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Entrectinib is a pharmaceutical drug that is used to treat cancer.
It is classified as a tyrosine kinase inhibitor and works by blocking the action of certain enzymes that are involved in cell division and growth.
These enzymes are called Trk kinases and are found in certain types of cancer cells.
By inhibiting the action of these enzymes, entrectinib can slow down or stop the growth and division of cancer cells, thereby slowing down the growth of the tumor.
The upstream and downstream products of entrectinib are a vital part of the chemical industry and are essential for the production and distribution of this drug.
Upstream products refer to the raw materials and chemicals that are used in the manufacturing process, while downstream products refer to the final product, in this case, entrectinib, and all its derivatives.
One of the upstream products of entrectinib is the active pharmaceutical ingredient (API), which is the actual active component of the drug.
The API for entrectinib is synthesized through a series of chemical reactions that involve the use of various starting materials and chemicals.
These starting materials are typically sourced from natural sources or synthesized in a laboratory.
The synthesis of the API involves a complex and multistep process that requires careful control and monitoring to ensure the quality and purity of the final product.
Downstream products of entrectinib include the finished dosage forms of the drug that are ready for distribution and consumption.
These dosage forms can include tablets, capsules, oral solutions, and other forms that are designed to make the drug more palatable or easier to administer.
The finished dosage forms are manufactured using the API as the starting material, and the process involves the use of various excipients, fillers, and other ingredients to create a pure and stable product.
The upstream and downstream products of entrectinib play a crucial role in ensuring the quality and safety of the final product.
The upstream products must meet strict quality standards to ensure that the API used in the manufacturing process is pure and free from any impurities that could compromise the efficacy of the drug.
Similarly, the downstream products must meet strict quality standards to ensure that the final product is safe, effective, and free from any contaminants or impurities.
The production and distribution of entrectinib also involve the use of various intermediates, such as the starting materials, reagents, and solvents that are used in the manufacturing process.
These intermediates are typically produced by chemical companies and are then supplied to the pharmaceutical companies that manufacture the final product.
The production and supply of these intermediates are also subject to strict quality standards and must meet certain specifications to ensure that they are suitable for use in the manufacturing process.
In conclusion, the upstream and downstream products of entrectinib play a vital role in the production and supply of this drug.
The upstream products, such as the API, are the raw materials that are used in the manufacturing process, while the downstream products, such as the finished dosage forms, are the final product that is ready for distribution and consumption.
The production and distribution of these products are subject to strict quality standards and must meet certain specifications to ensure the safety and efficacy of the final product.