Hot Products
Hot products from BioCrick which is a professional high-purity natural products manufacturer are well known to scientists around the world because of their high purity and stability. Each product is a chemical compound or substance produced by a living organism—that is, found in nature. In the broadest sense, natural products include any substance produced by life.Natural products remain the best sources of drugs and drug leads, and this remains true today despite the fact that many pharmaceutical companies have deemphasized natural products research in favor of HTP screening of combinatorial libraries during the past 2 decades. From 1940s to date, 131 (74.8%) out of 175 small molecule anticancer drugs are natural product-based/inspired, with 85 (48.6%) being either natural products or derived therefrom. From 1981 to date, 79 (80%) out of 99 small molecule anticancer drugs are natural product-based/inspired, with 53 (53%) being either natural products or derived therefrom. Among the 20 approved small molecule New Chemical Entities (NCEs) in 2010, a half of them are natural products.
Hot products from the professional high-purity natural products manufacturer
| Cat.No. | Product Name |
|---|---|
| BCC6920 | Oxotremorine M |
| Muscarinic receptor agonist. Also directly potentiates NMDA-mediated ion currents. | |
| BCC6921 | Senktide |
| NK3 tachykinin receptor agonist. Causes direct excitation of dopamine neurons; enhances dopaminergic function. Induces locomotor activity. | |
| BCC6922 | Zolantidine dimaleate |
| A potent, selective and brain penetrating H2 receptor antagonist. | |
| BCC6923 | Pirenzepine dihydrochloride |
| M1 muscarinic receptor selective antagonist. Inverse agonist activity reported. | |
| BCC6924 | AGN 192403 hydrochloride |
| I1 imidazoline binding site selective ligand with a potency at I1 comparable to moxonidine, but devoid of affinity for adrenoceptors and the I2 binding site. Interestingly, in animal models, this compound causes none of the physiological responses associated with the I1 binding site. | |
| BCC6926 | (RS)-AMPA hydrobromide |
| More water soluble hydrobromide salt of (RS)-AMPA. | |
| BCC6927 | (-)-Lobeline hydrochloride |
| High affinity, partial agonist with a Ki value of 4.4 nM in rat brain. | |
| BCC6929 | (R)-(+)-8-Hydroxy-DPAT hydrobromide |
| Full 5-HT1A serotonin receptor agonist; more active enantiomer. Reduces hippocampal 5-HT levels following systemic administration in rats in vivo. More active enantiomer of 8-Hydroxy-DPAT hydrobromide. 7-Hydroxy-DPAT hydrobromide also available. | |
