QNSWMJYOGMUVGO-REWXTUPXSA-N

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QNSWMJYOGMUVGO-REWXTUPXSA-N Basic information
Product Name:QNSWMJYOGMUVGO-REWXTUPXSA-N
Synonyms:QNSWMJYOGMUVGO-REWXTUPXSA-N
CAS:87725-72-2
MF:C24H35ClN2O5
MW:466.9981
EINECS:
Product Categories:
Mol File:87725-72-2.mol
QNSWMJYOGMUVGO-REWXTUPXSA-N Structure
QNSWMJYOGMUVGO-REWXTUPXSA-N Chemical Properties
Safety Information
MSDS Information
QNSWMJYOGMUVGO-REWXTUPXSA-N Usage And Synthesis
UsesTrandolapril Hydrochloride is an antihypertensive. Angiotensin converting enzyme (ACE) inhibitor.
in vivo

Trandolapril hydrochloride (3 mg/kg/day; p.o.; 7 d) reduces renal fibrosis in obstructive nephropathy in mice, by inhibiting renal interstitial matrix expression and myofibroblast activation, decreasing renal proinflammatory cytokine RANTES and TNF-α level[2].
Trandolapril hydrochloride (0.3 mg/kg/day; p.o.; 4 weeks) improves arterial mechanics in rats, prevents arterial hypertrophy, collagen and cellular fibronectin accumulation[3].
randolapril (0.3 mg/kg/day; p.o.; 4 months) exhibits a chronic anti-hypertension effects in rats, results in blood pressure decreasing[3].
Trandolapril hydrochloride (0.25 mg/kg; p.o.; twice a day; 4 months) inhibits Atherosclerosis in the Watanabe Heritable Hyperlipidemic Rabbit[4].

Animal Model:UUD (unilateral ureteral obstruction) model in Male CD-1 mice (18-22 g)[2]
Dosage:3 mg/kg
Administration:Oral gavage; daily, for 7 days
Result:Resulted in renal interstitial matrix expression (including fibronectin, type I, and type III collagen) decreasing, and inhibited myofibroblast activation by surprising a-smooth muscle actin (a-SMA) expression, decreased the RANTES (regulated on activation, normal T cell expressed and secreted) and TNF-α level.
Animal Model:SHR model (spontaneously hypertensive rats, 4-week-old)[3]
Dosage:0.3 mg/kg
Administration:Oral gavage; daily for 4 weeks
Result:Reduced collagen content in the aortic media and increased ariterial distensibility up to about 80%.
Animal Model:Watanabe heritable hyperlipidemic rabbit (3 months old)[4]
Dosage:0.25 mg/kg
Administration:Oral gavage; twice a day; 9 months
Result:Decreased in atherosclerotic involvement of the intimal surface, and also decreased cholesterol content in descending thoracic aorta.
QNSWMJYOGMUVGO-REWXTUPXSA-N Preparation Products And Raw materials
Tag:QNSWMJYOGMUVGO-REWXTUPXSA-N(87725-72-2) Related Product Information
QRFINCSKCRZION-WSZWBAFRSA-N PZPATWACAAOHTJ-CGLOQUBRSA-N QISHTWCSIVFJBU-UHFFFAOYSA-N QSIBSYLVSFILGA-RHQRLBAQSA-N Pyrrolo[1,2-f][1,2,4]triazin-4-amine JG26