Tasaka K, Kamei C, Nakano S, Takeuchi Y, Yamato M
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.
Methods Find Exp Clin Pharmacol. 1998 Mar;20(2):99-109. doi: 10.1358/mf.1998.20.2.485637.
Effects of certain resorcinol derivatives on tyrosinase activity, melanin formation and some other biological activities were studied in order to develop a new, potent depigmentor and/or antimelanoma drug. NKO-09, having isopentyl group in position 6 of resorcinal, exhibited a more potent effect than the compounds which have methyl (NKO-10), ethyl (NKO-11), hexyl (KOM-14), octyl (NKO-14), decyl (NKO-19), dodecyl (NKO-15) and tetradecyl (NKO-16) group in inhibiting the tyrosinase activities (both tyrosine hydroxylation and dopa oxidation). NKO-09 was more potent than hydroquinone in inhibiting the tyrosine hydroxylation; furthermore, NKO-09 inhibited the dopa oxidation different from hydroquinone. In the studies on melanin formation, protein synthesis and the growth of the melanoma cells, NKO-09 caused the most potent effect among the test compounds, except for the growth of the melanoma cells. KOM-14 was more potent than NKO-09 in the antimelanoma activity, and its effect was superior than that of 5-fluorouracil. From these findings, it is suggested that NKO-09 and KOM-14 can be used as an efficacious depigmentor and antimelanoma drug, respectively.
为开发一种新型、高效的色素脱失剂和/或抗黑色素瘤药物,研究了某些间苯二酚衍生物对酪氨酸酶活性、黑色素形成及其他一些生物学活性的影响。在间苯二酚的6位具有异戊基的NKO - 09,在抑制酪氨酸酶活性(酪氨酸羟化和多巴氧化)方面,比具有甲基(NKO - 10)、乙基(NKO - 11)、己基(KOM - 14)、辛基(NKO - 14)、癸基(NKO - 19)、十二烷基(NKO - 15)和十四烷基(NKO - 16)基团的化合物表现出更强的效果。NKO - 09在抑制酪氨酸羟化方面比氢醌更有效;此外,NKO - 09抑制多巴氧化的方式与氢醌不同。在黑色素形成、蛋白质合成及黑色素瘤细胞生长的研究中,除黑色素瘤细胞生长外,NKO - 09在受试化合物中产生的效果最为显著。KOM - 14在抗黑色素瘤活性方面比NKO - 09更有效,其效果优于5 - 氟尿嘧啶。从这些发现表明,NKO - 09和KOM - 14可分别用作有效的色素脱失剂和抗黑色素瘤药物。