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(R)-3-(tert-butoxycarbonylamino)-4-(4-chlorophenyl)butanoic acid, commonly known as Ezetimibe, is a cholesterol-lowering medication that functions by inhibiting the absorption of cholesterol from the small intestine. This action effectively reduces the amount of cholesterol entering the bloodstream, which can lower the risk of cardiovascular diseases such as heart attacks and strokes. Ezetimibe is typically prescribed alongside a healthy diet, exercise, and other cholesterol-lowering medications, and is available in tablet form. It is generally well-tolerated, with potential side effects including diarrhea, abdominal pain, and muscle pain. As a crucial component in managing high cholesterol and its associated health risks, Ezetimibe plays a significant role in the prevention and treatment of cardiovascular conditions.

1824131-52-3

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1824131-52-3 Usage

Uses

Used in Pharmaceutical Industry:
Ezetimibe is used as a cholesterol-lowering agent for the treatment of high cholesterol levels. It works by inhibiting the absorption of cholesterol from the small intestine, thereby reducing the amount of cholesterol that enters the bloodstream. This helps to decrease the risk of cardiovascular diseases such as heart attacks and strokes.
Used in Cardiovascular Health Management:
Ezetimibe is used as a preventive measure and treatment option for individuals at risk of or suffering from cardiovascular diseases. By reducing cholesterol levels in the blood, it contributes to the overall management of heart health and the mitigation of associated health risks.
Used in Combination Therapy:
Ezetimibe is often used in combination with a healthy diet, exercise, and other cholesterol-lowering medications to provide a comprehensive approach to managing high cholesterol and reducing the risk of cardiovascular diseases. This multifaceted treatment strategy enhances the effectiveness of cholesterol reduction and supports overall cardiovascular health.

Check Digit Verification of cas no

The CAS Registry Mumber 1824131-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,2,4,1,3 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1824131-52:
(9*1)+(8*8)+(7*2)+(6*4)+(5*1)+(4*3)+(3*1)+(2*5)+(1*2)=143
143 % 10 = 3
So 1824131-52-3 is a valid CAS Registry Number.

1824131-52-3Downstream Products

1824131-52-3Relevant academic research and scientific papers

Chiral synthesis method for chiral beta-amino acid and synthesis method for medicinal intermediate

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, (2018/01/11)

The invention relates to a chiral synthesis method for chiral beta-amino acid. The chiral synthesis method comprises the following steps: reacting a compound shown in formula (II) with an acylation reagent to prepare anhydride intermediate reaction liquid under the action of alkali; adding Meldrum's acid into the anhydride intermediate reaction liquid, and performing reaction to generate a compound shown in formula (III); reacting the compound shown in formula (III) with a compound shown in formula (IV) to generate a compound shown in formula (V); reducing the compound shown in formula (V) to generate a compound shown in formula (VI); performing acidic hydrolysis on the compound shown in formula (VI) to generate a compound shown in formula (I), i.e., the chiral beta-amino acid. The chiral synthesis method has the advantages of convenience for synthesis, low cost and simple process, and compared with a disclosed preparation method, is more suitable for industrial production.

Synthesis method of chiral N-Boc-3-amino-4-aryl-butyric acid

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Paragraph 0032; 0033; 0034; 0035; 0037; 0039, (2017/08/28)

The invention relates to a synthesis method of chiral N-Boc-3-amino-4-aryl-butyric acid. The method is as below: 1, conducting a cross metathesis reaction, an asymmetric conjugate addition reaction and an oxidation reaction on starting materials including an allyl aromatic compound and crotonaldehyde by a continuous reaction one-pot method to synthesize an N-Boc-3-aryl methyl-5-oxo isoxazole intermediate; or conducting an asymmetric conjugate addition reaction and an oxidation reaction on a starting material (E)-4-aryl-2-crotonaldehyde by a continuous reaction one-pot method to synthesize an N-Boc-3-aryl methyl-5-oxo isoxazole intermediate; and 2, subjecting (3R)-N-Boc-3-aryl methyl-5-oxo isoxazole intermediate by high-pressure hydrogenation to directly prepare the chiral N-Boc-3-amino-4-aryl-butyric acid. The synthesis method provided by the invention has the advantages of simple operation, mild reaction conditions, target product yield reaching 60-69%, and ee value of the target product reaching as high as 96%. The synthetic route has industrialization prospect.

UREA DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF

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Paragraph 0549; 0550; 0551; 0552, (2016/12/22)

The present invention provides a urea compound or a pharmacologically acceptable salt thereof that has a formyl peptide receptor like 1 (hereinafter may be abbreviated as FPRL1) agonist effect, a pharmaceutical composition containing the urea compound or the pharmacologically acceptable salt thereof, and a pharmaceutical use thereof. It has been found that a urea derivative represented by the general formula (I) below or a pharmacologically acceptable salt thereof has a superior FPRL1 agonist effect. Compound (I) or a pharmacologically acceptable salt thereof is highly useful for treatment, prevention, or suppression of inflammatory diseases, chronic airway diseases, cancers, septicemia, allergic symptoms, HIV retrovirus infection, circulatory disorders, neuroinflammation, nervous disorders, pains, prion diseases, amyloidosis, immune disorders and the like.

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