89 Results for "

Catechol

" in MedChemExpress (MCE) Product Catalog:
Products (89)

89 Results for "Catechol" in MCE Product Catalog:

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46
46 Publications Verification
Art. -Nr.: HY-B1473A
CAS. Nr.: 50-67-9
Synonyms: 5-Hydroxytryptamine; 5-HT
Serotonin is a monoamine neurotransmitter in the CNS and an endogenous 5-HT receptor agonist. Serotonin is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM.
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46
46 Publications Verification
Art. -Nr.: HY-B1473
CAS. Nr.: 153-98-0
Synonyms: 5-Hydroxytryptamine hydrochloride; 5-HT hydrochloride
Serotonin (5-Hydroxytryptamine) hydrochloride is a monoamine neurotransmitter in the CNS and an endogenous 5-HT receptor agonist, with blood-brain barrier permeability. Serotonin hydrochloride is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM.
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8
8 Cited Publications
Art. -Nr.: HY-14280
CAS. Nr.: 130929-57-6
Reinheit:  99.97%
Target:  

COMT

Forschungsgebiete:  

Neurological Disease Cancer

Entacapone is a potent, reversible, peripherally acting and orally active catechol-O-methyltransferase (COMT) inhibitor. Entacapone inhibits COMT from rat brain, erythrocytes and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC50s>50 μM). Entacapone can be used for the research of Parkinson's disease . Entacapone serves as a inhibitor of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders .
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3
3 Cited Publications
Art. -Nr.: HY-14896
CAS. Nr.: 923287-50-7
Reinheit:  99.06%
Synonyms: BIA 9-1067
Target:  

COMT

Forschungsgebiete:  

Neurological Disease

Opicapone (BIA 9-1067) is a potent third-generation catechol-O-methyltransferase (COMT) inhibitor for the research of Parkinson's disease and motor fluctuations. Opicapone decreases the ATP content of the cells with an IC50 of 98 μM .
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1
1 Cited Publications
Art. -Nr.: HY-B1473AS
CAS. Nr.: 58264-95-2
Synonyms: 5-Hydroxytryptamine-d4; 5-HT-d4
Serotonin-d4 is deuterium labeled Serotonin. Serotonin is a monoamine neurotransmitter in the CNS and an endogenous 5-HT receptor agonist. Serotonin is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM.
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1
1 Cited Publications
Art. -Nr.: HY-W012814
CAS. Nr.: 452-86-8
4-Methylcatechol is an intermediate in the degradation of some alkylbenzenes and an orally active suicide inhibitor of catechol 2,3-dioxygenase (C23O). 4-Methylcatechol induces apoptosis in melanoma cells through oxidative stress, but some studies have also shown that 4-Methylcatechol is carcinogenic. In addition, 4-Methylcatechol has antiplatelet and blood pressure-lowering activities. 4-Methylcatechol can also inhibit protein oxidation in beef but does not disulfide formation .
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1
1 Cited Publications
Art. -Nr.: HY-W014728
CAS. Nr.: 62-32-8
N-Methyldopamine hydrochloride is a precursor of adrenaline in the adrenal medulla. N-Methyldopamine hydrochloride is a modification of the dopamine (DA), and retains agonist activity at the DA1 receptor. N-Methyldopamine hydrochloride remains capable of universal surface coating and secondary reactions using the surface catechols. N-Methyldopamine hydrochloride can be used for heart failure research .
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1
1 Cited Publications
Art. -Nr.: HY-B1473S
CAS. Nr.: 2469263-61-2
Synonyms: 5-Hydroxytryptamine-d4 hydrochloride; 5-HT-d4 hydrochloride
Serotonin-d4 (5-Hydroxytryptamine-d4) hydrochloride is the deuterium labeled Serotonin (hydrochloride) (HY-B1473) . Serotonin (5-Hydroxytryptamine) hydrochloride is a monoamine neurotransmitter in the CNS and an endogenous 5-HT receptor agonist. Serotonin hydrochloride is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM .
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Art. -Nr.: HY-100562
CAS. Nr.: 2295-58-1
Reinheit:  98.57%
Target:  

5-HT Receptor COMT

Forschungsgebiete:  

Neurological Disease

Flopropione is a 5-HT receptor antagonist and also a catechol-o-methyltransferase (COMT) inhibitor . Flopropione also as an antispasmodic agent .
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Art. -Nr.: HY-157719
CAS. Nr.: 29907-86-6
Target:  

COMT

Forschungsgebiete:  

Others

S-Adenosylhomocysteine sulfoxide is an inhibitor of catechol-O-methyltransferase (COMT) with an IC50 value of 860 μM. S-Adenosylhomocysteine sulfoxide can be used in the research of methylation reaction modulators .
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Art. -Nr.: HY-106842
CAS. Nr.: 116313-94-1
Reinheit:  99.53%
Synonyms: OR-462
Target:  

