2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺

2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺

中文名称2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺
中文同义词2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺;化合物 T22685
英文名称CP 471,474
英文同义词PF-1626077;CP 471,474;2-[[[4-(4-Fluorophenoxy)phenyl]sulfonyl]amino]-N-hydroxy-2-methylpropanamide;2-(4-(4-Fluorophenoxy)phenylsulfonamido)-N-hydroxy-2-methylpropanamide;Propanamide, 2-[[[4-(4-fluorophenoxy)phenyl]sulfonyl]amino]-N-hydroxy-2-methyl-
CAS号210755-45-6
分子式C16H17FN2O5S
分子量368.38
EINECS号
相关类别Amines;Aromatics;Inhibitors;Intermediates & Fine Chemicals;Pfizer Compounds;Pharmaceuticals;Sulfur & Selenium Compounds;Heterocycles
Mol文件210755-45-6.mol
结构式2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺 结构式

2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺 性质

熔点135-137°C (dec.)
密度1.375±0.06 g/cm3(Predicted)
储存条件room temp
溶解度二甲基亚砜:≥20mg/mL
酸度系数(pKa)9.33±0.50(Predicted)
形态粉末
颜色白色至类白色

2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺 用途与合成方法

CP-471474 是一个口服有效的、广泛的 MMP 抑制剂,IC50 值分别为1170 nM (MMP-1)、0.7 nM (MMP-2)、16 nM (MMP-3)、13 nM (MMP-9) 和 0.9 nM (MMP-13)。

MMP-2

0.7 nM (IC 50 )

MMP-13

0.9 nM (IC 50 )

MMP-9

13 nM (IC 50 )

MMP-3

16 nM (IC 50 )

MMP-1

1170 nM (IC 50 )

CP-471474 plasma levels following subcutaneous injection are 2,020 ng/mL (1 h postdose) to 160 ng/mL (6 h postdose).
CP-471,474 significantly reduces both the extent and severity of inflammation at 2 months. At 4 months, a spontaneous reduction of the inflammatory response is observed in both treated and untreated animals, and consequently no difference is observed between both.
CP-471474 significantly decreases the destructive lesions mainly at 2 months and also at 4 months.

Animal Model: Guinea pigs weighing 400 to 450 g (COPD).
Dosage: 20 mg/kg (also supplemented daily by the diet (200 mg/200 g powdered chow)).
Administration: Subcutaneously (in 20% ethanol/80% polyethylene glycol), once a day during the entire course.
Result: Lungs derived from smoking animals treated with the compound demonstrated a statistically significant reduction in the destructive lesions.
Showed an increase of both pro–MMP-9 and its active form (lanes 5 to 8) as compared with control animals.

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危险类别码22
WGK Germany1

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2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺 上下游产品信息

"2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基] -N-羟基-2-甲基丙酰胺"相关产品信息
4-氟-3-苯氧基苯甲醛 4-苯氧基苯磺酰氯 苯氧乙醇
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