92 Results for "

EMD

" in MedChemExpress (MCE) Product Catalog:
Products (92)

92 Results for "EMD" in MCE Product Catalog:

Cat. No.: HY-103115
CAS No.: 443144-27-2
Synonyms: EMD 281014; LY 2422347 hydrochloride
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Pruvanserin hydrochloride (EMD 281014) is a selective serotonin 5-HT2A receptor antagonist with IC50 values of 0.35 nM and 1 nM for human and rat 5-HT2A receptors. Pruvanserin (hydrochloride) can be used for the research of schizophrenia .
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Cat. No.: HY-14771S
Synonyms: EMD 387008-d3
Imeglimin-d3 (EMD 387008-d3) is deuterium labeled Imeglimin. Imeglimin (EMD 387008) is an oral glucose-lowering agent. Imeglimin improves insulin sensitivity. Imeglimin also reduces reactive oxygen species (ROS) production, increases mitochondrial DNA and improves mitochondrial function .
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Cat. No.: HY-16141R
CAS No.: 188968-51-6
Synonyms: EMD 121974 (Standard)
Cilengitide (Standard) (EMD 121974 (Standard)) is the analytical standard of Cilengitide (HY-16141). This product is intended for research and analytical applications. Cilengitide (EMD 121974) is an integrin (integrin) inhibitor with blood-brain barrier permeability, with IC50 values against human targets as follows: 0.61 nM for αvβ3, 8.4 nM for αvβ5, 14.9 nM for α5β1, 5400 nM for αIIbβ3, 2050 nM for αvβ6, 2350 nM for αvβ8. Cilengitide inhibits the binding of integrins to vitronectin, fibronectin, fibrinogen and LAP (TGF-β), and serves as an internal standard for solid-phase integrin binding assays. Cilengitide inhibits tumor cell viability, induces apoptosis, reduces the phosphorylation levels of STAT3, AKT and mTOR, downregulates the expression of PD-L1, inhibits cell viability and angiogenesis, regulates anti-tumor immune responses and slows tumor growth. Cilengitide can be used in research related to glioblastoma, melanoma, advanced solid tumors and refractory brain tumors .
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Cat. No.: HY-14262S1
Synonyms: EMD 68843-d8; SB659746A-d8
Vilazodone-d8 hydrochloride is deuterated labeled Vilazodone (HY-14262). Vilazodone (EMD 68843; SB 659746A) is a potent, selective and orally active serotonin reuptake inhibitor (SSRI) and partial 5-HT1A receptor agonist. Vilazodone exhibits antidepressant efficacy in vivo can be used for the research of major depressive disorder (MDD) and affective disorders .
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Cat. No.: HY-70057R
CAS No.: 133865-89-1
Synonyms: FCE 26743 (Standard); EMD 1195686 (Standard)
Safinamide (Standard) is the analytical standard of Safinamide. This product is intended for research and analytical applications. Safinamide is a potent, selective, and reversible monoamine oxidase B (MAO-B) inhibitor (IC50=0.098 µM) over MAO-A (IC50=580 µM) . Safinamide also blocks sodium channels and modulates glutamate (Glu) release, showing a greater affinity at depolarized (IC50=8 µM) than at resting (IC50=262 µM) potentials. Safinamide has neuroprotective and neurorescuing effects and can be used for the study of parkinson disease, ischemia stroke etc.al .
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Cat. No.: HY-P2075
CAS No.: 126784-34-7
Target:  

Renin

Research Areas:  

Endocrinology

EMD 55068 is a renin antagonist. EMD 55068 inhibits the uptake of taurocholate .
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Cat. No.: HY-105539
CAS No.: 427889-61-0
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

EMD 86006 is a candidate for selective serotonin inhibitors. EMD 86006 has the potential for research on depressive disorders .
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Cat. No.: HY-129714
CAS No.: 129049-51-0
Target:  

Renin

Research Areas:  

