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Submit ReviewWAY 267464 dihydrochloride is a potent, selective non-peptide oxytocin receptor (OTR) agonist (Ki = 58.4 nM at human OTR). Exhibits anxiolytic-like effects. May have therapeutic potential for the treatment of psychosis and schizophrenia.
Sold for research purposes under agreement from Pfizer Inc.
分子量 | 654.59 |
公式 | C32H35N7O4.2HCl |
储存 | Store at -20°C |
纯度 | ≥97% (HPLC) |
CAS Number | 1432043-31-6 |
PubChem ID | 71555165 |
InChI Key | OTFWXMFLPMUDFP-UHFFFAOYSA-N |
Smiles | CN(N=C3)C1=C3CN(C(C4=CC=C(CNC(N5CCN(CC6=CC(O)=CC(O)=C6)CC5)=O)C(C)=C4)=O)C(C=CC=C2)=C2N1.Cl.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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 52.37 | 80 | |
water | 3.27 | 5 |
以下数据基于产品分子量 654.59。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.8 mM | 1.91 mL | 9.55 mL | 19.1 mL |
4 mM | 0.38 mL | 1.91 mL | 3.82 mL |
8 mM | 0.19 mL | 0.95 mL | 1.91 mL |
40 mM | 0.04 mL | 0.19 mL | 0.38 mL |
参考文献是支持产品生物活性的出版物。
Ring et al (2010) Receptor and behavioral pharmacology of WAY-267464, a non-peptide oxyt. receptor agonist. Neuropharmacology 58 6 PMID: 19615387
If you know of a relevant reference for WAY 267464 dihydrochloride, please let us know.
关键词: WAY 267464 dihydrochloride, WAY 267464 dihydrochloride supplier, WAY267464, dihydrochloride, oxytocin, agonists, OT, receptors, non-peptide, pfizer, Oxytocin, Receptors, 3933, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 WAY 267464 dihydrochloride 的部分引用包括:
Sandy et al (2022) Social isolation modulates appetite and avoidance behavior via a common oxytocinergic circuit in larval zebrafish. Nat Commun 13 2573 PMID: 35545618
Akihiro et al (2020) Physiological and pharmacological evaluation of oxytocin-induced milk ejection in mice. Exp Anim 69 345-353 PMID: 32213759
Tzu-Ming et al (2020) Utilizing Designed Receptors Exclusively Activated by Designer Drug Chemogenetic Tools to Identify Beneficial G Protein-Coupled Receptor Signaling for Fibrosis. J Pharmacol Exp Ther 375 357-366 PMID: 32848074
Xiao et al (2017) Biased OXTergic Modulation of Midbrain DA Systems. Neuron 95 368 PMID: 28669546
Huo et al (2018) Tph2-/- female mice restore socio-sexual recognition through upregulating ERα and OTR genes in the amygdala. PLoS One 13 e0193395 PMID: 29470551
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