Compound ID | 777

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CL-329998 (DMG-MINO)

Class: Glycylcycline

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Inhibited Gram positives and most Gram negative anaerobes
Description: Weiss WJ, Jjacobus NV, Petersen PJ, et al. In vitro activity of novel glycylcycline compounds against Enterococci and methicillin-resistant Staphylococci. 33rd-Intersci-Conf-Antimicrobial-Agents-Chemother 1993; 198.
Institute where first reported: Wyeth, USA
Year first mentioned: 1993
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 542.58
Iso. SMILES: CN(C)CC(=O)NC(=O)C1=C([C@@]2([C@@H](C[C@@H]3CC4=C(C=CC(=C4C(=C3C2=O)O)O)N(C)C)[C@@H](C1=O)N(C)C)O)O
InChI Key: XEQNXUPAPCDWFW-DALPMJHXSA-N
Can. SMILES: CN(C)CC(=O)NC(=O)C1=C([C@@]2([C@@H](C[C@@H]3CC4=C(C=CC(=C4C(=C3C2=O)O)O)N(C)C)[C@@H](C1=O)N(C)C)O)O
InChI: InChI=1S/C27H34N4O8/c1-29(2)11-17(33)28-26(38)20-23(35)21(31(5)6)14-10-12-9-13-15(30(3)4)7-8-16(32)19(13)22(34)18(12)24(36)27(14,39)25(20)37/h7-8,12,14,21,32,34,37,39H,9-11H2,1-6H3,(H,28,33,38)/t12-,14-,21-,27-/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/54684323
Citation:

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