Hot Natural Products & Bioactive Compounds
BioCrick offers high-purity natural products and bioactive compounds for scientific research. Our natural product collection includes compounds derived from plants, microorganisms and other biological sources and is widely used in pharmacological, biochemical and drug discovery research.
Natural products remain an important source of bioactive molecules and drug leads. BioCrick provides researchers with high-quality natural product compounds together with catalog numbers, product information and biological activity data.
Hot Products from BioCrick
Showing 1009 - 1016 of 9359 hot products
| Catalog No. | Product Name |
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| BCC4897 | CCG 50014 |
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Potent and selective inhibitor of regulator of G-protein signaling 4 (RGS4) protein (IC<sub>50</sub> values are 30.1 nM and 11.0 <span class='symbol'>μ</span>M for RGS4 and RGS8 respectively). Exhibits >20-fold selectivity for RGS4 over other RGS proteins.
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| BCC4899 | Ciclopirox |
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Pan-histone demethylase inhibitor. Exhibits no significant effect on histone deacetylases. Inhibits MYC-signaling and proliferation of neuroblastoma cells. Promotes Cdc25A-degradation in cancer cells. Antifungal.
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| BCC4901 | Diltiazem HCl |
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Antihypertensive and cardioprotective agent; an inhibitor of L-type Ca2+ channels.
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| BCC4902 | Doxercalciferol |
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Vitamin D<sub>2</sub> analog that acts as a vitamin D receptor activator (VDRA).
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| BCC4904 | Felbamate |
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Anticonvulsant, acting as an antagonist at the NMDA-associated glycine binding site.
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| BCC4905 | Fluconazole |
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Triazole antifungal agent. Effective against Candida strains in vitro and in vivo.
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| BCC4907 | Fluticasone propionate |
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High affinity, selective glucocorticoid receptor agonist (K<sub>d</sub> = 0.5 nM). Potently stimulates glucocorticoid receptor-mediated transactivation of gene expression and enhances human eosinophil apoptosis (EC<sub>50</sub> = 3.7 nM) <em>in vitro</em>. Inhibits mast cell accumulation in nasal mucosa following topical administration. Lipophilic anti-inflammatory agent with low oral bioavailability. Also potentiates K<sub>V</sub>1 channels (EC<sub>50</sub> = 37 nM).
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| BCC4910 | HC-030031 |
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Selective TRPA1 channel blocker that antagonizes AITC- and formalin-evoked calcium influx (IC<sub>50</sub> values are 6.2 and 5.3 <span class='symbol'>μ</span>M respectively). Does not block currents mediated by TRPV1, TRPV3, TRPV4, hERG or Na<sub>V</sub>1.2 channels. Inhibits AITC- and formalin-induced flinching <em>in vivo</em>.
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