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Aminopterin,CAS:54-62-6: A Promising Antifolate Agent

Introduction:Aminopterin is a pharmacological compound that belongs to the class of antifolate agents. It has gained significant attention in the field of medicine due to its potential therapeutic applications. This article aims to provide a comprehensive overview of aminopterin, including its chemical structure, mechanism of action, medical uses, and associated risks.Chemical Structure:Aminopterin, also known as 4-aminofolic acid, is a synthetic analogue of folic acid. It possesses a similar chemical structure to dihydrofolate, which is an essential component in the synthesis of nucleic acids [...]

Jun 12, 2025 Product News 552 Views Read More

Methyl 2,5,6-Trichloropyrimidine-4-carboxylate,Cas:89284-85-5: A Versatile Chemical Compound

Methyl 2,5,6-Trichloropyrimidine-4-carboxylate 89284-85-5: A Versatile Chemical Compound | Available at Finetech Industry LimitedIntroduction:Methyl 2,5,6-trichloropyrimidine-4-carboxylate is a chemical compound known for its versatility and wide-ranging applications. At FINETECH Industry Limited, we offer this compound to meet the diverse needs of industries. This article provides an overview of methyl 2,5,6-trichloropyrimidine-4-carboxylate, including its structure, synthesis methods, and potential applications, highlighting how you can contact us for your requirements.Chemical Structure:Met [...]

Jun 12, 2025 ---- News 535 Views Read More

Idarubicin: Mechanism of Action, Side Effects, and Clinical Applications in Cancer Treatment

Idarubicin 57852-57-0is a potent chemotherapy drug belonging to the anthracycline class, primarily used in the treatment of various types of cancer, including acute myeloid leukemia (AML) and acute lymphocytic leukemia (ALL). Its mechanism of action, side effects, and clinical applications make it a crucial component of cancer treatment regimens.Mechanism of Action:Idarubicin exerts its anticancer effects by interfering with the DNA and RNA synthesis of cancer cells. It does so by intercalating between DNA base pairs, inhibiting the activity of topoisomerase II enzyme, and generating free radi [...]

Jun 12, 2025 Product News 668 Views Read More