Mitotan
Synonym(s):Mitotane;o,p′-DDD;(2,4′-Dichlorodiphenyl)dichloroethane;o,p′-DDD;1-(2-Chlorophenyl)-1-(4-chlorophenyl)-2,2-dichloroethane
- CAS NO.:53-19-0
- Empirical Formula: C14H10Cl4
- Molecular Weight: 320.04
- MDL number: MFCD00000850
- EINECS: 200-166-6
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-10-31 18:15:48
What is Mitotan?
Absorption
About 40% oral Lysodren is absorbed
Description
Mitotane is an inhibitor of steroidogenesis that suppresses the growth of adrenocortical cells. It blocks the expression of several genes that encode proteins involved in steroidogenesis and disrupts mitochondrial respiratory chain activity in human adrenocortical cells. Mitotane has anti-neoplastic actions, alone or in combination with other compounds, and suppresses cortisol synthesis, although it also has significant toxicity in the gastrointestinal tract and nervous system. It is effective against adrenocortical carcinoma and Cushing’s Syndrome in clinical trials.
Chemical properties
Crystalline Solid
The Uses of Mitotan
Mitotane is an inhibitor of steroidogenesis that suppresses the growth of adrenocortical cells. It blocks the expression of several genes that encode proteins involved in steroidogenesis and disrupts mitochondrial respiratory chain activity in human adrenocortical cells. Mitotane has anti-neoplastic actions, alone or in combination with other compounds, and suppresses cortisol synthesis, although it also has significant toxicity in the gastrointestinal tract and nervous system. It is effective against adrenocortical carcinoma and Cushing’s Syndrome in clinical trials.
The Uses of Mitotan
An Antineoplastic. Used as an adrenolytic agent
The Uses of Mitotan
insecticide, antineoplastic
The Uses of Mitotan
aminobiphoshphanate for treatment of osteoporosis and Paget's bone disease
Background
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.
Indications
For treatment of inoperable adrenocortical tumours; Cushing's syndrome
What are the applications of Application
Mitotane is an adrenal cytotoxic agent
Indications
Mitotane (Lysodren) produces selective atrophy of the zona fasciculata and zona reticularis, which results in a decrease in the secretion of 17-hydroxycorticosteroids. Direct inhibition of cholesterol side-chain cleavage and 11/18-hydroxylase activities has also been demonstrated.
Indications
The observation that mitotane (Lysodren) could produce
adrenocortical necrosis in animals led to its use in
the palliation of inoperable adrenocortical adenocarcinomas.
A reduction in both tumor size and adrenocortical
hormone secretion can be achieved in about half of
the patients taking the drug. Because normal adrenocortical
cells also are affected, endogenous glucocorticoid
production should be monitored and replacement
therapy administered when appropriate.
Mitotane is incompletely absorbed from the gastrointestinal
tract after oral administration. However,
once absorbed, it tends to accumulate in adipose tissue.
Mitotane is slowly excreted and will appear in the urine
for several years.The major toxicities associated with its
use are anorexia, nausea, diarrhea, lethargy, somnolence,
dizziness, and dermatitis.
Definition
ChEBI: Mitotane is a diarylmethane.
Manufacturing Process
From dichloroacetaldehyde and 2-chlorphenylmagnesiumbromide was prepared 1-(2-chlorphenyl-2,2-dichloroethanol. By action of H2SO4 on 1-(2- chlorphenyl)-2,2-dichloroethanol in chlorobenzene was prepared 1,1-dichloro- 2,2-bis(2,4'-dichlorophenyl)ethane.
brand name
Lysodren (Bristol-Myers Squibb).
Therapeutic Function
Antineoplastic
General Description
Colorless powder.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Mitotan dehydrohalogenates with strong alkalis. Simple aromatic halogenated organic compounds are very unreactive; halogenated aliphatic compounds are moderately or very reactive. For both subgroups, reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
Fire Hazard
Flash point data for Mitotan are not available. Mitotan is probably combustible.
Pharmacokinetics
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.
