13 Results for "

DPI

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "DPI" in MCE Product Catalog:

64
64 Cited Publications
Cat. No.: HY-100965
CAS No.: 4673-26-1
Purity:  99.91%
Synonyms: DPI
Diphenyleneiodonium chloride is a NADPH oxidase (NOX) inhibitor and also functions as a TRPA1 activator with an EC50 of 1 to 3 μM. Diphenyleneiodonium chloride selectively inhibits intracellular reactive oxygen species.
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1
1 Cited Publications
Cat. No.: HY-19666
CAS No.: 97730-95-5
Synonyms: SDZ 201106
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

DPI 201-106 (SDZ 201106) is a cardiotonic agent with a synergistic sarcolemmal and intracellular mechanism of action. DPI 201-106 shows cardioselective modulation of voltage-gated sodium channels (VGSCs) resulting in a positive inotropic effect .
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Cat. No.: HY-P10761
CAS No.: 2941391-49-5
DPI-4452 is a CAIX-targeting cyclic peptide with a DOTA cage, and can be chelated with radionuclide for CAIX-expressing tumor PET-CT imaging and study. DPI-4452 specifically and selectively binds CAIX without interaction with an in vitro off-target receptor panel of 55 targets (IC50 for recombinant hCAIX: 130 nM). Radiolabeled DPI-4452 inhibits tumor growth in HT-29 and SK-RC-52 xenograft mouse models . DPI-4452 can be used for the synthesis/research of Radionuclide-Drug Conjugates (RDCs).
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Cat. No.: HY-19231
CAS No.: 182417-73-8
Synonyms: Org 41793
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

DPI-3290 (Org 41793) is a potent and specific opioid receptors agonist with Ki values of 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively. DPI-3290 is one of a series of novel centrally acting agents with potent antinociceptive activity .
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Cat. No.: HY-156988
CAS No.: 519058-13-0
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

DPI-287 is a selective delta-opioid receptor (DOP) agonist with a Ki value of 0.39 nM and can be used for pain research .
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Cat. No.: HY-157479
CAS No.: 2760731-35-7
Target:  

Bacterial

Research Areas:  

Infection

DPI-2016 is a antibacterial agent. DPI-2016 shows improved bactericidal activity (MIC, 0.25-8 μg/mL) against all bacterial strains compared to the aztreonam (HY-B0129) (MIC, 16->64 μg/mL) .
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Cat. No.: HY-19666R
CAS No.: 97730-95-5
Synonyms: SDZ 201106 (Standard)
DPI 201-106 (Standard) is the analytical standard of DPI 201-106. This product is intended for research and analytical applications. DPI 201-106 (SDZ 201106) is a cardiotonic agent with a synergistic sarcolemmal and intracellular mechanism of action. DPI 201-106 shows cardioselective modulation of voltage-gated sodium channels (VGSCs) resulting in a positive inotropic effect .
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Cat. No.: HY-P72176
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: DSP; PPKS2; Desmoplakin; DPII; DP; DPI; 250/210 KDa Paraneoplastic Pemphigus Antigen; Desmoplakin (DPI, DPII); KPPS2; DCWHKTA
Species:  
Source:  
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Cat. No.: HY-100965R
CAS No.: 4673-26-1
Synonyms: DPI (Standard)
Diphenyleneiodonium chloride (Standard) is the analytical standard of Diphenyleneiodonium chloride (HY-100965). This product is intended for research and analytical applications. Diphenyleneiodonium chloride is a NADPH oxidase (NOX) inhibitor and also functions as a TRPA1 activator with an EC50 of 1 to 3 μM. Diphenyleneiodonium chloride selectively inhibits intracellular reactive oxygen species.
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Cat. No.: HY-P82634
Synonyms: Desmoplakin I; Desmoplakin II; DPI; DPII; DSP; KPPS2; PPKS2

Host:  

Rabbit

Application:  

WB, ICC/IF, FC

Reactivity:  

Human, Rat

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Cat. No.: HY-P82634A
Synonyms: Desmoplakin I; Desmoplakin II; DPI; DPII; DSP; KPPS2; PPKS2

Host:  

Rabbit

Application:  

WB, ICC/IF, FC

Reactivity:  

Human, Rat

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Cat. No.: HY-183657
Target:  

Orphan GPCR

Research Areas:  

Neurological Disease

GPR3 inverse agonist-1 is a GPR3 inverse agonist with low micromolar potency in conformational analysis. GPR3 inverse agonist-1 inhibits GPR3-dependent Gs activity in HEK293A cells with an EC50 of 250 nM, and exhibits an EC50 of 2 μM in cAMP assays. GPR3 inverse agonist-1 induces concentration-dependent changes in BRET signals in GPR3 conformational biosensors (EC50 = 5 μM), reduces basal Gs activity downstream of GPR3, and competes for binding sites with the GPR3 agonist DPI (HY-100965). GPR3 inverse agonist-1 can be used in research related to Alzheimer's disease .
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Cat. No.: HY-183657A
Target:  

Orphan GPCR

Research Areas:  

Neurological Disease

GPR3 inverse agonist-1 TFA is a GPR3 inverse agonist with low micromolar potency in conformational analysis. GPR3 inverse agonist-1 TFA inhibits GPR3-dependent Gs activity in HEK293A cells with an EC50 of 250 nM, and exhibits an EC50 of 2 μM in cAMP assays. GPR3 inverse agonist-1 TFA induces concentration-dependent BRET signal changes in GPR3 conformational biosensors (EC50 = 5 μM), reduces basal Gs activity downstream of GPR3, competes for binding sites with the GPR3 agonist DPI (HY-100965). GPR3 inverse agonist-1 TFA can be used in research related to Alzheimer's disease .
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