Weight | 555.247 g/mol |
---|---|
Formula | C22H21Cl2IN4O |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 1 |
Aromatic Rings | 3 |
Rotatable Bonds | 4 |
AM251 (183232-66-8)
AM 251 · N-(piperidin-1-yl)-1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-1H-pyrazole-3-carboxamide · N-(piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide
Score:
#1181 in Neuroscience
,
#5093 in Biology
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- Sigma-Aldrich - AM251204.00 - 699.00 USD
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- 123I-labeled AM251: a radioiodinated ligand which binds in vivo to mouse brain cannabinoid CB1 receptors (European Journal of Pharmacology, 1996)
- Antidepressant-like and anorectic effects of the cannabinoid CB1 receptor inverse agonist AM251 in mice. (Behavioural Pharmacology, 2003)
- The cannabinoid CB1 antagonists SR 141716A and AM 251 suppress food intake and food-reinforced behavior in a variety of tasks in rats. (Behavioural Pharmacology, 2003)
- Binding of the non-classical cannabinoid CP 55,940, and the diarylpyrazole AM251 to rodent brain cannabinoid receptors (Life Sciences, 1997)
- Cannabinoid CB1 Receptor Antagonist AM251 Inhibits Cocaine-Primed Relapse in Rats: Role of Glutamate in the Nucleus Accumbens (The Journal of Neuroscience, 2006)
- Cannabinoid (CB)1 receptor antagonist, AM 251, causes a sustained reduction of daily food intake in the rat (Physiology & Behavior, 2004)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - AM 251
- N-(piperidin-1-yl)-1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-1H-pyrazole-3-carboxamide
- N-(piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide
- AM-251
-
SMILESCC1=C(N(N=C1C(=O)NN2CCCCC2)C3=C(C=C(C=C3)Cl)Cl)C4=CC=C(C=C4)I
-
InChIKeyBUZAJRPLUGXRAB-UHFFFAOYSA-N
- Pubchem - AM251
- Wikipedia - am-251
AM-251 is an inverse agonist at the CB1 cannabinoid receptor. AM-251 is structurally very close to SR141716A (rimonabant); both are biarylpyrazole cannabinoid receptor antagonists. In AM-251 the p-chloro group attached to the phenyl substituent at C-5 of the pyrazole ring is replaced with a p-iodo group.
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