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 2361 - 2368 of 9359 hot products

BioCrick hot natural products and bioactive compounds
Catalog No. Product Name
BCC6917 (-)-Quinpirole hydrochloride
Selective dopamine D2 receptor agonist (Ki values are 4.8, ~24, ~30 and 1900 nM at D2, D3, D4 and D1 receptors respectively).
BCC6918 2-Methylthioadenosine triphosphate tetrasodium salt
P2 purinoceptor agonist.
BCC6919 PD 168077 maleate
A potent D4 dopamine receptor agonist (Ki = 8.7 nM) with > 400-fold selectivity over D2 and > 300-fold selectivity versus D3 subtypes respectively. Induces synaptic translocation of CaMK II to postsynaptic sites in cultured prefrontal cortical neurons. Centrally active in vivo.
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.