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383415-79-0

中文名稱 TRP-TYR-LYS-HIS-VAL-ALA-SER-PRO-ARG-TYR-HIS-THR-VAL-GLY-ARG-ALA-ALA-GLY-LEU-LEU-MET-GLY-LEU
英文名稱 H-TRP-TYR-LYS-HIS-VAL-ALA-SER-PRO-ARG-TYR-HIS-THR-VAL-GLY-ARG-ALA-ALA-GLY-LEU-LEU-MET-GLY-LEU-OH
CAS 383415-79-0
分子式 C119H183N35O28S
分子量 2584.01
MOL 文件 383415-79-0.mol
更新日期 2024/12/22 20:23:45
383415-79-0 結(jié)構(gòu)式 383415-79-0 結(jié)構(gòu)式

基本信息

中文別名
神經(jīng)肽 W-23 (人)
神經(jīng)肽 W-23 (人), >95%
英文別名
NPW-23 (HUMAN)
NEUROPEPTIDE W-23 (HUMAN)
Neuropeptide W-23 (huMan) NPW-23 (huMan)
Neuropeptide W-23(human),WYKHVASPRYHTVGRAAGL MGL,NPW-23, >95%
TRP-TYR-LYS-HIS-VAL-ALA-SER-PRO-ARG-TYR-HIS-THR-VAL-GLY-ARG-ALA-ALA-GLY-LEU-LEU-MET-GLY-LEU
H-TRP-TYR-LYS-HIS-VAL-ALA-SER-PRO-ARG-TYR-HIS-THR-VAL-GLY-ARG-ALA-ALA-GLY-LEU-LEU-MET-GLY-LEU-OH
L-Leucine, L-tryptophyl-L-tyrosyl-L-lysyl-L-histidyl-L-valyl-L-alanyl-L-seryl-L-prolyl-L-arginyl-L-tyrosyl-L-histidyl-L-threonyl-L-valylglycyl-L-arginyl-L-alanyl-L-alanylglycyl-L-leucyl-L-leucyl-L-methionylglycyl-

物理化學性質(zhì)

儲存條件Desiccate at -20°C
形態(tài)Solid
顏色White to off-white
水溶解性Soluble to 1 mg/ml in sterile water

常見問題列表

生物活性
Neuropeptide W-23(human) 是 Neuropeptide W 的主要活性形式,為 NPBW1 和 NPBW2 的內(nèi)源性配體。
體外研究

NPW-23 increases the I Ca,L in transfected human embryonic kidney 293 cells and VSMCs via GPR7. NPW-23 increases the expression of pan phospho-PKC, intracellular diacylglycerol level, and the second messenger catalyzed by PLC.

體內(nèi)研究

NPW-23 increases pressure-induced vasotone of the rat mesenteric arteries. Importantly, the expression of NPW is decreased in the hypertensive rats. NPW-23 (0.3 nmol, 1.0 nmol, and 3.0 nmol) induces significant increases in mean arterial pressure (MAP) in conscious, freely moving male rats. Rats that receive either 1.0 or 3.0 nmol NPW-23 demonstrate a significant increase in total activity, ambulatory activity, and duration of stereotypy. NPW-23 fails to elevate MAP in rats pretreated with phentolamine. NPW-23-induced increases in total activity, ambulatory activity, and duration of stereotypy are reduced significantly by pretreatment with the orexin type 1 receptor (OX1R) antagonist, SB-408124.

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