Azathioprine
CAS No. 446-86-6
Azathioprine ( Azamune | Azoran | BW 57-322 | Imuran | NSC 39084 )
产品货号. M14531 CAS No. 446-86-6
硫唑嘌呤是一种免疫抑制化合物,抑制嘌呤合成和GTP结合蛋白Rac1激活,用于治疗器官移植和自身免疫性疾病。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | ¥300 | 有现货 |
|
| 1G | ¥399 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥397 | 有现货 |
|
生物学信息
-
产品名称Azathioprine
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述硫唑嘌呤是一种免疫抑制化合物,抑制嘌呤合成和GTP结合蛋白Rac1激活,用于治疗器官移植和自身免疫性疾病。
-
产品描述Azathioprine is an immunosuppressive drug, inhibiting purine synthesis and GTP-binding protein Rac1 activation, used in the treatment of organ transplantation and autoimmune diseases.(In Vitro):Azathioprine (0-50 μM, 48 hours) can induce severe intracellular GSH depletion with relevant concentrations in both primary rat and human hepatocytes.(In Vivo):Azathioprine (oral gavage, 25-400 mg/kg, everyday, 10days) can affect bone marrow cells, red blood cells, and peripheral blood cytokines and other related parameters in a dose-dependent manner, and can induce apoptosis in female CD-1 mice and ICR mice.
-
体外实验Azathioprine (0-50 μM, 48 hours) can induce severe intracellular GSH depletion with relevant concentrations in both primary rat and human hepatocytes. Cell Viability Assay Cell Line:Rat hepatocytes, Human hepatocytes Concentration:0-50 μM Incubation Time:24-48 hours Result:Showed the decrease in cell viability and intracellular GSH levels in rat hepatocytes as low concentration of 0.5 μM but no significant decrease in cell viability at concentrations below 50 μM as well as GSH depletion was obviously noted at a concentration as low as 1 μM in human hepatocytes.
-
体内实验Azathioprine (oral gavage, 25-400 mg/kg, everyday, 10days) can affect bone marrow cells, red blood cells, and peripheral blood cytokines and other related parameters in a dose-dependent manner, and can induce apoptosis in female CD-1 mice and ICR mice. Animal Model:Outbred female CD-1 mice, Female ICR mice Dosage:25-400 mg/kg Administration:Oral gavage; everyday; 10 days Result:Induced a decrease in erythrocyte-related parameters as well as leukocyte-related parameters in a dose-dependent manner.Induced 52.4%, 35.4%, 17.9%, 16.1% and 15.2% reduction in bone marrow cells at concentrations of 40, 60, 80, 100 and 120 mg/kg, respectively while fms-like tyrosine kinase-3(FLT-3) ligand (FL)-related cytokines were increased.
-
同义词Azamune | Azoran | BW 57-322 | Imuran | NSC 39084
-
通路Cell Cycle/DNA Damage
-
靶点GPR
-
受体HGPRT| Rac1
-
研究领域Inflammation/Immunology
-
适应症——
化学信息
-
CAS Number446-86-6
-
分子量277.26
-
分子式C9H7N7O2S
-
纯度>98% (HPLC)
-
溶解度DMSO: 54 mg/mL (194.76 mM)
-
SMILESO=[N+](C1=C(SC2=C3NC=NC3=NC=N2)N(C)C=N1)[O-]
-
化学全称6-((1-methyl-4-nitro-1H-imidazol-5-yl)thio)-7H-purine
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Tiede I, et al. J Clin Invest, 2003, 111(8), 1133-1145.
产品手册
关联产品
-
CRTh2 antagonist 1
CRTh2 antagonist 1 是 CRTh2 拮抗剂,IC50 值为 89 nM。
-
Dihydromunduletone
Dihydromunduletone (DHM) 是类胡萝卜素衍生物,是一种选择性,有效的粘附 G 蛋白偶联受体 (aGPCR) (GPR56 and GPR114/ADGRG5) 拮抗剂,对 GPR56 的 IC 50 值为 20.9 μM,但不抑制 GPR110 或 A 类 GPCR。
-
GPR81 agonist 1
GPR81 agonist 1 是一种高效、高选择性的 GPR81 激动剂,对人和小鼠 GPR81 的EC50 分别为 58 nM 和 50 nM。GPR81 agonist 1 抑制分化的 3T3-L1 脂肪细胞的脂解。GPR81 agonist 1 抑制小鼠的脂解并不会造成皮肤潮红。GPR81 agonist 1 对 GPR81 的选择性高于 GPR109a。
021-51111890
购物车()
sales@molnova.cn

