62'-Dihydroxyflavone
CAS No. 92439-20-8
62'-Dihydroxyflavone ( —— )
产品货号. M21418 CAS No. 92439-20-8
6,2'-DiHydroxyflavone 是一种新型的 GABAA 受体拮抗剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥150 | 有现货 |
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| 10MG | ¥207 | 有现货 |
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| 25MG | ¥319 | 有现货 |
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| 50MG | ¥461 | 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 |
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| 1 mL x 10 mM in DMSO | ¥402 | 有现货 |
|
生物学信息
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产品名称62'-Dihydroxyflavone
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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6,2'-DiHydroxyflavone 是一种新型的 GABAA 受体拮抗剂。
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产品描述62'-Dihydroxyflavone is a novel antagonist of GABAA receptor.
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体外实验6,2'-Dihydroxyflavone is a novel antagonist of GABAA receptor. 6,2'-Dihydroxyflavone inhibits [3H]-flunitrazepam binding to the rat cerebral cortex membranes with a Ki of 37.2±4.5 nM. The current elicited with the EC50 concentration of GABA is decreased to 73.6±1.9% of control by co-application of 5 μM 6,2'-Dihydroxyflavone (n=5), compare to a decrease to 65.9±3.0% by 1 μM FG-7142 (n=5). The EC50 for GABA dose response increases from 47.6 to 59.7 μM upon co-application of 5 μM 6,2'-Dihydroxyflavone, and the maximal GABA-current is decreased.
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体内实验6,2'-Dihydroxyflavone-treated mice exhibit significant differences from control mice with respect to the percentage of open arms entries [F(4,73)=8.01, P<0.0001] and the percentage of time spent in open arms [F (4,73)=5.19, P<0.002], but not the number of entries to closed arms [F(4,73)= 0.79,P=0.54]. The post-hoc NewmaneKeuls’ tests confirm that 6,2'-Dihydroxyflavone significantly decreases the percentage of open arm entries and time spent in open arms at the doses of 8 and 16 mg/kg. 6,2'-Dihydroxyflavone treatment similarly increases step-through latency [F(4,75)=4.71, P<0.002], suggesting enhanced cognitive performance.
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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GABAA
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研究领域——
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适应症——
化学信息
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CAS Number92439-20-8
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分子量254.24
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分子式C15H10O4
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纯度>98% (HPLC)
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溶解度DMSO:155 mg/mL (69.66 mM and warming)
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SMILESOc(cc1)cc2c1OC(c(cccc1)c1O)=CC2=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.Wang F et al. 62'-Dihydroxyflavone a subtype-selective partial inverse agonist of GABAA receptor benzodiazepine site. Neuropharmacology. 2007 Sep;53(4):574-82.
产品手册
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