
- BMS-833923
- LDE225 Diphosphate
- Purmorphamine
- LDE225 (NVP-LDE225,Erismodegib)
HhAntagGLI1-mediated transcription inhibitor |
Sample solution is provided at 25 µL, 10mM.
































Quality Control & MSDS
- View current batch:
- Purity = 98.95%
- COA (Certificate Of Analysis)
- HPLC
- MS (Retest)
- NMR (Nuclear Magnetic Resonance)
- MSDS (Material Safety Data Sheet)
- Datasheet
Chemical structure


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Cas No. | 496794-70-8 | SDF | Download SDF |
Synonyms | N/A | ||
Chemical Name | N-[4-chloro-3-[6-(dimethylamino)-1H-benzimidazol-2-yl]phenyl]-3,5-dimethoxybenzamide | ||
Canonical SMILES | CN(C)C1=CC2=C(C=C1)N=C(N2)C3=C(C=CC(=C3)NC(=O)C4=CC(=CC(=C4)OC)OC)Cl | ||
Formula | C24H23ClN4O3 | M.Wt | 450.92 |
Solubility | ≥13.3 mg/mL in DMSO, ≥52.3 mg/mL in EtOH with gentle warming, <2.69 mg/ml="" in="" h2o="">2.69> | Storage | Store at -20°C |
Physical Appearance | A solid | Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
IC50: from ~2 μM to >30 μM
HhAntag is a Hedgehog signaling antagonist. Ligand-dependent activation of the Hedgehog (Hh) signaling pathway has been associated with tumorigenesis in a number of human tissues.
In vitro: HhAntag has been evaluated for its effect on Hh pathway across a large panel of cancer cell lines. HhAntag demonstrated to be around 10-times more potent than cyclopamine at inhibiting the activity of Hh pathway. A range of cellular sensitivities to HhAntag was observed with IC50 values for growth inhibition ranging from ~2 μM to >30 μM. In contrast to previous reports, no tissue specificity of in vitro sensitivity to HhAntag was observed [1].
In vivo: Oral administration of HhAntag to mice with primary human xenografts resulted in significant growth delay in both pancreatic and colon adenocarcinoma models, with average tumour growth inhibitions of 29% and 48%, respectively. Moreover, the HhAntag doses required to inhibit the tumor growth were similar to the doses required to fully inhibit endogenous Hh target genes in tumour stroma or in surrogate normal tissues, indicating that such growth inhibition was a specific consequence of Hh inhibition [1].
Clinical trial: N/A
Reference:[1] Yauch RL,Gould SE,Scales SJ,Tang T,Tian H,Ahn CP,Marshall D,Fu L,Januario T,Kallop D,Nannini-Pepe M,Kotkow K,Marsters JC,Rubin LL,de Sauvage FJ. A paracrine requirement for hedgehog signalling in cancer. Nature.2008 Sep 18;455(7211):406-10.
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我知道所以你知道!
如果有,具体在哪个学校/单位/企业?
最近实验需要用到此设备。
如能告诉,不胜感谢!!!谢谢!!!
Luciferase
)
标记细胞或
DNA
,而荧光技术则采用绿色荧光蛋白、红色荧光蛋白等荧光报告基因和
FITC
、
Cy5
、
C
y7
等荧光素及量子点
(quantumdot
,
QD)
进行标记。
小动物活体成像技术是采用高灵敏度制冷
CCD
配合特制的成像暗箱和图像处理软件,使得可以直接监
控活体生物体内的细胞活动和基因行为。实验者借此可以观测活体动物体内肿瘤的生长及转移、
感染性
疾病发展过程、特定基因的表达等生物学过程。
由于具有更高量子效率
CCD
的问世,使活体动物体内光学成像技术具有越来越高的灵敏度,对肿瘤微
小转移灶的检测灵敏度极高;另外,该技术不涉及放射性物质和方法,非常安全。因其操作极其简单、
所得结果直观、
灵敏度高、
实验成本低等特点,
在刚刚发展起来的几年时间内,
已广泛应用于生命科学、
医学研究及药物开发等方面

