Compound ID | 1004

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N-ethoxy-benzylpenicillinamide

Class: Beta-lactam (penicillin)

Spectrum of activity: Gram-positive
Details of activity: Modified penicillin, Cell wall biosynthesis target.
Description: Grunberg, E and Beskid G. 1967. "Chemotherapuetic properties of N-Alkoxyamide Derivatives of Penicillin." ICAAC Conference.
Institute where first reported: Hofimann-La Roche Inc
Year first mentioned: 1967
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 377.46
Iso. SMILES: CCONC(=O)[C@H]1C(S[C@H]2N1C(=O)[C@H]2NC(=O)CC3=CC=CC=C3)(C)C
InChI Key: FLOMJSVKTIIALC-JKIFEVAISA-N
Can. SMILES: CCONC(=O)[C@H]1C(C)(C)S[C@@H]2[C@@H](C(=O)N12)NC(=O)CC3=CC=CC=C3
InChI: InChI=1S/C18H23N3O4S/c1-4-25-20-15(23)14-18(2,3)26-17-13(16(24)21(14)17)19-12(22)10-11-8-6-5-7-9-11/h5-9,13-14,17H,4,10H2,1-3H3,(H,19,22)(H,20,23)/t13-,14+,17-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/71463600
Citation: http://www.google.com/patents/US3177203

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