Membrane Transporter/Ion Channel
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.
- B5605 NS 3623Summary: human ether-a-go-go (hERG) KV11.1 potassium channel activator
- B5613 A 804598Summary: P2X7 antagonist,potent and selective
- B5620 DQP 1105Summary: NMDA receptor antagonist
- B5622 ML 218 hydrochlorideSummary: T-type calcium channels inhibitor
- B5628 ML 213Summary: KV7.2 (KCNQ2) and KV7.4 (KCNQ4) channel opener
- B5635 T16Ainh - A01Summary: inhibitor of Ca2+-dependent Cl- channel (CaCC) transmembrane protein 16A (TMEM16A)
- B5637 YM 244769Summary: inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)
- B5661 TC-I 2000Summary: TRPM8 channel blocker
- B5696 ML 204Summary: TRPC4 channels blocker
- B5700 ML SA1Summary: activator of TRPML channels