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 1033 - 1040 of 9359 hot products

BioCrick hot natural products and bioactive compounds
Catalog No. Product Name
BCC4955 NXY-059
Free radical trapping agent. Reduces infarct size and preserves brain function in several animal models of acute ischemic stroke. Neuroprotectant.
BCC4961 Suplatast Tosylate
Th2 cytokine inhibitor that attenuates IL-2, IL-5 and IL-13 production and has no effect on IFN-<span class='symbol'>&#947;</span> production. Acts as an immunoregulator that suppresses IgE production, eosinophil infiltration and histamine release. Exhibits antiasthmatic, anti-inflammatory and antifibrotic activity <em>in vivo</em> and is orally active.
BCC4962 Alfacalcidol
Metabolite and prodrug of vitamin D<sub>3</sub>. Improves mechanical bone strength and bone mass; suppresses osteoclastic bone resorption <em>in vivo</em>.
BCC4963 Alprostadil
Prostaglandin with some selectivity for EP3 and EP4 receptors (Ki values are 1.1, 2.1, 36, 10 and 33 nM for mouse EP3, EP4, EP1, EP2 and IP receptors respectively). Inhibits platelet aggregation and is a vasodilator in vivo.
BCC4970 Nanchangmycin
Antiviral. Inhibits Zika virus entry in a range of cell types including primary placental fibroblast cells, HUVECs and UtMECs (IC50 values are 0.1, 0.4 and 0.97 μM in U2OS, HBMECs and Jeg-3 cells respectively). Also inhibits cellular uptake of West Nile, dengue, sindbis and chikungunya viruses.
BCC4972 SB408124
Selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.
BCC4973 Ticlopidine HCl
Selective P2Y12 receptor antagonist. Inhibits ADP-induced platelet aggregation and displays antithrombotic activity following oral administration in vivo.
BCC4974 GW791343 HCl
P2X<sub>7</sub> allosteric modulator. Exhibits species-specific activity; acts as a negative allosteric modulator of human P2X<sub>7</sub> (pIC<sub>50</sub> = 6.9 - 7.2) and a positive allosteric modulator of rat P2X<sub>7</sub>.