Jones G H, Venuti M C, Young J M, Murthy D V, Loe B E, Simpson R A, Berks A H, Spires D A, Maloney P J, Kruseman M
J Med Chem. 1986 Aug;29(8):1504-11. doi: 10.1021/jm00158a031.
On the basis of previous observations that both 2,3-dihydro-2,2,3,3-tetrahydroxy-1,4-naphthoquinone (oxoline, 1) and 6-chloroisonaphthazarin (2) had demonstrated antipsoriatic activity in vivo, a series of structural derivatives of 2 were prepared and examined in the Scholtz-Dumas topical psoriasis bioassay. Of these six (5, 6, 9a, 10, 11a, 11b), the most effective compound was found to be 6-chloro-1,4-diacetoxy-2,3-dimethoxynaphthalene (RS-43179, lonapalene, 11a). An extensive series of 1,2,3,4-tetraoxygenated naphthalenes (16-74) incorporating variations of the ester, ether, and aryl substituents were prepared as analogues of 11a to examine the structural requirements for activity and were screened in vivo as inhibitors of arachidonic acid induced mouse ear edema, a topical bioassay capable of detecting 5-lipoxygenase inhibitors. Net lipophilicity, hydrolytic stability, and ring substitution play significant roles in determining the observed in vivo activity. Lonapalene (11a) is currently in clinical development as a topically applied nonsteroidal antipsoriatic agent.
基于之前的观察结果,即2,3 - 二氢 - 2,2,3,3 - 四羟基 - 1,4 - 萘醌(氧化萘啉,1)和6 - 氯异萘并萘醌(2)在体内均表现出抗银屑病活性,制备了一系列2的结构衍生物,并在Scholtz - Dumas局部银屑病生物测定法中进行了检测。在这六种化合物(5、6、9a、10、11a、11b)中,发现最有效的化合物是6 - 氯 - 1,4 - 二乙酰氧基 - 2,3 - 二甲氧基萘(RS - 43179,洛那帕琳,11a)。制备了一系列包含酯、醚和芳基取代基变化的1,2,3,4 - 四氧化萘(16 - 74)作为11a的类似物,以研究活性的结构要求,并在体内作为花生四烯酸诱导的小鼠耳水肿的抑制剂进行筛选,这是一种能够检测5 - 脂氧合酶抑制剂的局部生物测定法。净亲脂性、水解稳定性和环取代在决定观察到的体内活性方面起着重要作用。洛那帕琳(11a)目前正在作为一种局部应用的非甾体抗银屑病药物进行临床开发。