Cephalexin hydrate
SIGMA/C4895 - first-generation cephalosporin antibiotic
CAS Number: 1820673-23-1
Empirical Formula (Hill Notation): C16H17N3O4S · xH2O
Molecular Weight: 347.39 (anhydrous basis)
EC Number: 239-773-6
MDL Number: MFCD00056877
Linear Formula: C16H17N3O4S · xH2O
Product Type: Chemical
| antibiotic activity spectrum | Gram-negative bacteria |
| Gram-positive bacteria | |
| form | powder |
| InChI | 1S/C16H17N3O4S.H2O/c1-8-7 |
| InChI key | AVGYWQBCYZHHPN-FNOHQHCYSA |
| mode of action | cell wall synthesis | interferes |
| pKa | 5.2 |
| 7.3 | |
| Quality Level | 200 ![]() |
| SMILES string | S1C2N(C(=C(C1)C)C(=O)O)C( |
| storage temp. | 2-8°C |
| Application: | Cephalexin is a cephalosporin antibiotic used to study the effect of expression, binding, and inhibition of PBP3 and other penicillin-binding proteins (PBPs) on bacterial cell wall mucopeptide synthesis. |
| Biochem/physiol Actions: | Cephalexin disrupts the synthesis of the peptidoglycan layer of bacterial cell walls which is responsible for cell wall structural integrity. Peptidoglycan synthesis is facilitated by transpeptidases known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan. Cephalexin antibiotics mimic the D-Ala-D-Ala site, thereby competitively inhibiting PBP crosslinking of peptidoglycan. |
| General description: | Chemical structure: ß-lactam |
| Other Notes: | Storage of this product should be in airtight containers and protected from light. |
| Hazard Codes | Xn |
| Risk Statements | 42/43 |
| Safety Statements | 22-36/37-45 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | 2-8°C |
| UNSPSC | 51282503 |

