摘要:
The present invention provides indane acetic acid and their derivatives and methods for the treating and/or preventing of cognitive disorders based on the ApoE4 genotype of human subjects.
摘要:
An object of the present invention is to provide an amide compound or a salt thereof that controls a mite. The present invention provides an amide compound represented by Formula (1) : or a salt thereof, wherein R 1 represents C 1-6 alkyl or C 1-6 haloalkyl; R 2 and R 3 are identical or different and each represent hydrogen, halogen, cyano, nitro, C 1-6 alkyl, or the like; Q represents Q-1 or Q-2: R 4 represents hydrogen, C 1-6 alkyl, acetyl or the like; R 5 and R 6 are identical or different and each represent hydrogen, halogen, or C 1-6 alkyl, or the like; HET represents 5- or 6-membered heteroaryl, R 7 represents C 1-6 alkyl, C 1-6 haloalkyl, C 3-8 cycloalkyl, C 3-8 cycloalkyl C 1-6 alkyl, substituted or unsubstituted aryl, substituted or unsubstituted aryl C 1-6 alkyl X represents oxygen or sulfur; and n represents an integer of 0 to 2.
摘要:
Disclosed herein are compounds of Formula (I), methods of synthesizing compounds of Formula (I), and methods of using compounds of Formula (I) as an analgesic.
摘要:
The present disclosure provides compounds that are Large Multifunctional Protease 7 (LMP7) inhibitors and are therefore useful for the treatment of diseases treatable by inhibition of LMP7. Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.
摘要:
A compound, or pharmaceutically acceptable salt thereof, having a formula (I) wherein R 1 is H or optionally-substituted alkyl; R 2 is optionally-substituted alkyl; R 3 and R 4 are each independently H or optionally-substituted alkyl; R 5 is H, optionally-substituted alkyl, acyl, or alkoxycarbonyl; R 6 and R 7 are each independently H, deuterium, optionally- substituted alkyl, or R 6 and R 7 together form a carbocyclic; R 8 is optionally-substituted thiazolyl, optionally-substituted thiophenyl, or substituted phenyl, provided that if R 8 is 4-halophenyl, then R 2 is substituted alkyl or branched alkyl or at least one of R 6 or R 7 is not H; and R 30 , R 31 and R 32 are each independently H, deuterium, halogen, substituted sulfanyl, or optionally-substituted alkoxy.
摘要翻译:具有式(I)的化合物或其药学上可接受的盐,其中R 1为H或任选取代的烷基; R2是任选取代的烷基; R 3和R 4各自独立地为H或任选取代的烷基; R5是H,任选取代的烷基,酰基或烷氧基羰基; R6和R7各自独立地为H,氘,任选取代的烷基,或R6和R7一起形成碳环; R8是任选取代的噻唑基,任选取代的噻吩基或取代的苯基,条件是如果R8是4-卤代苯基,那么R 2是取代的烷基或支链烷基,或者R6或R7中的至少一个不是H; R 30,R 31和R 32各自独立地为H,氘,卤素,取代的硫烷基或任选取代的烷氧基。
摘要:
The present invention relates to novel tetrahydronaphthyl(thio) carboxamides, to processes for preparing these compounds, to compositions comprising these compounds, and to the use thereof as biologically active compounds, especially for control of harmful microorganisms in crop protection and in the protection of materials.
摘要:
The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores (II) from intermediates (I), wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Sc, NR S , C(O), C(O)C(O), Si(R 5 ) 2 , SO, S0 2 , PRS, BRS, C(R 5 ) 2 or P(O)R 5 and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (IT) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroary- lene substituents can be used. The core tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN) 2 or [C=C(CN) 2]2 . Organic electronic devices can be made including field-effect transistors. (Formula I, II)
摘要:
The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores, wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Sc, NR 5 , C(O), C(O)C(O), Si(R 5 ) 2 , SO, S0 2 , PR 5 , BR 5 , C(R 5 ) 2 or P(O)R s and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (II) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroarylene substituents can be used. The core tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN) 2 or [C=C(CN) 212 . Organic electronic devices can be made including field-effect transistors. Formula (II).
摘要:
Nitrated and non-nitrated compounds capable of protecting brain tissue from injury and useful as therapeutic agents to treat neurodegenerative diseases and conditions are disclosed. Methods of using the compounds in therapeutic treatments, and methods of preparing the compounds, also are disclosed.