Stroke Research

Stroke is classified as both a neurological and a cardiovascular disease, as it is a disruption in blood supply to the brain which causes the neurological abnormalities. There are two types of stroke; ischemic and hemorrhagic.

Stroke Research Products Targets

Products for Stroke Research - Page 8

  1. Cat.No. Product Name Information/Activity
  2. BCC2515 Zileuton Zileuton is a potent and selective inhibitor of 5-lipoxygenase with antiasthmatic properties. Zileuton chemical structure
  3. BCC5843 Atrial natriuretic factor (1-28) (rat) Atrial Natriuretic Peptide (ANP) (1-28), rat is a major circulating form of ANP in rats, potently inhibits Angiotensin II (Ang II)-stimulated endothelin-1 secretion in a concentration-dependent manner. Atrial natriuretic factor (1-28) (rat) chemical structure
  4. BCC5839 Atrial natriuretic factor (1-28) (human, porcine) 91917-63-4 Atrial natriuretic factor (1-28) (human, porcine) chemical structure
  5. BCC6034 Brain natriuretic peptide (1-32) (human) Nesiritide (Brain Natriuretic Peptide-32 human) is an agonist of natriuretic peptide receptors (NPRs), with Kd values of 7.3 and 13 pM for NPR-A and NPR-C, respectively. Brain natriuretic peptide (1-32) (human) chemical structure
  6. BCC6033 C-type natriuretic peptide (1-22) (human, rat, swine) C-Type Natriuretic Peptide (CNP) (1-22), human is the 1-22 fragment of C-Type Natriuretic Peptide. C-type natriuretic peptide is natriuretic peptide family peptide that is involved in the maintenance of electrolyte-fluid balance and vascular tone. C-type natriuretic peptide (1-22) (human, rat, swine) chemical structure
  7. BCC7068 BMY 45778 Non-prostanoid prostacyclin IP receptor partial agonist BMY 45778 chemical structure
  8. BCC7315 (±)-Cloprostenol sodium salt Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist. (±)-Cloprostenol sodium salt chemical structure
  9. BCC7843 16,16-Dimethyl Prostaglandin E2 16,16-Dimethyl prostaglandin E2 (16,16-dimethyl PGE2) is an orally active vertebrate Hematopoietic stem cells (HSCs) homeostasis critical regulator. 16,16-Dimethyl prostaglandin E2 can act through EP2/EP4 and has an interaction with the Wnt pathway. 16,16-Dimethyl Prostaglandin E2 chemical structure
  10. BCC7534 Epoprostenol Epoprostenol sodium (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH). Epoprostenol sodium is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation. Epoprostenol chemical structure
  11. BCC7247 Iloprost Iloprost (ZK 36374) is a synthetic analogue of prostacyclin PGI2. Iloprost chemical structure

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