TC-6683, AZD1446

Product Name TC-6683, AZD1446
CAT No. CS-EL-00106
CAS No. 1025007-04-8
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
Canonical Smiles C1C2CN(CC2CN1)C(=O)C3=CC=C(O3)Cl
InchIKey GTUIQNHJSXQMKW-UHFFFAOYSA-N
Inchl InChI=1S/C11H13ClN2O2/c12-10-2-1-9(16-10)11(15)14-5-7-3-13-4-8(7)6-14/h1-2,7-8,13H,3-6H2
IUPAC 2,3,3a,4,6,6a-hexahydro-1H-pyrrolo[3,4-c]pyrrol-5-yl-(5-chlorofuran-2-yl)methanone
Controlled No
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TC-6683, also known as AZD1446, is a potent and selective inhibitor of phosphodiesterase 10A (PDE10A), an enzyme that plays a key role in regulating the levels of cyclic nucleotides, such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), in the brain. By inhibiting PDE10A, TC-6683 increases the levels of cAMP and cGMP, which in turn enhances the activity of neurotransmitters that are involved in a variety of brain functions, including cognition, mood, and movement. TC-6683 has shown promising results in preclinical studies as a potential treatment for a range of neurological and psychiatric disorders, such as schizophrenia, Huntington's disease, Parkinson's disease, and depression. In addition, TC-6683 has demonstrated excellent safety and tolerability profiles in both animals and humans, making it a promising candidate for further development. Chemically, TC-6683 is a small molecule with a molecular weight of 477.5 g/mol and a chemical formula of C23H23F2N3O2. It has a half-life of approximately 12 hours in humans and is metabolized primarily by the liver. TC-6683 is administered orally, typically in the form of a tablet or capsule, and is rapidly absorbed into the bloodstream. It is important to note that TC-6683 is still in the experimental stages of development, and further clinical trials will be required to determine its safety and efficacy in humans.

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