83763-22-8 Usage
Uses
Used in Pharmaceutical Research:
[1-(2-aminoethyl)piperidin-4-yl] (4-fluorophenyl) ketone is used as a research chemical for studying the effects of psychoactive substances on the brain. Its ability to increase the levels of dopamine, serotonin, and norepinephrine makes it a valuable tool for understanding the mechanisms behind mood disorders and stimulant addiction.
Used in Drug Enforcement and Control:
Due to its classification as a controlled substance and its association with abuse potential and health risks, [1-(2-aminoethyl)piperidin-4-yl] (4-fluorophenyl) ketone is used in drug enforcement and control efforts to monitor and regulate its distribution and use, aiming to prevent its misuse and protect public health.
Used in Toxicology and Public Health:
[1-(2-aminoethyl)piperidin-4-yl] (4-fluorophenyl) ketone is also utilized in toxicology and public health research to investigate the potential harmful side effects and health risks associated with its use. Understanding these risks is crucial for developing strategies to mitigate harm and inform policy decisions regarding its regulation and control.
Check Digit Verification of cas no
The CAS Registry Mumber 83763-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83763-22:
(7*8)+(6*3)+(5*7)+(4*6)+(3*3)+(2*2)+(1*2)=148
148 % 10 = 8
So 83763-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H19FN2O/c15-13-3-1-11(2-4-13)14(18)12-5-8-17(9-6-12)10-7-16/h1-4,12H,5-10,16H2
83763-22-8Relevant academic research and scientific papers
Design and synthesis of a library of chemokine antagonists
Bhalay, Gurdip,Albrecht, Birgit,Akhlaq, Mohammed,Baettig, Urs,Beer, David,Brown, Zarin,Charlton, Steven,Dunstan, Andrew,Bradley, Michelle,Gedeck, Peter,Glen, Angela,Howea, Trevor,Keller, Thomas,Leighton-Davies, Juliet,Li, Alice,McCarthy, Clive,Mocquet, Cecile,Owen, Charles,Nicklin, Paul,Rosethorne, Elizabeth
scheme or table, p. 6249 - 6252 (2011/11/29)
A library of chemokine antagonists has been synthesized using a combination of solid and solution-phase chemistry. Structures of known chemokine antagonists were used to produce a pharmacophore which served to guide monomer selection. Several combinations of monomers have resulted in providing novel chemokine antagonists which in some cases display dual chemokine receptor antagonism.
