摘要:
Derivatives having potent antibacterial activities on gram-negative and gram-positive bacteria and, at the same time, favorable dynamics in vivo and a high safety; and excellent drugs. Compounds represented by general formula (I) and salts thereof, hydrates thereof, and antibacterial agents containing the same as the active ingredient. In said formula, R1 represents hydrogen or C¿1-6? alkyl optionally having substituent(s) selected from the group consisting of hydroxy, halogeno, C1-6 alkylthio and C1-6 alkoxy; R?2¿ represents hydrogen or amino optionally having one or two substituents selected from the group consisting of formyl, C¿1-6? alkyl and C2-6 acyl; and R?3¿ represents hydrogen, phenyl, acetoxymethyl, pivaloyloxymethyl, etoxycarbonyl, cholin, dimethylaminoethyl, 5-indanyl, phthalidinyl, 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl, 3-acetoxy-2-oxobutyl, C¿1-6? alkyl, C2-7 alkoxymethyl, or phenylalkyl composed of C1-6 alkylene and phenyl.
摘要:
Anti-acid-fast bacterial agents containing as the active ingredient compounds represented by the general formula (1), salts thereof or hydrates of the same. Namely, pyridonecarboxylic acid derivatives having an excellent antibacterial activity on tubercle bacillus and atypical acid-fast bacteria, favorable kinetics in vivo and a high safety.
摘要:
Compounds of general formula (I) and salts thereof, giving quinolone derivatives which exhibit high antibacterial activity against various bacteria including resistant ones and high safety, wherein R1 is cycloalkyl; R2 is hydrogen, amino, hydroxyl, mercapto, halogenomethyl, alkyl, alkenyl, alkynyl or alkoxy; R3 is amino, halogenomethyl, halogenomethoxy, alkyl, alkenyl, alkynyl or alkoxy; R4 is hydrogen or C¿1?-C6 alkyl; R?5 is C¿3-C6 cycloalkyl; and X is halogeno or hydrogen, with the proviso that these substituents may be further substituted; and Y is hydrogen, phenyl, acetoxymethyl, pivaloyloxymethyl, ethoxycarbonyl, choline, dimethylaminoethyl, 5-indanyl, phthalidinyl, 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl, 3-acetoxy-2-oxobutyl, C1-C6 alkyl, C2-C7 alkoxymethyl or phenylalkyl composed of C1-C6 alkylene and phenyl.
摘要:
(-)-7-[(7S)-7-Amino-5-azaspiro[2.4]heptan-5-yl]-6-fluoro-1-[(1R,2S)-2-fluoro-1-cyclopropyl]-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid monohydrochloride monohydrate and antibacterial agents containing the same. This compound is excellent in antibacterial activity and safety and highly stable to light and humidity, which makes it useful as an antibacterial agent.
摘要:
Compounds represented by general formula (I) carrying a tricylic amine substituent optionally having various substituents, their salts, hydrates thereof or drugs containing these compounds as the active ingredient. Because of having favorable antibacterial activities on gram-negative and gram-positive bacteria and being excellent both in the dynamics in vivo and safety, these compounds are useful in treating infectious diseases. In said formula (I), Q represents a partial structure which is preferably represented by formula (a); or (b) and may have various substituents.
摘要:
Quinolone derivatives having potent antibacterial effects on various bacteria including insensible bacilli, which are compounds represented by general formula (1), salts of the same, or hydrates of both: wherein R1 is an optionally substituted aromatic group; R?2 and R3¿ are each hydrogen or alkyl; R?4, R5 and R6¿ are each hydrogen, hydroxyl, halogeno, or the like; R?7 and R8¿ are each hydrogen or alkyl; R9 is alkyl, alkenyl, halogenoalkyl, or the like; R10 is hydrogen or alkylthio; R11 is hydrogen, amino, hydroxyl, or the like; X1 is halogeno or hydrogen; A1 is nitrogen or C-X2; X2 is hydrogen, amino, halogeno, or the like; A?2 and A3¿ are each ⊃C=C(-A?1=)-N(-R9¿)- or ⊃N-C(-A?1=)=C(-R9)-; R10 and R9 or R9 and X2¿ may be united to form a ring structure; and Y is hydrogen or an ester-forming group.
摘要:
N1-(Halogenocyclopropyl)-substituted pyridonecarboxylic acid derivatives represented by general formula (I), heterocyclic compounds useful as antibacterial agents, wherein X1 represents halo or hydrogen; X2 represents halo; R1 represents hydrogen, hydroxy, thiol, halomethyl, amino, alkyl or alkoxy; R2 represents a group of general formula (II) (wherein R?3 and R4¿ represent each hydrogen or alkyl; and n represents an integer of 1 or 2); A represents nitrogen or a group of general formula (III), (wherein X3 represents halo, cyano, amino, alkyl, halomethyl, alkoxy or halomethoxy); and R represents hydrogen, phenyl, acetoxymethyl, pivaloyloxymethyl, ethoxycarbonyl, choline, dimethylaminoethyl, 5-indanyl, phthalidinyl, 5-alkyl-2-oxo-1, 3-dioxol-4-ylmethyl, 3-acetoxy-2-oxobutyl, alkyl, alkoxymethyl or phenylalkyl.
摘要:
A compound represented by the following formula (I), which has antifungal activity in a wide spectrum by a novel mechanism, i.e., 1,6-ß-glucan synthesis inhibition, and can specifically or selectively exhibit such activity, a salt thereof, or a solvate of either; and an antifungal agent containing any of these.