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 2145 - 2152 of 9359 hot products
| Catalog No. | Product Name |
|---|---|
| BCC6696 | α-Methyl-5-hydroxytryptamine maleate |
|
5-HT2B receptor selective agonist with pKi values of 8.4, 6.1 and 7.3 at 5-HT2B, 5-HT2A and 5-HT2C receptors respectively.
|
|
| BCC6697 | N-Methylquipazine dimaleate |
|
5-HT3 agonist. Has almost the same affinity for 5-HT3 sites as quipazine but unlike the latter, does not bind to 5-HT1B sites.
|
|
| BCC6698 | (±)-Myristoylcarnitine chloride |
|
Homolog of acetylcarnitine chloride. Acylcarnitines are important intermediates in lipid metabolism.
|
|
| BCC6699 | PCA 4248 |
|
A specific PAF antagonist, more potent than the ginkolide BN-52021. Inhibits rabbit platelet aggregation with an IC<sub>50</sub> value of 1.05 <span class='symbol'>μ</span>M and has no significant activity on Ca<sup>2+</sup> channels. Active <em>in vivo</em>, antagonizing PAF-induced systemic hypotension and protein-plasma extravasation in rats.
|
|
| BCC6700 | (S)-(+)-α-Methylhistamine dihydrobromide |
|
Less active enantiomer of H<sub>3</sub> agonist R-(-)-<span class='symbol'>α</span>-methylhistamine; 120-fold less potent than R-(-) at H<sub>3</sub>.
|
|
| BCC6701 | Nα-Methylhistamine dihydrochloride |
|
Potent histamine agonist, particularly at H3 receptors (potency relative to histamine is 81, 185, and 270% at H1, H2 and H3 respectively). Also displays agonist properties at H4 receptors to which it binds with moderate affinity (Ki = 23 nM).
|
|
| BCC6702 | Methyl 2,5-dihydroxycinnamate |
|
Erbstatin analog. Inhibitor of EGF receptor-associated tyrosine kinases.
|
|
| BCC6703 | Tyrphostin B44, (-) enantiomer |
|
Potent inhibitor of epidermal growth factor receptor (EGFR) kinase (IC<sub>50</sub> = 0.4 <span class='symbol'>μ</span>M), more active than the (+) enantiomer. Selective over ErbB2.
|
|