Cephalexin

Cephalexin

Cat Number
PIGD-0256
CAS Number
15686-71-2

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CAS Number
15686-71-2
Storage
Store at -20℃
Synonyms
Cefalexin; Cephacillin; (6R,7R)-7-[[(2R)-2-amino-2-phenylacetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Formula
C16H17N3O4S
Molecular Weight
347.4
Smiles
O=C(N[C@@H]1C(N2[C@]1([H])SCC(C)=C2C(O)=O)=O)[C@H](N)C3=CC=CC=C3
Appearance
White to light yellow
Melting Point
196-198°C
Boiling Point
727.4±60.0°C(Predicted)
General Description
Cephalexin is a semisynthetic first-generation oral cephalosporin antibiotic of the beta-lactam class. Discovered in the late 1960s, it is one of the most commonly prescribed antibiotics. Cephalexin has high oral bioavailability and is generally well tolerated. It is active against several Gram-positive organisms, including Staphylococcus aureus (MSSA) and Streptococcus pneumoniae and some Gram-negative organisms, such as Escherichia coli and Klebsiella pneumoniae.
Mechanism of Action
The mode of action of cephalexin is by inhibiting cell wall synthesis. As a member of the beta-lactam class of antibiotics, cefalexin binds to penicillin-binding proteins (PBPs) on the inner membrane of the bacterial cell wall. It interferes with the transpeptidation enzyme that cross-links peptidoglycan strands. Unable to maintain a structurally sound cell wall due to a lack of peptidoglycan, bacteria eventually burst due to osmotic pressure and die.
Application
Cephalexin was discovered in 1967 and reached the market in 1969. It was approved by the FDA in 1971. Cephalexin may be used for treating lower respiratory tract infections, upper respiratory tract infections, gonorrhea, acute urinary tract infections, chronic urinary tract infections, scarlet fever, streptococcal septicemia, and β-lactamase induced infections caused by staphylococci. It is also used in skin infections and before and after surgery to prevent infection at the site.

Cephalexin is a beta-lactam antibiotic that works against bacteria by inhibiting cell wall synthesis. Beta-lactam antibiotics are classified as first-generation cephalosporins and include a beta-lactam ring in their chemical structure. Peptidoglycan found inside the bacterial cell contributes to mechanical support of the cell wall. Beta-lactam antibiotics inhibit peptidoglycan synthesis using the antibiotic's beta-lactam ring. More specifically, cephalexin uses its beta-lactam ring to bind penicillin-binding proteins (PBPs). The binding of PBPs inhibits synthesis of peptidoglycan by blocking the last step in synthesis known as the transpeptidation reaction. The transpeptidation reaction leads to cross-linking of bacterial peptidoglycan. By inhibiting this step, cephalexin inactivates cell viability causing bacterial cell autolysis.

References

  1. Herman T F, Hashmi M F. Cephalexin[M]//StatPearls [Internet]. StatPearls Publishing, 2023.

Antibiotics may be losing their effectiveness in fighting bacteria due to increased antibiotic resistance. For this reason, new methods to increase antibiotic potency were investigated. Scientists aimed to increase the effectiveness of the antibiotic cephalexin against pneumonia, which kills millions of children worldwide each year. Copper oxide nanoparticles were prepared by green synthesis through wild thyme extract. UV-vis spectroscopy, X-ray diffraction, and magnetic resonance were used to characterize the nanoparticles. Cephalexin was loaded onto CuO nanoparticles as a nanocomposite. The antibiotic-nanocomposite was found to exhibit superior antibacterial activity against clinical isolates of Klebsiella pneumoniae when compared to cephalexin alone. MIC values ranged from 1.8–2.2 mg ml−1. Complete inhibition was seen at 30 mg ml−1. The most effective suppression of pulmonary biofilm formation was exhibited at 20 mg ml−1. The result showed that cephalexin-CuO nanocomposite is a potent dual-functional candidate for advanced antibacterial and antioxidant therapeutic solutions.

Fig. 2 Ultraviolet-visible spectra of prepared copper oxide nanoparticles and cephalexin loaded on copper oxide nanoparticles. (Dali L, <i>et al</i>. 2026) Fig. 2 Ultraviolet-visible spectra of prepared copper oxide nanoparticles and cephalexin loaded on copper oxide nanoparticles. (Dali L, et al. 2026)

References

  1. Dali L, et al. Green synthesis of CuO nanoparticles using thyme extract and their application as cephalexin carriers against Klebsiella pneumoniae. Nanoscale Advances. 2026, 8(1): 97-110.

Can I request a formal quote for Cephalexin API?

Yes, please provide your required quantity for a Cephalexin API quote.

Does light exposure affect the stability of Cephalexin API?

Yes, Cephalexin API should be stored away from direct sunlight.

Is a certificate of analysis provided with Cephalexin API?

Every batch of Cephalexin API includes a detailed certificate of analysis.

How can I track my Cephalexin API shipment?

Use the provided tracking number to monitor your Cephalexin API.
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