About 9 results found for searched term "56-12-2" (0.06 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M4767 | aurantiamide-acetate | Cathepsin |
| Aurantiamide acetate is a selective and orally active cathepsin inhibitor isolated from Portulaca Oleracea L. Aurantiamide acetate has anti-inflammatory activity and can be used to study inflammatory diseases. | ||
| M4859 | Valrubicin | PKC |
| AD-32 | ||
| Valubicin (AD-32) is a chemotherapeutic compound for bladder cancer. | ||
| M14214 | γ-Aminobutyric acid | GABA Receptor |
| 4-Aminobutyric acid | ||
| γ-Aminobutyric acid (4-Aminobutyric acid) is a major inhibitory neurotransmitter in the adult mammalian brain, binding to the ionotropic GABA receptors (GABAA receptors) and metabotropic receptors (GABAB receptors). | ||
| M19383 | Aegeline | Antifungal |
| Aegeline, a main alkaloid, mimics the yeast SNARE protein Sec22p in suppressing α-synuclein and Bax toxicity in yeast. Aegeline restores growth of yeast cells suppressed by either αsyn or Bax. Antioxidant activity. | ||
| M20473 | Dolasetron | 5-HT Receptor |
| MDL-73147 | ||
| Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy. | ||
| M21037 | HPK1-IN-2 | Serine/Threonine Protease |
| HPK1-IN-2 is a potent and orally active inhibitor of hematopoietic progenitor kinase-1 (HPK1, a serine/threonine Ste20-related protein kinase), Lck and Flt3 with IC50 of <0.05 μM, IC50 of <0.5 μM and IC50 of <0.05 μM, respectively. HPK1-IN-2 exhibits antitumor activity. | ||
| M24616 | Seribantumab | EGFR/HER2 |
| SAR 256212; MM 121; Anti-Human ERBB3/ErbB 3 Recombinant Antibody | ||
| Seribantumab (MM 121) is a fully human IgG2 monoclonal antibody that targets HER3. Seribantumab blocks the activation of epidermal growth factor receptor (ErbB) family members and its downstream signal. Seribantumab inhibits neuregulin 1 (NRG1) fusion-dependent tumorigenesis in vitro and in vivo in breast, lung and ovarian patient-derived cancer models. | ||
| M29801 | Tutuilamide A | Elastase |
| Tutuilamide A is a potent porcine pancreatic elastase (PPE) inhibitor, with an IC50 of 1.2 nM. Tutuilamide A also inhibits human neutrophil elastase (HNE; IC50=0.73 nM) and kallikrein 7 (KLK7; IC50=5.0 nM). | ||
| M39970 | Vinaginsenoside R3 | Others |
| Vinaginsenoside R3 is a saponin composition of roots of Panax ginseng. Ginsengs have been not only used as therapeutic agents with tonic, anti-fatigue, and anti-gastric ulcer effect but also marketed as dietary supplements and raw materials of health food. | ||
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