1-(1-(3-ethoxyphenyl)propyl)-7-(pyrimidin-5-ylmethoxy)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid manufacturers
- ATZ-1993
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- $2180.00
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2026-05-11
- CAS:219705-77-8
- Purity:
- Supply Ability: 10g
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| | 1-(1-(3-ethoxyphenyl)propyl)-7-(pyrimidin-5-ylmethoxy)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid Basic information |
| | 1-(1-(3-ethoxyphenyl)propyl)-7-(pyrimidin-5-ylmethoxy)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid Chemical Properties |
| Boiling point | 725.6±60.0 °C(Predicted) | | density | 1.30±0.1 g/cm3(Predicted) | | pka | 3.84±0.20(Predicted) |
| | 1-(1-(3-ethoxyphenyl)propyl)-7-(pyrimidin-5-ylmethoxy)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid Usage And Synthesis |
| Uses | ATZ-1993 is an orally active, nonpeptide endothelin receptor subtype Aand endothelin receptor subtype B antagonist with pKi values of 8.69, 7.20, respectively. ATZ-1993 has the potential for the research of intimal hyperplasia after balloon denudation of the carotid artery[1]. | | in vivo | ATZ-1993 (30 mg/kg; drinking water, daily for 1 week) inhibits the intimal hyperplasia intimal hyperplasia after balloon denudation[1]. | Animal Model: | Japanese White male rabbits[1] | | Dosage: | 30 mg/kg | | Administration: | Drinking water, daily for 1 weeks | | Result: | Inhibited the intimal hyperplasia with the inhibition rate approximately 77%, increased in intima:media ratio and DNA content. |
| | IC 50 | ETA: 8.69 (pKi); ETB: 7.20 (pKi) | | References | [1] Azuma H, et al. ATZ1993, an orally active and novel nonpeptide antagonist for endothelin receptors and inhibition of intimal hyperplasia after balloon denudation of the rabbit carotid artery. Jpn J Pharmacol. 1999 Sep;81(1):21-8. DOI:10.1254/jjp.81.21 |
| | 1-(1-(3-ethoxyphenyl)propyl)-7-(pyrimidin-5-ylmethoxy)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid Preparation Products And Raw materials |
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