BMS-P5
CAS No. 1549811-36-0
BMS-P5 ( —— )
产品货号. M27535 CAS No. 1549811-36-0
BMS-P5 是一种具有口服活性的特异性肽基精氨酸脱亚胺酶 4 (PAD4) 抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2722 | 有现货 |
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| 10MG | ¥4026 | 有现货 |
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| 25MG | ¥6423 | 有现货 |
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| 50MG | ¥9153 | 有现货 |
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| 100MG | ¥12312 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称BMS-P5
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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BMS-P5 是一种具有口服活性的特异性肽基精氨酸脱亚胺酶 4 (PAD4) 抑制剂。
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产品描述BMS-P5 is a specific and orally active Peptidylarginine Deiminase 4 (PAD4) inhibitor.
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体外实验BMS-P5 blocks calcium ionophore-induced citrullination of histone H3.BMS-P5 is also able to inhibit formation of NETs induced by primary MM cells isolated from the BM of patients with MM. Cell Viability Assay Cell Line:Neutrophils.Concentration:10 μM and 100 μM.Incubation Time:30 min followed by addition of DP42 or 5TGM1 CM.Result:Prevented MM-induced NET formation.
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体内实验BMS-P5 (50 mg/kg, oral gavage) significantly improves survival of MM-bearing mice.BMS-P5 (50 mg/kg, oral gavage) may attenuate the presence of pro-tumorigenic proteins in the tumor microenvironment, and thus delay tumor progression. Animal Model:Syngeneic mouse model of MM.Dosage:50 mg/kg.Administration:Oral gavage, twice a day beginning on day 3 after tumor cell injection.Result:Significantly delayed development of symptoms and significantly prolonged survival of MM-bearing mice.
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同义词——
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通路Others
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靶点Other Targets
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受体COX|HO-1|NOS|Nrf2|PKC
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研究领域——
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适应症——
化学信息
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CAS Number1549811-36-0
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分子量509.04
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分子式C27H33ClN6O2
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纯度>98% (HPLC)
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溶解度——
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SMILESO=C(C1=CC(OC)=C2C(N=C(N2C)C3=CC4=CC=CN=C4N3CC5CC5)=C1)N6[C@H](CC[C@H](C6)N)C.Cl
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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.Nam JW, et al. Heat shock factor 1 inducers from the bark of Eucommia ulmoides as cytoprotective agents. Chem Biodivers. 2013 Jul;10(7):1322-7.
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