JMV 449

Pricing Availability   Qty
说明: Potent neurotensin receptor agonist
纯度: ≥95% (HPLC)
说明书
引用文献
评论
文献 (1)

生物活性 for JMV 449

JMV 449 is a potent, metabolically stable neurotensin receptor agonist peptide (IC50 = 0.15 nM for inhibition of [125I]-NT binding to neonatal mouse brain; EC50 = 1.9 nM for contraction of guinea pig ileum). Produces long-lasting hypothermic, neuroprotective and analgesic effects in mice following central administration in vivo.

技术数据 for JMV 449

分子量 746.96
公式 C38H66N8O7
序列 KKPYIL

(Modifications: Lys-1 - Lys-2 peptide bond replaced with Ψ(CH2-NH))

储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 139026-66-7
PubChem ID 164415
InChI Key TZCYVPLNMOJUIL-GULBXNHPSA-N
Smiles [H]N[C@@H](CCCCN)CN[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O

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 JMV 449

溶解性 Soluble to 0.80 mg/ml in water

产品说明书 for JMV 449

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参考文献 for JMV 449

参考文献是支持产品生物活性的出版物。

Lugrin et al (1991) Reduced peptide bond pseudopeptide analogues of neurotensin: binding and biological activities, and in vitro metabolic stability. Eur.J.Pharmacol. 205 191 PMID: 1812009

Dubuc et al (1992) JMV 449: a pseudopeptide analogue of neurotensin-(8-13) with highly potent and long-lasting hypothermic and analgesic effects in the mouse. Eur.J.Pharmacol. 219 327 PMID: 1425958

Torup et al (2003) Neuroprotective effect of the neurotensin analogue JMV-449 in a mouse model of permanent middle cerebral ischaemia. Neurosci.Lett. 351 173 PMID: 14623134


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关键词: JMV 449, JMV 449 supplier, Potent, neurotensin, receptor, agonists, NT, Receptors, JMV449, Neurotensin, 1998, Tocris Bioscience

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