Substance

ID:531

Names and Identifiers
Brand Name
ChlodithaneLysodrenChloditanKhlodithanChlodithanMitotanMitotanum [INN-Latin]
Synonyms
Mitotane
IUPAC Traditional name
mitotane
IUPAC name
1-chloro-4-[2,2-dichloro-1-(2-chlorophenyl)ethyl]benzene
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
6
Solubility
0.1 mg/L
Molecule Details
Drug Groups
approved
Description
A derivative of the insecticide dichlorodiphenyldichloroethane that specifically inhibits cells of the adrenal cortex and their production of hormones. It is used to treat adrenocortical tumors and causes CNS damage, but no bone marrow depression. [PubChem]
Indication
For treatment of inoperable adrenocortical tumours; Cushing's syndrome
Pharmacology
Mitotane is an oral chemotherapeutic agent indicated in the treatment of inoperable adrenal cortical carcinoma of both functional and nonfunctional types. Mitotane can best be described as an adrenal cytotoxic agent, although it can cause adrenal inhibition, apparently without cellular destruction. The administration of Mitotane alters the extra-adrenal metabolism of cortisol in man; leading to a reduction in measurable 17-hydroxy corticosteroids, even though plasma levels of corticosteroids do not fall. The drug apparently causes increased formation of 6-B-hydroxyl cortisol.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic and renal
Absorption
About 40% oral Lysodren is absorbed
Half Life
18-159 days
Protein Binding
6%
Elimination
A variable amount of metabolite (1%-17%) is excreted in the bile and the balance is apparently stored in the tissues.
External Links
Molecular Spectra
No Data Available
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References
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