摘要:
The present invention relates to a method for reducing the production of methane emanating from the digestive activities of a ruminant and/or for improving ruminant animal performance by using, as active compound at least one organic molecule substituted at any position with at least one nitrooxy group, or a salt thereof, which is administrated to the animal together with the feed. The invention also relates to the use of these compounds in feed and feed additives such as premix, concentrates and total mixed ration (TMR) or in the form of a bolus.
WHEREIN X IS O, S, -NH- OR -NCH3-;R IS A FREE OR ESTERIFIED HYDROXY GROUP, HYDROXYALKOXY, ACYLOXYALKOXY, ALKOXYALKOXY, DIALKYLAMINOALKOXY, PYRROLIDINOALKOXY, PIPERIDINOALKOXY, MORPHOLINOALKOXY, PIPERAZINOALKOXY, ACYLAMINO, AMINO, ALKYLSULFONYLAMINO, MONOALKYLAMINO, DIALKYLAMINO, CARBOXY, CARBALKOXY OR NITRO; AND R'' IS A HYDROGEN ATOM, A HALOGEN ATOM, AN ALKYL GROUP, OR A FREE, ETHERIFIED OR ESTERIFIED HYDROXY GROUP, HAVE ANTI-TRICHOMONADAL ACTIVITY.
摘要:
[Problem] The present invention addresses the problem of providing a novel compound. The present invention also addresses the problem of providing an OCT3 detection agent or an OCT3 activity inhibitor, which comprises the novel compound.[Solution] A compound represented by formula (A), a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof. R1-R2-R3-R4 (A)
摘要:
The present invention is novel selected hydroxamic acid derivatives of acyl residues of selected NSAIDS, i.e. having 5-lipoxygenase and cyclooxygenase inhibiting properties, pharmaceutical compositions for treating conditions advantageously affected by the inhibition and methods for treating these conditions in mammals, including humans suffering therefor.
摘要:
A nitrofuran derivative having the general formula ##SPC1##Wherein R is a group selected from the class consisting of hydroxyl group, hydroxyalkyl group, hydroxyalkoxylakyl group, hydroxyalkylaminoalkyl group, alkoxyalkyl group, sulfoalkyl group, which sulfoalkyl group may be that forming a salt, mercaptoalkyl group, an amino acid, and a residue resulting from the removal of the amino group from an amino acid amide, the amino group or carboxyl group of which residue may be that forming a salt. The nitrofuran derivative is useful as antimicrobial agent.
摘要:
WHEREIN X is O, S or NH, Y is -CH2- and R is nitro, benzoyloxy, alkoxycarbonyloxy, N-mono-alkylaminocarbonyloxy, N,Ndialkylaminocarbonyloxy or an N-substituted-aminoalkoxy group, having antimicrobial activity, e.g., against Trichomonas vaginalis.
摘要:
[Problem] The present invention addresses the problem of providing a novel compound. The present invention also addresses the problem of providing an OCT3 detection agent or an OCT3 activity inhibitor, which comprises the novel compound.[Solution] A compound represented by formula (A), a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof. R1-R2-R3-R4 (A)
摘要:
The present invention relates to a method for reducing the production of methane emanating from the digestive activities of a ruminant and/or for improving ruminant animal performance by using, as active compound at least one organic molecule substituted at any position with at least one nitrooxy group, or a salt thereof, which is administrated to the animal together with the feed. The invention also relates to the use of these compounds in feed and feed additives such as premix, concentrates and total mixed ration (TMR) or in the form of a bolus.
摘要:
Organic compounds showing the ability to inhibit viral glycoprotein (GP)-mediated entry of a filovirus into a host cell are disclosed. The disclosed filovirus entry inhibitor compounds are useful for treating, preventing, or reducing the spread of infections by filovirus including the type species Marburg virus (MARV) and Ebola virus (EBOV). Preferred inhibitors of the invention provide therapeutic agents for combating the Ivory Coast, Sudan, Zaire, Bundibugyo, and Reston Ebola virus strains.