78060-46-5 Usage
Uses
Used in Medicinal Chemistry:
6-CHLORO-2-PIPERAZIN-1-YL-QUINOLINE is used as a key component in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. It contributes to the development of new drugs with potential therapeutic applications.
Used in Drug Discovery and Development:
In the pharmaceutical industry, 6-CHLORO-2-PIPERAZIN-1-YL-QUINOLINE serves as a valuable asset in drug discovery and development processes. Its incorporation into drug molecules can enhance their pharmacological properties and improve their efficacy in treating specific medical conditions.
Used in Research:
6-CHLORO-2-PIPERAZIN-1-YL-QUINOLINE is utilized as a research tool to study drug-receptor interactions and drug metabolism. Understanding these interactions can help in optimizing drug design and improving therapeutic outcomes.
Used in Treatment of Medical Conditions:
Although further research is needed, 6-CHLORO-2-PIPERAZIN-1-YL-QUINOLINE may have potential applications in the treatment of certain medical conditions. Its pharmacological and biological activities could contribute to the development of novel therapeutic agents for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 78060-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78060-46:
(7*7)+(6*8)+(5*0)+(4*6)+(3*0)+(2*4)+(1*6)=135
135 % 10 = 5
So 78060-46-5 is a valid CAS Registry Number.
78060-46-5Relevant academic research and scientific papers
ANTHELMINTIC COMPOUNDS AND COMPOSITIONS AND METHOD OF USING THEREOF
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Paragraph 0458, (2014/05/25)
The present invention relates to novel anthelmintic compounds of formula (I) below: wherein Y and Z are independently a bicyclic carbocyclic or a bicyclic heterocyclic group, or one of Y or Z is a bicyclic carbocyclic or a bicyclic heterocyclic group and the other of Y or Z is alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, heterocyclyl or heteroaryl, and variables X1, X2, X3, X4, X5, X6, X7 and X8 are as defined herein. The invention also provides for veterinary compositions comprising the anthelmintic compounds of the invention, and their uses for the treatment and prevention of parasitic infections in animals.
Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1
Lee, Byoung Se,Chu, Soyoung,Lee, Byung Chul,Chi, Dae Yoon,Choe, Yearn Seong,Jeong, Kyung Ja,Jin, Changbae
, p. 1559 - 1562 (2007/10/03)
6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.
