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 2313 - 2320 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6868 | Diazoxide |
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Antihypertensive, activates ATP-dependent K<sup>+</sup> channels (K<sub>ir</sub>6). Induces activation of PKC<span class='symbol'>ε</span>, an intermediate in the opening of mitoK<sub>ATP</sub> channels, results in cardioprotection against hypoxia-induced death. Blocks desensitization of AMPA receptors.
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| BCC6869 | Tacrine hydrochloride |
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Potent cholinesterase inhibitor, a cognition enhancer in vivo.
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| BCC6870 | 1-Phenylbiguanide hydrochloride |
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5-HT3 receptor agonist.
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| BCC6871 | EGLU |
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Selective antagonist of presynaptically-mediated (1S,3S)-ACPD-induced depression of motoneuron excitation in neonatal rat spinal cord; presumed group II mGlu receptor antagonist. Also available as part of the Group II mGlu Receptor.
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| BCC6872 | CPPG |
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Potent group II/III mGlu receptor antagonist, with approximately 20-fold selectivity for group III over group II (IC<sub>50</sub> values of 2.2 and 46.2 nM respectively). A much less potent antagonist at group I receptors in neonatal rat cortical slices (K<sub>B</sub> = 0.65 ± 0.07 nM). Also available as part of the Group III mGlu Receptor.
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| BCC6873 | MPDC |
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Potent inhibitor of the Na+-dependent high-affinity synaptosomal glutamate transporter.
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| BCC6874 | RS 17053 hydrochloride |
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<span class='symbol'>α</span><sub>1A</sub>-adrenoceptor antagonist, with very high affinity for <span class='symbol'>α</span><sub>1A</sub> receptors (pK<sub>i</sub> and pA<sub>2</sub> estimates of 9.1 - 9.9) and a 30 - 100 fold selectivity over the <span class='symbol'>α</span><sub>1B</sub> and <span class='symbol'>α</span><sub>1D</sub> subtypes (pK<sub>i</sub> and pA<sub>2</sub> estimates 7.7 - 7.8).
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| BCC6875 | Imiloxan hydrochloride |
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A moderately potent, but highly selective <span class='symbol'>α</span><sub>2</sub>-adrenoceptor antagonist, the only reported selective antagonist at the <span class='symbol'>α</span><sub>2B</sub>-adrenoceptor not having potent <span class='symbol'>α</span><sub>1</sub>-adrenoceptor antagonist activity.
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