Methotrexate (CAS 59-05-2) stands as a pivotal compound in modern medicine, primarily recognized for its dual role as a potent chemotherapy agent and a crucial immunosuppressant for autoimmune conditions. Its efficacy in treating a wide spectrum of cancers, including leukemias, lymphomas, and solid tumors, stems from its mechanism of action as an antifolate. By competitively inhibiting dihydrofolate reductase (DHFR), Methotrexate disrupts the synthesis of purines and pyrimidines, essential for DNA and RNA production, thus halting the proliferation of rapidly dividing cells. This targeted approach is central to its methotrexate mechanism of action.
Beyond oncology, lower doses of Methotrexate have proven highly effective in managing chronic autoimmune diseases such as rheumatoid arthritis and psoriasis. In these conditions, it modulates the immune response, reducing inflammation and slowing disease progression. The precise methotrexate dosage is critical for efficacy and safety, with weekly administration being standard for non-oncologic indications to minimize toxicity. Patients and providers must be vigilant about potential adverse effects, including hepatotoxicity, pneumonitis, and bone marrow suppression, which necessitate regular monitoring. Understanding these methotrexate side effects and contraindications is paramount for safe patient care.
Drug interactions are another significant consideration when prescribing Methotrexate. Certain medications, such as NSAIDs and some antibiotics, can potentiate its toxicity. Therefore, a comprehensive review of a patient's medication regimen is essential. The methotrexate pregnancy warning is particularly severe, as the drug is teratogenic and can cause severe birth defects. Both male and female patients attempting to conceive must take strict precautions. For healthcare providers, staying updated on the latest guidelines regarding methotrexate drug interactions and safe administration protocols is vital for optimal patient outcomes. The availability of Methotrexate for purchase, coupled with ongoing research into its therapeutic potential, ensures its continued importance in medicine.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.