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Chloroacetaldehyde

from ifosfamide

Chloroacetaldehyde ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Chloroacetaldehyde ballicule

What it isA reactive metabolite of ifosfamide.

Why it mattersIt is the leading explanation for ifosfamide’s neurotoxicity (encephalopathy) and contributes to nephrotoxicity — toxicities cyclophosphamide largely lacks.

What it changesMethylene blue and supportive care address the encephalopathy; the metabolite is why ifosfamide, not cyclophosphamide, causes it.

Chloroacetaldehyde molecular structure (skeletal formula)
Molecular structure: Chloroacetaldehyde

NO BOXED WARNINGS

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

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