Abrocitinib (Synonyms: PF-04965842)
目录号: PL01610 纯度: ≥99%
CAS No. :1622902-68-4
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中文名称
Abrocitinib
英文名称
Abrocitinib
英文别名
Abrocitinib;73SM5SF3OR;N-{cis-3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide;N-(cis-3-(Methyl(7H-pyrrolo(2,3-d)pyrimidin-4-yl)amino)cyclobutyl)propane-1-sulfonamide;D7D;Abrocitinib [USAN];abrocitinib (proposed INN);GTPL9991;BDBM159748;SB18849;compound 25 [PMID: 29298069];PF04965842;PF 04965842;US9035074, 2;N-[cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl]propane-1-sulfonamide;N-[3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl]propane-1-sulfonamide;Cibinqo;Abrocitinib (JAN/USAN);PF-04965842(Abrocitinib;PF-04965842;N-[cis-3-(Methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)cyclobutyl]-1-propanesulfonamide;N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}-propane-1-sulfonamide
Cas No.
1622902-68-4
分子式
C14H21N5O2S
分子量
323.41
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Abrocitinib (PF-04965842) 是一种有效、可口服、选择性的 JAK1 抑制剂,对 JAK1 和 JAK2 的 IC50 值分别为 29 和 803 nM。Abrocitinib (PF-04965842) 可抑制 TYK2 的活性(IC50,1.253 μM) 和刺激后 STAT1,STAT3 和 STAT5 的磷酸化水平。可用于自身免疫症的研究。
生物活性
Abrocitinib (PF-04965842) is a potent, orally active and selective JAK1 inhibitor, with IC 50 s of 29 and 803 nM for JAK1 and JAK2, respectively. Abrocitinib (PF-04965842) exhibits less active effect on TYK2 (IC 50 , 1.253 μM), and inhibits phosphorylation of STAT1, STAT3 and STAT5 after stimulation. Effective in autoimmune disease.
性状
Solid
IC50 & Target[1][2]
JAK1 29 nM (IC50) JAK2 803 nM (IC50
体外研究(In Vitro)
Abrocitinib (Compound 25) inhibits IFNα-stimulated phosphorylation of STAT3, IFN-stimulated phosphorylation of STAT1 in human whole blood (HWB), as well as pSTAT5 in CD34+ spiked into HWB (JAK2), with IC50s of 189, 163 nM, 7.178 μM, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Abrocitinib (Compound 25; 5, 15, 50 mg/kg, p.o., daily for 7 days) significantly reduces paw swelling in rat adjuvant-induced arthritis model. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Vazquez ML, et al. Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases. J Med Chem. 2018 Feb 8;61(3):1130-115
溶解度数据
In Vitro: DMSO : 125 mg/mL (386.51 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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