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1443246-62-5

中文名称 1-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA
英文名称 VU0456810
CAS 1443246-62-5
分子式 C17H14F2N4O
分子量 328.32
MOL 文件 1443246-62-5.mol
更新日期 2024/04/29 17:03:07
1443246-62-5 结构式 1443246-62-5 结构式

基本信息

中文别名
化合物ML297
英文别名
ML297
VU0456810
CID 56642816
ML297 (VU0456810)
ML297 >=98% (HPLC)
ML297, Pubchem: CID 56642816
ML 297 (Synonyms: VU 0456810
ML 297
ML-297
ML297
VU0456810
VU-0456810
VU 0456810
GIRK Activator, ML297 - CAS 1443246-62-5 - Calbiochem
1-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA

物理化学性质

沸点377.8±42.0 °C(Predicted)
密度1.32±0.1 g/cm3(Predicted)
储存条件Sealed in dry,Store in freezer, under -20°C
溶解度DMSO:可溶15mg/mL,澄清
酸度系数(pKa)12.54±0.70(Predicted)
形态白色粉末
颜色白色至米色
稳定性Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.

安全数据

危险性符号(GHS)
GHS09
警示词警告
危险性描述H410
防范说明P273-P501
危险品标志N
危险类别码50/53
安全说明60-61
危险品运输编号UN 3077 9 / PGIII
WGK Germany3
1-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-1101921-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA
ML 297
1443246-62-55mg700元
2024/04/30HY-1101921-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA
ML 297
1443246-62-510mM * 1mLin DMSO770元
2024/04/30HY-1101921-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA
ML 297
1443246-62-510mg1100元

常见问题列表

生物活性
ML-297 (VU 0456810, CID 56642816)是一种有效的、选择性的 Kir3.1/3.2 (G protein-coupled inwardly rectifying potassium, GIRK1/2) 通道的激活剂,其对于GIRK1/2和GIRK1/4的EC50值分别为0.16 μM和1.8 μM。ML-297 具有治疗癫痫的潜力。
靶点
TargetValue
GIRK1/2
(Cell-free assay)
0.16 μM
GIRK1/4
(Cell-free assay)
1.8 μM
体外研究

ML 297 is completely inactive for GIRK 2/3 .
ML297 shows concentration-dependent efficacy in expressing GIRK1/2 cells and with an EC 50 of 162 nM.
ML297 shows a complete inability to modulate the activity of HEK-293 cells expressing GIRK 2 alone and GIRKGIRK 2/3 .

体内研究

ML297 (60 mg/kg; i.p.) shows a highly significant ability to both prevent convulsions and prevent fatality of the PTZ treatment.

Animal Model: 8-10 months old C57/BL6 male mice (approximately 30 g)
Dosage: 60 mg/kg
Administration: Intraperitoneal injection
Result: Most of the animals neither convulsions nor death.
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