Billich A, Fricker G, Müller I, Donatsch P, Ettmayer P, Gstach H, Lehr P, Peichl P, Scholz D, Rosenwirth B
Sandoz Research Institute, Vienna, Austria.
Antimicrob Agents Chemother. 1995 Jul;39(7):1406-13. doi: 10.1128/AAC.39.7.1406.
A series of inhibitors of human immunodeficiency virus type 1 (HIV-1) proteinase containing the 2-aralkyl-amino-substituted statine moiety as a novel transition-state analog was synthesized, with the aim to obtain compounds which combine anti-HIV potency with oral bioavailability. The reduced-size 2-aminobenzylstatine derivative SDZ PRI 053, which contains 2-(S)-amino-3-(R)-hydroxyindane in place of an amino acid amide, is a potent and orally bioavailable inhibitor of HIV-1 replication. The antiviral activity of SDZ PRI 053 was demonstrated in various cell lines, in primary lymphocytes, and in primary monocytes, against laboratory strains as well as clinical HIV-1 isolates (50% effective dose = 0.028 to 0.15 microM). Cell proliferation was impaired only at 100- to 300-fold-higher concentrations. The mechanism of antiviral action of the proteinase inhibitor SDZ PRI 0.53 was demonstrated to be inhibition of gag precursor protein processing. The finding that the inhibitory potency of SDZ PRI 053 in chronic virus infection, determined by p24 release, was considerably lower than that in de novo infection may be explained by the fact that the virus particles produced in the presence of SDZ PRI 053 are about 50-fold less infectious than those from untreated cultures. Upon intravenous administration, half-lives in blood of 100 and 32 min in mice and rats, respectively, were measured. Oral bioavailability of SDZ PRI 053 in rodents was 20 to 60%, depending on the dose. In mice, rats, and dogs, the inhibitor levels after oral administration remained far above the concentrations needed to efficiently block HIV replication in vitro for a prolonged period. This compound is thus a promising candidate for clinical use in HIV disease.
合成了一系列含有2-芳烷基氨基取代的他汀部分作为新型过渡态类似物的人免疫缺陷病毒1型(HIV-1)蛋白酶抑制剂,目的是获得兼具抗HIV效力和口服生物利用度的化合物。尺寸减小的2-氨基苄基他汀衍生物SDZ PRI 053,其含有2-(S)-氨基-3-(R)-羟基茚满以取代氨基酸酰胺,是一种有效的且具有口服生物利用度的HIV-1复制抑制剂。SDZ PRI 053的抗病毒活性在各种细胞系、原代淋巴细胞和原代单核细胞中得到证实,对实验室菌株以及临床HIV-1分离株均有效(50%有效剂量=0.028至0.15微摩尔)。仅在浓度高100至300倍时细胞增殖才受到损害。蛋白酶抑制剂SDZ PRI 0.53的抗病毒作用机制被证明是抑制gag前体蛋白的加工。通过p24释放测定发现,SDZ PRI 053在慢性病毒感染中的抑制效力远低于在初次感染中的抑制效力,这可能是因为在SDZ PRI 053存在下产生的病毒颗粒的感染性比未处理培养物产生的病毒颗粒低约50倍。静脉给药后,在小鼠和大鼠血液中的半衰期分别为100分钟和32分钟。SDZ PRI 053在啮齿动物中的口服生物利用度为20%至60%,取决于剂量。在小鼠、大鼠和狗中,口服给药后的抑制剂水平在很长一段时间内都远高于体外有效阻断HIV复制所需的浓度。因此,该化合物是用于HIV疾病临床治疗的有前景的候选药物。