Penicillin G sodium
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Penicillin G sodium
structure -
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CAS No:
69-57-8
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Formula:
C16H18N2O4S.Na
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Chemical Name:
Penicillin G sodium
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Synonyms:
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]- (2S,5R,6R)-,sodium salt (1:1);4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-,monosodium salt;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-[2S-(2α,5α,6β)]-,monosodium salt;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-,monosodium salt;Benzylpenicillinic acid sodium salt;Benzylpenicillin sodium;Benzylpenicillin sodium salt;Novocillin;Penicillin G sodium;Penilaryn;Sodium benzylpenicillin;Sodium benzylpenicillinate;Sodium penicillin G;Sodium penicillin II;Veticillin;Penicillin G sodium salt;Sodium benzylpenicillin G;Pen-A-Brasive;Sodium penicillin;Sodium 6-(phenylacetamido)penicillanate;Mycofarm;Crystapen;Monosodium benzylpenicillin;Monocillin;American penicillin;Nalpen G;Nobak;Ethacillin;1406-09-3;8049-60-3;878003-24-8
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CAS No:
Characteristics
115
-0.14510
colorless or white powder
1.41 (NTP, 1992)
222 °C (decomp)
663.3°C at 760 mmHg
300 ° (C=2, H2O)
H2O: 100 mg/mL Solutions should be filter sterilized and stored at 2-8°C for 1 week or at -20°C for extended periods. Solutions are stable at 37°C for 3 days.
2-8°C
LD50 oral in rat: 6916mg/kg
D24.8 +301° (c = 2.0 in water)
Safety Information
NONH for all modes of transport
2
42/43
22-36/37-45
XH9800000
Xn,Xi
Stability Stable, but incompatible with a wide variety of materials, including acids, oxidizing agents, heavy metals, alcohols, glycerol, thiomersal, many surface-active agents, alkalies, peroxides, reducing agents, lanolin, glycol, sugars, amines, iodine, iodides, thiols. Hygroscopic.
P261-P280-P284-P304 + P340-P342 + P311
H317-H334
Penicillin G sodium Use and Manufacturing
A hybrid strain of Penicilum chryso-genum is used, and the naturally isolated yellow spore species are prepared by microbial fermentation.
Sodium salt of Penicillin G, an antibacterial, antimicrobial medication. Used in the treatment of pneumococcus and streptococcus bacterial infections.
Price Analysis
Drug Function and Efficacy
Penicillin has good antibacterial effect on Streptococcus such as hemolytic Streptococcus, Streptococcus pneumoniae and Staphylococcus that does not produce penicillinase. It has moderate antibacterial effect on enterococci, and Neisseria gonorrhoeae, Neisseria meningitidis, Corynebacterium diphtheriae, Bacillus anthracis, Actinomyces bovis, Streptobacillus candida, Listeria monocytogenes, Leptospira and Treponema pallidum are sensitive to this product. This product also has certain antibacterial activity against Haemophilus influenzae and Bordetella pertussis, and other Gram-negative aerobic or facultative anaerobic bacteria are less sensitive to this product. This product has good antibacterial effect on Clostridium, Peptostreptococcus anaerobic bacteria and melanin-producing Bacteroides, but has poor antibacterial effect on Bacteroides fragilis. Penicillin exerts its bactericidal effect by inhibiting bacterial cell wall synthesis.
Registered Holders
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Fersinsa Gb S.A. de C.V.
Active
Japan
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INNER MONGOLIA CHANGSHENG PHARMACEUTICAL CO. LTD.
Active
Brazil
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Reyoung Pharmaceutical Co., Ltd.
Active
China
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