1364269-10-2 Usage
Uses
Used in Pharmaceutical Industry:
(R)-(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzamide is used as a potential pharmaceutical agent for [application reason]. (R)-(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzamide's unique structure and functional groups may offer novel therapeutic properties, which could be harnessed for the development of new drugs targeting various medical conditions.
Used in Chemical Research:
In the field of chemical research, (R)-(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzamide serves as a subject for studying its reactivity, stability, and potential interactions with other molecules. Understanding these properties can provide insights into the compound's behavior and possible applications in various chemical processes.
Used in Material Science:
(R)-(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzamide may be utilized in material science as a component in the development of new materials with specific properties. (R)-(Z)-4-(2-amino-5-(4-((dimethylamino)methyl)thiophen-2-yl)pyridin-3-yl)-2-((5,5,5-trifluoropent-3-en-2-yl)oxy)benzamide's unique structure and functional groups could contribute to the creation of materials with enhanced characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 1364269-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,2,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1364269-10:
(9*1)+(8*3)+(7*6)+(6*4)+(5*2)+(4*6)+(3*9)+(2*1)+(1*0)=162
162 % 10 = 2
So 1364269-10-2 is a valid CAS Registry Number.
1364269-10-2Relevant academic research and scientific papers
Design of potent and selective hybrid inhibitors of the mitotic kinase nek2: Structure-activity relationship, structural biology, and cellular activity
Innocenti, Paolo,Cheung, Kwai-Ming J.,Solanki, Savade,Mas-Droux, Corine,Rowan, Fiona,Yeoh, Sharon,Boxall, Kathy,Westlake, Maura,Pickard, Lisa,Hardy, Tara,Baxter, Joanne E.,Aherne, G. Wynne,Bayliss, Richard,Fry, Andrew M.,Hoelder, Swen
, p. 3228 - 3241 (2012/06/01)
We report herein a series of Nek2 inhibitors based on an aminopyridine scaffold. These compounds have been designed by combining key elements of two previously discovered chemical series. Structure based design led to aminopyridine (R)-21, a potent and selective inhibitor able to modulate Nek2 activity in cells.
