About 7 results found for searched term "55-98-1" (0.119 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3356 | Busulfan | DNA Alkylator/Crosslinker |
| Busulfan is a cell cycle non-specific alkylating antineoplastic agent. Busulfan causes DNA damage by cross-linking DNAs and DNA and proteins. Busulfan also inhibits thioredoxin reductase. | ||
| M3433 | Nitazoxanide | Anti-infection |
| NTZ; NSC 697855 | ||
| Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent (IC50 for canine influenza virus ranges from 0.17 to 0.21 μM). | ||
| M7127 | PFM 01 | Others |
| PFM 01 is a mRE11 endonuclease inhibitor. | ||
| M11284 | Cetaben | Others |
| Cetaben is a PPARα -independent peroxisome proliferator that can effectively reduce cholesterol and triglyceride concentrations. | ||
| M2051 | CP 945598 hydrochloride | Cannabinoid |
| Otenabant HCl; Otenabant hydrochloride | ||
| CP 945598 hydrochloride is a selective and high affinity CB1 antagonist (Ki values are 0.7 and 0.12 nM in binding and functional assays respectively). | ||
| M2552 | Otenabant | Cannabinoid |
| CP-945598; CP945598 | ||
| Otenabant (CP-945598) is a selective, high affinity, competitive CB1 receptor antagonist with Ki of 0.7 nM. | ||
| M21290 | BMS-986144 | HCV Protease |
| BMS-986144 is a third generation pan-genotypic NS3/4A protease inhibitor.BMS-986144 inhibits GT-1a, GT-1b, GT-2a, GT-3a, 1a R155X, 1b D168V replicon with EC50 values of 2.3, 0.7, 1.0, 12, 8.0, 5.8 nM, respectively.BMS-986144 has the potential to study HCV infection. | ||
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