4-IODO-6-PHENYLPYRIMIDINE

4-IODO-6-PHENYLPYRIMIDINE

中文名称4-IODO-6-PHENYLPYRIMIDINE
中文同义词化合物4-IPP;4-碘-6-苯基嘧啶;4-IPP,巨噬细胞迁移抑制因子(MIF)抑制剂
英文名称4-IODO-6-PHENYLPYRIMIDINE
英文同义词4-IODO-6-PHENYLPYRIMIDINE;4-IPP;MIF Antagonist III, 4-IPP;MIF Antagonist III, 4-IPP - CAS 41270-96-6 - Calbiochem;Pyrimidine, 4-iodo-6-phenyl-;4-IPP (4-Iodo-6-phenylpyrimidine);Inhibitor,osteoclastogenesis,4IPP,MIF,4-IPP,inhibit,4 IPP,RANKL,osteoblast
CAS号41270-96-6
分子式C10H7IN2
分子量282.08
EINECS号
相关类别
Mol文件Mol File
结构式4-IODO-6-PHENYLPYRIMIDINE 结构式

4-IODO-6-PHENYLPYRIMIDINE 性质

沸点380.2±30.0 °C(Predicted)
密度1.728±0.06 g/cm3(Predicted)
储存条件-20°C
溶解度在DMSO中的溶解度为10mg/mL(透明溶液,加热)
形态粉末
酸度系数(pKa)-0.54±0.17(Predicted)
颜色白色至米色
InChIKeyZTCJXHNJVLUUMR-UHFFFAOYSA-N

4-IODO-6-PHENYLPYRIMIDINE 用途与合成方法

4-IPP (4-Iodo-6-phenylpyrimidine)是 macrophage migration inhibitory factor (MIF) 的不可逆抑制剂,是MIF的特异性自杀底物。4-IPP可以抑制NF-κB配体(RANKL)诱导的破骨细胞的受体激活剂,并在体外增强成骨细胞介导的矿化和骨结节的形成。
TargetValue
MIF
()

4-IPP is a specific suicide substrate for MIF that binds covalently and irreversibly to MIF to inhibit its biologic activity.
4-IPP inhibits RANKL-induced p65 phosphorylation and nuclear translocation by preventing the interaction of MIF with thioredoxin-interacting protein-p65 complexes.
4-IPP can inhibit receptor activator of NF-κB ligand (RANKL)-induced osteoclastogenesis and potentiate osteoblast-mediated mineralization and bone nodule formation.
4-IPP (0.5-200μM;24-72 hours) inhibits osteoclastogenesis in a dose-dependent manner.
4-IPP(5-20μM; 5 days) inhibits RANKL-induced osteoclast differentiation and bone resorption .

Cell Cytotoxicity Assay

Cell Line: BMMs
Concentration: 0.5 μM, 1 μM, 2.5 μM, 5 μM, 10 μM, 25 μM, 50 μM, 100 μM, 200 μM
Incubation Time: 24 hours, 72 hours
Result: Inhibited osteoclastogenesis in a dose-dependent manner.

Western Blot Analysis

Cell Line: BMMs
Concentration: 5 μM,10 μM, 20 μM
Incubation Time: 1 day, 3 days, 5 days
Result: Inhibited RANKL-induced osteoclast differentiation and bone resorption.

4-IPP (1 mg/kg, 5 mg/kg; every 2 days; for 8 weeks) ameliorates the bone loss associated with estrogen deficiency by reducing osteoclastic activities and enhancing osteoblastic bone formation.

Animal Model: 8-weeks-old C57BL/6J male mice
Dosage: 1 mg/kg, 5 mg/kg
Administration: Intraperitoneal injection; every 2 days; for 8 weeks
Result: Alleviated OVX-induced osteoporosis.

安全信息

危险品标志Xn
危险类别码22-37/38-41
安全说明26-39
WGK Germany3

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-1100634-IPP1 mg400元
2024/04/30HY-1100634-IODO-6-PHENYLPYRIMIDINE
4-IPP
41270-96-65mg1150元

4-IODO-6-PHENYLPYRIMIDINE 上下游产品信息

"4-IODO-6-PHENYLPYRIMIDINE"相关产品信息
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