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 3281 - 3288 of 9359 hot products
| Catalog No. | Product Name |
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| BCC7852 | MJ 15 |
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Potent and selective CB1 receptor antagonist (Ki = 27.2 pM, IC50 = 118.9 pM for rat CB1 receptors). Exhibits potency in obesity and hyperlipidemia models; inhibits food intake and increases in body weight in diet-induced obese rats and mice.
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| BCC7853 | TCS 2510 |
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Highly selective EP<sub>4</sub> agonist (EC<sub>50</sub> = 2.5 nM; K<sub>i</sub> = 1.2 nM). Displays no significant binding at other prostaglandin receptors at concentrations up to 14 <span class='symbol'>μ</span>M.
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| BCC7854 | PF9 tetrasodium salt |
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Potent agonist of GPR17 (EC50 = 36 pM).
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| BCC7855 | ATPγS tetralithium salt |
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P2 purinergic receptor agonist. Nonhydrolyzable analog of ATP.
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| BCC7856 | LY 266097 hydrochloride |
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Selective 5-HT2B receptor antagonist (pKi = 9.3). More than 100-fold selective over 5-HT2A and 5-HT2C. Attenuates amphetamine-induced locomotion in the rat.
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| BCC7857 | Nalmefene hydrochloride |
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Opioid receptor antagonist; displays a longer half life than Naloxone. Exhibits neuroprotective effects after traumatic brain injury in the rat. Deuterated version, Nalmefene d3, also available.
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| BCC7858 | PE 154 |
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Potent fluorescent inhibitor of human acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) (IC<sub>50</sub> values are 280 pM and 16 nM respectively). Targets and labels <span class='symbol'>β</span>-amyloid plaques in histochemical analysis.
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| BCC7859 | PS 48 |
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Phosphoinositide-dependent protein kinase-1 (PDK1) activator (Kd = 10.3 μM). Binds exclusively to the PIF-binding pocket of PDK1, distinct from the ATP binding site.
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