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(trans)-8-({[5-(2-fluorophenyl)-2-pyrimidinyl]amino}methyl)-3-(2-pyridinyl)-1-oxa-3-azaspiro[4.5]decan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1177267-25-2

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1177267-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1177267-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,7,2,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1177267-25:
(9*1)+(8*1)+(7*7)+(6*7)+(5*2)+(4*6)+(3*7)+(2*2)+(1*5)=172
172 % 10 = 2
So 1177267-25-2 is a valid CAS Registry Number.

1177267-25-2Upstream product

1177267-25-2Relevant academic research and scientific papers

Discovery and structure-activity relationship of a novel spirocarbamate series of NPY Y5 antagonists

Leslie, Colin P.,Bentley, Jonathan,Biagetti, Matteo,Contini, Stefania,Di Fabio, Romano,Donati, Daniele,Genski, Thorsten,Guery, Sebastien,Mazzali, Angelica,Merlo, Giancarlo,Pizzi, Domenica A.,Sacco, Fabiola,Seri, Catia,Tessari, Michela,Zonzini, Laura,Caberlotto, Laura

, p. 6103 - 6107 (2010)

A novel series of trans-8-aminomethyl-1-oxa-3-azaspiro[4.5]decan-2-one derivatives was identified with potent NPY Y5 antagonist activity. Optimization of the original lead furnished compounds 23p and 23u, which combine sub-nanomolar Y5 activity with metabolic stability, oral bioavailability, brain penetration and strong preclinical profile for development. Both compounds significantly inhibited the food intake induced by a Y5 selective agonist with minimal effective doses of 3 mg/kg po.

Spiro Compounds As NPY Y5 Receptor Antagonists

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Page/Page column 79-80, (2009/08/18)

The present invention relates to novel compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein R is an aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano;Z1 is H, C1-C4 alkyl or F;Z is CH2, CH(C1-C4 alkyl), C(C1-C4 alkyl)2 or a bond;A is a 6-10 membered aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; or —C(═O)—X; or —O(CH2)0-1R1;B is hydrogen or is a 5-6 membered heteroaryl, or a 4-6 membered heterocycle, or phenyl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, hydroxyl, cyano; A and B being linked via any atom;R1 is —(C1-C4)alkyl(C1-C4)alkoxy; or C3-C8 cycloalkyl; or R1 is an aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; or R1 is a 4-6 membered heterocycle, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano;X is OR2 or NR3R4;R2 is C1-C4 alkyl;R3 is hydrogen or together with R4 and the nitrogen form a 5-6 saturated membered ring;R4 is C3-C8 cycloalkyl; processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them and their use in therapy, as NPY Y5 receptor antagonists and as agents for the treatment and/or prophylaxis of eating disorders such as a binge eating disorder.

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