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ChemicalBook--->CAS DataBase List--->192322-50-2

192322-50-2

192322-50-2 Structure

192322-50-2 Structure
IdentificationBack Directory
[Name]

CGP 71683 HYDROCHLORIDE
[CAS]

192322-50-2
[Synonyms]

CGP 71683
CGP71683HCl
UNII-45B73P82A3
CGP 71683 HYDROCHLORIDE
CGP 71683A hydrochloride
CGP-71683A; CGP 71683A; CGP71683A; UNII-45B73P82A3
N-[[TRANS-4-[[(4-AMINO-2-QUINAZOLINYL)AMINO]METHYL]CYCLOHEXYL]METHYL]-1-NAPHTHALENESULFONAMIDE HYDROCHLORIDE
1-Naphthalenesulfonamide, N-[[trans-4-[[(4-amino-2-quinazolinyl)amino]methyl]cyclohexyl]methyl]-, hydrochloride (1:1)
[Molecular Formula]

C26H30ClN5O2S
[MDL Number]

MFCD07783999
[MOL File]

192322-50-2.mol
[Molecular Weight]

512.07
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

H2O: ~14 mg/mL, soluble
[form ]

solid
[color ]

off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

CGP 71683 is an antagonist of neuropeptide Y (NPY) receptor Y5 (IC50 = 1.4 nM in a radioligand binding assay). It is selective for Y5 over Y1, Y2, and Y4 receptors (IC50s = 2,765, 7,187, and 5,637 nM, respectively). It inhibits NPY-induced increases in BT-549 cell growth and MDA-MB-231 cell migration when used at a concentration of 0.25 μM. CGP 71683 (10 mg/kg, i.p.) inhibits increases in food intake induced by intracerebroventricular administration of NPY in rats.
[Biological Activity]

Extremely selective, non-peptide NPY Y 5 receptor antagonist. Displays > 1000-fold selectivity over Y 1 , Y 2 and Y 4 receptors; IC 50 values are 1.4, 2765, 7187 and 5637 nM at cloned rat Y 5 , Y 1 , Y 2 and Y 4 receptors respectively. Potently inhibits NPY-induced food intake following i.p. administration in diabetic, free-feeding and fasted rats.
[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

CGP 71683 HYDROCHLORIDE(192322-50-2)1HNMR
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