Family · Pharmaceutical analytical standards
Temozolomide
An oral alkylating agent developed by Malcolm Stevens and his team at Aston University in Birmingham. Approved in 1999 in Europe and the United States, it is used mainly against glioblastoma and other brain tumours. This family brings together the active ingredient, pharmacopoeial impurities, metabolites, labelled standards and other impurities.
Did you know?It does not need the liver to become active: at the body's pH it opens up spontaneously into its active form, and it crosses the blood-brain barrier easily, reaching the brain.
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EDQM standards 1
The official European Pharmacopoeia standards for this family.
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Custom synthesis of impurities, metabolites and labelled compounds, with the same characterisation level.
