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502887-71-0

中文名称 MMP-9-IN-1
英文名称 MMP-9-IN-1
CAS 502887-71-0
分子式 C16H17F2N3O3S
分子量 369.39
MOL 文件 502887-71-0.mol
更新日期 2024/07/21 13:45:55
502887-71-0 结构式 502887-71-0 结构式

基本信息

中文别名
化合物MMP-9-IN-1
N-(4-(二氟甲氧基)苯基)-2-((6-氧代-4-丙基-1,6-二氢嘧啶-2-基)硫代)乙酰胺
英文别名
OUN87710
MMP-9-IN-1
Acetamide, N-[4-(difluoromethoxy)phenyl]-2-[(1,6-dihydro-6-oxo-4-propyl-2-pyrimidinyl)thio]-

物理化学性质

密度1.37±0.1 g/cm3(Predicted)
储存条件Inert atmosphere,2-8°C
溶解度DMSO: 125 mg/mL (338.40 mM)
酸度系数(pKa)7.80±0.50(Predicted)
形态Solid
颜色White to off-white

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
MMP-9-IN-1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-135232MMP-9-IN-1
MMP-9-IN-1
502887-71-05mg2900元
2024/04/30S0769MMP-9-IN-1
MMP-9-IN-1
502887-71-05mg2970元
2024/04/30HY-135232MMP-9-IN-1
MMP-9-IN-1
502887-71-010mg4500元

常见问题列表

生物活性
MMP-9-IN-1 (OUN87710)是一种 matrix metalloproteinase-9 (MMP-9) 的特异性抑制剂。MMP-9-IN-1 可选择性地靶向MMP-9的血红素(PEX)域,Kd值为2.1 μM。
靶点
TargetValue
MMP-9
(Cell-free assay)
2.1 μM(Kd)
体外研究

MMP-9-IN-1 (compound 2; 100 μM; 14 hours) does not cause notable cytotoxicity.
MMP-9-IN-1 (compound 2; 10 μM) significantly inhibits cell proliferation of HT-1080 and MDA-MB-435 cells.

Cell Cytotoxicity Assay

Cell Line: COS-1 monkey epithelial cell lines
Concentration: 100 μM
Incubation Time: 24 hours
Result: Treatment did not cause notable cytotoxicity.

Cell Proliferation Assay

Cell Line: HT-1080 and MDA-MB-435 cancer cells expressing endogenous MMP-9
Concentration: 10 μM
Incubation Time: 9 days
Result: Significant inhibition of cell proliferation.
体内研究

MMP-9-IN-1 (compound 2; 20 mg/kg; intraperitoneal and intratumoral injection alternately; 6 days/week; for 14 weeks) results in a profound delay in tumor growth in NCR-Nu mice bearing MDA-MB-435/GFP tumor.
MMP-9-IN-1 inhibits cancer cell metastasis in vivo.

Animal Model: 4-5 week-old female NCR-Nu mice bearing MDA-MB-435/GFP tumor
Dosage: 20 mg/kg
Administration: Intraperitoneal and intratumoral injection alternately; 6 days/week; for 14 weeks,
Result: Resulted in a profound delay in tumor growth.
Inhibited cancer cell metastasis.
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