Neuropeptide S (human) (TFA);
Neuropeptide S human TFA,一种神经肽,是一种有效的同源神经肽 S 受体 (NPSR) 激动剂。Neuropeptide S human TFA 可用于阿尔茨海默病 (AD) 的研究。
Neuropeptide S (human) (TFA) Chemical Structure
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100 mg | ; | 询价 | ; |
250 mg | ; | 询价 | ; |
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生物活性 |
Neuropeptide S human TFA, a neuropeptide, is a potent cognate neuropeptide S receptor (NPSR) agonist. Neuropeptide S human TFA can be used for Alzheimer’s disease (AD) research[1]. |
IC50 Target |
EC50: 9.4 nM (neuropeptide S receptor)[1] |
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体外研究 (In Vitro) |
Half-maximal effective concentrations (EC50) for mobilization of [Ca2+]i are 9.4 nM, 3.2 nM, and 3.0 nM for human, rat, and mouse Neuropeptide S (NPS), respectively[1]. Neuropeptide S (human) (4 pM-1.7 nM; 48 hours) retains full agonist activity with an EC50 of 6.7 nM, the binding of [125I] Y10-hNPS to CHO cells stably expressing hNPSR is saturable with high affinity (Kd = 0.33 nM)[1]. Neuropeptide S (human) (1 pM-3 μM; 48 hours) are used to compete with 0.15 nM [125II] Y10-NPS, [125II] Y10-NPS is displaceable by increasing concentrations of human NPS (IC50 = 0.42 nM) [1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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体内研究 (In Vivo) |
Neuropeptide S (human) (intracerebroventricular (i.c.v.) injection; 0.1 nM or 1 nM; 60 mins) causes a significant increase in locomotor activity, the total distance traveled, percentage of time moving, number of rearing events, and center entries are also significantly increased in mice[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
2301.52 |
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Formula |
C95H156N31F3O30S |
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Sequence |
Ser-Phe-Arg-Asn-Gly-Val-Gly-Thr-Gly-Met-Lys-Lys-Thr-Ser-Phe-Gln-Arg-Ala-Lys-Ser |
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Sequence Shortening |
SFRNGVGTGMKKTSFQRAKS |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
Please store the product under the recommended conditions in the Certificate of Analysis. |
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参考文献 |
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