Atovaquone D5

Product Name Atovaquone D5
Alternate Names Atovaquone Stable Isotopes, Stable Isotopes of Atovaquone
CAT No. CS-O-00760
CAS No. 1329792-63-3
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Atovaquone
Smileys O=C(C1=CC=CC=C1C2=O)C([C@@]3([2H])C([2H])([2H])C[C@H](C4=CC=C(Cl)C=C4)CC3([2H])[2H])=C2O
Controlled No
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Atovaquone D5 is a deuterated analog of Atovaquone, a medication used for the treatment and prevention of malaria. Atovaquone D5 is a chemical compound that contains five deuterium atoms instead of hydrogen atoms, which makes it useful for pharmacokinetic studies and metabolic analysis. Atovaquone D5 works by inhibiting the mitochondrial electron transport chain in the parasite responsible for malaria. It is a broad-spectrum antiparasitic drug that is effective against Plasmodium falciparum, the most lethal species of the malaria parasite. Atovaquone D5 is typically administered orally in tablet form and has a half-life of approximately 2-3 days. It is metabolized by the liver and excreted via the kidneys. The drug is not recommended for use in pregnant women or individuals with severe liver or kidney disease. Chemically, Atovaquone D5 is a yellow crystalline powder with a molecular weight of 290.35 g/mol. Its molecular formula is C22H14D5NO3. The compound is soluble in organic solvents such as ethanol, methanol, and acetonitrile, but insoluble in water. In conclusion, Atovaquone D5 is an important tool for understanding the pharmacokinetics and metabolism of Atovaquone, a widely used antimalarial drug. Its chemical properties make it useful for scientific research and drug development.

Related Compounds

cis-Atovaquone-d5 (contains 10% trans isomer) | Atovaquone 13C6 | Atovaquone D4 (naphthalene-D4) | cis-Atovaquone-d4 (Atovaquone EP Impurity B-d4) |

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