Ishii T, Hida T, Ishimaru T, Iinuma S, Sudo K, Muroi M, Kanamaru T, Okazaki H
Microbiology Research Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.
J Antibiot (Tokyo). 1991 Jun;44(6):589-99. doi: 10.7164/antibiotics.44.589.
A novel nonsteroidal aromatase inhibitor, TAN-931, was isolated from the culture filtrate of a soil isolate fungus, No. 8974. The strain was identified as Penicillium funiculosum No. 8974. TAN-931 inhibited human placental and rat ovarian aromatase activity, and the IC50 value was 17.2 and 162 microM, respectively. The inhibition of human placental aromatase was uncompetitive with respect to androstenedione conversion with a Ki value of 40 microM. When TAN-931 was subcutaneously administered at doses of 25, 50 and 100 mg/kg (once/day, x4) to 20-day-old female Sprague-Dawley rats treated with gonadotropin, the plasma estradiol-17 beta level and the weight of ovaries and uterus were markedly reduced in a dose-dependent manner. The in vivo inhibitory activity of TAN-931 was more potent than that of 4-hydroxyandrostenedione. Consecutive administration of TAN-931 (100 mg/kg, sc, twice/day, x 7) to 9-week-old male Sprague-Dawley rats did not induce any adrenal hypertrophy even though administration of aminoglutethimide caused 2-fold enlargement of the adrenal under the same conditions. Specific binding of TAN-931 to the estrogen receptor from a human breast cancer cell line, MCF-7, was not detected.
一种新型非甾体芳香化酶抑制剂TAN - 931,是从土壤分离真菌8974号的培养滤液中分离得到的。该菌株被鉴定为绳状青霉8974号。TAN - 931抑制人胎盘和大鼠卵巢芳香化酶活性,其IC50值分别为17.2和162微摩尔。就雄烯二酮转化而言,TAN - 931对人胎盘芳香化酶的抑制作用为非竞争性,Ki值为40微摩尔。当以25、50和100毫克/千克的剂量(每日一次,共4次)对用促性腺激素处理的20日龄雌性斯普拉格-道利大鼠皮下注射TAN - 931时,血浆雌二醇-17β水平以及卵巢和子宫的重量均呈剂量依赖性显著降低。TAN - 931的体内抑制活性比4 - 羟基雄烯二酮更强。对9周龄雄性斯普拉格-道利大鼠连续皮下注射TAN - 931(100毫克/千克,每日两次,共7次),即使在相同条件下给予氨鲁米特会导致肾上腺增大2倍,但TAN - 931并未引起任何肾上腺肥大。未检测到TAN - 931与人乳腺癌细胞系MCF - 7的雌激素受体有特异性结合。