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Tanespimycin is a chemotherapy drug that is used to treat cancer.
It is an antibiotic that belongs to a class of drugs called macrolide immunosuppressants.
Tanespimycin is produced through a complex chemical synthesis process that involves several steps and various intermediates.
Upstream products are the raw materials and intermediates that are used in the production of Tanespimycin.
The upstream products for Tanespimycin production include various reagents, solvents, and starting materials.
These materials are used to synthesize the precursor molecules that are required for the production of Tanespimycin.
The upstream products also include the equipment and machinery required for the synthesis process, such as reactors, filters, and purification columns.
One of the key upstream products for Tanespimycin production is a compound called thymidine.
Thymidine is a nucleoside that is used in the production of Tanespimycin.
It is synthesized through a series of chemical reactions that involve the oxidation of deoxyuridine to thymidine.
Thymidine is then converted into another compound called 2-deoxy-2-(3-dehydroquinoxalyl) adenine (DQA), which is a key intermediate in the synthesis of Tanespimycin.
Another important upstream product for Tanespimycin production is the chemical compound called D2.
D2 is a byproduct of the DQA synthesis process and is used to synthesize the final product, Tanespimycin.
The synthesis of D2 involves a series of chemical reactions that involve the condensation of several compounds, including DQA, thymine, and hydroxyurea.
The downstream products of Tanespimycin production are the final product itself, as well as any byproducts that are generated during the synthesis process.
The downstream products also include any derivatives or modified forms of the final product that may be used for pharmaceutical purposes.
Tanespimycin is the final product of the synthesis process.
It is a white to off-white powder that is used to treat various types of cancer, including non-Hodgkin's lymphoma and multiple myeloma.
Tanespimycin is administered intravenously and is usually given in combination with other chemotherapy drugs.
In addition to the final product, several byproducts are generated during the Tanespimycin synthesis process.
One of these byproducts is thymidine, which is a byproduct of the synthesis of DQA.
Thymidine can be separation