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 2273 - 2280 of 9359 hot products
| Catalog No. | Product Name |
|---|---|
| BCC6828 | Palmitoylethanolamide |
|
Endogenous lipid that acts as a selective GPR55 agonist (EC<sub>50</sub> values are 4, 19 800 and > 30 000 nM at GPR55, CB<sub>2</sub> and CB<sub>1</sub> receptors respectively). Substrate for fatty acid amide hydrolase (FAAH) and PEA-preferring acid amidase (PAA) and exhibits antinociceptive and anticonvulsant <em>in vivo</em>. Directly activates PPAR<span class='symbol'>α</span> (EC<sub>50</sub> = 3 <span class='symbol'>μ</span>M) producing robust anti-inflammatory actions.
|
|
| BCC6829 | ODQ |
|
A potent and selective inhibitor of NO-sensitive guanylyl cyclase.
|
|
| BCC6830 | Chlormethiazole hydrochloride |
|
Sedative and anticonvulsant which is neuroprotective in a number of animal models. Prevents the degeneration of serotonergic nerve terminals induced by MDMA ('Ecstasy').
|
|
| BCC6831 | ZM 226600 |
|
Potent K<sub>ir</sub>6 (K<sub>ATP</sub>) channel opener (EC<sub>50</sub> = 0.5 <span class='symbol'>μ</span>M), devoid of antiandrogen properties.
|
|
| BCC6832 | BD 1063 dihydrochloride |
|
<span class='symbol'>σ</span><sub>1</sub> receptor antagonist, approximately 50-fold selective over <span class='symbol'>σ</span><sub>2</sub> sites and ≥100-fold selective over opioid, PCP, muscarinic, dopamine, <span class='symbol'>α</span><sub>1</sub>, <span class='symbol'>α</span><sub>2</sub>, <span class='symbol'>β</span> adrenoceptor, 5-HT<sub>1</sub> and 5-HT<sub>2</sub> receptors. Prevents hyperlocomotion following cocaine administration in mice.
|
|
| BCC6833 | Cirazoline hydrochloride |
|
Selective <span class='symbol'>α</span><sub>1</sub> agonist. Also available as part of the <span class='symbol'>α</span><sub>1</sub>-Adrenoceptor and Mixed Adrenergic.
|
|
| BCC6834 | Rauwolscine hydrochloride |
|
Standard <span class='symbol'>α</span><sub>2</sub>-adrenergic antagonist (K<sub>i</sub> values are 3.5, 4.6, and 0.6 nM at cloned human <span class='symbol'>α</span><sub>2A</sub>, <span class='symbol'>α</span><sub>2B</sub>, and <span class='symbol'>α</span><sub>2C</sub>-adrenoceptors respectively). Partial agonist at 5-HT<sub>1A</sub> receptors. Also available as part of the <span class='symbol'>α</span><sub>2</sub>-Adrenoceptor. Diastereomer Yohimbine hydrochloride also available.
|
|
| BCC6835 | (RS)-(±)-Sulpiride |
|
Standard D<sub>2</sub>-like dopamine receptor antagonist. (<em>S</em>)-(-)-Sulpiride also available.
|
|