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 92

  1. Cat.No. Product Name Information/Activity
  2. BCC1863 Pitolisant hydrochloride Pitolisant hydrochloride is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM). Pitolisant hydrochloride chemical structure
  3. BCC7291 Carcinine ditrifluoroacetate 56897-53-1 Carcinine ditrifluoroacetate chemical structure
  4. BCC6781 Clobenpropit dihydrobromide Clobenpropit dihydrobromide is a potent histamine H3R antagonist/inverse agonist with a pEC50 of 8.07 for histamine H3LR. Clobenpropit dihydrobromide acts as partial agonist at histamine H4 receptors (Ki 13 nM). Clobenpropit dihydrobromide also binds to serotonin 5-HT3 receptors (Ki 7.4 nM) and α2A/α2C adrenoceptors (Ki 17.4/7.8 nM). Clobenpropit dihydrobromide increases apoptosis. Clobenpropit dihydrobromide chemical structure
  5. BCC7352 Conessine 546-06-5 Conessine chemical structure
  6. BCC7357 GT 2016 152241-24-2 GT 2016 chemical structure
  7. BCC7197 Impentamine dihydrobromide 149629-70-9 Impentamine dihydrobromide chemical structure
  8. BCC6793 Iodophenpropit dihydrobromide Iodophenpropit dihydrobromide is a potent and selective histamine H3 receptor antagonist. The binding of [125I]Iodophenpropit is selective, saturable, readily reversible, and of high affinity (KD 0.32 nM). Iodophenpropit dihydrobromide chemical structure
  9. BCC7842 JNJ 10181457 dihydrochloride 544707-20-2 JNJ 10181457 dihydrochloride chemical structure
  10. BCC6101 JNJ 5207852 dihydrochloride JNJ-5207852 is a selective and potent histamine H3 receptor (H3R) antagonist, with pKis of 8.9, 9.24 for rat and human H3R, respectively. JNJ 5207852 dihydrochloride chemical structure
  11. BCC7245 ROS 234 dioxalate 184576-87-2 ROS 234 dioxalate chemical structure

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