货号:A835423
同义名:
CID-230710; NSC 25850
ML204 is a selective antagonist of TRPC4 ion channel with IC50 of 0.96 μM and 2.6 μM in fluorescent and electrophysiological assays respectively.
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描述 | Transient receptor potential canonical (TRPC) channels are Ca2+-permeable nonselective cation channels implicated in diverse physiological functions, including smooth muscle contractility and synaptic transmission[3]. ML204 is a novel, potent, and selective TRPC4 channel inhibitor with apparent IC50 values of about 1 μM in fluorescent intracellular Ca2+ assays and about 3 μM in whole-cell voltage clamp experiments[3]. ML204 blocked TRPC4β activity induced through either Gi/o stimulation by μ-opioid, 5HT1A serotonin, and M2 muscarinic receptors or Gq/11 stimulation by the endogenous M3-like muscarinic receptors. It also blocked TRPC4β channels activated by intracellularly applied GTPγS (guanosine 5'-3-O-(thio) triphosphate) or Ca2+, which bypass receptor stimulation[3]. In isolated guinea pig ileal myocytes, ML204 blocked muscarinic cation currents activated by bath application of carbachol or intracellular infusion of GTPγS, demonstrating its effectiveness on native TRPC4 currents[3]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
4.42mL 0.88mL 0.44mL |
22.09mL 4.42mL 2.21mL |
44.19mL 8.84mL 4.42mL |
CAS号 | 5465-86-1 |
分子式 | C15H18N2 |
分子量 | 226.32 |
SMILES Code | CC1=CC(N2CCCCC2)=NC3=CC=CC=C13 |
MDL No. | MFCD00817920 |
别名 | CID-230710; NSC 25850; 2-piperidino-Lepidine |
运输 | 蓝冰 |
InChI Key | USYRQXDHKXGTCK-UHFFFAOYSA-N |
Pubchem ID | 230710 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
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