CAS:400827-64-7 7β - Amino - 3 - [4 - (pyridin - 2 - Thiazole Sulfone Radical)] - 3 - Cephem - 4 - Carboxylic Acid·2HCl

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CAS:400827-64-7 7β - Amino - 3 - [4 - (pyridin - 2 - Thiazole Sulfone Radical)] - 3 - Cephem - 4 - Carboxylic Acid·2HCl
Details
CAS  400827 - 64 - 7
MF C₁₆H₁₅ClN₄O₅S₃
MW 479.42424
Category
Cephalosporin Intermediates
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Description
 Name
7β - Amino - 3 - [4 - (pyridin - 2 - thiazole sulfone radical)] - 3 - cephem - 4 - carboxylic acid·2HCl
Synonyms
7β - Amino - 3 - [4 - (pyridin - 2 - thiazole sulfone radical)] - 3 - cephem - 4 - carboxylic acid·2HCl·
[4 - [(6R,7R) - 7 - amino - 2 - carboxy - 8 - oxo - 5 - thia - 1 - azabicyclo[4.2.0]oct - 2 - en - 3 - yl]thio] - methyl pyridinium chloride hydrate;
7β - Amino - 3 - [4 - (pyridin - 2 - thiazole sulfone radical)] - 3 - cephem - 4 - carboxylic acid·2HCl·
[4 - [(6R,7R) - 7 - amino - 2 - carboxy - 8 - oxo - 5 - thia - 1 - azabicyclo[4.2.0]oct - 2 - en - 3 - yl]thio] - methyl chloride hydrate; Ceftaroline main chain; Ceftaroline mother core; (dihydrochloride);
7 - [7 - Amino - 2 - carboxy - 8 - oxo - 5 - thia - 1 - azabicyclo[4.2.0]oct - 2 - en - 3 - yl]thiomethyl pyridinium chloride monohydrate; 7 - [7 - Amino - 2 - carboxy - 8 - oxo - 5 - thia - 1 - azabicyclo[4.2.0]oct - 2 - en - 3 - yl]thiomethyl pyridinium chloride;
7 - [7 - Amino - 2 - carboxy - 8 - oxo - 5 - thia - 1 - azabicyclo[4.2.0]oct - 2 - en - 3 - yl]thiomethyl pyridinium chloride hydrochloride
CAS 
400827 - 64 - 7
MF
C₁₆H₁₅ClN₄O₅S₃
MW
479.42424
EINECS 
447 - 990 - 4
Related Categories
Cephalosporin intermediate; Intermediate raw materials; Pharmaceutical fine chemical raw materials
Storage Conditions
Inert atmosphere, Room Temperature
Usage The ceftaroline nucleus is the primary raw material for the synthesis of ceftaroline fosamil. The antibacterial mechanism of ceftaroline fosamil involves binding to penicillin‑binding proteins, thereby exerting bactericidal activity. It exhibits strong antibacterial activity against Gram‑positive anaerobes, Staphylococcus aureus, Streptococcus pneumoniae, Gram‑negative anaerobes, MRSA, and other drug‑resistant Gram‑positive bacteria. It also shows inhibitory effects against Escherichia coli, Haemophilus influenzae, penicillin‑resistant pneumococci, Klebsiella oxytoca, and Klebsiella pneumoniae.

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