Membrane Transporter/Ion Channel


Membrane Transporters mediate the movement of ions and molecules via binding and moving the substance across the membrane. There are two main actions of transporter: facilitated diffusion (passive transport) and active transport. Membrane transporters which bind the hydrolysis of ATP to the transport of target molecules are referred to as ATPases. For instance, Na+,K+-ATPases or Na+,K+-pumps are responsible for the transport of Na+ out of and K+ into cells.
Ion channels are pore-forming membrane proteins which allow the flow of ions across the membrane. The ion channels can be broadly grouped into six families including calcium channels, chloride channels, potassium channels, sodium channels, gap junction proteins and porins. Not all ion channels are gated, such as certain type of K+ and Cl– channels, transient receptor potential superfamily of cation channels, the ryanodine receptors and the IP3 receptors, but most Na+, K+, Ca2+ and some Cl– channels are all gated by voltage. Ligand-gated channels are regulated in response to ligand binding (e.g. neurotransmitters signaling). These ligand-gated neurotransmitter receptors are known as ionotropic receptors. Various neurotransmitters couple to ionotropic receptors such as glutamate, acetylcholine, glycine, GABA, and serotonin.
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C8832 Procyclidine HClSummary: Procyclidine HCl is a synthetic anticholinergic muscarinic receptor antagonist used as a pharmacological probe in cholinergic signaling and neuropharmacology research. -
C8846 Eperisone hydrochlorideSummary: Eperisone hydrochloride is a centrally acting antispasmodic compound modulating spinal polysynaptic reflex pathways, widely utilized in neuropharmacology and neuromuscular signaling research. -
C8852 Revaprazan HydrochlorideSummary: Revaprazan Hydrochloride is a potassium-competitive acid blocker targeting gastric H?/K?-ATPase, utilized as a pharmacological tool in gastrointestinal physiology and acid-secretion research. -
C8877 Cloperastine hydrochlorideSummary: Cloperastine hydrochloride is a centrally acting antitussive small molecule used as a pharmacological probe in respiratory neuropharmacology and cough reflex pathway research. -
C8881 Landiolol hydrochlorideSummary: Landiolol hydrochloride is an ultra-short-acting, selective β1-adrenergic receptor antagonist used to investigate sympathetic signaling and cardiac electrophysiology in cardiovascular research. -
C8890 Levomilnacipran HydrochlorideSummary: Levomilnacipran Hydrochloride is a selective serotonin and norepinephrine reuptake inhibitor targeting monoamine transporters, widely utilized in neuropharmacology and neurotransmission mechanism research. -
C8892 AcetohexamideSummary: Acetohexamide is a first-generation sulfonylurea and ATP-sensitive potassium channel modulator used to investigate pancreatic β-cell insulin secretion and glucose metabolism pathways. -
C8898 Ethacrynate SodiumSummary: Ethacrynate sodium is a loop diuretic electrophile that inhibits glutathione S-transferase activity and is widely utilized in redox biology and cancer research. -
C8903 ZucapsaicinSummary: Zucapsaicin is a synthetic capsaicin analog and TRPV1 agonist used as a molecular probe in nociception and sensory neurobiology research. -
C8914 FursultiamineSummary: Fursultiamine is a lipophilic thiamine derivative used to investigate vitamin B1 metabolism, thiamine-dependent enzymatic pathways, and cellular bioenergetics in biochemical research.
