17 Results for "

MI1

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "MI1" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-106262B
Purity:  99.73%
Synonyms: KAI-9803 hydrochloride; BMS-875944 hydrochloride
Target:  

PKC

Delcasertib (KAI-9803) hydrochloride is a potent and selective δ-protein kinase C (δPKC) inhibitor. Delcasertib (KAI-9803) hydrochloride could ameliorate injury associated with ischemia and reperfusion in animal models of acute myocardial infarction (MI) .
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Cat. No.: HY-B1409
CAS No.: 87-33-2
Synonyms: ISDN
Target:  

NO Synthase

Research Areas:  

Cardiovascular Disease

Isosorbide dinitrate (ISDN) is an NO donor that prevents LV remodeling and degradation of cardiac function following myocardial infarction (MI) .
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Cat. No.: HY-B0592
CAS No.: 87679-37-6
Synonyms: RU44570
Trandolapril (RU44570) is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolaprilat. Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .
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Cat. No.: HY-119350B
CAS No.: 2815778-41-5
Purity:  99.07%
Synonyms: RUC-4 dihydrochloride
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

Zalunfiban (RUC-4) dihydrochloride is a potent, selective platelet αIIbβ3 antagonist (IC50=45 nM). Zalunfiban dihydrochloride can be used for the research of myocardial infarction (MI) .
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Cat. No.: HY-123422
CAS No.: 931399-19-8
Purity:  99.9%
Research Areas:  

Cardiovascular Disease

GSK360A is a potent and orally active HIF-PHD inhibitor with IC50 values of 10, 100, and 126 nM for PHD1, PHD2, and PHD3, respectively. GSK360A activates the HIF-1 alpha pathway and protect the failing heart after myocardial infarction (MI) .
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Cat. No.: HY-176716
CAS No.: 2988020-77-3
Research Areas:  

Cardiovascular Disease

ALDH2 activator 1 (Compound Z17) is an allosteric aldehyde dehydrogenase 2 (ALDH2) agonist. ALDH2 activator 1 enhances cardiac function and reduces myocardial necrosis in a mouse model of myocardial ischemia-reperfusion. ALDH2 activator 1 is promising for research of cardiovascular diseases such as myocardial infarction (MI) .
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Cat. No.: HY-111937
CAS No.: 433311-07-0
Research Areas:  

Cancer

MI-1 inhibits Menin-MLL interaction with an IC50 of 1.9 μM [1].
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Cat. No.: HY-106262
CAS No.: 949100-39-4
Synonyms: KAI-9803; BMS-875944
Target:  

PKC

Delcasertib (KAI-9803) is a potent and selective δ-protein kinase C (δPKC) inhibitor. Delcasertib (KAI-9803) could ameliorate injury associated with ischemia and reperfusion in animal models of acute myocardial infarction (MI) .
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Cat. No.: HY-119350
CAS No.: 1448313-27-6
Synonyms: RUC-4
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

Zalunfiban (RUC-4) is a potent, selective platelet αIIbβ3 antagonist (IC50=45 nM). Zalunfiban can be used for the research of myocardial infarction (MI) .
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Cat. No.: HY-119350C
CAS No.: 2376629-15-9
Synonyms: RUC-4 acetate
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

Zalunfiban (RUC-4) acetate is a potent, selective platelet αIIbβ3antagonist (IC50=45 nM). Zalunfiban acetate can be used for the research of myocardial infarction (MI) .
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Cat. No.: HY-B1409R
CAS No.: 87-33-2
Synonyms: ISDN (Standard)
Research Areas:  

Cardiovascular Disease

Isosorbide dinitrate (Standard) is the analytical standard of Isosorbide dinitrate. This product is intended for research and analytical applications. Isosorbide dinitrate (ISDN) is an NO donor that prevents LV remodeling and degradation of cardiac function following myocardial infarction (MI) .
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Cat. No.: HY-B0592A
CAS No.: 87725-72-2
Synonyms: RU44570 hydrochloride
Trandolapril (RU44570) hydrochloride is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolapril hydrochlorideat. Trandolapril hydrochloride is an orally active angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .
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Cat. No.: HY-B0592R
CAS No.: 87679-37-6
Synonyms: RU44570 (Standard)
Trandolapril (Standard) is the analytical standard of Trandolapril. This product is intended for research and analytical applications. Trandolapril (RU44570) is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolaprilat. Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .
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Cat. No.: HY-W744298
Trandolapril-d3 is the deuterium labeled Trandolapril (HY-B0592). Trandolapril (RU44570) is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolaprilat. Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .
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Cat. No.: HY-B0592S2
Synonyms: rac-RU44570-d5
rac-Trandolapril-d5 (rac-RU44570-d5) is deuterium labeled Trandolapril. Trandolapril (RU44570) is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolaprilat. Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .
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Cat. No.: HY-19224
CAS No.: 153235-15-5
Synonyms: HR 720
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

Fonsartan (HR720) is an AT1 receptor antagonist. Fonsartan can be used for the study of myocardial infarction (MI) .
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Cat. No.: HY-P86925
Synonyms: Inositol-3-phosphate synthase 1 EC:5.5.1.4 IPS 1 Myo-inositol 1-phosphate synthase MI-1-P synthase M; IP : synthase hIPS Myo-inositol 1-phosphate synthase A1 hINO1 ISYNA1 Inositol-3-phosphate synthase 1 EC:5.5.1.4 IPS 1 Myo-inositol 1-phosphate synthase MI-1-P synthase M; IP : synthase hIPS Myo-inositol 1-phosphate synthase A1 hINO1 ISYNA1 INO1

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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