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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1467057-23-3
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥770.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥318.0 |
| 规格: | 5 mg | 产品价格: | ¥700.0 |
| 规格: | 10 mg | 产品价格: | ¥1200.0 |
| 规格: | 25 mg | 产品价格: | ¥2400.0 |
| 规格: | 50 mg | 产品价格: | ¥4400.0 |
| 规格: | 100 mg | 产品价格: | ¥7100.0 |
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PF-06409577
CAS No. : 1467057-23-3
MCE 国际站:PF-06409577
产品活性:PF-06409577是有效,选择性的AMPK α1β1γ1 亚型变构激活剂,EC50 值为7 nM。
研究领域:Epigenetics | PI3K/Akt/mTOR
作用靶点:AMPK
In Vitro: PF-06409577 possesses similar potency toward the human and rat α1β1γ1 isoforms. In broad panel screening against other receptors, channels, PDEs and kinases, PF-06409577 exhibits minimal off-target pharmacology. PF-06409577 shows no detectable inhibition of hERG in a patch-clamp assay (100 μM) and is not an inhibitor (IC50>100 μM) of the microsomal activities of major human cytochrome P450 isoforms.
In Vivo: PF-06409577 demonstrates moderate plasma clearance in rats, dogs, and monkeys, and is well distributed with steady state distribution volume. Following oral administration of crystalline PF-06409577 in 0.5% methylcellulose suspension, PF-06409577 is rapidly absorbed in rats, dogs, and monkeys. The corresponding oral bioavailability values in rats, dogs, and monkeys, are 15%, 100%, and 59%, respectively. Dose responsive increases in pAMPK relative to total AMPK (tAMPK) in whole kidney tissue are observed with a maximal 3.8-fold response at 300 mg/kg PF-06409577 treatment. Oral administration of PF-06409577 (10, 30, and 100 mg/kg QD) results in dose-dependent reductions in proteinuria in the obese ZSF1 animals, with greater than 2-fold reduction in 24-hour urinary albumin loss compared to vehicle control after 60 days of treatment.
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文献和实验用张力计等测定。以水柱的长度(单位:厘米)表示土壤对水的吸力即基质势时,数字的幅度过大,因此 R. K. Schofield取其对数以 PF表示之。 100厘米的水柱相当于 100克 /平方厘米的压力, PF=2,永久凋萎点约相当于 15个大气压, PF=4.2。
血小板因子Ⅲ(PF3)有效性测定 【参考范围】被检者血浆与正常富含血小板血浆(PRP)及乏血小板血浆(PPP)分别反应,后者较前者凝血时间(检测器法)延长不超过5s.【影响因素】1.最好采用硅化或塑料注射器,玻璃试管等需涂硅处理或使用塑料制品。因为玻璃可以激活凝血反应。 2.较理想的抗凝剂应首选枸橼酸钠。 3.止血带不应扎得太紧,时间最好不超过5min,医学教|育网搜集整理并强调采血顺利,以防激活凝血反应。 4.PF3有效测定的准确性取决于富含
上海西唐生物科技有限公司 021-55229872, 65333639 www.westang.com 人血小板因子-4 ( PF-4 )ELISA 试剂盒 ( 用于血清、血浆、细胞培养上清液和其它生物体液内 ) 原理 本实验采用双抗体夹心 ABC-ELISA 法。用抗人 Platelet Factor 4 单抗包被于酶标板上,标准品和样品中的 PF-4与单抗结合,加入生物
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