FLUDARABINE PHOSPHATE
PURINE ANALOGUES · PROGRESSIVE CHRONIC LYMPHOCYTIC LEUKEMIA
FRESENIUS KABI
Drug class
Purine Analogues
Purine analogues are a class of antimetabolite medications chemically structured to mimic endogenous purine nucleosides and bases, such as adenine and guanine. Read more about Purine Analogues
75 drugs in this class 47 manufacturers
Drugs in Purine Analogues
CLADRIBINE
PURINE ANALOGUES · RELAPSING FORM OF MULTIPLE SCLEROSIS
APOTEX CORP
AZASAN (azathioprine)
PURINE ANALOGUES · RHEUMATOID ARTHRITIS ·+1
SALIX/BAUSCH HE
MERCAPTOPURINE
PURINE ANALOGUES · ACUTE LYMPHOID LEUKEMIA
NOVA LABORATORI
AZATHIOPRINE
PURINE ANALOGUES · RHEUMATOID ARTHRITIS ·+1
REMEDYREPACK, I
MERCAPTOPURINE
PURINE ANALOGUES · ACUTE LYMPHOID LEUKEMIA
GSMS, INC.
MERCAPTOPURINE
PURINE ANALOGUES · ACUTE LYMPHOID LEUKEMIA
FLORIDA PHARMAC
CLADRIBINE
PURINE ANALOGUES · RELAPSING FORM OF MULTIPLE SCLEROSIS
SANDOZ
IMURAN (azathioprine)
PURINE ANALOGUES · RHEUMATOID ARTHRITIS ·+1
LEGACY PHARMA I
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Purine analogues are a class of antimetabolite medications chemically structured to mimic endogenous purine nucleosides and bases, such as adenine and guanine.
Once incorporated into target cells and metabolically activated, they disrupt cellular proliferation by competing with natural substrates, inhibiting key enzymes in purine biosynthesis and DNA replication, and causing DNA strand termination or damage.
Therapeutically, these agents are primarily indicated for the treatment of hematologic malignancies, including acute leukemias, chronic lymphocytic leukemia, and hairy cell leukemia, as well as selected autoimmune conditions like multiple sclerosis and inflammatory bowel disease.
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fda.gov
Purine analogues are a class of antimetabolite medications chemically structured to mimic endogenous purine nucleosides and bases, such as adenine and guanine Once incorporated into target cells and metabolically activated, they disrupt cellular proliferation by competing with natural substrates, inhibiting key enzymes in purine biosynthesis and DNA replication, and causing DNA strand termination or damage
-
fda.gov
Purine analogues are a class of antimetabolite medications chemically structured to mimic endogenous purine nucleosides and bases, such as adenine and guanine Once incorporated into target cells and metabolically activated, they disrupt cellular proliferation by competing with natural substrates, inhibiting key enzymes in purine biosynthesis and DNA replication, and causing DNA strand termination or damage Therapeutically, these agents are primarily indicated for the treatment of hematologic mal...
-
fda.gov
Once incorporated into target cells and metabolically activated, they disrupt cellular proliferation by competing with natural substrates, inhibiting key enzymes in purine biosynthesis and DNA replication, and causing DNA strand termination or damage Therapeutically, these agents are primarily indicated for the treatment of hematologic malignancies, including acute leukemias, chronic lymphocytic leukemia, and hairy cell leukemia, as well as selected autoimmune conditions like multiple sclerosis ...
-
fda.gov
Therapeutically, these agents are primarily indicated for the treatment of hematologic malignancies, including acute leukemias, chronic lymphocytic leukemia, and hairy cell leukemia, as well as selected autoimmune conditions like multiple sclerosis and inflammatory bowel disease
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