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 67

  1. Cat.No. Product Name Information/Activity
  2. BCC6351 GMQ hydrochloride 5361-15-9 GMQ hydrochloride chemical structure
  3. BCC6054 Neuropeptide SF (mouse, rat) 230960-31-3 Neuropeptide SF (mouse, rat) chemical structure
  4. BCC6294 APETx2 713544-47-9 APETx2 chemical structure
  5. BCC1451 Capsazepine Capsazepine is a synthetic analogue of the sensory neurone excitotoxin, and an antagonist of TRPV1 receptor with an IC50 of 562 nM. Capsazepine chemical structure
  6. BCC7673 Phenamil 1161-94-0 Phenamil chemical structure
  7. BCC7515 Veratridine Veratridine (3-Veratroylveracevine), a alkaloid derived from plants in the family Liliaceae, is a sodium channel agonist. Veratridine inhibits the peak current of Nav1.7, with an IC50 of 18.39 µM. Veratridine chemical structure
  8. BCC5075 A-803467 A 803467 is a selective Nav1.8 sodium channel blocker with an IC50 of 8 nM; over 100-fold more selective vs. human Nav1.2, 1.3, 1.5 and 1.7. A-803467 chemical structure
  9. BCC7898 A 887826 A-887826 is a potent, selective, oral bioavailable and voltage-dependent Na(v)1.8 sodium channel blocker with an IC50 of 11 nM . A-887826 attenuates neuropathic tactile allodynia in vivo. A 887826 chemical structure
  10. BCC5067 Ambroxol HCl Na<sup>+</sup> channel blocker,AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. Phase 3. Ambroxol HCl chemical structure
  11. BCC4378 Carbamazepine Carbamazepine, a sodium channel blocker, is an anticonvulsant drug. Carbamazepine chemical structure

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