| Identification | Back Directory | [Name]
sodium [2S-[2alpha,5alpha,6beta(S*)]]-6-(azidophenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | [CAS]
35334-12-4 | [Synonyms]
Nalpen
Longatren
AZIDOCILLN
azidocillin sodium
Azidocillin sodium salt
(2S,5β)-6α-[[(R)-Azido(phenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid sodium salt
sodium [2S-[2alpha,5alpha,6beta(S*)]]-6-(azidophenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | [EINECS(EC#)]
252-516-2 | [Molecular Formula]
C16H16N5NaO4S | [MDL Number]
MFCD09839786 | [MOL File]
35334-12-4.mol | [Molecular Weight]
397.384 |
| Hazard Information | Back Directory | [Uses]
Azidocillin sodium, a semi-synthetic Penicillin, is an orally active β-lactam antibiotic. Azidocillin sodium bears an azide functionality and retains on-target activity within bacteria. Azidocillin sodium can be used to research osteitis caused by dental surgery, otitis media, enterococcal septicemia and other bacterial infectious diseases[1][2][3]. Azidocillin sodium is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | [Definition]
ChEBI: Azidocillin sodium is an organic sodium salt. It contains an azidocillin(1-). | [References]
[1] Bystedt H, et al. Concentration of azidocillin, erythromycin, doxycycline and clindamycin in dental alveolar serum after single oral doses. Int J Oral Surg. 1977 Apr;6(2):65-74. DOI:10.1016/s0300-9785(77)80001-x
[2] Spangler B, et al. Molecular Probes for the Determination of Subcellular Compound Exposure Profiles in Gram-Negative Bacteria. ACS Infect Dis. 2018 Sep 14;4(9):1355-1367. DOI:10.1021/acsinfecdis.8b00093
[3] Bengtsson E, et al. Azidocillin treatment of enterococcal septicemia. Scand J Infect Dis. 1972;4(2):143-8. DOI:10.3109/inf.1972.4.issue-2.15 |
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