Myocardial Infarction Research

Myocardial infarction (MI) - more commonly referred to as a heart attack - is an acute event caused by the interruption of blood supply to regions of the heart, leading to myocardial necrosis. Infarction of a substantial area of the myocardium can disrupt normal conductance of the heart, leading to cardiac arrest.In the majority of cases, an MI is immediately preceded by the presence of an occlusive thrombus within a coronary artery, blocking blood flow to the downstream tissue. The most common cause of an occlusive thrombus within a coronary artery is the rupture of an atherosclerotic plaque. However, the occlusion of a coronary artery may also result from coronary embolism. This can occur in patients following stent placement, angioplasty, and coronary artery bypass grafting.

Myocardial Infarction Research Products Targets

Products for Myocardial Infarction Research - Page 28

  1. Cat.No. Product Name Information/Activity
  2. BCC7181 SR 33805 oxalate 121346-33-6 SR 33805 oxalate chemical structure
  3. BCC4747 Verapamil HCl Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel antagonist. Verapamil HCl chemical structure
  4. BCN2207 Ascorbic acid PROTAC EED degrader-1 is a PROTAC targeting EED with a pKD of 9.02. PROTAC EED degrader-1 is a polycomb repressive complex 2 (PRC2) inhibitor (pIC50=8.17) targeting the EED subunit. Ascorbic acid chemical structure
  5. BCC3783 Gabapentin Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. Gabapentin chemical structure
  6. BCN2175 Pregabalin 148553-50-8 Pregabalin chemical structure
  7. BCC6689 L-NIO dihydrochloride L-NIO dihydrochloride is a potent, non-selective and NADPH-dependent nitric oxide synthase (NOS) inhibitor, with Kis of 1.7, 3.9, 3.9 μM for neuronal (nNOS), endothelial (eNOS), and inducible (iNOS), respectively. L-NIO dihydrochloride induces a consistentfocal ischemic infarctin rats. L-NIO dihydrochloride chemical structure
  8. BCC6795 Aminoguanidine hydrochloride Aminoguanidine hydrochloride is a diamine oxidase and NO synthase inhibitor, reduces levels of advanced glycation end products (AGEs) through interacting with 3-deoxyglucosone, is an investigational drug for the treatment of diabetic nephropathy. Aminoguanidine hydrochloride chemical structure
  9. BCC6823 AMT hydrochloride 21463-31-0 AMT hydrochloride chemical structure
  10. BCC6092 AR-C 102222 253771-21-0 AR-C 102222 chemical structure
  11. BCC7506 BYK 191023 dihydrochloride Potent and selective inhibitor of iNOS BYK 191023 dihydrochloride chemical structure

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