About 4 results found for searched term "PU-48" (0.12 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M42271 | PU-48 | Others |
| PU-48 is a potent urea transporters A (UT-A) inhibitor (IC50=0.32 μM). | ||
| M10482 | Forodesine hydrochloride | DNA/RNA Synthesis |
| BCX-1777 hydrochloride | ||
| Forodesine hydrochloride is a potent and orally active transition-state analog inhibitor of purine nucleoside phosphorylase, with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. | ||
| M13700 | Forodesine | DNA/RNA Synthesis |
| BCX-1777; Immucillin-H | ||
| Forodesine (BCX-1777) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. | ||
| M31284 | Puliginurad | URAT1 |
| YL-90148 | ||
| Puliginurad (YL-90148) is a potent, selective inhibitor of urate transporter protein (URAT) that can be used in studies related to hyperuricemia and gout by inhibiting the reabsorption of uric acid at the renal proximal tubule, thereby excreting more uric acid through the urine. | ||
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