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8-(1-(S)-(3,5-difluorophenylamino)ethyl)-N,N-dimethyl-2-((R)-2-methylmorpholino)-4-oxo-4H-chromene-6-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1296272-03-1

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  • 8-(1-(S)-(3,5-difluorophenylamino)ethyl)-N,N-dimethyl-2-((R)-2-methylmorpholino)-4-oxo-4H-chromene-6-carboxamide

    Cas No: 1296272-03-1

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1296272-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1296272-03-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,6,2,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1296272-03:
(9*1)+(8*2)+(7*9)+(6*6)+(5*2)+(4*7)+(3*2)+(2*0)+(1*3)=171
171 % 10 = 1
So 1296272-03-1 is a valid CAS Registry Number.

1296272-03-1Downstream Products

1296272-03-1Relevant articles and documents

Discovery of (R)-8-(1-(3,5-difluorophenylamino)ethyl)- N, N -dimethyl-2-morpholino-4-oxo-4 H -chromene-6-carboxamide (AZD8186): A potent and selective inhibitor of PI3Kβ and PI3Kδ for the treatment of PTEN-deficient cancers

Barlaam, Bernard,Cosulich, Sabina,Degorce, Sébastien,Fitzek, Martina,Green, Stephen,Hancox, Urs,Lambert-Van Der Brempt, Christine,Lohmann, Jean-Jacques,Maudet, Micka?l,Morgentin, Rémy,Pasquet, Marie-Jeanne,Péru, Aurélien,Plé, Patrick,Saleh, Twana,Vautier, Michel,Walker, Mike,Ward, Lara,Warin, Nicolas

, p. 943 - 962 (2015/01/30)

Several studies have highlighted the dependency of PTEN deficient tumors to PI3Kβ activity and specific inhibition of PI3Kδ has been shown activity against human B-cell cancers. We describe the discovery and optimization of a series of 8-(1-anilino)ethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxamides as PI3Kβ/δ inhibitors, which led to the discovery of the clinical candidate 13, also known as AZD8186. On the basis of the lower lipophilicity of the chromen-4-one core compared to the previously utilized pyrido[1,2-a]pyrimid-4-one core, this series of compounds displayed high metabolic stability and suitable physical properties for oral administration. Compound 13 showed profound pharmacodynamic modulation of p-Akt in PTEN-deficient PC3 prostate tumor bearing mice after oral administration and showed complete inhibition of tumor growth in the mouse PTEN-deficient PC3 prostate tumor xenograft model. 13 was selected as a clinical candidate for treatment of PTEN-deficient cancers and has recently entered phase I clinical trials.

CHROMENONE DERIVATIVES

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Page/Page column 85, (2011/05/05)

The invention concerns chromenone derivatives of Formula I or a pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, R6, R7, R8, n and R9 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.

CHROMENONE DERIVATIVES WITH ANTI-TUMOUR ACTIVITY

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Page/Page column 177-178, (2011/05/11)

The invention concerns chromenone derivatives of Formula (I) or a pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, R6, R7, R8, n and R9 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.

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