CAS NO: | 174484-41-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Tipranavir (PNU-140690) inhibits the enzymatic activity and dimerization ofHIV-1protease, exerts potent activity against multi-protease inhibitor (PI)-resistantHIV-1isolates withIC50s of 66-410 nM[1][2]. Tipranavir inhibits SARS-CoV-2 3CLproactivity[3]. | ||||||||||||||||
IC50& Target | IC50: 66-410 nM (HIV-1 isolates)[1] | ||||||||||||||||
体外研究 (In Vitro) | Tipranavir (PNU-140690) inhibits the enzymatic activity of HIV-1 protease, blocks the dimerization of protease subunits, and exerts potent activity against a wide spectrum of wild-type and multi-PI-resistant HIV-1 variants. When a mixture of 11 multi-PI-resistant (but TPV-sensitive) clinical isolates (HIV11MIX), which include HIVBand HIVC, is selected against Tipranavir, HIV11MIXrapidly (by 10 passages [HIV11MIXP10]) acquires high-level Tipranavir (PNU-140690) resistance and replicates at high concentrations of Tipranavir (PNU-140690). cHIVBI54Vand cHIVBI54V/V82Tare significantly resistant to Tipranavir (PNU-140690), with IC50s of 2.9 and 3.2 μM, respectively, which are 11- and 12-fold increases in comparison to the IC50against cHIVB, respectively[1]. | ||||||||||||||||
体内研究 (In Vivo) | Tipranavir (PNU-140690) is administered orally twice daily and must be given in combination with low-dose ritonavir (RTV) to boost Tipranavir bioavailability. In Tipranavir/r-cotreated mice, the Tipranavir (PNU-140690) abundance in the liver, spleen, and eyes is significantly higher than that in mice treated with Tipranavir alone. Tipranavir (PNU-140690) metabolites accounts for 31 and 38% in the serum and liver in the Tipranavir-alone group. In Tipranavir (PNU-140690) and Tipranavir (TPV/r)-cotreated mice, only 1 and 2% of metabolites are detected in the serum and liver. Sprague-Dawley rats are administered a single dose of [14C]Tipranavir (PNU-140690) with coadministration of RTV. The most abundant metabolite in feces is an oxidation metabolite. In urine, no single metabolite is found to be significantly present[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 602.66 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C31H33F3N2O5S | ||||||||||||||||
CAS 号 | 174484-41-4 | ||||||||||||||||
中文名称 | 替拉那韦 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 200 mg/mL(331.86 mM;Need ultrasonic) Ethanol : ≥ 50 mg/mL(82.97 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
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