OU749_γ-谷氨酰转移酶(GGT)抑制剂_519170-13-9_Apexbio

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Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request
生物活性
ຫໍສະໝຸດ Baidu
靶点 :
Metabolism
信号通路:
Transferase
产品描述:
OU749 is a competitive inhibitor of γ-glutamyl transpeptidase (GGT) [1]. Expression of γ-glutamyl transpeptidase (GGT) in tumors contributes to the resistance to radiation and chemotherapy. GGT is inhibited by glutamine analogues which compete with the substrate for the γ-glutamyl binding site [1]. OU749 inhibited human kidney GGT with an intrinsic Ki of 17.6 M [1]. In 786-O cells, a human
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特别声明
产品仅用于研究,
不针对患者销售,望谅解。
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COC1=CC=C(CC2=NN=C(NS(C3=CC=CC=C3)(=O)=O)S2)C=C1
Soluble in DMSO
Store at -20°C
For obtaining a higher solubility , please warm the tube at 37°C and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20°C for several months.
renal tumor cell line, OU749 showed more than 150-fold less toxic than the GGT inhibitor acivicin toward dividing cells. OU749 inhibited GGT isolated from human kidney in a dose-dependent manner [1]. OU749 was 7-fold less potent as inhibitor of GGT isolated from rat kidney and 10-fold less potent inhibiting GGT from mouse kidney [1]. OU749 did not inhibit degradation of glutathione by GGT from rat kidney. Inhibition of GGT by OU749 is species-specific [1]. OU749 showed no inhibitory effect on GGT from pig cells. OU749 inhibited human GGT expressed in mouse fibroblasts by a similar extent to the GGT from human cells, indicated that the species specificity was determined by differences in the primary structure of the protein rather than species-specific, post-translational modifications [1]. 参考文献: [1] King J B, West M B, Cook P F, et al. A novel, species-specific class of uncompetitive inhibitors of γ-glutamyl transpeptidase[J]. Journal of Biological Chemistry, 2009, 284(14): 9059-9065.
产品说明书
化学性质
产品名: Cas No.: 分子量: 分子式:
OU749 519170-13-9 361.4 C16H15N3O3S2
产品名: OU749 修订日期: 6/30/2016
化学名:
SMILES: 溶解性: 储存条件: 一般建议:
运输条件:
N-[5-[(4-methoxyphenyl)methyl]-1,3,4-thiadiazol-2-yl]-benzenesulfo namide
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