Methotrexate

Methotrexate

Methotrexate

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1 Kilogram

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Methotrexate 59-05-2 manufacturer , better price with good quality

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  • Appearance:Yellow Crystaline Powder
  • Application:Pharmaceuticals
  • PackAge:Depended
  • ProductionCapacity:300|Kilogram|Month
  • Storage:KEEP COLD
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Methotrexate Chemical Properties
mp  195°C
storage temp.  −20°C
solubility  H2O: insoluble
form  powder
Water Solubility  Insoluble. <0.1 g/100 mL at 19 ºC
Merck  5985
Stability: Stable, but light sensitive and hygroscopic. Incompatible with strong acids, strong oxidizing agents. Store at -15C or below.
CAS DataBase Reference 59-05-2(CAS DataBase Reference)
NIST Chemistry Reference Methotrexate(59-05-2)
EPA Substance Registry System L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl) methyl]methylamino]benzoyl]- (59-05-2)
 
Safety Information
Hazard Codes  T,F
Risk Statements  61-25-36/38-46-39/23/24/25-23/24/25-11
Safety Statements  53-26-36/37-45-36/37/39-36-16
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  MA1225000
F  3-8-10
HazardClass  6.1(b)
PackingGroup  III
HS Code  29335995
Hazardous Substances Data 59-05-2(Hazardous Substances Data)
MSDS Information
Provider Language
(+)-4-Amino-10-methylfolic acid English
SigmaAldrich English
 
