SORAFENIB TOSYLATE

PRODUCT IDENTIFICATION

CAS NO.

284461-73-0 (parent)
475207-59-1 (tosylate)

SORAFENIB

EINECS NO.  
FORMULA C21H16ClF3N4O3
MOL WT. 464.82

H.S. CODE

 

TOXICITY

 
SYNONYMS Nexavar;
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-((2-(methylcarbamoyl)pyridin-4-yl)oxy)phenyl)urea 4- methylbenzenesulfonate; 4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)phenoxy)- N2-methyl pyridine- 2-carboxamide 4-methylbenzenesulfonate; N-(4-Chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2- (N- methylcarbamoyl)-4-pyridyloxy)phenyl)urea 4-methylbenzenesulfonate;

CLASSIFICATION

Protein Kinase Inhibitor

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

white to off-white powder

MELTING POINT 230 C
BOILING POINT

 

RELATIVE DENSITY  
SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

 

REFRACTIVE INDEX

 

NFPA RATINGS

 

AUTOIGNITION

 

FLASH POINT

 

STABILITY Stable under normal conditions.

GENERAL DESCRIPTION & EXTERNAL LINKS

Types of chemotherapy drug;

  • Alkylating agents
  • Angiogenesis Inhibitors
  • Anti-metabolites
  • Anti-mitotics
  • Aromatase inhibitors
  • Biologic response modifiers
  • Differentiating agents
  • Hormonal therapies
  • Monoclonal antibodies
  • Platinum derivatives
  • Signaling inhibitors
  • Topoisomerase inhibitors

 

Treating the cancer by enhancing the immune system's ability to destroy it causes some cancers to shrink and may prolong survival (see Prevention and Treatment of Cancer: Immunotherapy). One such treatment, interleukin-2, is used for kidney cancer. Various combinations of interleukin-2, interferon, and other biologic agents and even vaccines developed from cells removed from the kidney cancer are being investigated. These treatments may be helpful for metastatic cancer, although the benefit is usually small. For people with metastatic cancer, recently developed treatments include the drugs sunitinib, sorafenib, and temsirolimus. These drugs alter molecular pathways that affect the tumor and are thus called targeted therapies. Rarely (in less than 1% of people), removing the affected kidney causes tumors elsewhere in the body to shrink. However, the slim possibility that tumor shrinkage will occur is not considered sufficient reason to remove a cancerous kidney when the cancer has already spread, unless removal is part of an overall plan that includes other systemic therapies.(http://www.mercksource.com/)

Sorafenib may stop the growth of tumor cells by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth. Estradiol can cause the growth of breast cancer. Hormone therapy using anastrozole may fight breast cancer by blocking the use of estradiol by the tumor cells. Sometimes when hormone therapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to hormone therapy. Giving sorafenib together with anastrozole may reduce drug resistance and allow the tumor cells to be killed. (http://www.clinicaltrials.gov/show/NCT00217399)

Sorafenib (Nexavar®) and sunitinib (Sutent®) are orally administered inhibitors of protein tyrosine kinases associated with the intracellular portions of certain transmembrane receptor molecules. Each targets the tyrosine kinase activity of more than one receptor, with effects that depend on each cell type’s receptor repertoire. Inhibiting these intracellular tyrosine kinases blocks signal transduction after a growth factor, cytokine, or other ligand binds to the receptor’s extracellular domain. In different cell types, this can inhibit tumor growth, metastasis, or angiogenesis (growth of new blood vessels). Both sorafenib and sunitinib are approved by the U.S. Food and Drug Administration (FDA) for the treatment of advanced renal cell carcinoma. Sunitinib also is indicated to treat gastrointestinal stromal tumor (GIST) after disease progression on or intolerance to imatinib. (http://www.bcbs.com/)

SALES SPECIFICATION

APPEARANCE

white to off-white powder

IDENTIFICATION

to pass

ASSAY

99.0%

HEAVY METALS

10ppm max

LOSS ON DRYING

0.5% max

RESIDUE ON IGNITION

0.2% max

TOTAL IMPURITY

1.0% max

MELTING POINT 230 C
TRANSPORTATION
PACKING
 
HAZARD CLASS  
UN NO.

 

PRICE INFORMATION