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6-chloromelatonin

Known as: N-(2-(6-chloro-5-methoxy-1H-indol-3-yl)ethyl)acetamide 
 
National Institutes of Health

Papers overview

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Highly Cited
2002
Highly Cited
2002
In rat caudal artery, contraction to melatonin results primarily from activation of MT(1) melatonin receptors; however, the role… Expand
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Highly Cited
2002
Highly Cited
2002
Melatonin's O-methyl and N-acetyl residues are not only the basis of its amphilicity enabling the molecule to enter all organs… Expand
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1998
1998
The endogenous indole melatonin and the melatonin receptor agonist 6-chloromelatonin block the proliferation of both dermal and… Expand
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Highly Cited
1997
Highly Cited
1997
Abstract We have identified subtype selective agonists, partial agonists and antagonists, which distinguish the human recombinant… Expand
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Highly Cited
1997
Highly Cited
1997
It has been suggested that the indole hormone melatonin (N-acetyl-5-methoxytryptamine, MLT) is an important natural antioxidant… Expand
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1993
1993
In order to explore the potential oncostatic properties of the pineal hormone, melatonin, we have investigated its binding… Expand
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1991
1991
Melatonin receptors were characterized in the brains of three mammals (rabbit, horse and sheep) by an in vitro binding technique… Expand
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Highly Cited
1989
Highly Cited
1989
Little is known of the neural sites of action for the pineal hormone, melatonin. Thus, we developed an in vitro autoradiographic… Expand
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Highly Cited
1988
Highly Cited
1988
In vitro autoradiography with 125I-labeled melatonin was used to examine melatonin binding sites in human hypothalamus. Specific… Expand
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Highly Cited
1988
Highly Cited
1988
The pharmacological potencies of 2-substituted N-acetyltryptamines were determined on the presynaptic melatonin receptor site of… Expand
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