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J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788 |
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Products Intro: |
Product Name:Avosentan CAS:290815-26-8 Package:100Mg,10Mg
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| avosentan Basic information |
Product Name: | avosentan | Synonyms: | N-(6-Methoxy-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)-pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide;N-(6-Methoxy-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)-pyrimidin-4-yl)-5-methylpyridine-2-sulfonam;2-Pyridinesulfonamide,N-[6-methoxy-5-(2-methoxyphenoxy)-2-(4-pyridinyl)-4-pyrimidinyl]-5-methyl-;avosentan;N-[6-Methoxy-5-(2-methoxyphenoxy)-2-(4-pyridinyl)-4-pyrimidinyl]-5-methyl-2-pyridinesulfonamide;Ro 67-0565;SPP-301;Avosentan (SPP301) | CAS: | 290815-26-8 | MF: | C23H21N5O5S | MW: | 479.51 | EINECS: | | Product Categories: | | Mol File: | 290815-26-8.mol | |
| avosentan Chemical Properties |
Boiling point | 575.5±60.0 °C(Predicted) | density | 1.363 | storage temp. | Store at -20°C | solubility | DMSO : 6.67 mg/mL (13.91 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble) | form | Powder | pka | 3.19±0.10(Predicted) |
| avosentan Usage And Synthesis |
Uses | Avosentan is a competitive antagonist of Endothelin-1 (ET-1) with a high selectivity for the ETA receptor. Avosentan may be a potential option in the treatment of glaucoma. | Enzyme inhibitor | This potent, selective and orally available endothelin A receptor blocker (FW = 479.51 g/mol; CAS 290815-26-8; Soluble in DMSO), also known by its code names SPP301 and Ro 67-0565, induces the dose-dependent reduction in the fractional renal excretion of sodium (up to 8.7% at 50 mg avosentan), with a paralleled dose-related increase in proximal sodium reabsorption. Avosentan reduces albuminuria, when added to standard treatment in patients with type 2 diabetes and overt nephropathy, but induces significant fluid overload and congestive heart failure. |
| avosentan Preparation Products And Raw materials |
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