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View all Histamine H<sub>1</sub> Receptors products.Highly potent H1 histamine receptor antagonist (Kd = 310 pM) and tricyclic antidepressant. Also binds to the H4 histamine receptor (pKi = 6.79).
This compound is a mixture of E/Z isomers (ratio: 85:15).
分子量 | 315.84 |
公式 | C19H21NO.HCl |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 1229-29-4 |
PubChem ID | 5281088 |
InChI Key | MHNSPTUQQIYJOT-CULRIWENSA-N |
Smiles | Cl[H].CN(C)CC\C=C1\C2=C(COC3=C1C=CC=C3)C=CC=C2 |
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。
Lurchins (1983) Review of clinical and animal studies comparing the cardiovascular effects of dox. and other tricyclic antidepressants. Am.J.Psychiatry 140 1006 PMID: 6346907
Nguyen et al (2001) Discovery of a novel member of the histamine receptor family. Mol.Pharmacol. 59 427 PMID: 11179435
Tran et al (1981) [3H]Doxepin interactions with histamine H1-receptors and other sites in guinea pig brain homogenates. Eur.J.Pharmacol. 70 501 PMID: 7238574
Merck Index 12 3492
关键词: Doxepin hydrochloride, Doxepin hydrochloride supplier, potent, H1, antagonists, binds, H4, Receptors, Histamine, histaminergic, 0508, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Doxepin hydrochloride 的部分引用包括:
Jones et al (2011) Roles of affinity and lipophilicity in the slow kinetics of prostanoid receptor antagonists on isolated smooth muscle preparations. Br J Pharmacol 162 863 PMID: 20973775
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