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Merck
CN

SML3927

Alalevonadifloxacin hydrochloride

≥98% (HPLC)

别名:

L-Alanine 1-[(5S)-2-carboxy-9-fluoro-6,7-dihydro-5-methyl-1-oxo-1H,5H-benzo[ij]quinolizin-8-yl]-4-piperidinyl ester hydrochloride, WCK 2349 hydrochloride

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关于此项目

经验公式(希尔记法):
C22H26FN3O5·HCl
化学文摘社编号:
分子量:
467.92
NACRES:
NA.77
UNSPSC Code:
51111800
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assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

Quality Level

Biochem/physiol Actions

Orally available L-alanine ester prodrug of Levonadifloxacin that is affective against Gram-positive and Gram-negative bacteria.


Alalevonadifloxacin, the L-alanine ester prodrug of levonadifloxacin, is an orally available and potent benzoquinolizine fluoroquinolone antibiotic that is affective against Gram-positive and Gram-negative bacteria, including methicillin- and quinolone-resistant Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae, and Moraxella catarrhalis and atypical pathogens. Alalevonadifloxacin targets staphylococcal DNA gyrase, unlike other quinolones, which primarily inhibit DNA topoisomerase IV.

Disclaimer

Hygroscopic

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Levonadifloxacin, a Novel Broad-Spectrum Anti-MRSA Benzoquinolizine Quinolone Agent: Review of Current Evidence
Drug design, development and therapy, 13, 4351-4365 (2019)
Design and synthesis of an oral prodrug alalevonadifloxacin for the treatment of MRSA infection
Bioorganic & Medicinal Chemistry Letters, 54, 128432-128432 (2021)
Intrapulmonary Pharmacokinetics of Levonadifloxacin following Oral Administration of Alalevonadifloxacin to Healthy Adult Subjects
Keith A Rodvold, Mark H Gotfried
Antimicrobial Agents and Chemotherapy, 62(3) (2018)

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