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 2209 - 2216 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6761 | Aminopotentidine |
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H2 antagonist (KB values are 220 and 280 nM at human and guinea pig H2 receptors respectively) and precursor for the synthesis of the [125I]-iodo derivative.
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| BCC6762 | N-Acetyl-N-acetoxy-4-chlorobenzenesulfonamide |
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A pro-drug of the potent vasorelaxant nitroxyl, H-N=O, which it slowly releases in neutral solution. HNO eventually dimerizes and dehydrates to N2O, without producing NO. Also a powerful inhibitor of aldehyde dehydrogenase.
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| BCC6763 | Tetrindole mesylate |
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Novel antidepressant, a selective inhibitor of MAO-A.
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| BCC6764 | Pirlindole mesylate |
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A highly selective reversible inhibitor of monoamine oxidase type A.
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| BCC6765 | BU 224 hydrochloride |
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High affinity ligand for the imidazoline I<sub>2</sub> binding site (K<sub>i</sub> = 2.1 nM). Putative I<sub>2</sub> antagonist; antagonizes the effects of imidazoline ligands on morphine antinociception. Produces ipsiversive rotational behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract.
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| BCC6766 | Pyrrolidinedithiocarbamate ammonium |
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This inhibitor of nuclear factor <span class='symbol'>κ</span>B (NF-<span class='symbol'>κ</span>B) prevents the increase in NO-synthase mRNA by interleukin-1, without affecting the formation of NO-synthase mRNA produced by cAMP.
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| BCC6767 | RS 23597-190 hydrochloride |
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A high affinity, selective competitive antagonist at 5-HT4 receptors.
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| BCC6768 | Imetit dihydrobromide |
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An extremely potent, high affinity agonist at H<sub>3</sub> and H<sub>4</sub> receptors (K<sub>i</sub> values are 0.3 and 2.7 nM respectively). Induces shape change in eosinophils with an EC<sub>50</sub> of 25 nM. Centrally active following systemic administration. Also available as part of the Histamine H<sub>3</sub> Receptor.
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