N-(3-methyl5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4((4-methylpiperazin-1-yl)methyl)benz

Product Name N-(3-methyl5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4((4-methylpiperazin-1-yl)methyl)benz
Alternate Names Imatinib Impurities, Impurities of Imatinib
CAT No. CS-O-13326
CAS No. Not Available
Category Impurities
Stock IN-Stock
Mol. Wt. 493.6 g/mol
Mol. For. C₂₉H₃₁N₇O
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Imatinib
Purity Not less than 90 %
Therapeutic Anti-Cancer / Oncology
Smileys O=C(C1=CC=C(CN2CCN(C)CC2)C=C1)NC3=CC(C)=CC(NC4=NC=CC(C5=CN=CC=C5)=N4)=C3
Controlled No
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N-(3-methyl5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4((4-methylpiperazin-1-yl)methyl)benz is a chemical compound that belongs to the class of benzamide derivatives. It is commonly used in the pharmaceutical industry for its therapeutic properties as a kinase inhibitor. Specifically, it is a potent inhibitor of the tyrosine kinase receptor, which plays a crucial role in the growth and proliferation of cancer cells. As such, it has been studied extensively for its potential use in the treatment of various types of cancer. Chemically, N-(3-methyl5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4((4-methylpiperazin-1-yl)methyl)benz consists of a benzene ring attached to a pyrimidine and a pyridine ring. It also contains a piperazine ring and a phenyl group, each of which is substituted with various other chemical groups. The compound is highly soluble in water and ethanol, and has a melting point of around 220-225°C. While the exact mechanism of action of N-(3-methyl5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4((4-methylpiperazin-1-yl)methyl)benz is not fully understood, it is believed to work by inhibiting the activity of specific enzymes involved in cancer cell growth and proliferation. It has shown promising results in preclinical studies and is currently undergoing clinical trials for the treatment of various types of cancer.

Related Compounds

Imatinib Impurity 3 | Imatinib EP Impurity D Tetrahydrochloride | N-Nitroso Imatinib impurity F | Imatinib Imidazole Impurity | Imatinib EP Impurity C Trihydrochloride | Imatinib N-Formyl Impurity | N-Nitroso Imatinib Nitro Intermediate | Imatinib Dimer | N-Boc-N-Desmethyl Imatinib | Imatinib impurity B | Des-4-methylpiperazin chloro Imatinib impurity | Imatinib EP Impurity D (chloride) | Imatinib Impurity 16 | Imatinib Guanidino Dihydrochloride Impurity | Imatinib EP Impurity D | Imatinib Dimethylamino Impurity | Imatinib Impurity 5 | Imatinib Hydrochloride Impurity G | N-(2-Methyl-5-nitrophenyl)-4-(pyridine-3-yl)pyridine-2-amine | Imatinib EP Impurity C | Imatinib (Pyridine)-N-oxide | Imatinib N-Desmethyl Impurity | N-Nitroso Imatinib | N-Desmethyl Imatinib Mesylate | Imatinib Impurity B | N-Desmethyl -N-Nitroso Imatinib | Imatinib (Piperazine)-N4-Oxide | Fluorescent derivative of imatinib | N-Nitroso Imatinib guanidine Intermediate | Imatinib DiPiperazine Impurity | N-Desmethyl -n-nitroso imatinib 1 | Imatinib (N-nitroso benzamide) | Imatinib N-Acetyl Impurity |

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