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Home > Fluorides > 1622-79-3

1622-79-3

1622-79-3 | 1-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-, hydrochloride (1:1)

CAS No: 1622-79-3 Catalog No: AG001SVX MDL No:MFCD00270922

Product Description

Catalog Number:
AG001SVX
Chemical Name:
1-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-, hydrochloride (1:1)
CAS Number:
1622-79-3
Molecular Formula:
C16H23ClFNO
Molecular Weight:
299.8113
MDL Number:
MFCD00270922
IUPAC Name:
1-(4-fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-one;hydrochloride
InChI:
InChI=1S/C16H22FNO.ClH/c1-13-8-11-18(12-9-13)10-2-3-16(19)14-4-6-15(17)7-5-14;/h4-7,13H,2-3,8-12H2,1H3;1H
InChI Key:
MQHYXXIJLKFQGY-UHFFFAOYSA-N
SMILES:
CC1CCN(CC1)CCCC(=O)c1ccc(cc1)F.Cl
EC Number:
216-599-9
UNII:
88G640374K
NSC Number:
760102

Properties

Complexity:
279  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
299.145g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
299.814g/mol
Monoisotopic Mass:
299.145g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
20.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0

Literature

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Cytochrome P450 2D6 dependent metabolization of risperidone is inhibited by melperone. European journal of clinical pharmacology 20060401
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P-glycoprotein is a factor in the uptake of dextromethorphan, but not of melperone, into the mouse brain: evidence for an overlap in substrate specificity between P-gp and CYP2D6. Journal of psychopharmacology (Oxford, England) 20041201
Discriminative stimulus properties of 1.25 and 5.0 mg/kg doses of clozapine in rats: examination of the role of dopamine, serotonin, and muscarinic receptor mechanisms. Pharmacology, biochemistry, and behavior 20040201
[Treatment of behavioral disorders in dementia with risperidone in psychogeriatric out-patients]. MMW Fortschritte der Medizin 20031009
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Melperone is an inhibitor of the CYP2D6 catalyzed O-demethylation of venlafaxine. Pharmacopsychiatry 20030101
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[Practical experiences in the therapy of postweaning edema disease in piglets]. Berliner und Munchener tierarztliche Wochenschrift 19961001
Dopamine D4 versus D2 receptor selectivity of dopamine receptor antagonists: possible therapeutic implications. European journal of pharmacology 19930604

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