Metabolic Disease

EMD 52297 is a Renin inhibitor, with acute hemodynamic and hormonal effects. EMD 52297 also acts as an ACE inhibitor .
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Cat. No.: HY-169827
CAS No.: 167364-01-4
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

EMD-132338 is a GPIIb/IIIa (αIIbβ3) antagonist that inhibits platelet aggregation. EMD-132338 can be utilized in antithrombosis research .
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Cat. No.: HY-103247
CAS No.: 1216884-39-7
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

EMD 66684 is an antagonist of Angiotensin II Type 1 (AT1) receptor. EMD 66684 shows potent binding affinities for the AT1 subtype Ang II receptor with an IC50 value of 0.7 nM. EMD 66684 also serves as an antiischemic cytoprotectant - .
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Cat. No.: HY-103247B
CAS No.: 187683-79-0
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

EMD-66684 potassium salt is a non-peptide angiotensin II receptor antagonist that demonstrates significant antihypertensive effects in spontaneously hypertensive rats. EMD-66684 potassium salt exhibits nanomolar affinity for angiotensin II receptors, comparable to losartan in potency. EMD-66684 potassium salt shows increased activity when modified with acetamides, leading to superior blood pressure reduction.
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Cat. No.: HY-19134
CAS No.: 133109-86-1
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

EMD 56551 is a potent and selective 5-HT1A receptor agonist. EMD 56551 exerts anxiolytic activity .
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Cat. No.: HY-170410
CAS No.: 178165-43-0
Target:  

iGluR

Research Areas:  

Neurological Disease

EMD-95885 is a selective NR2B-containing NMDA receptors antagonist with an IC50 of 3.9 nM. EMD-95885 does not interact with other sites on the NMDA receptor .
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Cat. No.: HY-114987
CAS No.: 61711-37-3
Target:  

iGluR

Research Areas:  

Neurological Disease

EMD 21657 is a derivative of Piracetam (HY-B0585). EMD 21657 inhibits LOT compound action potential, and enhances the local anesthetic effect of Hexanol (HY-W032022). EMD 21657 exhibits hemolytic effect, and can be used in research about alcoholic encephalopathy syndrome .
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Cat. No.: HY-10777
CAS No.: 811811-33-3
Target:  

Factor Xa

Research Areas:  

Cardiovascular Disease

EMD 495235 is a potent and orally active coagulation factor Xa inhibitor with an IC50 of 5.5 nM and a Ki of 6.8 nM. EMD 495235 shows anticoagulant activities .
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Cat. No.: HY-114990
CAS No.: 148714-88-9
Research Areas:  

Cardiovascular Disease

EMD 57439 is a selective PDE-III inhibitor. EMD 57439 does not significantly increase c-AMP concentration and has little effect on Ca(50) .
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Cat. No.: HY-103130A
CAS No.: 54635-62-0
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

EMD386088 free base is a potent serotonin 6 receptor (5-HT6R) agonist. EMD386088 free base induces cell death. EMD386088 free base regulates the activity of ERK1/2. EMD386088 free base has the potential for the research of alzheimer's disease (AD) and schizophrenia .
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Cat. No.: HY-123356
CAS No.: 768370-75-8
Target:  

Factor Xa

Research Areas:  

Cardiovascular Disease

EMD-503982 is an orally available FXa inhibitor .
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Cat. No.: HY-164394
CAS No.: 1100598-15-9
Target:  

c-Met/HGFR

Research Areas:  

Cancer

EMD 1204831 is a potent and highly selective c-Met inhibitor which selectively suppresses the c-Met receptor tyrosine kinase activity with an IC50 of 9 nM. EMD 1204831 can be utilized in cancer research .
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Cat. No.: HY-101473A
Target:  

Integrin

Research Areas:  

Cancer

EMD527040 (hydrochloride) is a highly potent and selective αvβ6 antagonist with anti-fibrotic activity. EMD527040 (hydrochloride) is used in the research of liver cancer and liver fibrosis .
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