Tsuchiya T, Hisano T, Tanaka A, Takahashi A
Toxicol Lett. 1987 Sep;38(1-2):97-102. doi: 10.1016/0378-4274(87)90116-0.
Benzimidazoles exhibited an inhibitory action on the chondrogenesis in a mouse limb bud cell culture system; further, nitro and chloro groups at the 5 position in 2-(2-pyridyl)benzimidazole were found to be potent substituents. However, 2-(2-pyridyl)benzoxazole and 5-methoxy-2-(2-pyridyl)benzothiazole exhibited no inhibitory action under our experimental conditions. Thus, imidazole NH proton seemed to be important in the inhibitory action in the mouse cell system. The concentrations of thiabendazole (TBZ), 5-hydroxy-TBZ (5-HY-TBZ) and N-methyl-TBZ necessary to reduce the amounts of cartilage proteoglycan by 50% (TP50) were estimated to be about 0.35, 0.25 and 0.70 mM, respectively, in the rat limb bud cell culture system. The TP50 of TBZ and 5-HY-TBZ in the rat cell system were 3- to 4-fold higher than those in the mouse cell system.
苯并咪唑在小鼠肢芽细胞培养系统中对软骨形成表现出抑制作用;此外,发现2-(2-吡啶基)苯并咪唑5位的硝基和氯基是有效的取代基。然而,在我们的实验条件下,2-(2-吡啶基)苯并恶唑和5-甲氧基-2-(2-吡啶基)苯并噻唑未表现出抑制作用。因此,咪唑NH质子在小鼠细胞系统的抑制作用中似乎很重要。在大鼠肢芽细胞培养系统中,使软骨蛋白聚糖量减少50%(TP50)所需的噻苯达唑(TBZ)、5-羟基-TBZ(5-HY-TBZ)和N-甲基-TBZ的浓度估计分别约为0.35、0.25和0.70 mM。大鼠细胞系统中TBZ和5-HY-TBZ的TP50比小鼠细胞系统中的高3至4倍。