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 2633 - 2640 of 9359 hot products
| Catalog No. | Product Name |
|---|---|
| BCC7193 | Eticlopride hydrochloride |
|
Selective dopamine D2/D3 receptor antagonist (Ki values are 0.50 and 0.16 nM respectively). Antipsychotic.
|
|
| BCC7195 | (R)-(+)-Blebbistatin |
|
Inactive enantiomer of the selective inhibitor of myosin II, (±)-blebbistatin.
|
|
| BCC7197 | Impentamine dihydrobromide |
|
Potent and highly selective histamine H3 receptor antagonist (pA2 = 8.4); displays > 30000-fold selectivity over H1 and H2 receptors. Can act as a partial agonist in SK-N-MC cells expressing human H3 receptors. Produces antinociception, possibly via a non-H1, -H2 or -H3 receptor-mediated mechanism, following central administration in vivo.
|
|
| BCC7198 | MRS 1845 |
|
Potent blocker of store-operated Ca2+ channels; inhibits capacitative Ca2+ influx in HL-60 cells (IC50 = 1.7 mM).
|
|
| BCC7199 | NSC 663284 |
|
Potent, selective inhibitor of Cdc25 dual specificity phosphatases (K<sub>i</sub> values are 29, 95 and 89 nM for human Cdc25A, Cdc25B<sub>2</sub> and Cdc25C respectively); > 20- and > 450-fold selective over VHR and PTP1B phosphatases respectively. Arrests cells at both G<sub>1</sub> and G<sub>2</sub>/M phase and blocks cdk2 and cdk1 activation. Blocks proliferation of a range of human tumor cell lines (IC<sub>50</sub> = 0.2 - 35 <span class='symbol'>μ</span>M).
|
|
| BCC7200 | U0124 |
|
Inactive analog of U0126. Used as a negative control. Does not inhibit MEK at concentrations up to 100 <span class='symbol'>μ</span>M.
|
|
| BCC7201 | Ipsapirone |
|
Selective 5-HT1A receptor agonist (Ki = 10 nM). Anxiolytic in vivo.
|
|
| BCC7202 | [D-Trp7,9,10]-Substance P |
|
Substance P analog that inhibits activation of Gq/11 by M1 muscarinic ACh receptors. Does not inhibit Gi/o activation by M2 ACh receptors.
|
|