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 2233 - 2240 of 9359 hot products

BioCrick hot natural products and bioactive compounds
Catalog No. Product Name
BCC6787 GBLD 345
A high affinity benzodiazepine agonist (IC50 against diazepam = 1 nM).
BCC6789 Carboxy-PTIO, potassium salt
A stable, water-soluble free radical that reacts stoichiometrically with NO. Almost twice as strong an inhibitor as N(<span class='symbol'>&omega;</span>)-nitroarginine or N-methylarginine.
BCC6790 (+)-UH 232 maleate
D<sub>2</sub> antagonist (K<sub>i</sub> = 72.7 nM in a ligand binding assay; apparent K<sub>B</sub> = 14.5 nM in a cAMP accumulation assay); displays preferential activity at central dopamine autoreceptors. Stimulates a marked acceleration of dopamine synthesis and turnover. Produces locomotor stimulation. Exhibits little or no activity at central noradrenalin and 5-HT receptors. Also D<sub>3</sub> partial agonist.
BCC6791 (S)-Methylisothiourea sulfate
Highly selective, potent competitive inhibitor of iNOS.
BCC6792 ICI 199,441 hydrochloride
Highly potent <span class='symbol'>&kappa;</span> agonist, 146-fold more active than U-50488 <em>in vitro</em>.
BCC6793 Iodophenpropit dihydrobromide
Selective H<sub>3</sub> antagonist with high affinity (K<sub>D</sub> = 0.3 nM). Also available as part of the Histamine H<sub>3</sub> Receptor.
BCC6794 NCS-382
<span class='symbol'>&gamma;</span>-Hydroxybutyric acid antagonist, anticonvulsant.
BCC6795 Aminoguanidine hydrochloride
Irreversible inhibitor of iNOS that displays some selectivity over eNOS and nNOS. Exhibits antioxidant and radioprotective effects in vivo.