CAS No. : 1234365-97-9
(Synonyms: AZD1722 (hydrochloride); RDX5791 (hydrochloride))
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| 10mg | $145 | In-stock |
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| 100mg | $698 | In-stock |
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| Cat. No. : | HY-15991A |
| M.Wt: | 1217.97 |
| Formula: | C50H68Cl6N8O10S2 |
| Purity: | >98 % |
| Solubility: | DMSO : 100 mg/mL (ultrasonic);H2O : 20 mg/mL (ultrasonic) |
Tenapanor (AZD1722) hydrochloride is a potent and orally active sodium/hydrogen exchanger isoform 3 (NHE3) inhibitor. Tenapanor hydrochloride reduces intestinal phosphate absorption predominantly through reduction of passive paracellular phosphate flux. Tenapanor hydrochloride has the potential for the research of hyperphosphatemia[1][2].
In Vivo: Tenapanor hydrochloride (0.15, 0.5 mg/kg; p.o.) reduces passive paracellular phosphate absorption in rats[1].
Tenapanor hydrochloride (0.15 mg/kg; p.o.; twice-daily for 11 consecutive days) increases the reduction in urinary phosphorus excretion in rats[2].
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