100-33-4
基本信息
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
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
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) |  GHS07 |
| 警示词 | 警告 |
| 危险性描述 | H315-H302-H335-H319 |
| 防范说明 | P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P |
| 危险品运输编号 | 3249 |
| 危险等级 | 6.1(b) |
| 包装类别 | III |
| 毒害物质数据 | 100-33-4(Hazardous Substances Data) |
常见问题列表
IC50: 2.5 μM (
Leishmania infantum
)
Protein tyrosine phosphatases (PTPases)
Phosphatase of regenerating liver (PRL)
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. |
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. |