Methotrexate Usage And Synthesis
Treatment of cancer and rheumatoid arthritis Methotrexate is a drug used for the treatment of cancer, also known as cytotoxic drugs. In order to reduce its cytotoxicity, it can be used in conjunction with calcium leucovorin. It is primarily used for the treatment of acute leukemia (acute lymphocytic leukemia), breast cancer, malignant mole and choriocarcinoma, head and neck cancer, bone cancer, leukemia, spinal cord meningeal infiltration, lung cancer, reproductive system cancer, liver cancer, refractory psoriasis vulgaris, dermatomyositis, body myositis, ankylosing spondylitis inflammation, Crohn's disease, psoriasis and psoriatic arthritis, Behcet's disease and autoimmune disease. 
Methotrexate is an immunosuppressant and can be used for easing the process of rheumatism with a particularly excellent efficacy in treating synovial inflammation of rheumatoid arthritis and is the most frequently used drugs for treating rheumatoid diseases.
The main side effects of methotrexate include: nausea, vomiting and diarrhea, liver damage, mouth ulcers, pneumonia, sepsis, and Nocardia, mild fatigue and headaches, dry skin.
History of discovery Methotrexate is the first effective anti-metabolites for treatment of tumor with good efficacy in treating choriocarcinoma and acute lymphoblastic leukemia. In 1940s, the scientists discovered that the active ingredient of Lactobacillus casei in inhibiting mice tumor-transplanted sarcoma S180 and spontaneous breast cancer is pterin tri-glutamic acid with the later one having a weak anti-folate effect. It has also observed of bone marrow suppression upon lack of folic acid. Folic acid can promote the development of leukemia. Therefore, people initially tried to identify anti-cancer drugs from folate antimetabolites. In 1947, aminopterin had been subject to clinical trials and found to be effective in treating childhood leukemia. Then it was found of that methotrexate has high therapeutic index in treating the mouse leukemia L1210. In 1950s, it had been applied to the clinical trial and had quickly substituted the aminopterin for the treatment of leukemia and had been later further expanded for treating other tumors. It has been one of the most intensively studied anticancer drugs. 
In the field of rheumatoid, though in 1951, Gubner had successfully applied aminopterin for the methotrexate treatment of rheumatoid arthritis and psoriasis. However, at the time, methotrexate was still considered as the anti-metabolic anti-cancer drugs, therefore, it is natural that people think it has a really high toxicity. Another reason is the emergence of hormones, resulting in almost all the attention being focused on hormone therapy. Only a few researchers in the field of rheumatology include Rex Hoffmeister et al had began to apply a small dose of methotrexate for treatment of autoimmune diseases.
The above information is edited by the Chemicalbook of Dai Xiongfeng.
Immunosuppressants Methotrexate is an anti-folate anti-metabolite with a strong immunosuppressive effect. It is first anti-folate agents that have been successfully applied to clinical field. It is effective for not only treating leukemia but also for treating solid tumors and is a kind of basic clinical anti-tumor drugs. Methotrexate can selectively act on the proliferation of cells, preventing cell division and proliferation of immune mother cells. It has inhibitory effect against humoral and cellular immunity and also has strong anti-inflammatory effect. It has inhibitory effect on the primary immune response and secondary immune response, delayed hypersensitivity and graft-versus-host reaction. Applying medication at the same time of antigen-stimulation or after one to two days can yield the strongest immunosuppressive medication with being invalid prior to antigen stimulation. Clinically it is mainly used in treatment of autoimmune diseases such as rheumatoid arthritis, systemic lupus erythematosus and dermatomyositis. In addition, methotrexate is also effective for treating acute leukemia, choriocarcinoma, osteosarcoma, breast cancer, and testicular cancer and so on. It is a commonly used cycle specific drugs in combination chemotherapy.
Pharmacological effects Methotrexate is an antifolate antineoplastic drug with inhibitory effect on a variety of animal tumor. Experiments have shown that this drug work through competitive inhibition on the dihydrofolate reductase. Dihydrofolate reductase is a key enzyme in DNA synthesis, and in particular being indispensable in the process of conversion of folate to tetrahydrofolate and deoxyuridine methylation into thymidine. This drug can selectively act on the DNA synthesis period (i.e. S phase), belonging to a cycle specific drugs. Recently it has been considered that the product has a second point of action, namely G1/S transition period; it can also inhibit IL-2 synthesis and neutrophil chemotaxis, therefore having immunosuppressive and anti-inflammatory effects. Upon large doses, it can further have direct toxicity on non-proliferating cells especially liver cells. It is clinically commonly used in as an antidote. 
Methotrexate (MTX for short) has a similar structure as folic. The 4’ hydroxy and 10’ hydrogen in NH respectively correspond to the NH3 group and CH3 in the MTX. MTX can bind with the dihydrofolate reductase, blocking the reduction of folate and dihydrofolate into activated form of tetrahydrofolate, thereby inhibiting the intracellular one-carbon transfer, and affecting the newly synthesized purine nucleotide and conversion of deoxyuridine to deoxythymidine nucleotides, further blocking the DNA and RNA synthesis. The plasma concentration of MTX is 10-8mol/L, and can effectively block the incorporation of deoxyuridine into DNA via deoxythymidine nucleotide with the inhibitory concentration of purine synthesis being 10-7mol / L. The combination of MTX with dihydrofolate reductase is reversible but very strong. In order to fight against the binding of MTX, dihydrofolate should have an at least 1000 fold as high as MTX. In vitro, when MTX is less than the concentration of complete inhibition of DNA synthesis, it can induce the differentiation of human choriocarcinoma cell, increasing the generation of human chorionic gonadotropin. MTX is a cell cycle-specific drug with its major effect acting on S-phase cell with specific effect on the G1 phase as well and having delayed effect on the G1 / S.
Pharmacokinetics This product has an excellent oral absorption with the plasma concentration reaching peak after 30 ~ 60min. Large-dose administration or simultaneous administration without food yield a poor absorption. After intramuscular injection, the blood concentration can be maintained for a longer period with drug disappearing slowly after intrathecal injection, the cerebrospinal fluid concentration can be maintained for about 6d. This product, after absorption, has 60% to 85% for binding with plasma protein. Simultaneously taking aspirin or sulfa drugs can lead to high blood concentration of this product with consequent increase in both efficacy and toxicity. Poor kidney function may also increase the toxicity of this product. A small amount of this product can be able to penetrate through the blood-brain barrier. This drug is mainly distributed in the liver, kidney with also a fraction existing in the main bone marrow. Drug has plasma half-life of 2h. Drug is primarily excreted in the prototype by the urine with the urine excretion amount being 90% within 48h while excretion amount of biliary and fecal being minimal.
