4 Results for "

S-COMT

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "S-COMT" in MCE Product Catalog:

Cat. No.: HY-128410
CAS No.: 842-01-3
Purity:  99.35%
Target:  

COMT

Research Areas:  

Neurological Disease

4-Phenyl-7,8-dihydroxycoumarin is a coumarin-based non-nitro catechol-type COMT inhibitor with an IC50 of 1.8 μM against rat S-COMT. 4-Phenyl-7,8-dihydroxycoumarin can be used in studies on the binding mechanism of COMT inhibitors and Parkinson's disease .
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Cat. No.: HY-E70007
CAS No.: 9012-25-3
Synonyms: COMT
Catechol O-methyltransferase, porcine liver (COMT), the magnesium-dependent transfer of methyl groups from S-adenosyl methionine to a hydroxyl group on dopamine, converting it to 3-methoxytyramine. Catechol O-methyltransferase has two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). Catechol O-methyltransferase is to regulate epinephrine, norepinephrine, and dopamine levels in the brain .
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Cat. No.: HY-168154
Target:  

COMT

Research Areas:  

Cancer

COMT-IN-2 (compund 9) is the potent COMT inhibitor, showing selective inhibition of brain (IC50=24 nM) and liver (IC50=81 nM) MB-COMT compared to the liver S-COMT (IC50=620 nM) isoform .
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Cat. No.: HY-W761397
CAS No.: 117568-28-2
Target:  

COMT

Research Areas:  

Neurological Disease

COMT-IN-3 is a competitive inhibitor of soluble catechol-O-methyltransferase (S-COMT). COMT-IN-3 coordinates with the Mg 2+ ion at the COMT active site via its catechol hydroxyl group, and its nitro group, as a strong electron-withdrawing substituent, further enhances the binding affinity. COMT-IN-3 interacts with the hydrophobic residues Trp38, Met40, and Trp143 at the back of the active site via its neutral nitrile tail, thereby competitively inhibiting COMT activity. COMT-IN-3 can be used in research related to Parkinson's disease .
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