Cardiovascular Research

The cardiovascular, or circulatory, system is a closed elastic circuit consisting of the heart, blood vessels (arteries, capillaries and veins) and the blood. The primary function is to pump oxygenated blood to the tissues throughout the body and reabsorb waste carbon dioxide for its removal. This function is performed by the use of pulmonary and systemic circulation.

Cardiovascular Research Products Areas

Products for Cardiovascular Research - Page 99

  1. Cat.No. Product Name Information/Activity
  2. BCC2358 Ac-IEPD-AFC Ac-IEPD-AFC (IEPD) is a substrate of Granzyme B. Ac-IEPD-AFC chemical structure
  3. BCC2359 Ac-LEHD-AFC 210345-03-2 Ac-LEHD-AFC chemical structure
  4. BCC3600 PAC-1 PAC-1 is an activator of procaspase-3 induces apoptosis in cancer cells with EC50 of 2.08 μM. PAC-1 chemical structure
  5. BCC2360 PETCM PETCM is an activator of caspase-3 and acts as an cytochrome c (cyto c)-dependent manner. PETCM promotes Apaf-1 oligomerization and induces cell apoptosis in HeLa cells. PETCM chemical structure
  6. BCN2678 Embelin Embelin is a cell-permeable benzoquinone compound that exhibits antitumor properties. Embelin chemical structure
  7. BCC8042 UC 112 UC-112 is a novel potent IAP(Inhibitor of apoptosis) inhibitor; potently inhibit cell growth in two human melanoma (A375 and M14) and two human prostate (PC-3 and DU145) cancer cell lines(IC50=0.7-3.4 uM). UC 112 chemical structure
  8. BCN5984 Triptolide Triptolide is a diterpenoid triepoxide extracted from the root of Tripterygium wilfordii with immunosuppressive, anti-inflammatory and antiproliferative effects. Triptolide is a NF-κB activation inhibitor. Triptolide chemical structure
  9. BCC2241 Pifithrin-α (PFTα) Pifithrin-α hydrobromide is a p53 inhibitor which blocks its transcriptional activity and prevents cells from apoptosis. Pifithrin-α hydrobromide is also an aryl hydrocarbon receptor (AhR) agonist. Pifithrin-α (PFTα) chemical structure
  10. BCC2407 Cyclic Pifithrin-α hydrobromide Pifithrin-β hydrobromide (PFT β hydrobromide) is a potent p53 inhibitor with an IC50 of 23 μM. Cyclic Pifithrin-α hydrobromide chemical structure
  11. BCC2412 Pifithrin-μ Pifithrin-μ is an inhibitor of p53 and HSP70, with antitumor and neuroprotective activity. Pifithrin-μ chemical structure

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