计算溶液所需的质量、体积或浓度。
活性类型 | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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F414459-5mg |
5mg |
现货 ![]() |
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F414459-10mg |
10mg |
现货 ![]() |
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F414459-25mg |
25mg |
现货 ![]() |
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F414459-50mg |
50mg |
现货 ![]() |
| |
F414459-100mg |
100mg |
现货 ![]() |
|
别名 | 3-氨基-N-(4-氟苯基)-6-(2-噻吩基)-4-(三氟甲基)-噻吩并[2,3-b]吡啶-2-羧酰胺 | 3-氨基-N-(4-氟苯基)-6-(噻吩-2-基)-4-(三氟甲基)噻吩并[2,3-b]吡啶-2-羧酰胺 |
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英文别名 | NCGC00099374 | NCGC00099374-01 | AS-57575 | MFCD01416826 | 3-amino-N-(4-fluorophenyl)-6-(thiophen-2-yl)-4-(trifluoromethyl)thieno[2,3-b]pyridine-2-carboxamide | HMS1798G15 | FDI-6, >=98% (HPLC) | ZATJMMZPGVDUOM-UHFFFAOYSA-N | FOXM1 Inhibitor III (FDI-6) | |
规格或纯度 | ≥98% |
英文名称 | FDI-6 |
生化机理 | FDI-6 (NCGC00099374) 是一种叉头盒蛋白 M1 转录因子(FOXM1)抑制剂,IC50 为 22.5 μM。 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
产品介绍 |
Information FDI-6 FDI-6 (NCGC00099374) is an inhibitor of the Forkhead box protein M1 transcription factor (FOXM1) with IC50 of 22.5 μM. Targets FOXM1 (Cell-free assay) 22.5 μM In vitro FDI-6 (NCGC00099374) is characterized in depth and is shown to bind directly to FOXM1 protein, to displace FOXM1 from genomic targets in MCF-7 breast cancer cells, and induces concomitant transcriptional down-regulation. Global transcript profiling of MCF-7 cells by RNA-seq shows that FDI-6 specifically down-regulates FOXM1-activated genes with FOXM1 occupancy confirmed by ChIP-seq. In vivo Inhibiting FOXM1 with FDI-6 inhibits liver cancer cell growth in vivo. Cell Research(from reference) Cell lines:MCF-7 cells Concentrations:20 μM, 40 μM Incubation Time:6 h |
ALogP | 5.117 |
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hba_count | 2 |
HBD Count | 2 |
Rotatable Bond | 4 |
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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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PubChem SID | 504763247 |
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分子类型 | 小分子 |
IUPAC Name | 3-amino-N-(4-fluorophenyl)-6-thiophen-2-yl-4-(trifluoromethyl)thieno[2,3-b]pyridine-2-carboxamide |
INCHI | InChI=1S/C19H11F4N3OS2/c20-9-3-5-10(6-4-9)25-17(27)16-15(24)14-11(19(21,22)23)8-12(26-18(14)29-16)13-2-1-7-28-13/h1-8H,24H2,(H,25,27) |
InChi Key | ZATJMMZPGVDUOM-UHFFFAOYSA-N |
Canonical SMILES | C1=CSC(=C1)C2=NC3=C(C(=C2)C(F)(F)F)C(=C(S3)C(=O)NC4=CC=C(C=C4)F)N |
Isomeric SMILES | C1=CSC(=C1)C2=NC3=C(C(=C2)C(F)(F)F)C(=C(S3)C(=O)NC4=CC=C(C=C4)F)N |
分子量 | 437.43 |
Reaxy-Rn | 32458479 |
Reaxys-RN link address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=32458479&ln= |
溶解性 | Solubility (25°C) In vitro DMSO: 87 mg/mL (198.88 mM); Water: Insoluble; Ethanol: Insoluble; |
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DMSO(mg / mL) Max Solubility | 87 |
DMSO(mM) Max Solubility | 198.888965091558 |
Water(mg / mL) Max Solubility | <1 |
分子量 | 437.400 g/mol |
XLogP3 | 5.600 |
氢键供体数Hydrogen Bond Donor Count | 2 |
氢键受体数Hydrogen Bond Acceptor Count | 9 |
可旋转键计数Rotatable Bond Count | 3 |
精确质量Exact Mass | 437.028 Da |
单同位素质量Monoisotopic Mass | 437.028 Da |
拓扑极表面积Topological Polar Surface Area | 124.000 Ų |
重原子数Heavy Atom Count | 29 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 602.000 |
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 |
象形图 | GHS07 |
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信号词 | Warning |
危险声明 |
H319: 引起严重眼睛刺激 H302: 吞食有害 |
预防措施声明 |
P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P501: 将内容物/容器处理到。。。 P264: 处理后要彻底洗手。 P270: 使用本产品时,请勿进食、饮水或吸烟。 P330: 漱口 P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。 P301+P317: 如果被吞咽:请寻求医疗帮助。 P337+P317: 如果眼睛刺激持续:寻求医疗帮助。 |
Reaxy-Rn | 32458479 |
Reaxys-RN link address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=32458479&ln= |
Purity(HPLC) | 98-100(%) |
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Appearance(F414459) | bright yellow powder |
Proton NMR spectrum | Conforms to structure |
FNMR spectrum | Conforms to Structure |