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- 详细信息
- 技术资料
- 保质期:
2 years
- 英文名:
JK184
- 库存:
10
- 供应商:
上海伟进生物科技有限公司
- CAS号:
315703-52-7
- 保存条件:
-20℃
- 规格:
5mg
Biological Activity
JK184, a cell-permeable imidazopyridine derivative compound, is a potent downstream hedgehog (Hh) signaling antagonist that inhibits Shh-N-mediated Gli-transcription (IC50= 30 nM) and shows suppression of GLI1 and Ptch1 mRNA expression in a dose-dependent manner. JK184 has been found to function by inhibiting class IV alcohol dehydrogenase (Adh7), with an IC50 of 210 nM. JK184 exhibits antiproliferation activities in a wide range of cancer cell lines with abnormally activated Hh signaling (GI50= 3-21 nM) as well as in human xenografts in vivo [1]. JK184 is shown to modulate Hedgehog target gene expression by depolymerizing microtubules [2].
Chemical Properties
| Cas No.: 315703-52-7 |
M. Wt.: 350.44 |
| Formula: C19H18N4OS |
Purity: ≥98% |
| Synonym: Hh Signaling Antagonist VII |
|
| Chemical Name: N-(4-Ethoxyphenyl)-4-(2-methylimidazo[1,2-a]pyridin-3-y l)-2-thiazolamine |
|
| Appearance: Beige solid |
|
| Solubility: Soluble to 100 mM in DMSO and to 25 mM in ethanol |
|
| Storage: Store solid at +4 ºC |
|
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