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1225062-23-6

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1225062-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1225062-23-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,0,6 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1225062-23:
(9*1)+(8*2)+(7*2)+(6*5)+(5*0)+(4*6)+(3*2)+(2*2)+(1*3)=106
106 % 10 = 6
So 1225062-23-6 is a valid CAS Registry Number.

1225062-23-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-6-bromopyrazine-2-carbohydrazide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1225062-23-6 SDS

1225062-23-6Downstream Products

1225062-23-6Relevant articles and documents

Discovery of 1-(4-(5-(5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)-1-ethyl-1,2,4-triazol-3-yl)piperidin-1-yl)-3-hydroxypropan-1-one (AZD8835): A potent and selective inhibitor of PI3Kα and PI3Kδ for the treatment of cancers

Barlaam, Bernard,Cosulich, Sabina,Delouvrié, Bénédicte,Ellston, Rebecca,Fitzek, Martina,Germain, Hervé,Green, Stephen,Hancox, Urs,Harris, Craig S.,Hudson, Kevin,Lambert-Van Der Brempt, Christine,Lebraud, Honorine,Magnien, Fran?oise,Lamorlette, Maryannick,Le Griffon, Antoine,Morgentin, Rémy,Ouvry, Gilles,Page, Ken,Pasquet, Georges,Polanska, Urszula,Ruston, Linette,Saleh, Twana,Vautier, Michel,Ward, Lara

, p. 5155 - 5162 (2015)

Starting from potent inhibitors of PI3Kα having poor general kinase selectivity (e.g., 1 and 2), optimisation of this series led to the identification of 25, a potent inhibitor of PI3Kα (wild type, E545K and H1047R mutations) and PI3Kδ, selective versus PI3Kβ and PI3Kγ, with excellent general kinase selectivity. Compound 25 displayed low metabolic turnover and suitable physical properties for oral administration. In vivo, compound 25 showed pharmacodynamic modulation of AKT phosphorylation and near complete inhibition of tumour growth (93% tumour growth inhibition) in a murine H1047R PI3Kα mutated SKOV-3 xenograft tumour model after chronic oral administration at 25 mg/kg b.i.d. Compound 25, also known as AZD8835, is currently in phase I clinical trials.

CHEMICAL COMPOUNDS

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Page/Page column 111; 112, (2014/08/07)

The invention concerns compounds of Formula (I) (Formula (I)) or pharmaceutically-acceptable salts thereof, wherein R1 and R2 have any of the meanings defined herein before in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of cell proliferative disorders.

Compounds Useful as Inhibitors of ATR Kinase

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Paragraph 0240; 0242, (2013/05/21)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, a

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