Dynorphin A
CAS No. 80448-90-4
Dynorphin A ( —— )
产品货号. M30699 CAS No. 80448-90-4
Endogenous kappa receptor agonist.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1815 | 有现货 |
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| 10MG | ¥2404 | 有现货 |
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| 25MG | ¥4259 | 有现货 |
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| 50MG | ¥6538 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称Dynorphin A
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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Endogenous kappa receptor agonist.
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产品描述Endogenous kappa receptor agonist.
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体外实验Dynorphin A (10 μM, 4 h/72 h) increases caspase-3 activity and the level of cytochrome c released from mitochondria in mouse striatal neurons, and induces neuronal death.dynorphin A (33 μM, 4 h) elevates [Ca2+]i and causes a significant loss of neurons.dynorphin A (1 μM) inhibits the release of vasopressin (VP) from the isolated neural lobe. Cell Viability Assay Cell Line:Mouse striatal neurons Concentration:10 μM Incubation Time:0, 24, 48, 72 h Result:Induced neuronal death (identified by the fragmentation and destruction of the cell body and neurites).
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体内实验Dynorphin A (intracerebroventricular injection, 1 μg of 2 μL, a single dose) inhibits vasopressin (VP) release in 24 h water-deprived male rats.Dynorphin A (intracerebroventricular injection, 500 pmol/5 μL per day for 4 d) alleviates stress-induced behavioral impairments in ddY mice accompanied by regulation of the 5-HTergic system in the brain. Animal Model:24 h water-deprived male rats Dosage:1 μg of 2 μL Administration: Intracerebroventricular injection Result:Inhibited vasopressin (VP) release 30 min upon injection. Animal Model:Male ddY mice Dosage:15, 150, 1500 pmol/5 μL per day for 4 days Administration:Intracerebroventricular injection Result: Attenuated the repeated stress-induced escape failures from the shock.
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同义词——
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通路Apoptosis
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靶点Caspase
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number80448-90-4
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分子量2147.51
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分子式C99H155N31O23
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纯度>98% (HPLC)
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溶解度water:0.80 mg/mL
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SMILES[H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)NCC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O
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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. Dhawan et al (1996) International union of pharmacology XII. Classification of opioid receptors. Pharmacol.Rev. 48 567 PMID:
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