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1-[3-Cyano-4-(2,2-dimethyl-propoxy)-phenyl]-1H-pyrazole-4-carboxylic acid manufacturers
- Niraxostat
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- $127.00
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2026-04-20
- CAS:206884-98-2
- Purity: 98.13%
- Supply Ability: 10g
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| | 1-[3-Cyano-4-(2,2-dimethyl-propoxy)-phenyl]-1H-pyrazole-4-carboxylic acid Basic information |
| | 1-[3-Cyano-4-(2,2-dimethyl-propoxy)-phenyl]-1H-pyrazole-4-carboxylic acid Chemical Properties |
| Boiling point | 500.5±45.0 °C(Predicted) | | density | 1.20±0.1 g/cm3(Predicted) | | pka | 3.68±0.10(Predicted) | | form | Solid | | color | White to off-white |
| | 1-[3-Cyano-4-(2,2-dimethyl-propoxy)-phenyl]-1H-pyrazole-4-carboxylic acid Usage And Synthesis |
| Uses | Niraxostat (Y-700; Piraxostat) is an orally active xanthine oxidoreductase (XOR) inhibitor used in the study of hyperuricemia and other diseases in which XOR may be involved[1]. | | in vivo | Niraxostat (Y-700; 1 mg/kg) has high oral bioavailability (84.1%) and is almost not excreted through the kidneys. It is mainly eliminated through the liver[1]. Niraxostat (Y- 700; 1-10 mg/kg; oral; single dose) dose-dependently reduces plasma urate levels in oxonate-treated rats [1]. Niraxostat (Y-700 ; 0.3-3 mg/kg; Oral; Single dose) In normal rats, dose-dependently reduces urinary excretion of urate and allantoin while increasing excretion of hypoxanthine and xanthine [1].
Pharmacokinetic Analysis of Niraxostat (Y-700) in normal rats[1]
| Route | Dose (mg/kg) | tmax (h) | Cmax (μg/ml) | AUC0-∞ (μg/h/ml) | t1/2 (h) | | PO | 0.3 | 0.5 | 0.43 | 2.07 | 5.0 | | PO | 1 | 0.3 | 1.8 | 7.01 | 3.2 | | PO | 3 | 0.5 | 6.49 | 30.31 | 2.7 | | IV | 1 | / | 3.97 | 8.34 | 2.5 |
| | References | [1] Fukunari A, et al. Y-700 [1-[3-Cyano-4-(2,2-dimethylpropoxy)phenyl]-1H-pyrazole-4-carboxylic acid]: a potent xanthine oxidoreductase inhibitor with hepatic excretion. J Pharmacol Exp Ther. 2004 Nov;311(2):519-28. DOI:10.1124/jpet.104.070433 |
| | 1-[3-Cyano-4-(2,2-dimethyl-propoxy)-phenyl]-1H-pyrazole-4-carboxylic acid Preparation Products And Raw materials |
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