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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| S414160-1mg |
1mg |
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| S414160-5mg |
5mg |
现货 ![]() |
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| S414160-10mg |
10mg |
现货 ![]() |
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| S414160-25mg |
25mg |
现货 ![]() |
| |
| S414160-50mg |
50mg |
现货 ![]() |
| |
| S414160-100mg |
100mg |
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|
| 英文别名 | BDBM177786 | S 055746 | s55746 | S-55746 | US9120791, Example 1 | 1448584-12-0 | S55746 (BLC201) | S55746 (S 055746,BCL201) | (S)-N-(4-hydroxyphenyl)-3-(6-(3-(morpholinomethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)benzo[d][1,3]dioxol-5-yl)-N-phenyl-5 |
|---|---|
| 规格或纯度 | ≥98% |
| 英文名称 | S55746 |
| 生化机理 | S55746(S 055746,BCL201)是一种新型口服活性 BCL-2 特异性抑制剂(Ki = 1.3 nM),对 BCL-XL 的亲和力较差,与 MCL-1、BFL-1(BCL2A1/A1)无明显结合。与 BCL-XL 相比,S55746 对 BCL-2 的选择性从约 70 倍到 400 倍不等。 |
| 储存温度 | -20°C储存 |
| 运输条件 | 超低温冰袋运输 |
| 产品介绍 |
S55746 (BCL201) 是一种有效、可口服、选择性的 BCL-2 抑制剂,其 Ki 值和 Kd 值分别为 1.3 nM 和 3.9 nM。S55746 (BCL201) 具有抗肿瘤活性且毒性低。 Information S55746 (S 055746,BCL201) is a novel, orally activeBCL-2specific inhibitor (Ki = 1.3 nM) with poor affinity for BCL-XL and no significant binding to MCL-1, BFL-1 (BCL2A1/A1). The selectivity of S55746 for BCL-2 versus BCL-XL ranges from ~70 to 400 folds. Targets Bcl-2 (Cell-free assay) 1.3 nM(Ki) In vitro S55746 occupies the hydrophobic groove of BCL-2. In a panel of hematological cell lines, S55746 induces hallmarks of apoptosis including externalization of phosphatidylserine, caspase-3 activation and PARP cleavage. S55746 potently induces RS4;11 cell killing after 72 h of treatment with an IC50 of 71.6 nM and exhibits a much weaker activity in H146 (IC50 = 1.7 μM), a BCL-XL-dependent cell line, which expresses a low level of BCL-2 and high level of BCL-XL. It has no cytotoxic activity on BCL-XL-dependent cells, such as platelets. In vivo S55746 administered by oral route daily in mice demonstrates robust anti-tumor efficacy in two hematological xenograft models (RS4;11 and Toledo models) with no weight lost and no change in behavior. Cell Research(from reference) Cell lines:RS4;11 cells Concentrations:0.01, 0.03, 0.1, 0.3, 1 μM Incubation Time:2 hours |
| 纯度 | ≥98% |
| IC50 | Bcl-2, Ki: 1.3 nM |
|---|---|
| ALogP | 6.817 |
| HBD Count | 1 |
| Rotatable Bond | 7 |
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
| PubChem SID | 488202277 |
|---|---|
| 分子类型 | 小分子 |
| IIUPAC Name | N-(4-hydroxyphenyl)-3-[6-[(3S)-3-(morpholin-4-ylmethyl)-3,4-dihydro-1H-isoquinoline-2-carbonyl]-1,3-benzodioxol-5-yl]-N-phenyl-5,6,7,8-tetrahydroindolizine-1-carboxamide |
| INCHI | 1S/C43H42N4O6/c48-34-15-13-32(14-16-34)47(31-10-2-1-3-11-31)43(50)37-23-39(45-17-7-6-12-38(37)45)35-24-40-41(53-28-52-40)25-36(35)42(49)46-26-30-9-5-4-8-29(30)22-33(46)27-44-18-20-51-21-19-44/h1-5,8-11,13-16,23-25,33,48H,6-7,12,17-22,26-28H2/t33-/m0/s1 |
| InChi Key | VYXJULKGMXJVGI-XIFFEERXSA-N |
| Smiles | C1CCN2C(=C(C=C2C3=CC4=C(C=C3C(=O)N5CC6=CC=CC=C6CC5CN7CCOCC7)OCO4)C(=O)N(C8=CC=CC=C8)C9=CC=C(C=C9)O)C1 |
| Isomeric SMILES | C1CCN2C(=C(C=C2C3=CC4=C(C=C3C(=O)N5CC6=CC=CC=C6C[C@H]5CN7CCOCC7)OCO4)C(=O)N(C8=CC=CC=C8)C9=CC=C(C=C9)O)C1 |
| PubChem CID | 71654876 |
| 分子量 | 710.82 |
| 溶解性 | Solubility (25°C) In vitro DMSO: 100 mg/mL (140.68 mM); Water: Insoluble; Ethanol: Insoluble; |
|---|---|
| DMSO(mg / mL) Max Solubility | 100 |
| DMSO(mM) Max Solubility | 140.682591936074 |
| Water(mg / mL) Max Solubility | <1 |
| 分子量 | 710.800 g/mol |
| XLogP3 | 5.800 |
| 氢键供体数Hydrogen Bond Donor Count | 1 |
| 氢键受体数Hydrogen Bond Acceptor Count | 7 |
| 可旋转键计数Rotatable Bond Count | 7 |
| 精确质量Exact Mass | 710.31 Da |
| 单同位素质量Monoisotopic Mass | 710.31 Da |
| 拓扑极表面积Topological Polar Surface Area | 96.700 Ų |
| 重原子数Heavy Atom Count | 53 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 1250.000 |
| 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 | 1 |
| 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 |
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 | |
| 分析证书 | S414160 |