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4-<(7-chloro-4-quinolinyl)amino>-2-<(1-pyrrolidinyl)methyl>phenol 1-oxide is a complex organic compound with the molecular formula C22H22ClN3O2. It is characterized by a phenol core, with a 7-chloro-4-quinolinyl group attached to the 4-position and a pyrrolidinylmethyl group at the 2-position. The molecule also features a hydroxyl group and a 1-oxide functional group, which contributes to its unique chemical properties. 4-<(7-chloro-4-quinolinyl)amino>-2-<(1-pyrrolidinyl)methyl>phenol 1-oxide is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting various diseases. Its structure and properties make it a subject of interest for chemists and biologists alike, as it may possess specific biological activities or serve as a precursor in the synthesis of other medicinally relevant compounds.

1051-72-5

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1051-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1051-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1051-72:
(6*1)+(5*0)+(4*5)+(3*1)+(2*7)+(1*2)=45
45 % 10 = 5
So 1051-72-5 is a valid CAS Registry Number.

1051-72-5Downstream Products

1051-72-5Relevant academic research and scientific papers

Anticholinesterase activity of 4-aminoquinolines related to amodiaquine and their respective N-oxides

Go,Ngiam,Lim

, p. 81 - 85 (2007/10/02)

The inhibitory activities of a series of substituted 4-aminoquinolines related to the antimalarial agent amodiaquine and their respective N-oxides toward acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) have been determined and discussed in terms of their proposed mode of interaction with the enzyme surface. A marked difference was noted in the AChE and BChE inhibitory potencies of these compounds. The strong anti-AChE activity of amodiaquine has been explained by a specific two-point interaction with the anionic site and acidic group of AChE. However, such an interaction appears to be absent in the case of the amodiaquine inhibition of BChE, suggesting differences in the ability of the enzymes to accommodate similar inhibitory molecules.

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