9 Results for "

NG 108-15

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "NG 108-15" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-102064
CAS No.: 77145-61-0
Purity:  99.86%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

SR 57227A is a potent, orally active and selective 5-HT3 receptor agonist, with ability to cross the blood brain barrier. SR 57227A has affinities (IC50) varying between 2.8 and 250 nM for 5-HT3 receptor binding sites in rat cortical membranes and on whole NG 108-15 cells or their membranes. Anti-depressant effects .
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1
1 Cited Publications
Cat. No.: HY-10815
CAS No.: 1204401-49-9
Purity:  99.89%
Research Areas:  

Neurological Disease Cancer

σ1 Receptor antagonist-1 is a highly potent and selective sigma 1 receptor antagonist (pKi=10.28). σ1 Receptor antagonist-1 inhibits cell growth, arrests cell cycle at G0/G1 phase and induces apoptosis of MCF-7/ADR cells .
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Cat. No.: HY-W587488
CAS No.: 84-21-9
Synonyms: 3′-AMP
Adenosine 3’-monophosphate (3’-AMP) is a nucleotide. Adenosine 3’-monophosphate is a cyclic AMP production agonist. Adenosine 3’-monophosphate increases cyclic AMP levels concentration-dependently in NG108-15 cells. Adenosine 3’-monophosphate can be used in the determination of acid phosphatase activity of human serum, which is estabilished as a laboratory procedure in the diagnosis of prostate cancer, metastatic mammary cancer and Gaucher’s disease. Adenosine 3’-monophosphate inhibits human aortic and coronary vascular smooth muscle cell proliferation via A2B receptors .
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Cat. No.: HY-P10815
Research Areas:  

Others

IP3RCYT is an IP3R inhibitory peptide, which can inhibit the binding of cytochrome C to IP3R with an IC50 about 100 nM. IP3RCYT regulates calcium signaling within cells. P3RCYT inhibits apoptosis in HeLa and Jurkat cells treated with Staurosporine (HY-15141) or Membrane-bound Fas ligand (FasL) .
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Cat. No.: HY-102064R
CAS No.: 77145-61-0
Research Areas:  

Neurological Disease

SR 57227A (Standard) is the analytical standard of SR 57227A (HY-102064). This product is intended for research and analytical applications. SR 57227A is a potent, orally active and selective 5-HT3 receptor agonist, with ability to cross the blood brain barrier. SR 57227A has affinities (IC50) varying between 2.8 and 250 nM for 5-HT3 receptor binding sites in rat cortical membranes and on whole NG 108-15 cells or their membranes. Anti-depressant effects .
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Cat. No.: HY-N10815
CAS No.: 69618-94-6
Anthriscinol is a natural product that can be isolated from Anthriscus sylvestris HOFFM .
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Cat. No.: HY-NP108
Synonyms: Rat Type II collagen, immunization grade
Highly purified type II collagen, from rat sternal cartilage (Rat Type II collagen, immunization grade) is an immune grade collagen derived from rat sternal cartilage, which can stimulate the animal's immune system to produce specific antibodies against this collagen. Collagen is also a substrate for hydrolysis by MMPs .
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Cat. No.: HY-RS10815
Research Areas:  

Others

POGZ Human Pre-designed siRNA Set A contains three designed siRNAs for POGZ gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-L108
3,059 compounds

Depression is a serious global affective disorder and one of the most common neurological diseases whose clinical manifestations are low mood, loss of interest, anhedonia, loss of energy, and fatigue, people with major depressive disorder (MDD) can even have suicidal thoughts and behaviors.

Currently available antidepressants have significant limitations, including a long time lag for a therapeutic response (weeks to months) and low response rates. This is particularly problematic for a disease with a high suicide rate. Therefore, the development of new antidepressant drugs is particularly urgent.

MCE offers a unique collection of 3,059 compounds with antidepressant activities or targeting the unique targets of depression. MCE Antidepressant Compound Library is a useful tool for exploring the mechanism of depression and discovering new drugs for depression.