Compound ID | 753

HMR 3004

Synonym(s): RU 64004

Class: Macrolide (ketolide)

Spectrum of activity: Gram-positive
Details of activity: Antistreptococcal activity; when tested against Campylobacter spp., RU 664004 was not as active as faropenem, erythromycin, clarithromycin, azithromycin or ofloxacin. When its activity against S. pneumoniae, E. faecalis and E. faecium, RU 664004 was better than erythromycin
Description: Schulin T, Wennersten CB, Eliopoulos GM, et al. In vitro activity of RU 64004, a new ketolide antibiotic against Gram-positive bacteria. 36th-Intersci-Conf-Antimicrobial-Agents-Chemother 1996; 138.
Institute where first reported: Hoechst Marion Roussel (Sanofi-Aventis, France); Aventis (Sanofi Aventis, France)
Year first mentioned: 1996
Highest developmental phase: Phase 2
Development status: Inactive
Chemical structure(s):
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Molecular weight: 796.99
Iso. SMILES: CCC1[C@@]2([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H](C(=O)[C@H](C(=O)O1)C)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)OC)C)C)N(C(=O)O2)NCCCC4=CC=NC5=CC=CC=C45)C
InChI Key: NEXGHZNDZNYBRI-IGXXTDCFSA-N
Can. SMILES: CCC1[C@]2(C)[C@@H]([C@@H](C)C(=O)[C@H](C)C[C@](C)([C@@H]([C@@H](C)C(=O)[C@@H](C)C(=O)O1)O[C@H]3[C@@H]([C@H](C[C@@H](C)O3)N(C)C)O)OC)N(C(=O)O2)NCCCC4=CC=NC5=C4C=CC=C5
InChI: InChI=1S/C43H64N4O10/c1-12-33-43(8)37(47(41(52)57-43)45-20-15-16-29-19-21-44-31-18-14-13-17-30(29)31)26(4)34(48)24(2)23-42(7,53-11)38(27(5)35(49)28(6)39(51)55-33)56-40-36(50)32(46(9)10)22-25(3)54-40/h13-14,17-19,21,24-28,32-33,36-38,40,45,50H,12,15-16,20,22-23H2,1-11H3/t24-,25-,26+,27+,28-,32+,33?,36-,37-,38-,40+,42-,43-/m1/s1

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