13 Results for "

ECE1

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

13 Results for "ECE1" in MCE Product Catalog:

Cat. No.: HY-P3749
CAS No.: 323577-36-2
Target:  

Fluorescent Dye

Research Areas:  

Others

Mca-(ala7,lys(dnp)9)-bradykinin is a sensitive fluorogenic substrate for ECE-1 (endothelin-converting enzyme-1). The incorporation of a (7-methoxycoumarin-4-yl)acetyl (Mca) fluorescent group and a 2,4-dinitrophenyl (Dnp) quenching group has resulted in a large fluorescence increase upon substrate cleavage [1].
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Cat. No.: HY-RS04133
Research Areas:  

Others

ECE1 Human Pre-designed siRNA Set A contains three designed siRNAs for ECE1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS18611
Research Areas:  

Others

Ece1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ece1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-178732
CAS No.: 1463913-43-0
AB-22, a vinyl sulfate compound, is an orally active antifungal agent. AB-22 inhibits hyphal growth and biofilm initiation by inhibiting the gene expression of ALS3, HWP1, and ECE1 in Candida albicans SC5314 cells. AB-22 can be used for the research of infrction, such as systemic candidiasis [1].

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Cat. No.: HY-RS25097
Research Areas:  

Others

Ece1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ece1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-N11772
CAS No.: 875455-92-8
Mutanocyclin is a potent antifungal agent. Mutanocyclin inhibits Candida albicans (C. albicans) filamentation. Mutanocyclin decreases the mRNA expression of HWP1, ECE1, FLO8, TEC1. Mutanocyclin inhibits yeast-form in ex vivo mouse [1].
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Cat. No.: HY-Y1783
CAS No.: 109-83-1
Synonyms: N-Methylethanolamine
2-(Methylamino) ethanol (N-Methylethanolamine) is an orally active Phospholipase D inhibitor and analog of Ethanolamine (HY-Y0524). 2-(Methylamino) ethanol reduces the mRNA levels of ACE, ppET-1 and ECE-1, and inhibits MMP-2 activity. 2-(Methylamino) ethanol inhibits Collagen synthesis. 2-(Methylamino) ethanol attenuates ventricular hypertrophy, prevents increased myocardial stiffness and hemodynamic deterioration. 2-(Methylamino) ethanol can capture industrial acid gases and react with carbon dioxide to form carbamates and bicarbonates. 2-(Methylamino) ethanol can be used in studies related to hypertensive heart failure (diastolic heart failure) [1] .
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Cat. No.: HY-107762
CAS No.: 261619-50-5
CGS35066 is a potent and selective aminophosphonate inhibitor of endothelin-converting enzyme-1 (ECE-1). CGS 35066 inhibits the activity of human ECE-1 and rat kidney neutral endopeptidase 24.11 (NEP) in vitro with IC50 values of 22 nM and 2.3 μM, respectively [1].
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Cat. No.: HY-119545
CAS No.: 179598-53-9
PD159790 is a selective endothelin-converting enzyme-1 (ECE-1) inhibitor, with an EC50 of 28.1 μM [1] .
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Cat. No.: HY-P70035
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ECE1; Endothelin-Converting Enzyme 1; Prev. ECE; Endothelin Converting Enzyme 1; ECE-1
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-18211
CAS No.: 849066-09-7
CGS 35601 is the inhibitor for endothelin-converting enzyme-1 (ECE-1), neutral endopeptidase 24.11 (NEP), and angiotensin-converting enzyme (ACE), with IC50s of 55, 2, and 22 nM, respectively. CGS 35601 suppresses the big endothelin-1 (big ET-1)- and angiotensin I-induced pressor response, and enhances circulation of atrial natriuretic peptide (ANP), regulates the cardiovascular function in SD rats [1].
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Cat. No.: HY-N11772R
CAS No.: 875455-92-8
Mutanocyclin (Standard) is the analytical standard of Mutanocyclin (HY-N11772). This product is intended for research and analytical applications. Mutanocyclin is a potent antifungal agent. Mutanocyclin inhibits Candida albicans (C. albicans) filamentation. Mutanocyclin decreases the mRNA expression of HWP1, ECE1, FLO8, TEC1. Mutanocyclin inhibits yeast-form in ex vivo mouse [1].
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Cat. No.: HY-184728
Target:  

Fungal PKA

Research Areas:  

Infection

Antifungal agent-169 (compound 5p) is an antifungal agent that inhibits fluconazole (HY-B0101)-susceptible Candida albicans SC5314 with an MIC50 of 0.28 μM. Antifungal agent-169 reduces the expression levels of cAMP-PKA pathway-related genes including RAS1, EFG1, BCR1, ECE1 and HWP1 in Candida albicans. Antifungal agent-169 inhibits biofilm formation and hyphal growth of Candida albicans. Antifungal agent-169 can be used in studies related to Candida albicans infection [1].
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