计算溶液所需的质量、体积或浓度。
This is a demo store. No orders will be fulfilled.
| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| M647964-1mg |
1mg |
期货 ![]() |
| |
| M647964-5mg |
5mg |
期货 ![]() |
| |
| M647964-10mg |
10mg |
期货 ![]() |
| |
| M647964-25mg |
25mg |
期货 ![]() |
| |
| M647964-50mg |
50mg |
期货 ![]() |
| |
| M647964-100mg |
100mg |
期货 ![]() |
|
| 别名 | 甲哌嗪 | BA2845 |
|---|---|
| 英文别名 | Pacatal Base | Lacumin | Pakatal | mepasin | MPMP | CAS-60-89-9 | Pacatal | Nothiazine | Paxital | Pecatal | Meprazine | Mesapin | (N-Methyl-3-piperidyl)methylphenothiazine | Pecazine | Pacatol | Mepazine Base | MEPAZINE |
| 规格或纯度 | Moligand™, ≥99% |
| 英文名称 | Mepazine |
| 生化机理 | 美帕秦(Pecazine)是一种强效的选择性 MALT1 蛋白酶抑制剂,对 GSTMALT1 全长和 GSTMALT1 325-760 的 IC 50 s 分别为 0.83 和 0.42 μM。美帕秦通过增强细胞凋亡影响 ABC-DLBCL 细胞的活力。 |
| 储存温度 | -20°C储存 |
| 运输条件 | 超低温冰袋运输 |
| 产品介绍 |
Mepazine (Pecazine) is a potent and selective MALT1 protease inhibitor with IC 50 s of 0.83 and 0.42 μM for GSTMALT1 full length and GSTMALT1 325-760, respectively. Mepazine affects viability of ABC-DLBCL cells by enhancing apoptosis In Vitro Mepazine (5-20 μM; 4 days) causes a decrease of cell viability in the activated B cell subtype of diffuse large B cell lymphoma (ABCDLBCL) cells, without significantly affecting GCB-DLBCL cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: ABC-DLBCL cell lines (HBL1, OCI-Ly3, U2932, TMD8, OCI-Ly10) and GCB-DLBCL cell lines (BJAB, Su-DHL-6, Su-DHL-4) Concentration: 5, 10, and 20 μM Incubation Time: 4 days Result: Caused a decrease of cell viability in the ABC-DLBCL cells HBL1, OCI-Ly3, U2932, and TMD8, without significantly affecting GCB-DLBCL cells. In Vivo Mepazine (16 mg/kg; intraperitoneal administration) interferes with growth and induces apoptosis of ABC-DLBCL cell line OCI-Ly10 in NOD/scid IL-2Rg (NSG) mice with a murine DLBCL xenogeneic tumor model. Daily administration of Mepazine strongly impairs the expansion of the ABC-DLBCL cell line OCI-Ly10 . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: 6- to 8-week-old female NOD.Cg- Prkdc scid Il2rg tm1Wjl /SzJ (NSG) mice with a murine DLBCL xenogeneic tumor model Dosage: 400 μg per animal (25 g), corresponding to approximately 16 mg/kg. Administration: Intraperitoneal administration; started 1 or 12 days after transplantation and given continuously every 24 hr; daily application Result: Daily administration strongly impaired the expansion of the ABC-DLBCL cell line OCI-Ly10. Form:Solid IC50& Target:MALT1 |
| 纯度 | ≥99% |
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
| 分子类型 | 小分子 |
|---|---|
| IIUPAC Name | 10-[(1-methylpiperidin-3-yl)methyl]phenothiazine |
| INCHI | 1S/C19H22N2S/c1-20-12-6-7-15(13-20)14-21-16-8-2-4-10-18(16)22-19-11-5-3-9-17(19)21/h2-5,8-11,15H,6-7,12-14H2,1H3 |
| InChi Key | CBHCDHNUZWWAPP-UHFFFAOYSA-N |
| Smiles | CN1CCCC(C1)CN2C3=CC=CC=C3SC4=CC=CC=C42 |
| Isomeric SMILES | CN1CCCC(C1)CN2C3=CC=CC=C3SC4=CC=CC=C42 |
| 关联CAS | 24360-97-2;2975-36-2 |
| 分子量 | 310.46 |
| 溶解性 | DMSO : 100 mg/mL (322.10 mM; Need ultrasonic) |
|---|---|
| 分子量 | 310.500 g/mol |
| XLogP3 | 5.600 |
| 氢键供体数Hydrogen Bond Donor Count | 0 |
| 氢键受体数Hydrogen Bond Acceptor Count | 3 |
| 可旋转键计数Rotatable Bond Count | 2 |
| 精确质量Exact Mass | 310.15 Da |
| 单同位素质量Monoisotopic Mass | 310.15 Da |
| 拓扑极表面积Topological Polar Surface Area | 31.800 Ų |
| 重原子数Heavy Atom Count | 22 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 352.000 |
| 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 | 1 |
| 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 |