Abstract: Trovafloxacin acid salts are prepared via the hydrolysis of imine intermediates using mineral acid including, but not limited to, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, nitric acid, sulfuric acid, phosphoric acid, hydrochloric acid, hydrobromic acid, tartaric acid, citric acid, acetic acid, and maleic acid. Trovafloxacin acid salts are useful as antibiotic agents.
Type:
Grant
Filed:
August 26, 1999
Date of Patent:
March 19, 2002
Assignee:
Pfizer Inc.
Inventors:
Timothy Norris, Keith M. DeVries, Peter R. Rose
Abstract: The present invention relates to novel 2,3 disubstituted-4(3H)-quinazolinone compounds of the formula I:
wherein, R1, R2 and R3 are as defined in the specification; and to the pharmaceutically acceptable salts of compounds of formula I, and to pharmaceutical compositions and methods of treating neurodegenerative and CNS-trauma related conditions.
Type:
Grant
Filed:
November 23, 1999
Date of Patent:
October 16, 2001
Assignee:
Pfizer Inc
Inventors:
Mark L. Elliott, Willard M. Welch, Bertrand L. Chenard
Abstract: This invention relates to pharmaceutical compositions for rectal administration containing semi-synthetic glycerides produced by interesterification, and, as the active ingredient, triazole derivatives of the formula ##STR1## wherein R.sup.1 is phenyl optionally sustituted with from one to three substituents independently selected from the group consisting of F, Cl, Br, I, CF.sub.3,(C.sub.1 -C.sub.4)alkyl, (C.sub.1 -C.sub.4)alkoxy, and 5-chloropyrid-2-yl; X is OH, F, Cl or Br; R.sub.2 is H.sub.2, CH.sub.3 or F; and R.sub.3 is H or F.
Type:
Grant
Filed:
October 13, 1992
Date of Patent:
November 1, 1994
Assignee:
Pfizer Inc.
Inventors:
Walter F. Fries, Gunther F. D. Pfaff, Jorg C. Pfitzner, Gerhard Simon
Abstract: Macrolides of formula (I) and methods of treatment of resistance to transplantation, fungal infections and autoimmune diseases such as rheumatoid arthritis and psoriasis using said macrolides of formula (I), ##STR1## wherein n is 1 or 2; A and B taken together form .dbd.O or A and B taken separately are each H or A is OH and B is H; R.sup.1 is a group of the formula ##STR2## R.sup.2 is OH or a desosaminyloxy group; and R.sup.3 is an alkyl or allyl group.
Abstract: Compounds of the formula ##STR1## and pharmaceutical compositions comprising them, wherein R.sup.1, Z, X, W and Y are as defined below. The compounds are useful in the treatment of psychosis and anxiety.