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Submit ReviewHigh affinity and selective presynaptic choline transporter (CHT) inhibitor (Ki = 92 nM). Exhibits selectivity for CHT over dopamine, serotonin and noradrenalin transporters; acetylcholinesterase and cholineacetyltransferase; and a panel of 65 other GPCRs, ion channels and transporters.
分子量 | 423.93 |
公式 | C21H29N3O4.HCl |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1962928-20-6 |
PubChem ID | 121513888 |
InChI Key | UKLCTDBUTADGBD-UHFFFAOYSA-N |
Smiles | COC1=CC=C(C(NCC3=CC(C(C)C)=NO3)=O)C=C1OC2CCN(C)CC2.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Ennis et al (2015) Identification and characterization of ML352: a novel, noncompetitive inhibitor of the presynaptic choline transporter. ACS Chem.Neurosci. 6 417 PMID: 25560927
Bollinger et al (2015) Synthesis and structure-activity relationships of a series of 4-methoxy-3-(piperidin-4-yl)oxy benzamides as novel inhibitors of the presynaptic choline transporter. Bioorg.Med.Chem.Lett. 25 1757 PMID: 25801932
关键词: ML 352 hydrochloride, ML 352 hydrochloride supplier, ML352, hydrochloride, 1649450-12-3, high, affinity, selective, presynaptic, choline, transporter, CHT, Acetylcholine, Transporters, 5725, Tocris Bioscience
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