Name | N-[2(S)-(acetylhtiomethyl)-3-(2-methylphenyl)-1-oxopropyl]-L-methionine ethyl ester |
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Synonyms |
N-(2(S)-(ACETYLTHIOMETHYL)-3-(2-METHYLPHENYL)-1-OXOPROPYL)-L-METHIONINE ETHYL ESTER
N-[2(S)-acetylthiomethyl-3-(2-methylphenyl)propionyl]-(S)-methionine ethyl ester |
Description | SCH 42495 is an orally active neutral metalloendopeptidase (NEP) inhibitor with antihypertensive effect. SCH 42495 is the orally active ethylester prodrug of SCH 42354[1]. |
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Related Catalog | |
Target |
NEP[1] |
In Vitro | SCH 42354 selectively inhibits hydrolysis of leu-enkephalin and ANF (IC50 of 8.3 and 10.0 nM, respectively) in vitro[1]. |
In Vivo | SCH 42495 (30 mg/kg; oral gavage; twice daily) causes a significant reduction in the pulmonary vascular remodelling and ventricular hypertrophy in hypoxic rats after 10 days[2]. Treatment with SCH 42495 (30 mg/kg; oral gavage; twice daily) leads to a decrease in cardiovascular remodelling secondary to chronic hypoxia in rats[2]. SCH 42495 (oral doses of 1, 3, or 10 mg/kg) produces significant reductions in blood pressure in DOCA-N a hypertensive rats of 22±6, 43±7, and 62±12 mm Hg, respectively[1]. Animal Model: Hypoxic rats[2] Dosage: 30 mg/kg Administration: Oral gavage; twice daily for 10 days Result: Caused a significant reduction in the pulmonary vascular remodelling and ventricular hypertrophy. Led to a decrease in cardiovascular remodelling secondary to chronic hypoxia. |
References |
Molecular Formula | C20H29NO4S2 |
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Molecular Weight | 411.57900 |
Exact Mass | 411.15400 |
PSA | 123.07000 |
LogP | 3.62530 |