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2-[4-(6-Heptanoylimidazo[1,2-a]pyridin-8-yl)phenyl]acetic acid is a novel compound with potential therapeutic applications, characterized by its unique chemical structure that features a heptanoyl imidazol[1,2-a]pyridine moiety attached to a phenyl group. This structure endows the compound with specific properties that make it a promising candidate for the development of treatments for certain medical conditions.

1933533-18-6

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1933533-18-6 Usage

Uses

Used in Pharmaceutical Industry:
2-[4-(6-Heptanoylimidazo[1,2-a]pyridin-8-yl)phenyl]acetic acid is used as a novel inhibitor of serine palmitoyl transferase (SPT) for the treatment of type 2 diabetes and dyslipidemia. Its application is based on its ability to target and inhibit the enzyme SPT, which plays a crucial role in the biosynthesis of sphingolipids. By inhibiting SPT, 2-[4-(6-heptanoylimidazo[1,2-a]pyridin-8-yl)phenyl]acetic acid can potentially modulate the levels of sphingolipids, which are known to be involved in the pathophysiology of type 2 diabetes and dyslipidemia, thus offering a new approach to managing these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1933533-18-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,3,3,5,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1933533-18:
(9*1)+(8*9)+(7*3)+(6*3)+(5*5)+(4*3)+(3*3)+(2*1)+(1*8)=176
176 % 10 = 6
So 1933533-18-6 is a valid CAS Registry Number.

1933533-18-6Downstream Products

1933533-18-6Relevant academic research and scientific papers

Imidazopyridine and Pyrazolopiperidine Derivatives as Novel Inhibitors of Serine Palmitoyl Transferase

Genin, Michael J.,Gonzalez Valcarcel, Isabel C.,Holloway, William G.,Lamar, Jason,Mosior, Marian,Hawkins, Eric,Estridge, Thomas,Weidner, Jeffrey,Seng, Thomas,Yurek, David,Adams, Lisa A.,Weller, Jennifer,Reynolds, Vincent L.,Brozinick, Joseph T.

, p. 5904 - 5910 (2016)

To develop novel treatments for type 2 diabetes and dyslipidemia, we pursued inhibitors of serine palmitoyl transferase (SPT). To this end compounds 1 and 2 were developed as potent SPT inhibitors in vitro. 1 and 2 reduce plasma ceramides in rodents, have

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