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 51

  1. Cat.No. Product Name Information/Activity
  2. BCC5614 CKI 7 dihydrochloride 1177141-67-1 CKI 7 dihydrochloride chemical structure
  3. BCN2964 Cyclopamine Cyclopamine is a Hedgehog (Hh) pathway antagonist with an IC50 of 46 nM in the Hh cell assay. Cyclopamine chemical structure
  4. BCC3618 DAPT (GSI-IX) DAPT (GSI-IX) is a potent and orally active γ-secretase inhibitor with IC50s of 115 nM and 200 nM for total amyloid-β (Aβ) and Aβ42, respectively. DAPT inhibits the activation of Notch 1 signaling and induces cell differentiation. DAPT also induces autophagy and apoptosis. DAPT has neuroprotection activity and has the potential for autoimmune and lymphoproliferative diseases, degenerative disease and cancers treatment. DAPT (GSI-IX) chemical structure
  5. BCC1184 Dexamethasone (DHAP) Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18L expression on monocytes. Dexamethasone (DHAP) chemical structure
  6. BCC8079 Dibutyryl-cAMP, sodium salt Bucladesine sodium salt (Dibutyryl-cAMP sodium salt) is a stabilized cyclic AMP (cAMP) analog and a selective PKA activator. Bucladesine sodium salt raises the intracellular levels of cAMP. Bucladesine sodium salt is also a phosphodiesterase (PDE) inhibitor. Bucladesine sodium salt has anti-inflammatory activity and can be used for impaired wound healing. Dibutyryl-cAMP, sodium salt chemical structure
  7. BCC5329 DMH-1 DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/107.9/<5/47.6 nM for ALK1/ALK2/ALK3/ALK6, respectively. DMH-1 chemical structure
  8. BCC4361 Dorsomorphin 2HCl Dorsomorphin dihydrochloride (Compound C dihydrochloride) is a potent, selective and ATP-competitive AMPK inhibitor, with a Ki of 109 nM. Dorsomorphin dihydrochloride inhibits BMP pathway by targeting the type I receptors ALK2, ALK3, and ALK6. Dorsomorphin dihydrochloride induces autophagy. Dorsomorphin 2HCl chemical structure
  9. BCC6904 1-EBIO 10045-45-1 1-EBIO chemical structure
  10. BCC6097 EC 23 EC23 (AGN 190205) is a stable synthetic retinoid analogue and induces neuronal differentiation. EC 23 chemical structure
  11. BCC5341 FH1(BRD-K4477) FH1(BRDK4477) is a small molecule that can enhance the functions of cultured hepatocytes. FH1(BRD-K4477) chemical structure

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