What are the categories of Polyaluminum Chloride (PAC)
Polyaluminum Chloride (PAC) Activator
An analytical standard for melatonin is standard melatonin( Standard). This publication contains research and analytical applications. The pineal gland releases melatonin receptors, which activates it. Sleeping-related meladipine has potent antioxidant and anti-inflammatory properties. A novel selective ATF-6 inhibitor, mitochondrialatonin, downregulates COX-2 and causes apoptosis in human hepatoma cells. Endoplasmic reticulum stress inhibits the palmitic acid-induced( HY-N0830) mouse granulosa cell apoptosis.
Standard melatonin
HY-131947
Antagonist DH97-7
With Ki values of 252 nM and 1100 nM for MT2 and MT1, respectively, DH97 is a potent melatonin receptor 2( MT2) antagonist.
DH97-7
HY-169382
Inhibitor of the melatonin-tamoxifen conjugate
A potent antagonist of ER( IC50=863 nM), the melatonin-tamoxifen conjugate( compound 16c) is known as the "metal-tamoxifen-compound conjugate "( compound 16c). In cells that express the hMT1 receptor, the melathifen-tamoxifen conjugate has the ability to bind to the MLT receptor( Ki=3.1 nM) and promote ERK activation and promoting -arrestin (EC50=914 nM) (EC50=98 nM). Compared to the common cell lines MCF-7, MDA-MB-231, and HT-1080, the IC50s of the melatonin-tamoxifen conjugate are 6.8M, 6.4%, and 1.7%, respectively.
Combination of melatonin and ammonia
HY-122136
Antagonist S26131 99.99%
S26131( compound 5) is a highly potent and selective MT1 melatonin ligand. The Ki values for MT1 and MT2 are 0.5 and 112 nM, respectively. S26131 behaves as an MT1 and MT2 antagonist.
S26131
HY-B0075S
Melatonin-d4
Melatonin d4
Activator ≥99.0%
Melatonin-d4 is a deuterated form of melatonin. Melatonin is a hormone made by the pineal gland that activates the melatonin receptor. It has antioxidant and anti-inflammatory properties. Melatonin is a novel selective ATF-6 inhibitor that induces apoptosis in human hepatoma cells via COX-2 downregulation.
Melatonin-d4
HY-101358
8-M-PDOT Agonist 99.54%
8-M-PDOT( AH-002) is a selective melatonin MT2 receptor agonist. 8-M-PDOT is 5.2 times more selective for MT2 than for MT1 receptors. 8-M-PDOT binds to human recombinant MT1 and MT2 receptors with pKi values of 8.23 and 8.95, respectively. 8-M-PDOT has anxiolytic activity.
8-M-PDOT
HY-101176
2-Iodomelatonin
2-Iodomelatonin
Agonist 99.04%
2-Iodomelatonin is a potent agonist of melatonin receptor 1( MT1) with a Ki of 28 pM and is more than 5-fold selective for MT1 over MT2.2-Iodomelatonin can be used to identify, characterize, and localize melatonin binding sites in brain and peripheral tissues.
2-Iodomelatonin
HY-14803
Tasimelteon
Tasimelteon
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