- INH6
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- $1.00 / 1KG
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2019-12-31
- CAS:1001753-24-7
- Min. Order: 1KG
- Purity: Min98% HPLC
- Supply Ability: g/kg/ton
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| | N-(4-Mesitylthiazol-2-yl)benzaMide Basic information |
| Product Name: | N-(4-Mesitylthiazol-2-yl)benzaMide | | Synonyms: | N-(4-Mesitylthiazol-2-yl)benzaMide;INH6;N-[4-(2,4,6-trimethylphenyl)-2-thiazolyl]-benzamide;N-[4-(2,4,6-trimethylphenyl)thiazol-2-yl]benzamide;INH-6; INH6;N-(4-Mesitylthiazol-2-yl)benzaMide USP/EP/BP;Apoptosis,Inhibitor,INH 6,INH6,INH-6,inhibit;Benzamide, N-[4-(2,4,6-trimethylphenyl)-2-thiazolyl]- | | CAS: | 1001753-24-7 | | MF: | C19H18N2OS | | MW: | 322.42 | | EINECS: | | | Product Categories: | Inhibitors | | Mol File: | 1001753-24-7.mol |  |
| | N-(4-Mesitylthiazol-2-yl)benzaMide Chemical Properties |
| Melting point | 192-193 °C | | density | 1.216±0.06 g/cm3(Predicted) | | storage temp. | Desiccate at -20°C | | solubility | ≥32.2 mg/mL in DMSO; insoluble in H2O; ≥3.55 mg/mL in EtOH with gentle warming and ultrasonic | | form | Powder | | pka | 7.07±0.70(Predicted) | | CAS DataBase Reference | 1001753-24-7 |
| | N-(4-Mesitylthiazol-2-yl)benzaMide Usage And Synthesis |
| Uses | INH6 is a Hec1 inhibitor that targets the Hec1/Nek2 pathway and causes chromosome mis-alignment as well as cell death. | | Biological Activity | inh6 is a potent inhibitor of hec1/nek2 [1].hec1 is an oncogene that involved in spindle checkpoint signaling and is overexpressed in many human cancers. nek2 is a serine/threonine-protein kinase that phosphorylates hec1, which is critical for its mitotic function and cell survival [1].inh6 is a potent hec1/nek2 inhibitor. inh6 inhibited hec1/nek2 function through protein degradation that led to chromosome mis-segregation and cell death. in mda-mb468 and mda-mb231 human breast cancer cell lines, hela human cervical cancer line and k562 human erythromyeloblastoid leukemia cell line, inh6 exhibited significantly anti-proliferation activities with ic50 values of 2.1, 1.7, 2.4 and 2.5 μm, respectively. in hela cell extract, inh6-conjugated matrix selectively co-precipitated with cellular hec1, which suggested that inh6 bound to cellular hec1. in hela cells, inh6 (6.25 μm) reduced nek2 by 50% at 8-11 h. in addition, inh6 slightly reduced hec1 over time. also, inh6 increased mitotic population with multipolar spindle configurations. in hela cells expressing the chromosome marker protein h2b-gfp, inh6 increased chromosome misalignment. in hela cells, inh6 exhibited progressive morphological changes of dying cells and induced apoptosis by 20% [1]. | | target | Hec1/Nek2 complex | | references | [1]. qiu xl, li g, wu g, et al. synthesis and biological evaluation of a series of novel inhibitor of nek2/hec1 analogues. j med chem, 2009, 52(6): 1757-1767. |
| | N-(4-Mesitylthiazol-2-yl)benzaMide Preparation Products And Raw materials |
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