Ramachandran J, Behrens C
Biochim Biophys Acta. 1977 Feb 28;496(2):321-8. doi: 10.1016/0304-4165(77)90314-2.
The catalytic dehalogenation of iodinated derivatives of corticotropin in the presence of tritium was investigated. In 0.1 M acetic acid, complete and rapid removal of iodine was achieved in the presence of freshly prepared palladium or palladium oxide as catalyst, but the specific radioactivity of the product was only 10-20% of the theoretically attainable value. Synthetic human corticotropin containing a 3,5-diiodo tyrosine in position 23 in place of tyrosine was successfully dehalogenated in solvent mixture 0.1 M acetic acid: hexamethylphosphoramide: dimethylformamide (1 : 10 : 90, v/v) in the presence of palladium oxide and calcium carbonate. The product was obtained in 30% yield after purification by carboxymethyl cellulose chromatography. The tritiated hormone had a specific radioactivity of 46 Ci/mmol (80% of the theoretical value) and was as potent as synthetic human corticotropin in stimulating steroidogenesis and lipolysis.
研究了在氚存在下促肾上腺皮质激素碘化衍生物的催化脱卤反应。在0.1 M乙酸中,以新鲜制备的钯或氧化钯为催化剂可实现碘的完全快速去除,但产物的比放射性仅为理论可达到值的10 - 20%。在23位含有3,5 - 二碘酪氨酸而非酪氨酸的合成人促肾上腺皮质激素,在氧化钯和碳酸钙存在下,于0.1 M乙酸:六甲基磷酰胺:二甲基甲酰胺(1 : 10 : 90,v/v)的溶剂混合物中成功脱卤。通过羧甲基纤维素色谱纯化后,产物的产率为30%。氚标记的激素比放射性为46 Ci/mmol(为理论值的80%),在刺激类固醇生成和脂解方面与合成人促肾上腺皮质激素效力相当。