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产地 | 中国 |
品牌 | 爱必信(absin) |
货号 | abs813433 |
用途 | 见爱必信官网 |
英文名称 | 见爱必信官网 |
包装规格 | 100mg,100mg,100mg,200mg,200mg,200mg,50mg,50mg,50mg,25mg,25mg,25mg |
纯度 | >98%% |
CAS编号 | 22560-50-5 |
别名 | 氯屈膦酸二钠 |
是否进口 | 否 |
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抑制剂描述: 产品名称:Clodronate disodium 产品别名:见爱必信官网 英文别名:Clodronate disodium 靶点:Others CAS:22560-50-5 纯度:>98% 外观:见爱必信官网 保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. 描述: Clodronate Disodium是一种二磷酸盐,抑制骨吸收,是一种抗溶骨试剂。 溶解性:Water :66 mg/mL (228.5 mM) 体外研究:
Clodronate significantly decreases total viability of cultures of J774 cells with EC50 of 300 μM, while liposome-encapsulated Clodronate decreases total viability of cultures of J774 cells with EC50 of 1 μM. Clodronate and liposome-encapsulated Clodronate is metabolized to a nonhydrolyzable adenosine triphosphate (ATP) analog, adenosine 5'-(beta, gamma-dichloromethylene) triphosphate, which can be detected in J774 cell extracts by using fast protein liquid chromatography. Clodronate induces apoptosis in isolated osteoclasts. Clodronate, when administered in liposomes, also induces apoptosis in rat peritoneal macrophages in vitro and in liver macrophages of mice in vivo but not in murine macrophage-like RAW-264 cells. Clodronate delivered into macrophages by liposome will kill these cells as a result of intracellular accumulation and irreversible metabolic damage. Clodronate encapsulated in liposomes (clodrolip) efficiently depletes the phagocytic cells in the murine F9 teratocarcinoma and human A673 rhabdomyosarcoma mouse tumour models resulting in significant inhibition of tumour growth ranging from 75 to >92%, depending on therapy and schedule. Clodronate, a bisphosphonate that lacks a nitrogen, does not inhibit protein isoprenylation but can be metabolized intracellularly to a beta-gamma-methylene (AppCp-type) analog of ATP, which is cytotoxic to macrophages in vitro. Clodronate is metabolited to AppCCl(2)p, and AppCCl(2)p inhibits mitochondrial oxygen consumption by a mechanism that involves competitive inhibition of the ADP/ATP translocase. 体内研究:
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