Compound ID | 1005

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N-propoxy-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: 391.49
Iso. SMILES: CCCOC1(C(SC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)(C)C)C(=O)N
InChI Key: QVSVMVFOYYQALW-UHFFFAOYSA-N
Can. SMILES: CCCOC1(C(=O)N)C(C)(C)SC2C(C(=O)N21)NC(=O)CC3=CC=CC=C3
InChI: InChI=1S/C19H25N3O4S/c1-4-10-26-19(17(20)25)18(2,3)27-16-14(15(24)22(16)19)21-13(23)11-12-8-6-5-7-9-12/h5-9,14,16H,4,10-11H2,1-3H3,(H2,20,25)(H,21,23)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/211220
Citation: http://www.google.com/patents/US3177203

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