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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
---|---|---|---|---|
C129430-50mg |
50mg | 期货 | | |
C129430-250mg |
250mg | 期货 | | |
C129430-1g |
1g | 期货 | |
别名 | 克林沙星 |
---|---|
英文别名 | PD127391; PD 127391; PD-127391;7-(3-Amino-1-pyrrolidinyl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid |
规格或纯度 | ≥95% |
英文名称 | Clinafloxacin |
生化机理 | Clinafloxacin inhibits both Topo II (DNA gyrase)and topoisomerase IV dually in Streptococcus pneumoniae. The compound has a broad-spectrum activity against gram-negative and gram-positive bacteria, aerobes and anaerobes. Studies comparing the inhibitory effects of the fluoroquinolones: clinafloxacin, trovafloxacin, sparfloxacin, and ciprofloxacin demonstrated clinafloxacin having the greatest inhibition of Topo II (DNA gyrase) and topoisomerase IV. |
储存温度 | 2-8°C储存 |
运输条件 | 冰袋运输 |
产品介绍 |
Clinafloxacin 可以抑制肺炎双球菌中 DNA旋转酶和拓扑异构酶IV。A fluoroquinolone that inhibits both DNA gyrase and topoisomerase IV. Clinafloxacin inhibits both DNA gyrase and topoisomerase IV dually in Streptococcus pneumoniae. |
IUPAC Name | 7-(3-aminopyrrolidin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid |
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INCHI | InChI=1S/C17H17ClFN3O3/c18-13-14-10(5-12(19)15(13)21-4-3-8(20)6-21)16(23)11(17(24)25)7-22(14)9-1-2-9/h5,7-9H,1-4,6,20H2,(H,24,25) |
InChi Key | QGPKADBNRMWEQR-UHFFFAOYSA-N |
Canonical SMILES | C1CC1N2C=C(C(=O)C3=CC(=C(C(=C32)Cl)N4CCC(C4)N)F)C(=O)O |
WGK Germany | 3 |
RTECS | VB1800600 |
PubChem CID | 60063 |
分子量 | 365.79 |
CAS Registry No. | 105956-97-6 |
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PubChem CID | 60063 |
ChEMBL Ligand | CHEMBL278255 |
Antibiotic DB | 515 |
DrugCentral Ligand | 677 |
溶解性 | DMSO 0.03 mg/mL Water Ethanol |
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象形图 |
Health Hazard |
---|---|
信号词 | Warning |
危险声明 |
H361: Suspected of damaging fertility or the unborn child |
预防措施声明 | P280,P405,P501,P203,P318 |
WGK Germany | 3 |
RTECS | VB1800600 |
输入批号以搜索COA:
1. Asahina Y, Takei M, Kimura T, Fukuda Y. (2008) Synthesis and antibacterial activity of novel pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid derivatives carrying the 3-cyclopropylaminomethyl-4-substituted-1-pyrrolidinyl group as a C-10 substituent.. J Med Chem, 51 (11): (3238-49). [PMID:18457383] |