SHA 68

Pricing Availability   Qty
说明: Selective Neuropeptide S receptor antagonist
化学名: N-[(4-Fluorophenyl)methyl]tetrahydro-3-oxo-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxamide
纯度: ≥98% (HPLC)
说明书
引用文献 (2)
评论

生物活性 for SHA 68

SHA 68 is a selective neuropeptide S receptor (NPSR) antagonist (IC50 values are 22.0 and 23.8 nM for human NPSR Asn107 and Ile107 variants respectively). Displays no activity against a range of 14 GPCRs, including vasopressin and oxytocin receptors.

化合物库 for SHA 68

SHA 68 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for SHA 68

分子量 445.49
公式 C26H24FN3O3
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 847553-89-3
PubChem ID 11374217
InChI Key SFRQIPRTNYHJHP-UHFFFAOYSA-N
Smiles O=C(NCC4=CC=C(F)C=C4)N1CC2N(C(OC(C5=CC=CC=C5)2C3=CC=CC=C3)=O)CC1

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.

溶解性数据 for SHA 68

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 44.55 100
ethanol 44.55 100

制备储备液 for SHA 68

以下数据基于产品分子量 445.49。 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.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.24 mL 11.22 mL 22.45 mL
5 mM 0.45 mL 2.24 mL 4.49 mL
10 mM 0.22 mL 1.12 mL 2.24 mL
50 mM 0.04 mL 0.22 mL 0.45 mL

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关键词: SHA 68, SHA 68 supplier, SHA68, neuropeptides, S, NPSRs, NPS, antagonists, selective, Neuropeptide, Receptors, 4510, Tocris Bioscience

2 篇 SHA 68 的引用文献

引用文献是使用了 Tocris 产品的出版物。 SHA 68 的部分引用包括:

Jing et al (2020) Neuropeptide S Displays as a Key Neuromodulator in Olfactory Spatial Memory. Chem Senses 45 195-202 PMID: 32010937

Ruzza et al (2018) Pharmacological profile of the neuropeptide S receptor: Dynamic mass redistribution studies. Pharmacol Res Perspect 6 e00445 PMID: 30534379


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