Tioguanine
Clinical data | |
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Routes of administration | oral |
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Pharmacokinetic data | |
Bioavailability | 30% (range 14% to 46%) |
Metabolism | Intracellular |
Elimination half-life | 80 minutes (range 25-240 minutes) |
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DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C5H5N5S |
Molar mass | 167.193 g/mol |
WikiDoc Resources for Tioguanine |
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Most recent articles on Tioguanine |
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Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Tioguanine at Clinical Trials.gov Clinical Trials on Tioguanine at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Tioguanine
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Definitions |
Patient Resources / Community |
Patient resources on Tioguanine Discussion groups on Tioguanine Patient Handouts on Tioguanine Directions to Hospitals Treating Tioguanine Risk calculators and risk factors for Tioguanine
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Causes & Risk Factors for Tioguanine |
Continuing Medical Education (CME) |
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Experimental / Informatics |
Overview
Tioguanine (INN), formerly Thioguanine (BAN), is a drug that is used in the treatment of cancer. It belongs to the family of drugs called antimetabolites. It is a guanine analog. Its principal use is in acute leukaemias and chronic myeloid leukaemia.
Pharmacology
As a guanine analogue, it is transformed inside the cell into to 6-thioguanilyic acid (TGMP) which, by pseudofeedback interference with purine biosynthesis, interferes with the synthesis of guanine nucleotides. Some of its activity may also be due to the incorporation of thioguanine nucleotides into both RNA and DNA, but the end result is inducing cell cycle arrest and apoptosis. It is metabolized by via methylation by thiopurine methyltransferase.
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