SML1581
莫西沙星 盐酸盐
≥98% (HPLC), synthetic fluoroquinolone antibacterial, powder
别名:
12-8039, Avalox, BAY12-8039, 盐酸盐
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关于此项目
经验公式(希尔记法):
C21H24FN3O4· HCl
化学文摘社编号:
分子量:
437.89
Beilstein:
8377447
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
产品名称
莫西沙星 盐酸盐, 98-102% (HPLC)
质量水平
方案
98-102% (HPLC)
表单
powder
储存条件
desiccated
颜色
light yellow to yellow
溶解性
H2O: slightly soluble
储存温度
−20°C
SMILES字符串
Cl.COc1c(N2C[C@@H]3CCCN[C@@H]3C2)c(F)cc4C(=O)C(=CN(C5CC5)c14)C(O)=O
InChI
1S/C21H24FN3O4.ClH/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24;/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28);1H/t11-,16+;/m0./s1
InChI key
IDIIJJHBXUESQI-DFIJPDEKSA-N
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一般描述
莫西沙星是第四代合成氟喹诺酮类抗菌剂。莫西沙星与其他喹诺酮类药物不同,其是一种8-甲氧基喹诺酮。
应用
盐酸莫西沙星已被用于研究其对已生长至高密度细菌的抗菌作用。
生化/生理作用
莫西沙星已被证明可有效治疗鼻窦炎、社区获得性呼吸道感染、肺炎和慢性支气管炎的急性加重。与其他氟喹诺酮(如环丙沙星和氧氟沙星)相比,它具有更好的抗革兰氏阳性活性。莫西沙星可用于治疗细菌性皮肤感染。它可以适当渗透到周围组织和炎性液体中。氟喹诺酮类可通过与酶-DNA复合物结合来稳定由DNA回旋酶和拓扑异构酶IV产生的DNA链断裂。 与哺乳动物DNA促旋酶相比,莫西沙星对细菌DNA促旋酶的亲和力高100倍。莫西沙星是一种抗生素,可抗革兰氏阳性和革兰氏阴性细菌。莫西沙星在治疗耐多药结核病中的研究正在进行中。
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
涉药品监管产品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Understanding and sensitizing density-dependent persistence to quinolone antibiotics.
Gutierrez A, et al.
Molecular Cell, 68(6), 1147-1154 (2017)
Ana Topete et al.
Journal of controlled release : official journal of the Controlled Release Society, 326, 245-255 (2020-07-20)
Posterior capsule opacification (PCO) still remains the most frequent long term complication after cataract surgery, while endophthalmitis is rare but severe and should be prevented at all cost. Intraocular lenses (IOLs) with different designs (eg. edge and body-haptics angle) and
An HPLC Method for the Determination of Moxifloxacin in Breast Milk by Fluorimetric Detection with Precolumn Derivatization.
Tekkeli SEK
Acta Chromatographica , 10-10 (2016)
Moxifloxacin.
Muijsers R B and Jarvis B
Drugs, 62(6), 967-973 (2002)
Francis S Mah
Current opinion in ophthalmology, 15(4), 316-320 (2004-07-03)
The fourth-generation fluoroquinolones, moxifloxacin and gatifloxacin, were introduced in 2003 promising improved spectrum of activity and delayed development of resistance. Although these topical agents have recently been introduced in commercial form, there is already a growing body of evidence showing
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