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 1265 - 1272 of 9359 hot products
| Catalog No. | Product Name |
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| BCC5662 | IPAG |
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Potent <span class='symbol'>σ</span>-receptor antagonist.
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| BCC5663 | 2-Methyl-5-hydroxytryptamine hydrochloride |
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5-HT3 agonist (Ki = 1200 nM) and potent 5-HT6 ligand (Ki = 46 nM).
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| BCC5664 | Metaphit |
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Acylator of PCP and <span class='symbol'>σ</span>-receptors.
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| BCC5665 | (R)-(-)-α-Methylhistamine dihydrobromide |
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Very potent, high affinity H<sub>3</sub> agonist (K<sub>D</sub> = 50.3 nM) that displays > 200-fold selectivity over H<sub>4</sub> receptors. Inhibits H<sub>3</sub>-mediated histamine synthesis and release in the CNS and stimulates H<sub>4</sub>-mediated eosinophil shape change (EC<sub>50</sub> = 66 nM). Part of the Histamine H<sub>3</sub> Receptor. (<em>S</em>)-(+)-<span class='symbol'>α</span>-Methylhistamine dihydrobromide also available.
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| BCC5666 | L-690,330 |
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A potent inhibitor of inositol monophophatase; stable to hydrolysis. Induces autophagy in COS-7 cells independently of mTOR inhibition.
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| BCC5667 | L-690,488 |
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Cell-permeable prodrug of the potent inositol monophosphatase inhibitor L-690,330; penetrates cells more effectively than its metabolite.
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| BCC5668 | BU 239 hydrochloride |
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High affinity ligand for the imidazoline I<sub>2</sub> binding site.
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| BCC5669 | DPPE fumarate |
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Binds with high affinity to the antiestrogen binding site but not to the estrogen receptor. Induces of sterol accumulation in MCF7 cells. An inhibitor of histamine binding at the intracellular histamine (Hlc) site.
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