CAS NO: | 134865-74-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | 4-P-PDOT is a potent, selective and affinityMelatonin receptor(MT2)antagonist. 4-P-PDOT is >300-fold more selective forMT2thanMT1. 4-P-PDOT significantly counteracts Melatonin-mediated antioxidant effects (GSH/GSSG ratio, phospho-ERK, Nrf2 nuclear translocation, Nrf2 DNA-binding activity)[1][2][3][4]. | ||||||||||||||||
IC50& Target | MT2 receptor[1] | ||||||||||||||||
体外研究 (In Vitro) | In CHO-mt1 cells the amidotetraline 4-P-PDOT (10 mM) has no effect on forskolin-stimulated cyclic AMP levels, either alone, or in the presence of Melatonin. In contrast, in CHO-MT2 cells, 4-P-PDOT is an agonist, producing a concentration-dependent inhibition of forskolin stimulated cyclic AMP, with a pEC50value of 8.72 and intrinsic activity of 0.86[1]. Cell Viability Assay[5]
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体内研究 (In Vivo) | 4-P-PDOT (0.5-1.0 mg/kg; intravenous injection;klothomutant mice) treatment significantly reverses antioxidant effects mediated by Melatonin. And significantly reverses the changes in the levels of these GSH-related parameters. 4-P-PDOT treatment significantly reverses the memory function of Melatonin-treatedklothomutant mice. 4-P-PDOT also counteracts Melatonin-mediated attenuation in response to the decreases in phospho-ERK expression, Nrf2 nuclear translocation, Nrf2 DNA-binding activity, and GCL mRNA expression in the hippocampi ofklothomutant mice[2].
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分子量 | 279.38 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H21NO | ||||||||||||||||
CAS 号 | 134865-74-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 41.67 mg/mL(149.15 mM;Need ultrasonic) 配制储备液
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