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 2265 - 2272 of 9359 hot products
| Catalog No. | Product Name |
|---|---|
| BCC6820 | MTPG |
|
Group II/group III metabotropic glutamate receptor antagonist, showing selectivity for group II in electrophysiological studies.
|
|
| BCC6821 | L-732,138 |
|
Potent and highly selective competitive tachykinin NK1 receptor antagonist (IC50 = 2.3 nM).
|
|
| BCC6822 | MDL 11,939 |
|
Orally active 5-HT2A receptor antagonist; displays selectivity for 5-HT2A receptors over 5-HT2C receptors (Ki values are 0.54, 2.5, 81.6 and ~10,000 nM at rabbit 5-HT2A, human 5-HT2A, rabbit 5-HT2C and human 5-HT2C receptors respectively).
|
|
| BCC6823 | AMT hydrochloride |
|
Potent, selective and reversible inhibitor of iNOS (IC50 = 3.6 nM; approximately 30 and 40 times selective over nNOS and eNOS respectively).
|
|
| BCC6824 | EIT hydrobromide |
|
Potent, selective and reversible inhibitor of isoform II NO synthase (IC50 = 13 nM; approximately 20- and 30-fold selective over isoforms I and III respectively).
|
|
| BCC6825 | AM 92016 hydrochloride |
|
A specific blocker of the time dependent delayed rectifier potassium current, devoid of any <span class='symbol'>β</span>-adrenoceptor blocking activity. Exhibits proarrhythmic and prohypertensive activity <em>in vivo</em>.
|
|
| BCC6826 | Luzindole |
|
Melatonin antagonist.
|
|
| BCC6827 | Oleamide |
|
Endogenous sleep-inducing lipid. Acts as an agonist at the CB<sub>1</sub> cannabinoid receptor (EC<sub>50</sub> = 1.64 <span class='symbol'>μ</span>M). Also appears to potentiate the actions of 5-HT on 5-HT<sub>2A</sub> and <sub>2C</sub> receptors, and act via an allosteric regulatory site on 5-HT<sub>7</sub> receptors.
|
|