Modulators of receptors, ion channels, transporters and G-protein signaling.
2-Chloro-ATP is a soluble guanylate cyclase inhibitor that increases intracellular calcium concentration at low...
5R(6S)-EET is the metabolite of Arachidonic acid ( HY-109590 ). 5R(6S)-EET activates the synthesis of endogenous...
trans-Latanoprost (5,6-trans-Latanoprost) is the trans isomer of Latanoprost ( HY-B0577 ). trans-Latanoprost is...
IGS-1.76 efficiently inhibits the human NCS-1/Ric8a complex. IGS-1.76 shows a significantly increased affinity for...
BMS-986104 is a potent and selective S1P1 receptor modulator. BMS-986104 is effective in a mouse EAE model, which is...
Quindecamine (UCL 1407) is a potent IK Ca blocker with an IC 50 of 0.85 μM.
GPR34 agonist 1 (Compound M1), a lysophosphatidylserine analogue, is an efficient GPR34 agonist.
ABT-299 is a prodrug of a platelet-activating factor (PAF) antagonist that exhibits significant inhibitory activity...
CYM5181 is a novel S1P1 agonist with a pEC 50 value of -8.47.
α,α-DiBn-DL-Gly (Dibenzylglycine) is an achiral α-substituted phenylalanine derivative, non-substrate weak inhibitor...
NPS-467 is a calcium-sensing receptor ( CaR ) activator and stereospecific agent with only its R-enantiomer active....
Potassium ionophore III (BME-44) is a specific potassium ion carrier with high selectivity for sodium and ammonium...
Ciproquazone (SL-573) is a compound that inhibits prostaglandin biosynthesis. Its relative inhibitory potency is...
TAS2R14 agonist is a potent TAS2R14 partial agonist with an EC 50 of 116.6 ±23.6 nM.
Peonidin-3-O-galactoside chloride is an anthocyanin with antioxidant properties and blood-brain barrier...
VUF8507 is an allosteric modulator for adenosine A3 receptor with a K i of 204 nM.
PSB11 hydrochloride is an antagonist with reverse excitatory activity for human A3 Adenosine Receptor with high...
ETH 157 is a neutral sodium-selective carrier. ETH 157 exhibits sufficient Na + / K + selectivity and enhanced Na +...
Hadacidin is a competitive inhibitor of adenylate synthase . Hadacidin binds to the active site of adenylate...
AGN-201904Z is a compound that inhibits gastric acid secretion and is a new type of proton pump inhibitor that can...
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