Clinical application It is effective in treating acute leukemia with better efficacy in pediatric patients. It has a good efficacy in treating choriocarcinoma and malignant mole. Large dose administration is effective in treating osteosarcoma, soft tissue sarcoma, lung cancer, testicular cancer, breast cancer, and ovarian cancer. It is also effective in treating head and neck cancer, liver cancer and gastrointestinal cancer. Arterial infusion of this product has goo efficacy in treating head and neck cancer and liver cancer. However, it is rarely used for treating psoriasis and psoriasis.
Dosage 1, early treatment of leukemia usually applies multiple dose of treatment; adult oral 2.5 ~ 10 mg / d with total amount of 50 ~ 150 mg. Children: 1.25 ~ 5mg / d, tend to apply large-scale intermittent dosing regimen, administered therapy, oral administration or intramuscular injection 2 times per week with 0.25 ~ 0.75 mg / kg at each time; adults usually take 20 ~ 25 mg per time; sheath injection of 10 ~ 15 mg / time; children: 6 ~ 12mg / times according to the ages; for therapeutic use once a day and continue for 3 d; for prevention, apply once every 4-8 weeks. 
2, Choriocarcinoma, adult: 10 ~ 30mg; use intramuscular injection or oral administration once daily for continuous 5d. You can repeat the treatment course according to the reaction of the patient. 
3, solid cancer, preferably for continuous arterial infusion while giving intermittent intramuscular injection of leucovorin (CF); the usual dose is 25 ~ 50mg / d, CF6 ~ 9mg, apply intramuscular injection once every 4 ~ 6h. 
4, apply large-dose for treating osteosarcoma and combine with CF detoxification. The general dose of this product is generally 3 ~ 20g / m2. It can be dissolved in 500 ~ 1000 mL of 5% glucose injection for intravenous infusion of 4h. After dropping of 2 ~ 6h, you can begin to use CF with a dose of 6 ~ 12mg for intramuscular injection (or oral) once each 6h for a total of 3 d. In order to ensure that the drug can be rapidly excreted from the body, we should replenish electrolytes, water and sodium bicarbonate at I d before or every 1 ~ 2d during the infusion to make the daily urine output be over 3000ml and ensure that it is alkaline. For the blood and plasma concentration of methotrexate, liver function, and kidney function, we should apply daily inspection. 
5, treatment of psoriasis has been rarely applied due to side effects. For treating psoriasis, orally administer 1.25 mg per time with 2 to 3 times per day and 6 ~ 9d as a course of treatment.
Adverse reactions and precautions 1. Gastrointestinal reactions include oral mucosal erosion, ulcers, vomiting, and diarrhea with blood in the stool being observed in severe cases. 
2. Inhibition of bone marrow granulocyte system with pancytopenis happening in severe cases. 
3. Excessive head and neck artery injection or intrathecal injection can cause convulsions. 
4. high-dose or long-term medication can cause liver and kidney damage.
5. Additionally, there are hair loss, rashes, and pigmentation, exfoliative dermatitis may also occur; in a few conditions, reproductive dysfunction, irregular menstruation can be observed. It can cause teratogenic fetus or abortion during the early half of pregnancy. 6. Upon intrathecal injection, systemic administration should be paused in order to avoid accumulation of drug for poisoning.
7. Patients of liver and kidney dysfunction should be disabled; pregnant women should take with caution. 
8. Salicylates, sulfonamides, phenytoin, tetracycline, chloramphenicol and aminobenzoic acid can enhance the efficacy of the drug with folic acid may reduce the efficacy of the drug.
Drug Interactions 1, Alcohol and other drugs which can cause liver damage, if used in combination with this product, may further increase liver toxicity. 
2, since methotrexate can cause increased blood uric acid levels, for patients with gout or hyperuricemia, you should respectively increase the dose of allopurinol and colchicine. 
3, the product can enhance the anti-clotting effect, and can even cause lack of liver coagulation factors (and) thrombocytopenia, and therefore we should be cautious for using it in combination with other anticoagulants. 
4, with the simultaneous administration of Phenylbutazone and sulfa drugs, because of it competition with protein binding, this product may cause increased serum concentration and lead to toxicity. 
5, Oral administration of the kanamycin can increase the absorption of this drug upon oral administration, and oral neomycin may reduce its absorption. 
6, Combination with a weak organic acid and salicylate can inhibit the renal excretion of this product, further resulting in increased serum concentrations of the drug. We should reduce the dosage appropriately according to the actual case. 
7, Drugs like triamterene and pyrimethamine can have anti-folate effects with simultaneous use of this product being able to increase its side effects.
8, Combination with fluorouracil or first using fluorouracil before administering this drug can both produce antagonism. But if first use this drug and then administer fluorouracil after 4 ~ 6h can have synergistic effect. Similarly, this drug, if being used in combination with L-asparaginase can also lead to reduced efficiency, as with the latter 10 days or within 24h after administration of this product to L-asparaginase Instead applying the L-asparaginase at ten days after using the later one or at 24 h within using this product can enhance the efficacy and reduce its side effects on the digestive tract and bone marrow. It has been reported recently applying cytarabine at 24 h before using this product or 10 mins after can increase the anti-cancer activity of this product. We should be cautious when applied methotrexate in combination with radiotherapy or other kinds of drugs on bone marrow suppression.
Chemical Properties It is orange-yellow crystalline powder. It has a melting point of 185-204 ℃. It is easily soluble in dilute alkali, acid or alkali metal carbonate solution, and slightly soluble in dilute hydrochloric acid but almost insoluble in water, ethanol, chloroform, and ethyl ether.
Production method It is obtained from the cyclization between 2, 4, 5, 6-tetraaminopyrimidine and dibromo propionaldehyde and further condensation with p-N-Methylaminobenzoylglutamic acid.
Chemical Properties Yellow Crystaline Powder
Usage A Folic acid antagonist. Used as a antineoplastic and antirheumatic.
Usage Anti-cancer
Usage dietary supplement, crosses the blood-brain barrier, potential activities as anxiolytic and vasodilator
Usage A deuterated folic acid antagonist
Usage Used as a antineoplastic and antirheumatic. A folic Acid antagonist
General Description Odorless yellow to orange-brown crystalline powder.
Air & Water Reactions Methotrexate is sensitive to hydrolysis, oxidation and light. Insoluble in water.
Reactivity Profile Methotrexate decomposes in very acidic or alkaline conditions. Methotrexate is incompatible with strong oxidizing agents and strong acids.
Fire Hazard Flash point data for Methotrexate are not available; however, Methotrexate is probably combustible.
Biological Activity Cytotoxic agent. Inhibits thymidylate synthetase and de novo purine synthesis. Potent folic acid antagonist; inhibits dihydrofolate reductase. Also inhibits Ras carboxyl methylation in DKOB8 cells, leading to decreased p44 and Akt activation.
 
Methotrexate Preparation Products And Raw materials
Raw materials 2,4,5,6-TETRAAMINOPYRIMIDINE-->p-Methylaminobenzoylglutamic acid

 

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