L-type and N-type Ca2+ channel blocker used to treat hypertension. It also improves insulin sensitivity, suppresses nociception, and inhibits progression of glomerulonephritis. (C003B-255778)

Cilnidipine is a dihydropyridine that exhibits antihypertensive, vasodilatory, antinociceptive, and nephroprotective activities. Cilnidipine acts as an antagonist at L-type and N-type voltage-gated Ca2+ channels. In subjects with hypertension, cilnidipine decreases blood pressure and urinary albumin excretion. Cilnidipine also increases expression of eNOS ex vivo in thoracic arteries. In animal models of non insulin-dependent diabetes, cilnidipine improves insulin sensitivity, indicating potential anti-diabetic activity as well. This compound inhibits nociception in animal models undergoing the formalin test. Additionally, in vitro, cilnidipine decreases production of AP-1, TGF-ß, and fibronectin, inhibiting proliferation of mesangial cells; in similar animal models, cilnidipine inhibits progression of glomerulonephritis. Grade: ≥98%

UPC:

51433912

Condition:

New

Weight:

1.00 Ounces

HazmatClass:

No

Quantity:

1

Unit of Measurement:

EA

WeightUOM:

LB

MPN:

C3446-250 mg

CAS:

132203-70-4