基本属性 生物活性靶点体外研究体内研究 用途与合成方法 曲伐沙星 价格(试剂级) 上下游产品信息 供应商 供应信息 相关产品
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曲伐沙星

曲伐沙星

中文名称:曲伐沙星
英文名称:TROVAFLOXACIN
CAS号:147059-72-1
分子式:C20H15F3N4O3
分子量:416.36
EINECS号:
Mol文件:147059-72-1.mol
曲伐沙星 结构式

曲伐沙星 性质

熔点 >195oC (dec.)
沸点 630.5±55.0 °C(Predicted)
密度 1.612±0.06 g/cm3(Predicted)
储存条件 -20°C Freezer, Under inert atmosphere
溶解度 可溶于乙腈(少许)、DMSO(少许)
形态 固体
酸度系数(pKa) 5.80±0.70(Predicted)
颜色 淡米色至浅米色
CAS 数据库 147059-72-1

曲伐沙星 用途与合成方法

Trovafloxacin 是一种广谱喹诺酮类抗生素,对革兰氏阳性,革兰氏阴性和厌氧菌具有有效的活性。Trovafloxacin 可阻断 DNA 促旋酶 (DNA gyrase) 和拓扑异构酶 IV (topoisomerase IV) 的活性。Trovafloxacin 也是一种有效的,选择性的,口服活性的 Pannexin 1 通道 (PANX1) 抑制剂,对 PANX1 内向电流的 IC50 为 4 μM。Trovafloxacin 不抑制 connexin 43 gap junction 或 PANX2。Trovafloxacin 通过抑制 PANX1 导致凋亡细胞碎片失调。

IC50: 4 μM (Pannexin 1 channel (PANX1))
Gram-positive, Gram-negative and anaerobic organisms
DNA gyrase
Topoisomerase IV

Trovafloxacin (20 µM; 24 hours; HepG2 cells) and tumor necrosis factor (TNF; 4 ng/mL) incubation induces apoptosis and increases leakage of lactate dehydrogenase (LDH) in HepG2 cells.
Trovafloxacin (20 µM; 24 hours; HepG2 cells) and TNF (4 ng/mL) incubation increases expression of early NF-κB-related factors A20 and IκBα.
Trovafloxacin prolongs TNF-induced activation of MAPKs and IKKα/β activation in HepG2.
Trovafloxacin is a potent inhibitor of TO-PRO-3 uptake by apoptotic cells. Trovafloxacin also inhibits ATP release from apoptotic cells. Trovafloxacin does not inhibit caspase 3/7 activation, or caspase-mediated PANX1 cleavage during apoptosis.
Trovafloxacin is equally active against both penicillin-susceptible and -resistant pneumococci, with MICs of 0.06-0.25 mg/mL reported for more than 700 isolates. The MICs of Trovafloxacin at which 90% of isolates are inhibited for 55 isolates of pneumococci is 0.125 μg/mL.

Apoptosis Analysis

Cell Line: HepG2 cells
Concentration: 20 µM
Incubation Time: 24 hours
Result: Showed a gradual increase of Annexin V-staining and an increased leakage of lactate dehydrogenase (LDH) at 24 h.

RT-PCR

Cell Line: HepG2 cells
Concentration: 20 µM
Incubation Time: 24 hours
Result: Caused a higher increase in the transcription of A20 and IκBα in HepG2 cells.

Trovafloxacin (150 mg/kg; oral administration; male C57BL/6 J mice) treatment disrupts TNF-induced p65 nuclear translocation. Trovafloxacin treatment increases expression of early NF-κB-related factors A20 and IκBα.
Trovafloxacin, when administered in combination with lipopolysaccharide (LPS) or TNF to mice induces severe liver toxicity associated with vast apoptotic areas in the liver, increased serum levels of alanine amino transferases (ALT) and pro-inflammatory cytokines.

Animal Model: Male C57BL/6 J mice (9-11-week-old) injected with recombinant murine TNF ion
Dosage: 150 mg/kg
Administration: Oral administration
Result: Showed a greater number of cells with increased nuclear/cytoplasmic p65 ratio in liver.
化学性质 
盐酸特伐沙星(Trovafloxacin Hydrochloride):C20H15F3N4O3?HCl。 [146961-34-4]。从乙腈-甲醇得淡黄色结晶,熔点246℃(分解)。
用途 
喹诺酮类抗菌药。
生产方法 
450ml THF、50ml水、127ml甲磺酸和7-氯-1-(2,4-二氟苯基)-7-氟-1,4-二氢-4-氧代-1,8-喹啉-3-羧酸乙酯一起回流1h,冷至25℃。过滤收集结晶,用THF洗,真空干燥,得7-氯-1-(2,4-二氟苯基)-7-氟-1,4-二氢-4-氧代-1,8-喹啉-3-羧酸,收率89%,mp 250℃。
500mg 7-氯-1-(2,4-二氟苯基)-7-氟-1,4-二氢-4-氧代-1,8-喹啉-3-羧酸、624mg(1α,5α,6α)-6-氨基-3-氮杂二环[3.1.0]己烷二甲苯磺酸盐、0.6ml三乙胺和5ml甲醇,一起回流16h。过滤收集形成的白色固体,在THF中回流,再过滤收集。得450ml特伐沙星,收率75%,mp 225~228℃(分解)。

曲伐沙星 价格(试剂级)

更新日期 产品编号 产品名称 CAS号 包装 价格
2024-11-08 HY-A0170 1 mg 360
2024-11-08 HY-A0170 5 mg 900

曲伐沙星 上下游产品信息

曲伐沙星供应商 更多

青岛国海生物制药有限公司
黄金产品
联系电话:0532-68019710
产品介绍:
中文名称:聚苯乙烯磺酸钙
上海喀露蓝科技有限公司
联系电话:18149758185 18149758185
产品介绍:
英文名称:Trovafloxacin
CAS:147059-72-1
纯度:98%
包装信息:1g;10g;100g
上海贺康生物技术有限公司
联系电话: 18939837085
产品介绍:
中文名称:曲伐沙星
英文名称:Trovafloxacin
CAS:147059-72-1
纯度:98+%
包装信息:1g, 5g, 10g, 25g, 100g, 1kg, 1000kg
备注:C7988
上海伯韵医药科技有限公司
联系电话:021-54581719 13817873692
产品介绍:
中文名称:曲氟沙星
英文名称:Trovafloxacin
CAS:147059-72-1
纯度:97% HPLC
包装信息:5G:10G:50G:100G:500G:1KG:5KG
北京普西唐生物科技有限公司
联系电话:010-60605840 18892239720
产品介绍:
中文名称:曲伐沙星
英文名称:Trovafloxacin
CAS:147059-72-1
纯度:98%
包装信息:10mg;50mg

最新发布供应信息

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