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 2353 - 2360 of 9359 hot products
| Catalog No. | Product Name |
|---|---|
| BCC6909 | 1-BCP |
|
A centrally active selective potentiator of AMPA-mediated responses. Facilitates memory retention in rats.
|
|
| BCC6910 | CHPG |
|
A selective mGlu<sub>5</sub> metabotropic glutamate receptor agonist, completely inactive at mGlu<sub>1a</sub> receptors expressed in CHO cells. Active <em>in vivo</em>. CHPG sodium salt also available.
|
|
| BCC6911 | Zinterol hydrochloride |
|
Potent and selective <span class='symbol'>β</span><sub>2</sub>-adrenoceptor agonist (pK<sub>B</sub> values are 8.3 and < 5.7 for <span class='symbol'>β</span><sub> 2</sub> and <span class='symbol'>β</span><sub>1</sub> receptors respectively, as measured in human artery).
|
|
| BCC6912 | A 61603 hydrobromide |
|
Potent <span class='symbol'>α</span>-adrenoceptor agonist that is at least 35-fold more potent at <span class='symbol'>α</span><sub>1A</sub> than at <span class='symbol'>α</span><sub>1B</sub> or <span class='symbol'>α</span><sub>1D</sub> sites. Induces dose response increases in spontaneous Ca<sup>2+</sup> transients in rat ventricular myocytes <em>in vitro</em> (EC<sub>50</sub> = 6.9 nmol/L). Also available as part of the <span class='symbol'>α</span><sub>1</sub>-Adrenoceptor.
|
|
| BCC6913 | GR 55562 dihydrochloride |
|
A selective competitive 5-HT<sub>1B</sub> (5-HT<sub>1D<span class='symbol'>β</span></sub>) silent antagonist with pK<sub>B</sub> values of 7.3 and 6.3 for human cloned 5-HT<sub>1B</sub> and 5-HT<sub>1D</sub> receptors respectively and only weak binding at a number of other 5-HT subtypes.
|
|
| BCC6914 | WIN 64338 hydrochloride |
|
The first potent, non-peptide, competitive bradykinin B2 receptor antagonist. In organ bath studies, WIN 64338 inhibits [3H]-bradykinin binding on guinea pig trachea with nanomolar affinity but is not active in the rabbit aorta (the classical bradykinin B1 preparation).
|
|
| BCC6915 | BW 723C86 hydrochloride |
|
Selective 5-HT2B receptor agonist.
|
|
| BCC6916 | (S)-(-)-Pindolol |
|
5-HT1A/1B receptor antagonist, with roughly equal affinity for each subtype. A partial agonist at mouse and human β3-adrenoceptors. More active enantiomer of pindolol.
|
|