摘要:
A novel compound having an excellent antagonistic effect on a corticotropin-releasing-factor receptor. It is a compound represented by the following formula or a salt thereof. (I) In the formula, R1 represents hydrogen, C¿1-6? alkyl, C1-6 alkoxy, etc.; R?2¿ represents halogeno, cyano, nitro, C¿1-10? alkyl, C2-10 alkenyl, C2-10 alkynyl, etc.; R?3¿ represents an optionally substituted C¿6-14? aromatic hydrocarbon group or an optionally substituted, 5- to 14-membered aromatic heterocyclic group; and X, Y, and Z each independently represents nitrogen or CR?4¿ (wherein R4 represents hydrogen, halogeno, cyano, nitro, optionally halogenated C¿1-6? alkyl, etc.), provided that at least two of X, Y, and Z represent CR?4¿.
摘要:
Compounds represented by general formula (I) are provided, which exhibit antagonism against corticotropin-releasing factor receptor, wherein A, B and C are each independently -(CR1R2)m- (wherein R?1 and R2¿ are each C¿1-6? alkyl or the like, and m is an integer of 1 to 4), -NR?3¿- (wherein R3 is hydrogen or the like), or the like; E and G are each independently a heteroatom such as nitrogen, -(CR6R7)p- (wherein R?6 and R7¿ are each hydrogen or the like, and p is an integer of 0 to 2), or the like; J is a carbon atom substituted with aryl or the like, or a nitrogen atom; K and L are each independently carbon or nitrogen; M is hydrogen, optionally substituted alkyl, or the like; and the partial structures ----- are each a single or double bond.
摘要:
Heterocycle-fused benzothiazine derivatives represented by general formula (I) and salts thereof or hydrates of the same which are efficacious in preventing and treating diseases in which histamine, leukotriene, etc. participate, wherein the ring Het represents an unsaturated heterocycle; R?1 and R2¿ are the same or different and each represents halogeno, optionally substituted alkyl, alkoxy, cyano, etc.; D represents optionally substituted lower alkylene, etc.; Q represents amino, carboxy, a heterocycle, etc.; and x is an integer of 1 or 2.
摘要:
A novel compound having excellent JNK inhibitory activity. It is a compound represented by the following general formula or a salt thereof. (I) In the formula, R1 represents -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb, and Rc each independently represents hydrogen, halogeno, hydroxy, optionally substituted C1-6 alkyl, etc.); Cy means a 5- or 6-membered aromatic heterocycle; and V's each independently means -L-X-Y [wherein L means a single bond, optionally substituted C1-6 alkylene, etc.; X means a single bond, -A- (wherein A represents NR2, O, CO, S, SO, or SO2), etc.; and Y means hydrogen, halogeno, nitro, etc.].
摘要:
Compounds represented by the general formula (I), salts thereof, and hydrates of both: (I) wherein R1 is methoxy, ethyl, methylthio, or the like; R?2, R3 and R4¿ are each hydrogen, halogeno, or the like; R?5 and R6¿ are each a group represented by the general formula: -X5-X6-X7 (wherein X5 is a single bond or CO-; X6 is a single bond, -NR3a-, or the like; X?7 and R3a¿ are each hydrogen, C¿1-10? alkyl, or the like); and Ar is phenyl, pyridyl, or the like.
摘要:
A novel 1H-indazole compound having excellent JNK inhibitory activity. It is a compound represented by the following general formula (I), a salt thereof, or a hydrate of either: (I) wherein R means C6-14 aromatic cyclic hydrocarbon group; R , R , and R each independently means hydrogen, halogeno, cyano, etc.; L means a single bond, C1-6 alkylene, etc.; X means a single bond, a group represented by -CO-NH- or -NH-CO-, etc.; and Y means C3-8 cycloalkyl, a C6-14 aromatic cyclic hydrocarbon group, a 5- to 14-membered aromatic heterocyclic group, etc.