Phenacetin是非阿片类镇痛化合物,具有抗炎活性。
Phenacetin is a non-opioid analgesic without anti-inflammatory properties.
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] Kanumuri Siva Rama Raju et. Al. No effect on pharmacokinetics of tamoxifen and 4-hydroxytamoxifen by multiple doses of red clover capsule in rats. Scientific reports, 5, 16126 (2015).
[2] Veenu Bala et. Al. N-Alkyl/aryl-4-(3-substituted-3-phenylpropyl)piperazine-1-carbothioamide as dual-action vaginal microbicides with reverse transcriptase inhibition. European Journal of Medicinal Chemistry, 101, 640-650 (2015).
[3] Ayorinde Adehin and Oluseye O Bolaji. Polymorphisms of CYP1A2 and CYP2A6 activity: phenotypes and the effect of age and sex in a Nigerian population. 30(3), 203-210 (2015)
分子式 C10H13NO2 |
分子量 179.22 |
CAS号 62-44-2 |
储存方式 ﹣20 ℃冷藏长期储存。冰袋运输 |
溶剂(常温) |
DMSO 35 mg/mL |
Water <1 mg/mL |
Ethanol 35 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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