Peldesine
CAS No. 133432-71-0
Peldesine ( BCX 34 )
产品货号. M26363 CAS No. 133432-71-0
Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥2341 | 有现货 |
|
10MG | ¥3750 | 有现货 |
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25MG | ¥6205 | 有现货 |
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50MG | ¥8667 | 有现货 |
|
100MG | ¥11745 | 有现货 |
|
500MG | ¥23328 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称Peldesine
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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
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产品简述Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase.
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产品描述Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase. Peldesine inhibits T-cell proliferation with an IC50 of 800 nM. Peldesine can be used in research on cutaneous T-cell lymphoma, psoriasis and HIV infection.(In Vitro):The IC50s are 36 nM, 5 nM, and 32 nM for human, rat, and mouse red blood cell purine nucleoside phosphorylase, respectively. In Jurkat cells, Peldesine (BCX 34; 0-50 μM; 72 hours) inhibits the T-cell proliferation completely at a concentration of less than 10 μM, in the presence of dGuo (10 μM). In contrast, the B-cell proliferation is not affected by Peldesine.(In Vivo):Peldesine is orally active in elevating plasma inosine in rats (2-fold at 30 mg/kg), in suppressing ex vivo RBC PNP activity in rats (98% at 3 h. 100 mg/kg), and in suppressing ex vivo skin PNP in mice (39% at 3 h, 100 mg/kg). Oral bioavailability of Peldesine in rats is 76%.
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同义词BCX 34
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通路Others
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靶点Other Targets
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受体GSTP1; Gutathione S-transferase
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研究领域——
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适应症——
化学信息
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CAS Number133432-71-0
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分子量241.3
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分子式C12H11N5O
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纯度>98% (HPLC)
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溶解度——
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SMILESNc1nc2c(Cc3cccnc3)c[nH]c2c(=O)[nH]1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Ruscoe JE, et al. Pharmacologic or genetic manipulation of glutathione S-transferase P1-1 (GSTpi) influences cell proliferation pathways. J Pharmacol Exp Ther. 2001 Jul;298(1):339-45.
产品手册
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