2438 Results for "

decrease

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

2438 Results for "decrease" in MCE Product Catalog:

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

5-HT Receptor

Áreas de investigación:  

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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Referencia número: HY-114567
No. CAS: 1093294-48-4
Target:  

CDK

Áreas de investigación:  

Neurological Disease Metabolic Disease

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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Referencia número: HY-116457
No. CAS: 1421-14-3
Synonyms: Sombrevin; Fabantol
Target:  

GABA Receptor

Áreas de investigación:  

Cardiovascular Disease Neurological Disease

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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Referencia número: HY-117078
No. CAS: 25001-57-4
Pureza:  99.63%
Target:  

Apoptosis

Áreas de investigación:  

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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Referencia número: HY-117856
No. CAS: 1426047-44-0
Pureza:  99.57%
Target:  

Prion Protein

Áreas de investigación:  

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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Referencia número: HY-128678
No. CAS: 488847-28-5
Pureza:  99.43%
Target:  

Na+/Ca2+ Exchanger

Áreas de investigación:  

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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Referencia número: HY-135375
No. CAS: 887196-29-4
Target:  

Drug Metabolite

Áreas de investigación:  

Metabolic Disease Inflammation/Immunology

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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Referencia número: HY-136185
No. CAS: 873950-19-7
Target:  

Drug Metabolite

Áreas de investigación:  

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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Referencia número: HY-145873
No. CAS: 2759037-58-4
Target:  

Fungal

Áreas de investigación:  

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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Referencia número: HY-14747
No. CAS: 625114-41-2
Synonyms: RO4389620; R-1440
Target:  

Glucokinase

Áreas de investigación:  

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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Referencia número: HY-154387
No. CAS: 1219485-46-7
Synonyms: 1-IsoPT
Áreas de investigación:  

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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Referencia número: HY-178853
No. CAS: 87112-04-7
Target:  

Others

Áreas de investigación:  

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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Referencia número: HY-N0465S
No. CAS: 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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Referencia número: HY-N10772
No. CAS: 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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Referencia número: HY-N3009R
No. CAS: 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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Referencia número: HY-P4497
No. CAS: 71835-80-8
Target:  

ERK

Áreas de investigación:  

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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Referencia número: HY-114913
No. CAS: 60168-88-9
Synonyms: EL 222
Áreas de investigación:  

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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Referencia número: HY-124863A
No. CAS: 241476-71-1
Target:  

SphK

Áreas de investigación:  

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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Referencia número: HY-134577
No. CAS: 3811-25-4
Pureza:  99.33%
Target:  

Adrenergic Receptor

Áreas de investigación:  

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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Referencia número: HY-150192
No. CAS: 21489-20-3
Target:  

Adrenergic Receptor

Áreas de investigación:  

Neurological Disease Endocrinology

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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