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 1657 - 1664 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6059 | 4,4-Pentamethylenepiperidine hydrochloride |
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M2 proton channel blocker (IC<sub>50</sub> = 0.92 <span class='symbol'>μ</span>M). Inhibits influenza virus M2 protein (AM2).
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| BCC6060 | MDL 72527 |
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Polyamine oxidase (POA) inhibitor. Does not inhibit monoamine oxidase or D-Amino acid oxidase. Displays anticancer and neuroprotective activity in vivo.
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| BCC6061 | Boc-MLF |
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Antagonist of formyl peptide receptor 1 (FPR1). Reduces superoxide production induced by fMLF with an EC<sub>50</sub> of 0.63 <span class='symbol'>μ</span>M. Almost completely blocks fMLF-stimulated primary granule exocytosis.
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| BCC6062 | GSK 264220A |
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Endothelial lipase and lipoprotein lipase inhibitor (IC<sub>50</sub> values are 0.13 and 0.10 <span class='symbol'>μ</span>M respectively).
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| BCC6063 | CP 20961 |
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Non-immunogenic adjuvant; used to induce arthritis in Lewis (LEW) and DA rats.
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| BCC6064 | DADLE |
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Prototypical <span class='symbol'>δ</span>-opioid receptor agonist that also displays activity at the <span class='symbol'>μ</span>-opioid receptor. Displays antinociceptive activity <em>in vivo</em>.
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| BCC6065 | Hemopressin (human, mouse) |
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Bioactive endogenous peptide substrate for endopeptidase 24.15 (ep24.15), neurolysin (ep24.16) and ACE. K<sub>i</sub> values are 27.76, 3.43 and 1.87 <span class='symbol'>μ</span>M respectively. Potent hypotensive <em>in vivo</em>. Also acts as a selective CB<sub>1</sub> receptor inverse agonist. Displays antinociceptive activity <em>in vivo</em>.
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| BCC6066 | ITX3 |
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Selective inhibitor of TrioN RhoGEF activity. Inhibits TrioN-mediated GTP exchange on RhoG and Rac1, formation of TrioN-induced cellular structures in REF52 fibroblasts and NGF-mediated neurite outgrowth in PC12 cells in vitro.
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