计算溶液所需的质量、体积或浓度。
活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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T126330-5mg |
5mg |
现货 ![]() |
| |
T126330-25mg |
25mg |
现货 ![]() |
| |
T126330-100mg |
100mg |
现货 ![]() |
|
别名 | 费德拉替尼(SAR302503、TG101348) |
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英文别名 | 7.ALPHA.-METHYLNORETHINDRONE | FEDRATINIB [WHO-DD] | NSC800099 | NSC-800099 | N-Tert-butyl-3-(5-methyl-2-(4-(2-pyrrolidin-1-yl-ethoxy)-phenylamino)-pyrimidin-4-ylamino)-benzenesulfonamide | Fedratinib (TG101348) | 936091-26-8 (free base) | s2736 | Z203728 |
规格或纯度 | Moligand™, ≥98% |
英文名称 | Fedratinib (SAR302503, TG101348) |
生化机理 | TG-101348 是一种强效、高选择性的 JAK2 抑制剂。 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
作用类型 | 抑制剂 |
作用机制 | 酪氨酸蛋白激酶 JAK2 抑制剂 |
产品介绍 |
TG-101348 (SAR302503)是JAK2选择性抑制剂,IC50为3 nM,作用于JAK2比作用于JAK1和JAK3选择性高35和334倍,同时还能抑制BRD4,IC50为340 nM。A selective inhibitor of JAK2 tyrosine kinase TG-101348 (SAR302503) is a selective inhibitor of JAK2 with IC50 of 3 nM, 35- and 334-fold more selective for JAK2 versus JAK1 and JAK3, TG-101348 also inhibit BRD4 with IC50 of 340 nM. |
ALogP | 4.8 |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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分子类型 | 小分子 |
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IUPAC Name | N-tert-butyl-3-[[5-methyl-2-[4-(2-pyrrolidin-1-ylethoxy)anilino]pyrimidin-4-yl]amino]benzenesulfonamide |
INCHI | InChI=1S/C27H36N6O3S/c1-20-19-28-26(30-21-10-12-23(13-11-21)36-17-16-33-14-5-6-15-33)31-25(20)29-22-8-7-9-24(18-22)37(34,35)32-27(2,3)4/h7-13,18-19,32H,5-6,14-17H2,1-4H3,(H2,28,29,30,31) |
InChi Key | JOOXLOJCABQBSG-UHFFFAOYSA-N |
Canonical SMILES | CC1=CN=C(N=C1NC2=CC(=CC=C2)S(=O)(=O)NC(C)(C)C)NC3=CC=C(C=C3)OCCN4CCCC4 |
Isomeric SMILES | CC1=CN=C(N=C1NC2=CC(=CC=C2)S(=O)(=O)NC(C)(C)C)NC3=CC=C(C=C3)OCCN4CCCC4 |
PubChem CID | 16722836 |
分子量 | 524.68 |
溶解性 | DMSO 105 mg/mL Water <1 mg/mL Ethanol 21 mg/mL |
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分子量 | 524.700 g/mol |
XLogP3 | 4.800 |
氢键供体数Hydrogen Bond Donor Count | 3 |
氢键受体数Hydrogen Bond Acceptor Count | 9 |
可旋转键计数Rotatable Bond Count | 11 |
精确质量Exact Mass | 524.257 Da |
单同位素质量Monoisotopic Mass | 524.257 Da |
拓扑极表面积Topological Polar Surface Area | 117.000 Ų |
重原子数Heavy Atom Count | 37 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 787.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 1 |
Purity(HPLC) | 98-100(%) |
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Appearance(T126330) | White to Grey solid |
NMR spectrum | Conforms to Structure |
通过匹配包装上的批号来查找并下载产品的 COA,每批产品都进行了严格的验证,您可放心使用!
批号(Lot Number) | 证书类型 | 日期 | 货号 |
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分析证书 | 23-01-12 | T126330 |
1. Wernig G, Kharas MG, Okabe R, Moore SA, Leeman DS, Cullen DE, Gozo M, McDowell EP, Levine RL, Doukas J et al.. (2008) Efficacy of TG101348, a selective JAK2 inhibitor, in treatment of a murine model of JAK2V617F-induced polycythemia vera.. Cancer Cell, 13 (4): (311-20). [PMID:18394554] [10.1021/op500134e] |
2. Ciceri P, Müller S, O'Mahony A, Fedorov O, Filippakopoulos P, Hunt JP, Lasater EA, Pallares G, Picaud S, Wells C et al.. (2014) Dual kinase-bromodomain inhibitors for rationally designed polypharmacology.. Nat Chem Biol, 10 (4): (305-12). [PMID:24584101] [10.1021/op500134e] |
3. Bose P, Alfayez M, Verstovsek S. (2019) New Concepts of Treatment for Patients with Myelofibrosis.. Curr Treat Options Oncol, 20 (1): (5). [PMID:30675650] [10.1021/op500134e] |