Flurocitabine hydrochloride is an antitumor agent that exerts its effects by undergoing hydrolysis in vivo to yield two active metabolites: arabinosyl-fluorocytosine (ara-FC) and arabinosyl-fluorouracil (ara-FU). These metabolites are involved in disrupting nucleic acid synthesis, making Flurocitabine hydrochloride a valuable tool in cancer research. Its ability to target tumor growth positions it as a significant compound for studies focused on chemotherapy and the development of novel anticancer therapies.
Flurocitabine hydrochloride is an antitumor agent that exerts its effects by undergoing hydrolysis in vivo to yield two active metabolites: arabinosyl-fluorocytosine (ara-FC) and arabinosyl-fluorouracil (ara-FU). These metabolites are involved in disrupting nucleic acid synthesis, making Flurocitabine hydrochloride a valuable tool in cancer research. Its ability to target tumor growth positions it as a significant compound for studies focused on chemotherapy and the development of novel anticancer therapies.
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