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α-CGRP (mouse, rat)
CAS No. 83651-90-5
α-CGRP (mouse, rat) ( ——— )
产品货号. M38004 CAS No. 83651-90-5
α-CGRP (mouse, rat), a neuropeptide (calcitonin gene-related peptide (CGRP)) mainly expressed in neuromuscular junction, is a potent vasodilator. α-CGRP (mouse, rat) can lead to a fall in blood pressure and an increase in heart rate by peripheral administration, also relax colonie smooth muscle. α-CGRP (mouse, rat) has the potential in cardiovascular, pro-inflammatory, migraine and metabolic studies.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称α-CGRP (mouse, rat)
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注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
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产品简述α-CGRP (mouse, rat), a neuropeptide (calcitonin gene-related peptide (CGRP)) mainly expressed in neuromuscular junction, is a potent vasodilator. α-CGRP (mouse, rat) can lead to a fall in blood pressure and an increase in heart rate by peripheral administration, also relax colonie smooth muscle. α-CGRP (mouse, rat) has the potential in cardiovascular, pro-inflammatory, migraine and metabolic studies.
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产品描述α-CGRP (mouse, rat), a neuropeptide (calcitonin gene-related peptide (CGRP)) mainly expressed in neuromuscular junction, is a potent vasodilator. α-CGRP (mouse, rat) can lead to a fall in blood pressure and an increase in heart rate by peripheral administration, also relax colonie smooth muscle. α-CGRP (mouse, rat) has the potential in cardiovascular, pro-inflammatory, migraine and metabolic studies.
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体外实验α-CGRP (mouse, rat) (0.25, 0.5, 1 μg/kg/min, 静脉注射) 剂量依赖性地降低了平均动脉血压，同时心率和全身血管传导增加，而心输出量保持不变。α-CGRP (mouse, rat) 在 Kainic acid (KA) 诱导的海马 CA3 区锥体细胞死亡的调控中发挥重要作用。
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体内实验α-CGRP (mouse, rat) 可调节 2 组先天淋巴样细胞反应。α-CGRP (mouse, rat) 可调节胰岛素分泌，降低 2 型糖尿病的风险。
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同义词———
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通路Others
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靶点Other Targets
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受体CGRP Receptor
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研究领域———
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适应症———
化学信息
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CAS Number83651-90-5
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分子量3806.25
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分子式C162H262N50O52S2
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纯度>98% (HPLC)
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溶解度H2O : ≥ 100 mg/mL (26.27 mM)
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SMILES———
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化学全称———
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Whitby K, et al. Castanospermine, a potent inhibitor of dengue virus infection in vitro and in vivo. J Virol. 2005 Jul;79(14):8698-706.?
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