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GSK484 hydrochloride
CAS No. 1652591-81-5
GSK484 hydrochloride ( GTPL8577,AOB6992 )
产品货号. M22058 CAS No. 1652591-81-5
GSK484 盐酸盐 (GTPL8577) 是一种特异性、可逆的肽基精氨酸脱亚胺酶 4 (PAD4) 抑制剂。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1280 | 有现货 |
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10MG | ¥1936 | 有现货 |
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25MG | ¥3904 | 有现货 |
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50MG | ¥5581 | 有现货 |
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100MG | ¥7954 | 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 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称GSK484 hydrochloride
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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GSK484 盐酸盐 (GTPL8577) 是一种特异性、可逆的肽基精氨酸脱亚胺酶 4 (PAD4) 抑制剂。
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产品描述GSK484 hydrochloride (GTPL8577) is a specifc and reversible peptidyl arginine deiminase 4 (PAD4) inhibitor. It demonstrates high-affinity binding to PAD4 with IC50s of 50 nM in the absence of Calcium.GSK484 demonstrates high-affinity binding to the low-calcium form of PAD4 with IC50s of 50 nM and 250 nM in the absence of Calcium (0 mM) and Calcium (2 mM), respectively. GSK484 also inhibits PAD4 citrullination (at 0.2 mM Calcium) of benzoyl-arginine ethyl ester (BAEE) substrate in a concentration-dependent manner.To address whether PAD4 inhibition can suppress cancer-associated kidney injury, MMTV-PyMT mice are treated with the PAD4 inhibitor GSK484 at 4 mg/kg daily for one week. This dose suppresses the elevated number of neutrophils undergoing NETosis in peripheral blood in mice with cancer. In parallel, the total protein level in urine from MMTV-PyMT mice is significantly reduced compared with untreated tumor-bearing mice. Administration of GSK484 at a dose of 4 mg/kg daily during one week reverts signs of kidney dysfunction in tumor-bearing mice to the same extent as DNase I treatment, without any detectable signs of toxicity.
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体外实验——
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体内实验——
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同义词GTPL8577,AOB6992
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通路Others
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靶点Other Targets
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受体PAD4
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研究领域——
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适应症——
化学信息
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CAS Number1652591-81-5
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分子量510.03
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分子式C27H30ClN5O3
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纯度>98% (HPLC)
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溶解度DMSO:60 mg/mL (117.64 mM; Need ultrasonic)
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SMILESCl.COC1=CC(=CC2=C1N(C)C(=N2)C1=CC2=CC=CC=C2N1CC1CC1)C(=O)N1CC[C@@H](O)[C@@H](N)C1
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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. Lewis HD, et al. Inhibition of PAD4 activity is sufficient to disrupt mouse and human NET formation. Nat Chem Biol. 2015 Mar;11(3):189-91.
产品手册
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