COMT

Nitecapone (OR-462) is an orally active and short-acting catechol-O-methyltransferase (COMT) inhibitor with gastroprotective and antioxidant properties. Nitecapone (OR-462) scavenges reactive oxygen and nitric radicals and prevents lipid peroxidation .
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Art. -Nr.: HY-133597
CAS. Nr.: 2138-22-9
Reinheit:  99.26%
Target:  

Drug Derivative

Forschungsgebiete:  

Others

4-Chlorocatechol is a major degradation product of 4-chloro-2-aminophenol (4C2AP). 4-Chlorocatechol is also a substrate for catechol 1,2-dioxygenases and chlorocatechol dioxygenase .
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Art. -Nr.: HY-106405
CAS. Nr.: 274925-86-9
Reinheit:  99.89%
Synonyms: BIA 3-202
Target:  

COMT

Forschungsgebiete:  

Metabolic Disease

Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of COMT, and it is potential for the treatment of Parkinson's disease .
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Art. -Nr.: HY-125339
CAS. Nr.: 125628-97-9
Reinheit:  98.0%
Target:  

COMT Apoptosis

Forschungsgebiete:  

Neurological Disease Cancer

Ro 41-0960 is a CNS-penetrant, orally active catechol-O-methyl transferase (COMT) inhibitor. Ro 41-0960 reduces dopamine catabolism, increases striatal dopamine and DOPAC levels, decreases striatal HVA levels, induces apoptosis, inhibits proliferation and extracellular matrix formation in uterine fibroid cells. Ro 41-0960 arrests or shrinks uterine fibroid lesions in rats. Ro 41-0960 can be used for the research of Parkinson’s disease, uterine leiomyomas, and breast cancer .
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Art. -Nr.: HY-W116576
CAS. Nr.: 934-00-9
3-Methoxycatechol is a catechol derivative with endothelium-dependent vasodilatory and antihypertensive activities. 3-Methoxycatechol activates GPR35, triggering dynamic mass redistribution and β-arrestin translocation. 3-Methoxycatechol inhibits tau self-interaction and scavenges free radicals such as DPPH. 3-Methoxycatechol combined with NaNO2 enhances forestomach proliferative lesions and papilloma formation, reduces glandular stomach lesions, and promotes esophageal lesion development. 3-Methoxycatechol can be used for research related to hypertension and papilloma .
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Art. -Nr.: HY-D0798
CAS. Nr.: 115-41-3
Forschungsgebiete:  

Others

Catechol violet is an iron ion chelating agent and colorimetric complexing reagent. Catechol violet can be used as a chromogenic, absorption spectroscopic, and spectrophotometric reagent for the determination of aluminum, forming a ternary complex with aluminum and cetyltrimethylammonium bromide, and quantifying the release of iron ions from nanocarriers by colorimetry. Catechol violet is a phenolic model aqueous pollutant and can be photocatalytically degraded under visible light by a molybdenum disulfide-bacterial cellulose nanocomposite with hydrogen peroxide .
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Art. -Nr.: HY-B1481
CAS. Nr.: 7279-75-6
Synonyms: Isoetarine mesylate
Isoetharine (Isoetarine) mesylate is an orally active selective agonist of β-adrenergic receptors. Isoetharine mesylate is a catechol-like agent and catechol O-methyltransferase (COMT) mediates its methylation. Isoetharine mesylate can promote the production of cAMP which stimulates the relaxation of smooth muscle cells and can be used as an emphysema, bronchitis and bronchodilator .
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Art. -Nr.: HY-W006000
CAS. Nr.: 1198-55-6
Target:  

Drug Metabolite

Forschungsgebiete:  

Others

Tetrachlorocatechol is a metabolite of pentachlorophenol. Tetrachlorocatechol is one of the most toxic chlorinated catechol produced by the chlorobleaching of pulp and frequently found in the kraft pulp mill effluents .
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Art. -Nr.: HY-D2344
CAS. Nr.: 325721-44-6
Synonyms: 3-Benzothiazole-daphnetin
3-BTD (3-Benzothiazole-daphnetin) is a Catechol-O-methyltransferase (COMT) two-photon fluorescence probe. 3-BTD can also be used for biological imaging of endogenous COMT in living cells and tissue sections .
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Art. -Nr.: HY-100959
CAS. Nr.: 7659-29-2
Reinheit:  99.72%
Synonyms: OR-486; 3,5-DinitropyroCatechol
Target:  

COMT

Forschungsgebiete:  

Neurological Disease Endocrinology

3,5-Dinitrocatechol (OR-486) is an orally active, blood-brain barrier-permeable selective catechol-O-methyltransferase (COMT) inhibitor. 3,5-Dinitrocatechol can be used in research related to Parkinson's disease, pheochromocytoma and adult cataract .
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