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2699607-22-0

2699607-22-0 Structure

2699607-22-0 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2699607-22-0
[Synonyms]

[Molecular Formula]

C16H19KN2O5S
[MOL File]

2699607-22-0.mol
[Molecular Weight]

390.5
Chemical PropertiesBack Directory
[solubility ]

PBS (pH 7.2): 10 mg/ml
[form ]

A solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H334-H317
[Precautionary statements ]

P261-P264-P270-P272-P280-P284-P301+P312-P330-P302+P352-P304+P341-P333+P313-P321-P342+P311-P363-P501
Hazard InformationBack Directory
[Description]

Penicillin V-d5 is intended for use as an internal standard for the quantification of penicillin V by GC- or LC-MS. Penicillin V is a β-lactam antibiotic that inhibits the growth of bacteria.1,2,3 In vitro, penicillin V inhibits the growth of clinical isolates of Streptococci (MICs = 0.004-0.008 mg/L) and C. difficile (MICs = 1 to >256 mg/L).1,2 Penicillin V also inhibits growth of S. aureus in vitro (MIC = 0.016 mg/L) and in vivo in a thigh model of infection in mice.3 It inhibits the growth of S. pyogenes in mice following one or two dose therapy with curative dose (CD50) values of 0.207 and 0.031 mg, respectively.4 Penicillin V (100 mg/kg per day, p.o.) prevents experimental acute otitis media in rats when administered prior to infection by pneumococci.5 Formulations containing penicillin V have been used to treat bacterial infections of the skin, throat, ear, mouth, and respiratory tract.
[Uses]

Penicillin V-d5 (potassium) is the deuterium labeled Penicillin V Potassium[1]. Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[2][3][4][5].
[References]

1. Kamme, C., and Petersson, A.C. In vitro effect on group A streptococci of loracarbef versus cefadroxil, cefaclor and penicillin V Scand. J. Infect. Dis. 25(1),37-42(1993).
2. Norén, T., Alriksson, I., Akerlund, T., et al. In vitro susceptibility to 17 antimicrobials of clinical Clostridium difficile isolates collected in 1993-2007 in Sweden Clin. Microbiol. Infect. 16(8),1104-1110(2010).
3. Overbosch, D., Mattie, H., and Van Furth, R. Comparative pharmacodynamics and clinical pharmacokinetics of phenoxymethylpenicillin and pheneticillin Br. J. Clin. Pharmacol. 19(5),657-668(1985).
4. Powell, H.M., and Culbertson, C.G. Effectiveness of phenoxymethyl penicillin V, and sodium penicillin G against hemolytic Streptococcus infection in white mice Proc. Soc. Exp. Biol. Med. 90(1),186-187(1955).
5. Hermansson, A., Prellner, K., and Hellstr?m, S. Prevention of experimental acute otitis media with penicillin V Acta Otolaryngol. 109(1-2),119-123(1990).
2699607-22-0 suppliers list
Company Name: Artis Biotech Co. Ltd.  
Tel: 19138486554 18108108965
Website: www.artis-standards.com/
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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Company Name: ChengDu SinoStandards Bio-Tech Co.,Ltd. ,  
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Website: www.ebuylabs.com/
Company Name: LGC Science (Shanghai) Ltd.  
Tel: 17717235263
Website: https://www.lgcstandards.com/CN/en/Pharmaceutical/cat/279492
Company Name: Cayman Chemical Company  
Tel: 800-364-9897
Website: www.caymanchem.com
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Website: www.caymanchem.com
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