8 Results for "

phosphodiesterase 7

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "phosphodiesterase 7" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-134124
CAS No.: 92614-59-0
Purity:  95.8%
Research Areas:  

Metabolic Disease

Glutathione ethyl ester is a cell-permeable GSH donor and provides an efficient supply of GSH to the oocyte. Glutathione ethyl ester shows positive effect on the in vitro production of embryos by enhancement of the antioxidative defense .
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Cat. No.: HY-112555
CAS No.: 107522-19-0
Purity:  ≥99.0%
Research Areas:  

Neurological Disease

PDE7-IN-2 (compound 2) is a potent PDE7 (phosphodiesterase 7) inhibitor with IC50 value of 2.1 µM. PDE7-IN-2 has the potential for the research of parkinson’s disease .
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Cat. No.: HY-114727
CAS No.: 18741-24-7
Purity:  98.55%
Research Areas:  

Inflammation/Immunology

PDE7-IN-4 is a phosphodiesterase 7 (PDE7) inhibitor with activity that increases intracellular cyclic adenosine monophosphate (cAMP) levels. PDE7-IN-4 shows potential inhibitory effects in neurotransmission and anti-inflammatory applications. PDE7-IN-4 exerts its biological activity by acting on the cAMP/cAMP response element binding protein (CREB) pathway. The development of PDE7-IN-4 aims to improve its pharmacokinetic characteristics to more effectively target neurodegenerative diseases and other inflammation-related diseases .
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Cat. No.: HY-P2424
CAS No.: 144396-38-3
Synonyms: CCK-J
Target:  

Calcium Channel

Research Areas:  

Others

Cholecystokinin-J (CCK-J), a cholecystokinin, stimulates Ca 2+ release .
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Cat. No.: HY-P703577
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PDE7A; High Affinity CAMP-Specific PDE 1; phosphodiesterase 7A; TM22; HCP1; High Affinity CAMP-Specific 3',5'-Cyclic phosphodiesterase 7A; High Affinity 3',5'-Cyclic-AMP phosphodiesterase 7A; phosphodiesterase Isozyme 7; CAMP-Specific phosphodiesterase 7A
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P76902
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ENPP7; Alkaline Sphingomyelin phosphodiesterase; Ectonucleotide Pyrophosphatase/phosphodiesterase 7; Intestinal Alkaline Sphingomyelinase; Alk-SMase; Alkaline Sphingomyelinase; NPP7; E-NPP 7; Ectonucleotide Pyrophosphatase/phosphodiesterase Family Member
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-P77358
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ENPP7; Alkaline Sphingomyelin phosphodiesterase; Ectonucleotide Pyrophosphatase/phosphodiesterase 7; Intestinal Alkaline Sphingomyelinase; Alk-SMase; Alkaline Sphingomyelinase; NPP7; E-NPP 7; Ectonucleotide Pyrophosphatase/phosphodiesterase Family Member
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-119514
CAS No.: 423744-89-2
BC12 is a barbituric acid derivative and a phosphodiesterase 7 (PDE7) inhibitor, with an IC50 of 0.77 μM against human targets. BC12 inhibits the enzymatic activity of PDE7, but this activity is not the driver of its immunomodulatory effects on T lymphocytes. BC12 blocks the upregulation of IL-2 transcription in activated T cells. BC12 modulates the transcriptional response of T cells upon stimulation, exerting anti-inflammatory and pro-stress effects. BC12 inhibits the proliferation of primary mouse T cells and the IL-2 secretion of human peripheral blood T lymphocytes. BC12 exerts immunosuppressive and immunomodulatory effects on T lymphocyte function. BC12 can be used in research related to T lymphocyte-mediated diseases .
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