-BUTHIONINE-(S,R)-SULFOXIMINE
描述: L-Buthionine-(S,R)-sulfoximine 是一种细胞渗透性和不可逆的 γ-谷氨酰半胱氨酸合成酶抑制剂,通过消耗 GSH 诱导细胞中的氧化应激,可降低细胞内谷胱甘肽的水平,其对黑色素瘤、乳腺卵巢癌标本的 IC50值分别为1.9 μM、8.6 μM 和29 μM。
体外活性: IC50 values (microM) for L-buthionine-S,R-sulfoximine (BSO) on melanoma, breast and ovarian tumor specimens were 1.9, 8.6, and 29, respectively. The IC90 for melanoma was 25.5 microM, a level 20-fold lower than steady-state levels achieved clinically [1]. GSH loss induced by L-buthionine-S,R-sulfoximine (BSO) leads to overproduction of reactive oxygen species (ROS) and triggers apoptosis of MYCN-amplified neuroblastoma cells [2].
体内活性: Systemic BSO administration selectively altered GSH homeostasis and EAAT3 levels in the mice cerebellum. Intraperitoneal treatment of mice with 6?mmol/kg of BSO depleted GSH and GSSG in the liver at 2?h of treatment [3].
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : Insoluble
H2O : 10 mM
关键字: Ferroptosis | stress | GSH | Inhibitor | eye-spot | inhibit | oxidative | L-BUTHIONINE-SULFOXIMINE | glutamylcysteine | LBUTHIONINE(S,R)SULFOXIMINE | L BUTHIONINE (S,R) SULFOXIMINE | L-BSO | L-Buthionine sulfoximine | BSO
相关产品: D-glutamine | UAMC-3203 hydrochloride | Deferasirox | PD146176 | TBHQ | Troglitazone | PRIMA-1 | Butylhydroxyanisole | Siramesine hydrochloride | U-73122
相关库: HIF-1 Signaling Pathway Compound Library | Cell Cycle Compound Library | Bioactive Compounds Library Max | Anti-Ovarian Cancer Compound Library | Ferroptosis Compound Library | Inhibitor Library | Apoptosis Compound Library | NO PAINS Compound Library | Covalent Inhibitor Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途