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Indolidan

Catalog No. T32160   CAS 100643-96-7
Synonyms: LY 195115

Indolidan (LY 195115) induces cardiovascular and adrenal hyperplastic lesions in Fischer 344 rats. Indolidan increases the risk of cardiovascular disease.

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Indolidan Chemical Structure
Indolidan, CAS 100643-96-7
Pack Size Availability Price/USD Quantity
1 mg In stock $ 160.00
5 mg In stock $ 390.00
10 mg In stock $ 590.00
25 mg In stock $ 943.00
50 mg In stock $ 1,280.00
100 mg In stock $ 1,730.00
500 mg In stock $ 3,460.00
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Purity: 99.60%
Purity: 99.51%
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Biological Description
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Description Indolidan (LY 195115) induces cardiovascular and adrenal hyperplastic lesions in Fischer 344 rats. Indolidan increases the risk of cardiovascular disease.
In vivo Male and female Fischer 344 rats were treated with the positive inotropic agents, isomazole or indolidan, in the diet for 104 weeks. The doses were 0.0, 11.5, 23.5, or 48.0 mg/kg and 0.0, 0.12, 0.40, or 1.3 mg/kg, respectively. Only 17% of the males treated with 48.0 mg/kg isomazole survived the duration of the study. The male component of the indolidan study was terminated at 22 months, with only 18% of the high-dose males surviving. Sixty-five percent of the males treated with 48.0 mg/kg isomazole and 70% of the males treated with 1.3 mg/kg indolidan were found to have severe periarteritis, often with thrombi located mainly in the mesenteric arteries. Fifty-four percent of the male rats treated with 48.0 mg/kg isomazole and 55% of the male rats treated with 1.3 mg/kg indolidan died from cardiovascular disease compared to 1-2% among the control males. Animals in the low- and middle-dose groups of both studies had a lower incidence of cardiovascular disease than did those in the high-dose group. Additional lesions associated with the long-term administration of both drugs were markedly increased incidence of adrenal medullary proliferative lesions (both hyperplasia and pheochromocytomas) and increased incidence of chronic progressive glomerulonephrosis. These lesions, like those in the cardiovascular system, occurred in a dose-dependent manner and were more frequent in males than in females.[5]
Synonyms LY 195115
Molecular Weight 257.29
Formula C14H15N3O2
CAS No. 100643-96-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Haynes J Jr, et al. 5-(N-ethylcarboxamido)adenosine desensitizes the A2b-adenosine receptor in lung circulation. Am J Physiol. 1999;276(6):1877-1883. 2. Naka Y, et al. cAMP-mediated vascular protection in an orthotopic rat lung transplant model. Insights into the mechanism of action of prostaglandin E1 to improve lung preservation. Circ Res. 1996;79(4):773-783. 3. Ashikaga T, et al. Comparison of indolidan analog binding sites of drug antibody and sarcoplasmic reticulum with inhibition of cyclic AMP phosphodiesterase. J Recept Signal Transduct Res. 1996;16(5-6):315-337. 4. Rousseau E, et al. Specific cyclic nucleotide phosphodiesterase inhibitors differently modulate contractile kinetics in airway smooth muscle. Can J Physiol Pharmacol. 1995;73(12):1784-1794. 5. Sandusky GE Jr, et al. Cardiovascular and adrenal proliferative lesions in Fischer 344 rats induced by long-term treatment with type III phosphodiesterase inhibitors (positive inotropic agents), isomazole and indolidan. Fundam Appl Toxicol. 1991;16(1):198-209. 6. Corder CN, et al. Clinical effect of indolidan in congestive heart failure. Int J Clin Pharmacol Ther Toxicol. 1992;30(10):405-409.

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Keywords

Indolidan 100643-96-7 LY 195115 LY195115 LY-195115 inhibitor inhibit

 

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