Penicillin G sodium salt
CAS No. 69-57-8
Penicillin G sodium salt( —— )
Catalog No. M15662 CAS No. 69-57-8
Benzylpenicillin sodium is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 44 | In Stock |
|
| 200MG | 63 | In Stock |
|
| 500MG | 104 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePenicillin G sodium salt
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NoteResearch use only, not for human use.
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Brief DescriptionBenzylpenicillin sodium is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections.
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DescriptionBenzylpenicillin sodium is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on gamma-aminobutyric acid mediated synaptic transmission.(In Vitro):The Ultraviolet-visible (UV-Vis) absorption spectrum of the Penicillin G sodium salt-TEM-1 system is markedly different to that of Penicillin G sodium salt and TEM-1 β-lactamase, indicating the formation of new complexes between Penicillin G sodium salt and TEM-1 β-lactamase. The UV-Vis absorption of TEM-1 β-lactamase increases and a slight red-shift occurs as the concentration of Penicillin G sodium salt increasing, indicating that the interaction between Penicillin G sodium salt and TEM-1 β-lactamase results in subtle conformational changes of TEM-1 β-lactamase.(In Vivo):In the logistic regression model, the probability of a positive swab in the control group is 1.6 times higher than that in the pigs treated with Penicillin G sodium salt (P<0.05). In the control group, the risk of a swab having 10 to 99 colonies per plate, compare to having zero per plate, is 2.3 times greater than that in the pigs treated with Penicillin G sodium salt (P=0.022).
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In VitroThe Ultraviolet-visible (UV-Vis) absorption spectrum of the Penicillin G sodium salt-TEM-1 system is markedly different to that of Penicillin G sodium salt and TEM-1 β-lactamase, indicating the formation of new complexes between Penicillin G sodium salt and TEM-1 β-lactamase. The UV-Vis absorption of TEM-1 β-lactamase increases and a slight red-shift occurs as the concentration of Penicillin G sodium salt increasing, indicating that the interaction between Penicillin G sodium salt and TEM-1 β-lactamase results in subtle conformational changes of TEM-1 β-lactamase.
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In VivoIn the logistic regression model, the probability of a positive swab in the control group is 1.6 times higher than that in the pigs treated with Penicillin G sodium salt (P<0.05). In the control group, the risk of a swab having 10 to 99 colonies per plate, compare to having zero per plate, is 2.3 times greater than that in the pigs treated with Penicillin G sodium salt (P=0.022).
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Synonyms——
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorPBPs| GABAR
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number69-57-8
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Formula Weight356.37
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Molecular FormulaC16H17N2NaO4S
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Purity>98% (HPLC)
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SolubilityWater: 71 mg/mL (199.23 mM); DMSO: 71 mg/mL (199.23 mM)
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SMILESCC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[Na+]
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Jiang X, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Apr 5;140:474-8.
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