CAS 525-94-0
:Penicillin N
Description:
Penicillin N, with the CAS number 525-94-0, is a naturally occurring antibiotic belonging to the beta-lactam class of antibiotics. It is produced by the fungus Penicillium chrysogenum and is characterized by its beta-lactam ring structure, which is essential for its antibacterial activity. Penicillin N exhibits a broad spectrum of activity against various Gram-positive bacteria and some Gram-negative bacteria, making it effective in treating a range of bacterial infections. The compound is sensitive to beta-lactamase enzymes produced by certain bacteria, which can confer resistance. Penicillin N is typically administered via injection due to its instability in acidic environments, which limits its oral bioavailability. Its pharmacological properties include bactericidal action, where it inhibits bacterial cell wall synthesis, leading to cell lysis and death. While it has been largely replaced by more stable and effective penicillin derivatives in clinical use, Penicillin N remains significant in research and as a precursor in the synthesis of other antibiotics.
Formula:C14H21N3O6S
InChI:InChI=1S/C14H21N3O6S/c1-14(2)9(13(22)23)17-10(19)8(11(17)24-14)16-7(18)5-3-4-6(15)12(20)21/h6,8-9,11H,3-5,15H2,1-2H3,(H,16,18)(H,20,21)(H,22,23)/t6-,8-,9+,11-/m1/s1
InChI key:InChIKey=MIFYHUACUWQUKT-GPUHXXMPSA-N
SMILES:C(O)(=O)[C@@H]1N2[C@@]([C@H](NC(CCC[C@H](C(O)=O)N)=O)C2=O)(SC1(C)C)[H]
Synonyms:- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(5R)-5-amino-5-carboxy-1-oxopentyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-
- Cephalosporin N
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(D-5-amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(5-amino-5-carboxy-1-oxopentyl)amino]-3,3-dimethyl-7-oxo-, [2S-[2α,5α,6β(S*)]]-
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(5-amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-, D-
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