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Ion Channel/Membrane Transporter

Chemical Structure Cat. No. Product Name CAS No.
Uridine 5'-diphosphoglucose disodium salt Chemical Structure
BCP37401 Uridine 5'-diphosphoglucose disodium salt 28053-08-9
Uridine 5′-diphosphoglucose disodium salt is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms.
Verapamil Chemical Structure
BCP37129 Verapamil 52-53-9
Verapamil is a calcium channel blocker that is a class IV anti-arrhythmia agent.
BAY-1797 Chemical Structure
BCP36916 BAY-1797 2055602-83-8
BAY-1797 is a potent, orally active, and selective P2X4 antagonist, with an IC50 of 211 nM against human P2X4. BAY-1797 displays no or very weak activity on the other P2X ion channels. BAY-1797 shows anti-nociceptive and anti-inflammatory effects.
NPPB Chemical Structure
BCP36797 NPPB 107254-86-4
NPPB is a blocker of the outwardly rectifying chloride channel (ORCC).
Isourolithin B Chemical Structure
BCP36684 Isourolithin B 855255-55-9
Urolithin C Chemical Structure
BCP36683 Urolithin C 165393-06-6
Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion.
Clomethiazole Chemical Structure
BCP36337 Clomethiazole 533-45-9
Chlormethiazole is an potent and orally active GABAA agonist. Chlormethiazole inhibits cytochrome P450 isoforms: CYP2A6 and CYP2E1 in human liver microsomes. Chlormethiazole is an anticonvulsant agent and has the potential for treating convulsive status epilepticus.
Spermidine trihydrochloride Chemical Structure
BCP36231 Spermidine trihydrochloride 334-50-9?
Spermidine trihydrochloride is a polyamine that binds to NMDA receptor.
GSK2193874 Chemical Structure
BCP36070 GSK2193874 1336960-13-4
GSK2193874 is an orally active, potent, and selective TRPV4 antagonist with IC50s of 2 nM and 40 nM for rTRPV4 and hTRPV4.
Golexanolone Chemical Structure
BCP36048 Golexanolone 2089238-18-4
Golexanolone is a GABA-A receptor modulating steroid antagonist that selectively antagonizes the enhanced activation of GABAA receptors by neurosteroids such as allopregnanolone and THDOC.
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