Sorafenib
Cat.No:IS0220 Solarbio
CAS:284461-73-0
Molecular Formula:C21H16ClF3N4O3
Molecular Weight:464.83
Storage:Powder:-20℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
Qty:
Size:
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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > MAPK > SorafenibCAS:284461-73-0
Molecular Formula:C21H16ClF3N4O3
Molecular Weight:464.83
Storage:Powder:-20℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
Qty:
Size:
| CAS | 284461-73-0 |
| Name | Sorafenib |
| Molecular Formula | C21H16ClF3N4O3 |
| Molecular Weight | 464.83 |
| Solubility | Soluble in DMSO ≥5mg/mL |
| Purity | HPLC≥98% |
| Appearance | White to off-white Solid |
| Storage | Powder:-20℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
| EC | EINECS 608-209-4 |
| MDL | MFCD06411450 |
| SMILES | O=C(NC(C=C1)=CC=C1OC2=CC(C(NC)=O)=NC=C2)NC3=CC=C(Cl)C(C(F)(F)F)=C3 |
| InChIKey | MLDQJTXFUGDVEO-UHFFFAOYSA-N |
| InChI | InChI=1S/C21H16ClF3N4O3/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23,24)25/h2-11H,1H3,(H,26,30)(H2,28,29,31) |
| PubChem CID | 216239 |
| Target Point | Ferroptosis;Raf |
| Passage | Apoptosis;MAPK |
| Background | It is a potent Raf inhibitor and a multi-kinase inhibitor, which has inhibitory effect on VEGFR2,VEGFR3,PDGFRβ,FLT3 and c-Kit. It was also a ferroptosis agonist that induced autophagy and apoptosis. |
| Biological Activity | Sorafenib (Bay 43-9006) 是有效的多激酶抑制剂,抑制Raf-1,B-Raf 和 VEGFR-3 的 IC50 分别为6 nM,20 nM,22 nM。[1-4] |
| Data Literature Source | [1]. Wilhelm SM,et al. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis. Cancer Res. 2004 Oct 1;64(19):7099-109. [2]. El-Ashmawy NE,et al. Sorafenib effect on liver neoplastic changes in rats: more than a kinase inhibitor. Clin Exp Med. 2016 Apr 16. [3]. Jin W,et al. Long non-coding RNA TUC338 is functionally involved in sorafenib-sensitized hepatocarcinoma cells by targeting RASAL1. Oncol Rep. 2017 Jan;37(1):273-280. [4]. Li M,et al. Activation of an AKT/FOXM1/STMN1 pathway drives resistance to tyrosine kinase inhibitors in lung cancer. Br J Cancer. 2017 Aug 29. |
| Unit | Bottle |
| Specification | 10mg 10mM*1mL in DMSO 50mg 100mg |
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
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