About 5 results found for searched term "71-91-0" (0.126 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M20564 | Tetraethylammonium bromide | Potassium Channel |
| TEAB, TEA bromide | ||
| Tetraethylammonium bromide is used as the source of tetraethylammonium ions in pharmacological and physiological studies, but is also used in organic chemical synthesis. It blocks selective potassium channels. | ||
| M42114 | STAT6-IN-3 | STAT |
| STAT6-IN-3 is a STAT6 inhibitor (IC50= 44 nM). | ||
| M10871 | PF-07104091 | CDK |
| Tagtociclib | ||
| Pf-07104091 is an oral bioavailable, selective CDK2 inhibitor with a Ki value of 1.16 nM against CDK2/ Clin E1. Pf-07104091 has antitumor activity against cyclinE amplified cancers. | ||
| M28178 | A 71915 | Peptides |
| A 71915 is a highly potent and competitive natriuretic peptide receptor A (ANP, NPRA) antagonist (pKi= 9.18). A 71915 displaces [125I]ANP dose dependently, with a Ki of 0.65 nM. A71915( pA2= 9.48) against rat ANP-induced cGMP production in NB-OK-1 cells. | ||
| M30609 | FG 7142 | GABA Receptor |
| ZK 39106; LSU-65 | ||
| FG 7142 (ZK 39106; LSU-65), a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM). FG 7142 (ZK 39106; LSU-65) also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM). FG 7142 (ZK 39106; LSU-65) can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex. | ||
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