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(3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)(piperidin-1-yl)methanone is a synthetic compound characterized by a complex molecular structure that features a piperidine ring, an isoxazole ring, and a ketone functional group. (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)(piperidin-1-yl)methanone is recognized for its potential biological activity and is commonly utilized in pharmaceutical research and drug development.
Used in Pharmaceutical Research and Drug Development:
(3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)(piperidin-1-yl)methanone is used as a compound of interest in pharmaceutical research and drug development due to its potential biological activity and possible applications as a central nervous system stimulant or an analgesic.
Used in Laboratory and Research Settings:
In laboratory and research settings, (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)(piperidin-1-yl)methanone is used for studying its complex structure and potential physiological effects, with a necessary emphasis on careful handling and use to ensure safety.

153948-82-4

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153948-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153948-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153948-82:
(8*1)+(7*5)+(6*3)+(5*9)+(4*4)+(3*8)+(2*8)+(1*2)=164
164 % 10 = 4
So 153948-82-4 is a valid CAS Registry Number.

153948-82-4Downstream Products

153948-82-4Relevant academic research and scientific papers

The first low μM SecA inhibitors

Chen, Weixuan,Huang, Ying-ju,Gundala, Sushma Reddy,Yang, Hsiuchin,Li, Minyong,Tai, Phang C.,Wang, Binghe

experimental part, p. 1617 - 1625 (2010/05/17)

SecA ATPase is a critical member of the Sec family, which is important in the translocation of membrane and secreted polypeptides/proteins in bacteria. Small molecule inhibitors can be very useful research tools as well as leads for future antimicrobial agent development. Based on previous virtual screening work, we optimized the structures of two hit compounds and obtained SecA ATPase inhibitors with IC50 in the single digit micromolar range. These represent the first low micromolar synthetic inhibitors of bacterial SecA and will be very useful for mechanistic studies.

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