Nafarelin is a gonadotropin-releasing hormone (GnRH) agonists that stimulates secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH).
Nafarelin is a gonadotropin-releasing hormone (GnRH) agonists that stimulates secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). Nafarelin can Induce atrophy and regression of experimentally induced endometriosis in rat and shrinks hypertrophic tissue in benign prostatic hyperplasia. Nafarelin decreases or ablates the physical symptoms associated with endometriosis, and pregnancy rates.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Mizutani T et al. Effect of gonadotropin-releasing hormone agonists, nafarelin, buserelin, and leuprolide, on experimentally induced endometriosis in the rat. Int J Fertil Menopausal Stud. 1995 Mar-Apr;40(2):106-11.
[2] Chrisp P et al. Nafarelin. A review of its pharmacodynamic and pharmacokinetic properties, and clinical potential in sex hormone-related conditions. Drugs. 1990 Apr;39(4):523-51.
分子式 C66H83N17O13 |
分子量 1322.48 |
CAS号 76932-56-4 |
储存方式 -20 ℃长期冷藏储存。冰袋运输 |
溶剂(常温) |
DMSO Soluble |
Water <1 mg/mL |
Ethanol <1 mg/mL |
体内溶解度
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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