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3-(3,4,5-trimethoxybenzyl)indolin-2-one is a complex organic compound with the molecular formula C18H19NO5. It is a derivative of indolin-2-one, featuring a 3,4,5-trimethoxybenzyl group attached to the indoline core. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure. The presence of three methoxy groups on the benzyl ring provides a significant level of lipophilicity, which can influence its solubility and interaction with biological targets. The compound's structure also suggests that it may have potential in medicinal chemistry, particularly in the development of drugs targeting the central nervous system or other therapeutic areas where modulating receptor activity is crucial.

3359-50-0

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3359-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3359-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3359-50:
(6*3)+(5*3)+(4*5)+(3*9)+(2*5)+(1*0)=90
90 % 10 = 0
So 3359-50-0 is a valid CAS Registry Number.

3359-50-0Downstream Products

3359-50-0Relevant academic research and scientific papers

3-aryl-indolinones derivatives as antiplasmodial agents: synthesis, biological activity and computational analysis

Luczywo, Ayelen,González, Lucía G.,Aguiar, Anna C. C.,Oliveira de Souza, Juliana,Souza, Guilherme E.,Oliva, Glaucius,Aguilar, Luis F.,Casal, Juan J.,Guido, Rafael V. C.,Asís, Silvia E.,Mellado, Marco

, (2021)

Malaria is an infectious illness, affecting vulnerable populations in Third World countries. Inspired by natural products, indole alkaloids have been used as a nucleus to design new antimalarial drugs. So, eighteen oxindole derivatives, aza analogues were obtained with moderate to excellent yields. Also, the saturated derivatives of oxindole and aza derivatives via H2/Pd/C reduction were obtained in good yields, leading to racemic mixtures of each compound. Next, the inhibitory activity against P. falciparum of 18 compounds were tested, founding six compounds with IC50 20 μM. The most active of these compounds was 8c; however, their unsaturated derivative 7c was inactive. Then, a structure-activity relationship analysis was done, founding that focused LUMO lobe on the specific molecular zone is related to inhibitory activity against P. falciparum. Finally, we found a potential inhibition of lactate dehydrogenase by oxindole derivatives, using molecular docking virtual screening.

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