Poor bioavailability of CGS 8216 in a water/tween vehicle following intraperitoneal injection.
作者信息
Lister R G, LeDuc B W, Greenblatt D J, File S E
出版信息
Psychopharmacology (Berl). 1987;91(2):260-1. doi: 10.1007/BF00217076.
PMID:3107044
Abstract
摘要
相似文献
1
Poor bioavailability of CGS 8216 in a water/tween vehicle following intraperitoneal injection.腹腔注射后，CGS 8216在水/吐温载体中的生物利用度较低。
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Behavioral effects of vehicles: DMSO, ethanol, Tween-20, Tween-80, and emulphor-620.赋形剂的行为效应：二甲基亚砜、乙醇、吐温-20、吐温-80和乳化剂-620。
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Lack of effect of flumazenil and CGS 8216 on the anxiolytic-like properties of loreclezole.氟马西尼和CGS 8216对氯雷唑抗焦虑样特性无影响。
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本文引用的文献
1
A pharmacokinetic study of CGS-8216, a benzodiazepine receptor ligand, in the rat.苯二氮䓬受体配体CGS - 8216在大鼠体内的药代动力学研究。
Psychopharmacology (Berl). 1984;84(3):420-2. doi: 10.1007/BF00555224.
2
Metabolic fate of CGS 8216, a benzodiazepine receptor antagonist, in rat and in man.苯二氮䓬受体拮抗剂CGS 8216在大鼠和人体内的代谢命运。
Psychopharmacology (Berl). 1986;88(4):529-30. doi: 10.1007/BF00178521.
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