2438 Results for "

decrease

" in MedChemExpress (MCE) Product Catalog:
Products (2438)

2438 Results for "decrease" in MCE Product Catalog:

Cat. No.: HY-101630A
CAS No.: 120444-72-6
Synonyms: EGIS-3886 fumarate
Target:  

5-HT Receptor

연구분야:  

Others

Deramciclane fumarate is an antagonist of 5-HT Receptor. Deramciclane fumarate is an inverse agonist of 5-HT2C Receptor with an IC50 of 168 nM. Deramciclane fumarate also decreases basal phosphoinositide hydrolysis .
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Cat. No.: HY-114567
CAS No.: 1093294-48-4
Target:  

CDK

GW780056X is a CDK12 inhibitor. GW780056X decreases nuclear foci count in DM1 cells. GW780056X can be used for the research of myotonic dystrophy type 1 .
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Cat. No.: HY-116457
CAS No.: 1421-14-3
Synonyms: Sombrevin; Fabantol
Propanidid (Sombrevin; Fabantol) is a γ-aminobutyric acid type A (GABAA) receptor agonist and a short-acting non-barbiturate general agent that can suppress or relieve pain. Propanidid can decrease the arterial pressure .
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Cat. No.: HY-117078
CAS No.: 25001-57-4
Purity:  99.63%
Target:  

Apoptosis

연구분야:  

Cancer

justicidin A is a nature product that could be isolated form Justicia procumbens. justicidin A decreases the level of Ku70 leading to translocation of Bax from the cytosol to mitochondria to induce apoptosis. justicidin A can be used in research of cancer .
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Cat. No.: HY-117856
CAS No.: 1426047-44-0
Purity:  99.57%
Target:  

Prion Protein

연구분야:  

Infection

IND24 is a potent antiprion agent with an EC50 value of 1.27 µM. IND24 decreases abnormal, misfolded, pathogenic forms of benign normally occurring prion protein on the cell surface or inside the cell .
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Cat. No.: HY-128678
CAS No.: 488847-28-5
Purity:  99.43%
Target:  

Na+/Ca2+ Exchanger

연구분야:  

Cardiovascular Disease

ORM-10103 is a specific inhibitor of the Na+/Ca2+ exchanger (NCX), which decreases the NCX current with estimated IC50s of 55 and 67 nM at -80 and at 20 mV, respectively .
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Cat. No.: HY-135375
CAS No.: 887196-29-4
O-Methyl Atorvastatin (hemicalcium) is an impurity of Atorvastatin. Atorvastatin is an orally active 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, has the ability to effectively decrease blood lipids .
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Cat. No.: HY-136185
CAS No.: 873950-19-7
Target:  

Drug Metabolite

연구분야:  

Others

Atorvastatin Epoxy Tetrahydrofuran Impurity is an impurity isolated oxidative degradation products of Atorvastatin (HY-B0589) . Atorvastatin is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids.
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Cat. No.: HY-145873
CAS No.: 2759037-58-4
Target:  

Fungal

연구분야:  

Infection

BI-10 is an antifungal compound. BI-10 combined with Fluconazole can inhibit hyphal growth, result in ROS accumulation, and decrease mitochondrial membrane potential (MMP) as well as altering membrane permeability .
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Cat. No.: HY-14747
CAS No.: 625114-41-2
Synonyms: RO4389620; R-1440
Target:  

Glucokinase

연구분야:  

Metabolic Disease

Piragliatin (RO4389620) is an activator for glucokinase, which reduces endogenous glucose production, increases β-cell function and glucose utilization, and thus decreases the blood glucose levels. Piragliatin exhibits antidiabetic efficacy .
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Cat. No.: HY-154387
CAS No.: 1219485-46-7
Synonyms: 1-IsoPT
연구분야:  

Cancer

1-Isopropyltryptophan (1-IsoPT) is a IDO1 inhibitor. 1-Isopropyltryptophan decreases the expression of IFN-γ stimulated ID0-1 and ID0-2 mRNA .
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Cat. No.: HY-178853
CAS No.: 87112-04-7
Target:  

Others

연구분야:  

Inflammation/Immunology

3,4-Dihydroxybenzeneethanimidamide can selectively react with Gly-Pro, the substrate for prolidase, and the prolidase activity is measured by monitoring the decrease in FL intensities. 3,4-Dihydroxybenzeneethanimidamide can be used for the study of inflammation .
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Cat. No.: HY-N0465S
CAS No.: 1189487-82-8
Olaquindox-d4 is the deuterium labeled Olaquindox (HY-N0465) . Olaquindox, a quinoxalin derivative, is an orally active antibiotic. Olaquindox stimulates growth and decreases intestinal mucosal immunity of piglets .
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Cat. No.: HY-N10772
CAS No.: 73343-42-7
Albanin A, a flavonoid, suppresses glutamate release by decreasing Ca 2+/calmodulin/adenylate Cyclase 1 (AC1) activation in synaptosomes and exerts neuroprotective effect in vivo. Albanin A has anti-inflflammatory activity .
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Cat. No.: HY-N3009R
CAS No.: 58822-47-2
Secoxyloganin (Standard) is the analytical standard of Secoxyloganin. This product is intended for research and analytical applications. Secoxyloganin, isolated from Lonicera japonica Thunb, inhibits the blood flow (BF) decrease. Secoxyloganin has allergy-preventive activity .
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Cat. No.: HY-P4497
CAS No.: 71835-80-8
Target:  

ERK

연구분야:  

Cancer

Prolylserine, a dipeptide, is an inhibitor of melanogenesis production in Mel-Ab cells. Prolylserine decreases expression of microphthalmia-associated transcription factor (MITF) and tyrosinase, induces phorphosylation of ERK, but not cAMP response element binding protein (CREB) .
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Cat. No.: HY-114913
CAS No.: 60168-88-9
Synonyms: EL 222
연구분야:  

Infection Endocrinology

Fenarimol (EL 222) is a potent and orally active fungicide. Fenarimol also is a androgen receptor inhibitor with an IC50 value of 19 µM. Fenarimol decreases the mRNA expression of PBP C3, ODC, IGF-1 .
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Cat. No.: HY-124863A
CAS No.: 241476-71-1
Target:  

SphK

연구분야:  

Inflammation/Immunology

(R)-AAL is an immunomodulator. (R)-AAL decreases circulating T lymphocytes in rats, with an ID50 value of 0.009 mg/kg. (R)-AAL is a substrate of sphingosine kinase (SphK), which catalyzes the phosphorylation of (R)-AAL .
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Cat. No.: HY-134577
CAS No.: 3811-25-4
Purity:  99.33%
Target:  

Adrenergic Receptor

연구분야:  

Endocrinology

Clorprenaline is a potent agonist of β2-adrenergic. Clorprenaline promotes animal muscular mass growth and decreases fat accumulation. Clorprenaline is a potential new lean meat-boosting feed additive .
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Cat. No.: HY-150192
CAS No.: 21489-20-3
Talsupram is a selective noradrenaline inhibitor that has a high affinity for the noradrenaline transporter. Talsupram exhibits anti-hyperalgesic effects. Talsupram can decrease ethanol intake to the levels prior to REM-induced deprivation in rat model .
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