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Alogliptin trifluoroacetate is a pharmaceutical compound that serves as a prodrug for alogliptin, a potent and selective dipeptidyl peptidase-4 (DPP-4) inhibitor. DPP-4 inhibitors play a crucial role in managing type 2 diabetes by slowing the inactivation of incretin hormones, which in turn stimulates insulin secretion and reduces glucagon levels, leading to improved glycemic control. Alogliptin trifluoroacetate is specifically designed to enhance the solubility and bioavailability of alogliptin, facilitating its absorption in the body and making it more effective in treating diabetes. Alogliptin trifluoroacetate is an important part of the therapeutic arsenal for managing blood sugar levels in patients with type 2 diabetes.

1246610-76-3

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1246610-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1246610-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,6,1 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1246610-76:
(9*1)+(8*2)+(7*4)+(6*6)+(5*6)+(4*1)+(3*0)+(2*7)+(1*6)=143
143 % 10 = 3
So 1246610-76-3 is a valid CAS Registry Number.

1246610-76-3Downstream Products

1246610-76-3Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF ALOGLIPTIN

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Page/Page column 27, (2010/11/05)

The present invention is based on the discovery of a process for preparing pyrimidin- dione compounds, especially alogliptin and its derivatives, which comprises the reaction of a urea derivative of formula (VIII) with a malonic acid or its derivatives to form intermediates of formulae (VII) or (VII-A), which are subsequently converted to a compound of formula (II) upon introduction of a leaving group X. Compound (II) then reacts with an amine to form compound (I), which is optionally converted to its salts of formula (IV).

DIPEPTIDYL PEPTIDASE INHIBITORS

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Page/Page column 22, (2009/12/02)

Methods of making compounds of the formula (I) wherein the variables are as defined herein. Also, methods of making compounds that may be used to inhibit dipeptidyl peptidase.

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