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 2401 - 2408 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6958 | DAMGO |
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Highly selective peptide agonist for the <span class='symbol'>μ</span> opioid receptor.
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| BCC6959 | Neuropeptide Y 13-36 (porcine) |
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Neuropeptide Y2 receptor agonist.
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| BCC6960 | [Sar9,Met(O2)11]-Substance P |
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Potent selective NK1 tachykinin receptor agonist.
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| BCC6961 | Galanin (1-30) (human) |
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Endogenous peptide with multiple endocrine, metabolic and behavioral effects. Has been shown to have an action on intestinal smooth muscle, insulin and somatostatin release, and synaptic neurotransmission.
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| BCC6962 | PACAP 1-38 |
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Endogenous neuropeptide showing considerable homology with vasoactive intestinal peptide (VIP) but with a greater potency for stimulation of adenylyl cyclase.
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| BCC6963 | BQ-123 |
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Selective ETA endothelin receptor antagonist (Ki values are 1.4 and 1500 nM at ETA and ETB receptors respectively). Reduces ischemia-induced ventricular arrhythmias in a rat model.
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| BCC6964 | NF 279 |
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A potent and selective P2X<sub>1</sub> antagonist (IC<sub>50</sub> = 19 nM). Displays good selectivity over P2X<sub>2</sub>,(IC<sub>50</sub> = 0.76 <span class='symbol'>μ</span>M), P2X<sub>3</sub> (IC<sub>50</sub> = 1.62<span class='symbol'>μ</span>M), P2X<sub>4</sub> (IC<sub>50</sub> > 300 <span class='symbol'>μ</span>M), P2Y receptors and ecto-nucleotidases.
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| BCC6965 | Nω-Propyl-L-arginine hydrochloride |
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Highly selective and potent inhibitor of nNOS (Ki = 57 nM). Displays 3158-fold and 149-fold selectivity over iNOS and eNOS respectively. Hypotensive in vivo.
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