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methyl 3-(6-((4-methoxyphenyl)(methyl)carbamoyloxy)-1H-indol-3-yl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1415333-75-3

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1415333-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415333-75-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,3,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1415333-75:
(9*1)+(8*4)+(7*1)+(6*5)+(5*3)+(4*3)+(3*3)+(2*7)+(1*5)=133
133 % 10 = 3
So 1415333-75-3 is a valid CAS Registry Number.

1415333-75-3Relevant academic research and scientific papers

INDOLE, INDOLINE DERIVATIVES, COMPOSITIONS COMPRISING THEM AND USES THEREOF

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Page/Page column 26; 29; 41, (2013/10/22)

The invention provides indole and indoline derivatives and slats thereof, compositions comprising them and uses thereof for the treatment of diseases and disorders.

Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease

Yanovsky, Inessa,Finkin-Groner, Efrat,Zaikin, Andrey,Lerman, Lena,Shalom, Hila,Zeeli, Shani,Weill, Tehilla,Ginsburg, Isaac,Nudelman, Abraham,Weinstock, Marta

, p. 10700 - 10715 (2013/02/22)

The cascade of events that occurs in Alzheimer's disease involving oxidative stress and the reduction in cholinergic transmission can be better addressed by multifunctional drugs than cholinesterase inhibitors alone. For this purpose, we prepared a large number of derivatives of indoline-3-propionic acids and esters. They showed scavenging activity against different radicals in solution and significant protection against cytotoxicity in cardiomyocytes and primary cultures of neuronal cells exposed to H2O2 species and serum deprivation at concentrations ranging from 1 nM to 10 μM depending on the compound. For most of the indoline-3-propionic acid derivatives, introduction of N-methyl-N-ethyl or N-methyl-N-(4-methoxyphenyl) carbamate moieties at positions 4, 6, or 7 conferred both acetyl (AChE) and butyryl (BuChE) cholinesterase inhibitory activities at similar concentrations to those that showed antioxidant activity. The most potent AChE inhibitors were 120 (3-(2-aminoethyl) indolin-4-yl ethyl(methyl)carbamate dihydrochloride) and 94 (3-(3-methoxy-3-oxopropyl)-4-(((4-methoxyphenyl)(methyl) carbamoyl)oxy)indolin- 1-ium hydrochloride) with IC50s of 0.4 and 1.2 μM, respectively.

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