Ampicillin sodium

TargetMol
Product Code: TAR-T6386
Supplier: TargetMol
CodeSizePrice
TAR-T6386-1g1g£111.00
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Ampicillin Sodium is the sodium salt form of ampicillin, a broad-spectrum semisynthetic derivative of aminopenicillin. Ampicillin sodium inhibits bacterial cell wall synthesis by binding to penicillin binding proteins, thereby inhibiting peptidoglycan synthesis, a critical component of the bacterial cell wall.
CAS:
69-52-3
Formula:
C16H18N3NaO4S
Molecular Weight:
371.39
Pathway:
Microbiology/Virology
Purity:
0.9987
SMILES:
[Na+].CC1(C)SC2C(NC(=O)C(N)c3ccccc3)C(=O)N2C1C([O-])=O
Target:
Antibacterial; Antibiotic

References

Zhou J, Huang J, Huang H, et al.Fiber-integrated cantilever-based nanomechanical biosensors as a tool for rapid antibiotic susceptibility testing.Biomedical Optics Express.2023, 14(5): 1862-1873. Zhang Z, Ye J, Liu X, et al.Huangqi Guizhi Wuwu decoction alleviates oxaliplatin-induced peripheral neuropathy via the gut-peripheral nerve axis.Chinese Medicine.2023, 18(1): 1-15. Lee KE, et al. The neuroprotective mechanism of ampicillin in a mouse model of transient forebrain ischemia. Korean J Physiol Pharmacol. 2016 Mar;20(2):185-92. Gotz V, et al. Am J Hosp Pharm, 1979, 36(6), 754-757. Lund B, et al. Ampicillin in portal and peripheral blood and bile after oral administration of ampicillin andpivampicillin. Eur J Clin Pharmacol. 1974;7(2):133-5. Chopra SL, et al. Effect of Ampicillin on E. Coli of Swine Origin. Can J Comp Med Vet Sci. 1963 Sep;27(9):223-7. Sutcliffe JG, et al. Proc Natl Acad Sci U S A, 1978, 75(8), 3737-3741.