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100-33-4

中文名称 喷他脒
英文名称 Pentamidine
CAS 100-33-4
分子式 C19H24N4O2
分子量 340.42
MOL 文件 100-33-4.mol
更新日期 2024/12/18 10:44:13
100-33-4 结构式 100-33-4 结构式

基本信息

中文别名
喷他脒
4,4'-二脒基二苯氧基戊烷
4,4'-(戊烷-1,5-二基双(氧基))二苯脒
英文别名
NSC 9921
MP 601205
PENTAMIDINE
4,4’-diamidinodiphenoxypentane
4,4’-(pentamethylenedioxy)di-benzamidin
p,p’-(pentamethylenedioxy)dibenzamidine
4,4’-(pentamethylenedioxy)dibenzamidine
4,4'-(1,5-Pentanediylbisoxy)dibenzamidine
p,p’-(pentamethylene-dioxy)bis-benzamidine
4-[5-(4-amidinophenoxy)pentoxy]benzamidine
所属类别
原料药:抗丝虫病及抗利什曼原虫病药

物理化学性质

熔点186 °C (dec.)
沸点476.22°C (rough estimate)
密度1.1805 (rough estimate)
折射率1.6620 (estimate)
储存条件-20°C Freezer, Under Inert Atmosphere
溶解度可溶于DMSO、甲醇(少量)
酸度系数(pKa)pKa 11.4 (Uncertain)
形态固体
颜色白色至灰白色

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS07
警示词警告
危险性描述H315-H302-H335-H319
危险品运输编号3249
危险等级6.1(b)
包装类别III

图谱信息

常见问题列表

生物活性
Pentamidine (MP-601205) 是一种抗微生物剂,会干扰 DNA 的生物合成。Pentamidine 抑制寄生虫 Leishmania infantum,IC50 为 2.5 μM。Pentamidine 是一种有效的选择性蛋白酪氨酸磷酸酶 (PTPases) 和再生肝磷酸酶 (PRL) 抑制剂。Pentamidine 可用于冈比亚锥虫病,抗锑利什曼病和卡氏肺孢子虫肺炎的研究。抗肿瘤活性,抗菌活性。
靶点

IC50: 2.5 μM ( Leishmania infantum )
Protein tyrosine phosphatases (PTPases)
Phosphatase of regenerating liver (PRL)

体外研究

Pentamidine (0-10 µg/mL; 6 days; WM9, DU145, C4-2, Hey, WM480, and A549 cells) treatment inhibits the growth of cancer cells in a concentration-dependent manner.
The cytotoxic properties of Pentamidine isethionate towards the promastigotes of the protozoan parasite Leishmania infantum is determined. The leishmanicidal activity of Pentamidine isethionate is 60 times higher after 72 h of incubation than that of Cisplatin. Pentamidine isethionate induces a higher amount of programmed cell death (PCD) than Cisplatin, which is associated with inhibition of DNA synthesis and cell-cycle arrest in the G2/M phase. Binding of Pentamidine isethionate to calf-thymus DNA (CT-DNA) induces conformational changes in the DNA double helix, consistent with a B-->A transition. The interaction of Pentamidine isethionate with ubiquitin leads to a 6% increase in the beta-sheet content of the protein.

Cell Viability Assay

Cell Line: WM9, DU145, C4-2, Hey, WM480, and A549 cells
Concentration: 0-10 µg/mL
Incubation Time: 6 days
Result: The growth of all six of the cell lines in culture was inhibited in a concentration-dependent manner with complete growth inhibition of the cell lines occurring at 10 µg/mL.
体内研究

Pentamidine (0.25 mg/mouse; intramuscular injection; every 2 days; for 4 weeks; athymic nude mice) treatment markedly inhibits the growth of WM9 human melanoma tumors in nude mice.

Animal Model: Athymic nude mice (6 weeks old) injected with WM9 cells
Dosage: 0.25 mg/mouse
Administration: Intramuscular injection; every 2 days; for 4 weeks
Result: Markedly inhibited the growth of WM9 human melanoma tumors in nude mice.
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