- Molecular NameTemozolomide
- SynonymMethazolastone; Temozolamide; Temozolodida [Spanish]; temozolomide; Temozolomidum [Latin]
- Weight194.154
- Drugbank_IDDB00853
- ACS_NO85622-93-1
- Show 2D model
- LogP (experiment)N/A
- LogP (predicted, AB/LogP v2.0)-0.89
- pkaN/A
- LogD (pH=7, predicted)-0.89
- Solubility (experiment)N/A
- LogS (predicted, ACD/Labs)(ph=7)-0.84
- LogSw (predicted, AB/LogsW2.0)15.18
- Sw (mg/ml) (predicted, ACD/Labs)6.74
- No.of HBond Donors3
- No.of HBond Acceptors8
- No.of Rotatable Bonds1
- TPSA116.8
- StatusFDA approved
- AdministrationN/A
- PharmacologyAn oral alkylating agent which can be used for the treatment of Grade IV astrocytoma -- an aggressive brain tumor, also known as glioblastoma multiforme.
- Absorption_value100.0
- Absorption (description)Rapid and complete absorption in the gastrointestinal tract
- Caco_2N/A
- Bioavailability96.0
- Protein binding15.0
- Volume of distribution (VD)0.4 L/kg; 17 L/m2
- Blood/Plasma Partitioning ratio (D_blood)N/A
- MetabollsmSpontaneously hydrolyzed at physiologic pH to the active species, 3-methyl-(triazen-1-yl)imidazole-4-carboxamide (MTIC) and to temozolomide acid metabolite.
- Half life1.8 h (temozolomide); 2.5 min (MTIC).
- ExcretionN/A
- Urinary ExcretionN/A
- CleranceN/A
- ToxicityDuring the concomitant phase (Temozolomide + radiotherapy) of the treatment of newly diagnosed glioblastoma multiforme, adverse events including thrombocytopenia, nausea, vomiting, anorexia and constipation, were more frequent in the Temozolomide + radiotherapy arm than in the radiotherapy arm.
- LD50 (rat)N/A
- LD50 (mouse)N/A