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4-(2-(5-chloro-1,3-dioxoisoindolin-2-yl)ethyl)benzenesulfonamide is a complex organic chemical compound with the molecular formula C14H11ClN2O5S. It is characterized by a benzene ring with a sulfonamide group attached at the 4-position, and a 5-chloro-1,3-dioxoisoindolin-2-yl group connected to the 2-position of an ethyl chain. 4-(2-(5-chloro-1,3-dioxoisoindolin-2-yl)ethyl)benzenesulfonamide is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of certain drugs. Its structure provides a unique set of properties that can be exploited in medicinal chemistry, making it a compound of interest for researchers and developers in the field.

6881-89-6

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6881-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6881-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6881-89:
(6*6)+(5*8)+(4*8)+(3*1)+(2*8)+(1*9)=136
136 % 10 = 6
So 6881-89-6 is a valid CAS Registry Number.

6881-89-6Relevant academic research and scientific papers

Design, synthesis, molecular modeling and anti-hyperglycemic evaluation of phthalimide-sulfonylurea hybrids as PPARγ and SUR agonists

El-Zahabi, Mohamed Ayman,Elbendary, Eman R.,Bamanie, Faida H.,Radwan, Mohamed F.,Ghareib, Salah A.,Eissa, Ibrahim H.

, (2019)

New series of phthalimide-sulfonylurea hybrids were prepared and examined for their in vivo anti-hyperglycemic activities in STZ-induced hyperglycemic rats using glibenclamide as a reference drug. Compounds 6c, 6d, 6g, 6h, 6j and 6k induced significant reduction in the blood glucose levels of diabetic rats ranging from 24.43 to 21.43%. Moreover, molecular docking and pharmacophore approaches were carried out to examine binding modes and fit values of the prepared compounds against PPARγ and SUR, respectively. Compounds 6c, 6d, 6j and 6m exhibited the highest binding free energies against PPARγ. Compounds 6c, 6j, 6k, 6l, and 6n showed the highest fit values against the generated pharmacophore model. Also, QSAR technique was carried out to estimate the proposed PPARγ binding affinities and insulin-secreting abilities. The synthesized compounds showed promising estimated activities. In-silico ADMET studies were performed to investigate pharmacokinetics of the synthesized compounds. They showed considerable human intestinal absorption with low BBB penetration.

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