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Antimicrobial Agents and Chemotherapy, March 1999, p. 454-459, Vol. 43, No. 3
Infectious Disease Research Section,
Antimicrobial Chemotherapy, Wyeth-Ayerst Research, Pearl River, New
York 10965
Received 24 April 1998/Returned for modification 18 September
1998/Accepted 9 December 1998
CL 188,624, CL 190,294, and CL 191,121 are novel aminomethyl
tetrahydrofuranyl (THF)-1
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
In Vitro Activities of Aminomethyl-Substituted
Analogs of Novel Tetrahydrofuranyl Carbapenems
-methylcarbapenems. The in vitro
antibacterial activities of these THF carbapenems were
evaluated and compared with those of biapenem, imipenem, and meropenem
against 554 recent clinical isolates obtained from geographically
distinct medical centers across North America. The antibacterial
activities of the THF carbapenems were equivalent to that
of biapenem, and the THF carbapenems were slightly more
active than imipenem and less active than meropenem against most of the
members of the family Enterobacteriaceae but lacked
significant activity against Pseudomonas isolates. In general, CL 191,121 was two- to fourfold more active than
CL 188,624 and CL 190,294 against the staphylococcal and enterococcal
isolates tested. CL 191,121 was twofold less active than imipenem
against methicillin-susceptible staphylococci and was as activity as
imipenem against Enterococcus faecalis isolates. Biapenem
and meropenem were two- and fourfold less active than CL 191,121, respectively, against the methicillin-susceptible staphylococci and
E. faecalis. All the carbapenems displayed
equivalent good activities against the streptococci. Biapenem was
slightly more active than the other carbapenems against
Bacteroides fragilis isolates. Time-kill curve studies
demonstrated that the THF carbapenems were
bactericidal in 6 h against Escherichia coli and
Staphylococcus aureus isolates. The postantibiotic effect
exerted by CL 191,121 was comparable to or slightly longer than that of
imipenem against isolates of S. aureus, E. coli, and Klebsiella pneumoniae.
*
Corresponding author. Mailing address: Wyeth-Ayerst
Research, 401 N. Middletown Rd., Pearl River, NY 10965. Phone:
(914) 732-2719. Fax: (914) 732-5671. E-mail:
weissw{at}war.wyeth.com.
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