28266
左氧氟沙星
98.0-102.0% anhydrous basis (HPLC)
别名:
(−)-Ofloxacin
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关于此项目
经验公式（希尔记法）:
C18H20FN3O4
化学文摘社编号:
分子量:
361.37
UNSPSC Code:
51102829
NACRES:
NA.85
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7327015
biological source
synthetic
Quality Segment
assay
98.0-102.0% anhydrous basis (HPLC)
form
powder or crystals
color
light yellow-white to yellow-white
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
enzyme | inhibits
SMILES string
OC(C(C1=O)=CN2C(C1=CC(F)=C3N4CCN(C)CC4)=C3OC[C@@H]2C)=O
InChI
1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m0/s1
InChI key
GSDSWSVVBLHKDQ-JTQLQIEISA-N
Gene Information
human ... KCNH1(3756)
Application
Levofloxacin is a broad-spectrum antibiotic used in pharmacokinetic , antibiotic resistance , and resistance prevention studies. Antibiotic against bacterial respiratory tract infections.
Biochem/physiol Actions
Levofloxacin is active against Gram-positive and Gram-negative bacteria. It inhibits DNA gyrase (type II topoisomerase) and topoisomerase IV, thereby inhibiting cell division.
Packaging
10mg, 1g, 10g
Other Notes
Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Resp. Sens. 1A - Skin Sens. 1A
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves