质量水平
检测方案
≥98% (HPLC)
形式
powder
颜色
white to beige
溶解性
DMSO: 20 mg/mL, clear
运输
wet ice
储存温度
−20°C
SMILES字符串
C[C@@H](C(N)=O)[C@H](N)C1=NC2=CC(C(C)(C)C)=CC=C2N1
InChI
1S/C15H22N4O/c1-8(13(17)20)12(16)14-18-10-6-5-9(15(2,3)4)7-11(10)19-14/h5-8,12H,16H2,1-4H3,(H2,17,20)(H,18,19)/t8-,12+/m1/s1
InChI key
APWZIFIAVVFPNT-PELKAZGASA-N
生化/生理作用
PF-06305591 is a potent and highly selective sodium channel Nav1.8 inhibitor.
PF-06305591 is safe and has acceptable absorption, distribution, metabolism, and elimination (ADME) properties.
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Alan D Brown et al.
Bioorganic & medicinal chemistry, 27(1), 230-239 (2018-12-13)
The voltage gated sodium channel NaV1.8 has been postulated to play a key role in the transmission of pain signals. Core hopping from our previously reported phenylimidazole leads has allowed the identification of a novel series of benzimidazole NaV1.8 blockers.
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