摘要:
The present disclosure is directed to compounds of Formula (I) as Bruton's kinase inhibitors and their preparation, as well as compositions comprising compounds of Formula (I).
摘要:
Disclosed herein are hydroxythienoquinolones and related compounds and their pharmaceutically acceptable salts useful as antiviral agents and having the general formula (I) in which the variables R 2 , R 6 , and R 7 are defined herein. Certain compounds provided herein possess potent antibacterial, antiprotozoal, or antifungal activity and are particularly efficacious for the treatment of MRSA infections. The invention also provides pharmaceutical compositions, pharmaceutical compositions containing a hydroxythienoquinolone in combination with one or more other active agent, and methods of treating microbial infections in animals by administering an effective amount of a hydroxythienoquinolone or related compound to an animal suffering from a microbial infection.
摘要:
Compounds of formula (1) are provided: (1) where R1 through R7 are defined herein. The compounds of formula (I) are 5HT2c agonists or partial agonists, and are useful for treating a variety of disorders.
摘要:
The present invention provides compounds of formula (I) , wherei n R1, R2, R3, R4, Y, b, and c have any of the values defined in the specification, as well as pharmaceutical compositions comprising the compounds. The invention also provides therapeutic methods for treating diseases wherein modulation of 5-HT activity is desired, as well as processes and intermediates useful for preparing compounds of formula I.
摘要:
The invention relates to an improved method for the production of 6-aryl-4H-s-triazolo[3,4-c]-thieno[2,3-e]-1,4-diazepines of formula I, where R1 to R3 have the meanings given in claim 1 and novel intermediate products used during said method.
摘要:
Die Erfindung betrifft neue herbizid wirksame Verbindungen der Formel I worin B für ein Imidazolon der Formel oder A und B gemeinsam für ein anelliertes Imidazolon der Formel stehen und die Reste X, R¹, R² und A darüber hinaus die im Text angegebene Bedeutung haben und R³ für C₁-C₄-Alkyl und R⁴ für eine mit 1 bis 5-Fluoratomen substituierte Methyl- oder Ethyl-Gruppe steht, Verfahren zu deren Herstellung; Mittel enthaltend Verbindungen der Formel I, Verfahren zur Bekämpfung von Unkräutern sowie neue Zwischenprodukte für die Herstellung der Verbindungen der Formel I.
摘要:
Disclosed in the present invention are a thiophene ring compound, a preparation method therefor and an application thereof. The structure of the thiophene ring compound of the present invention is as shown in formula I. The compound of the present invention has good affinity and agonistic activity against at least one of a dopamine receptor and a 5-hydroxytryptamine receptor.