Pharmacology
Mitotane, a derivative of the insecticide DDT, quickly lowers the level of corticosteroids, and is metabolized in the blood and urine and used on non-operable metastatic prostate carcinomas. Synonyms of this drug are lysodren and others.
Clinical Use
Mitotane is the drug of choice for the treatment of
primary adrenal carcinoma when surgery or radiation
therapy is not feasible. Its effectiveness
in curtailing adrenal activity is due to an action on
adrenocortical mitochondria to impair cytochrome
P450 steps in steroid biosynthesis. Mitotane requires
metabolic transformation to exert its therapeutic action,
and the differential ability of tumors to metabolize
the drug may determine its clinical effectiveness. It is
advised to measure serum mitotane levels and urinary
free cortisol excretion to ensure adequate therapeutic
concentrations. Mitotane increases circulating cholesterol
by inhibiting cytochrome P450–mediated reactions
and therefore contributes to the cardiovascular
events that are a significant cause of mortality in untreated
Cushing’s syndrome.
Mitotane, being closely related to the organochlorine
insecticides, shares its inductive effects on the liver
microsomal drug-metabolizing enzyme system, and its
use may therefore alter the requirement for concomitantly
administered drugs that are also metabolized by
this pathway.
Side Effects
Mitotane is capable of inducing remission of Cushing’s disease, but only after several weeks of therapy and at the price of severe gastrointestinal distress. Moreover, more than half of patients relapse following cessation of therapy. Other side effects include lethargy, mental confusion, skin rashes, and altered hepatic function. Being a lipid-soluble substance, mitotane remains stored in body tissues for extended periods. This may account for the marked patient-to-patient variability in its therapeutic and/or toxic effects.
Synthesis
Mitotane, 1,1-dichloro-2-(o-chlorophenyl)ethane (30.5.8), is made by alkylating chlorobenzene with 1-(2-chlorophenyl)-2,2-dichloroethane (30.5.7) in the presence of sulfuric acid. The necessary 1-(2-chlorophenyl)-2,2-dichloroethanol (30.5.7) is in turn made from reacting 2-chlorophenylmagnesiumbromide with dichloroacetic aldehyde.
Veterinary Drugs and Treatments
In veterinary medicine, mitotane is used primarily for the medical treatment of pituitary-dependent hyperadrenocorticism (PDH), principally in the dog. It has also been used for the palliative treatment of adrenal carcinoma in humans and dogs.
Drug interactions
Potentially hazardous interactions with other drugs
Anticoagulants: possibly reduced anticoagulant effect
of coumarins.
Antipsychotics: avoid with clozapine (increased risk
of agranulocytosis).
Diuretics: avoid with spironolactone.
Metabolism
Hepatic and renal
Metabolism
Metabolised in the liver and other tissues and excreted as metabolites in urine and bile. From 10-25% of a dose has been recovered in the urine as a water-soluble metabolite and 1-17% in the faeces as metabolites
Purification Methods
Purify Mitotane by recrystallisation from pentane, MeOH or EtOH. It is soluble in isooctane and CCl4. [Haller et al. J Am Chem Soc 67 1600 1945, Beilstein 5 IV 1883.]
Properties of Mitotan
Melting point: | 77-78 °C(lit.) |
Boiling point: | 405.59°C (rough estimate) |
Density | 1.3118 (rough estimate) |
refractive index | 1.6000 (estimate) |
storage temp. | Inert atmosphere,Room Temperature |
solubility | DMSO: soluble20mg/mL, clear |
form | powder |
color | white to beige |
Water Solubility | <0.1 g/100 mL at 24 ºC |
Merck | 13,6237 / 13,6237 |
BRN | 2056007 |
CAS DataBase Reference | 53-19-0(CAS DataBase Reference) |
NIST Chemistry Reference | Mitotane(53-19-0) |
EPA Substance Registry System | o,p'-DDD (53-19-0) |
Safety information for Mitotan
Signal word | Warning |
Pictogram(s) |
Health Hazard GHS08 |
GHS Hazard Statements |
H351:Carcinogenicity |
Precautionary Statement Codes |
P280:Wear protective gloves/protective clothing/eye protection/face protection. |
Computed Descriptors for Mitotan
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