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 1577 - 1584 of 9359 hot products
| Catalog No. | Product Name |
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| BCC5978 | α-Conotoxin PnIA |
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Selective antagonist of <span class='symbol'>α</span>3<span class='symbol'>β</span>2 nAChR receptors (IC<sub>50</sub> values are 9.56 and 252 nM for <span class='symbol'>α</span>3<span class='symbol'>β</span>2 and <span class='symbol'>α</span>7 receptors respectively).
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| BCC5979 | α-Conotoxin EI |
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Selective antagonist of neuromuscular nicotinic receptors <span class='symbol'>α</span>1<span class='symbol'>β</span>1<span class='symbol'>γδ</span>. Displays selectivity for <span class='symbol'>α</span>/<span class='symbol'>δ</span> sites over <span class='symbol'>α</span>/<span class='symbol'>γ</span> sites in Torpedo.
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| BCC5980 | Conantokin-R |
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Potent, non-competitive NMDA receptor antagonist (IC<sub>50</sub> = 93 nM) that has been suggested to have NR2 subunit selectivity. Inhibits inward currents evoked by NMDA in central nervous system neurons (IC<sub>50</sub> = 350 nM) and exhibits broad anticonvulsant and antiparkinsonian activity <em>in vivo</em> at doses devoid of behavioral toxicity.
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| BCC5981 | d[Leu4,Lys8]-VP |
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Selective vasopressin V<sub>1B</sub> receptor agonist (K<sub>i</sub> values are 0.16, 64, 100 and 3800 nM for V<sub>1B</sub>, oxytocin, V<sub>2</sub> and V<sub>1A</sub> receptors respectively). Displays weak antidiuretic, vasopressor and <em>in vitro</em> oxytocic activities.
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| BCC5982 | Ketamine hydrochloride |
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Non-competitive NMDA receptor antagonist (EC<sub>50</sub> values are 13.6 and 17.6 <span class='symbol'>μ</span>M for NR1/NR2A and NR1/NR2B subunit combinations respectively). Dissociative anesthetic. S-enantiomer also available.
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| BCC5983 | Neuropeptide FF |
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Endogenous antiopioid peptide and agonist at NPFF<sub>1</sub> and NPFF<sub>2</sub> receptors (K<sub>i</sub> values are 2.82 and 0.21 nM respectively). Exhibits anorexigenic effects following i.c.v. administration.
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| BCC5984 | K 114 |
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Potent amyloid fibril-specific fluorescent dye (EC<sub>50</sub> = 20 - 30 nM). Exhibits minimal fluorescence in aqueous buffers and fluoresces brightly in the presence of A<span class='symbol'>β</span>, <span class='symbol'>α</span>-synuclein and tau <em>in situ</em>. (Optimum wavelength = 550 nm).
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| BCC5985 | [Orn5]-URP |
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Urotensin-II (UT) receptor pure antagonist (pEC<sub>50</sub> = 7.24). Displays no agonist activity unlike other U-II/URP analogs. Inhibits the action of U-II in the rat aorta ring assay.
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