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Melogliptin is a prescription medication that belongs to the class of dipeptidyl peptidase-4 (DPP-4) inhibitors. It is used to treat type 2 diabetes by controlling blood sugar levels. Melogliptin works by increasing the levels of incretin hormones in the body, which regulate blood sugar by stimulating insulin release and decreasing sugar production in the liver. It is available in tablet form and is typically taken once a day.

868771-57-7

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  • 2-Pyrrolidinecarbonitrile,4-fluoro-1-[2-[[(1R,3S)-3-(1H-1,2,4-triazol-1-ylmethyl)cyclopentyl]amino]acetyl]-,(2S,4S)-

    Cas No: 868771-57-7

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  • 2-Pyrrolidinecarbonitrile,4-fluoro-1-[2-[[(1R,3S)-3-(1H-1,2,4-triazol-1-ylmethyl)cyclopentyl]amino]acetyl]-,(2S,4S)-

    Cas No: 868771-57-7

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  • 2-Pyrrolidinecarbonitrile,4-fluoro-1-[2-[[(1R,3S)-3-(1H-1,2,4-triazol-1-ylmethyl)cyclopentyl]amino]acetyl]-,(2S,4S)-

    Cas No: 868771-57-7

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868771-57-7 Usage

Uses

Used in Pharmaceutical Industry:
Melogliptin is used as an oral antihyperglycemic agent for the treatment of type 2 diabetes. It helps to control blood sugar levels by increasing the levels of incretin hormones, which in turn stimulate insulin release and decrease sugar production in the liver.
Used in Diabetes Management:
Melogliptin is used as a medication for managing type 2 diabetes, helping patients to maintain their blood sugar levels within a healthy range. It is an essential component of a comprehensive diabetes management plan, which may also include diet, exercise, and regular monitoring of blood sugar levels.
Common side effects of Melogliptin may include headache, upper respiratory tract infection, and urinary tract infection. It is crucial to follow the dosage instructions provided by a healthcare professional and to discuss the potential risks and benefits of using Melogliptin before starting treatment. Regular monitoring of blood sugar levels is also important while taking this medication.

Check Digit Verification of cas no

The CAS Registry Mumber 868771-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,7,7 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 868771-57:
(8*8)+(7*6)+(6*8)+(5*7)+(4*7)+(3*1)+(2*5)+(1*7)=237
237 % 10 = 7
So 868771-57-7 is a valid CAS Registry Number.

868771-57-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-1-[2-[[(1R,3S)-3-(1,2,4-triazol-1-ylmethyl)cyclopentyl]amino]acetyl]pyrrolidine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names UNII-I3N8016NKU

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:868771-57-7 SDS

868771-57-7Downstream Products

868771-57-7Relevant articles and documents

NOVEL PROCESSES FOR THE PREPARATION OF DPP IV INHIBITORS

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Page/Page column 39, (2008/06/13)

The present invention relates to novel processes for preparing DPP-IV inhibitors having the structure of formula I, and pharmaceutically acceptable salt thereof, which are useful for treatment of Type 2 diabetes.

NOVEL DIPEPTIDYL PEPTIDASE IV INHIBITORS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND PROCESS FOR THEIR PREPARATION

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Page/Page column 83-84, (2008/06/13)

The present invention relates to novel compounds useful as dipeptidyl peptidase IV (DPP-IV) inhibitors of the formula: (I) wherein Y is -S(O)m, -CH2-, CHF, or -CF2; m is 0, 1, or 2; X is a bond, C1-C5 alkyl (e.g., -CH2-), or -C(=0)-; the dotted line [----] in the carbocyclic ring represents an optional double bond; R1 is substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkylalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocyclic ring, substituted or unsubstituted heterocyclylalkyl, substituted or unsubstituted heteroarylalkyl, CN, -COOR3, CONR3R4, -OR3, -NR3R4, or NR3COR3; R2 is hydrogen, cyano, COOH, or an isostere of a carboxylic acid (such as SO3H, CONOH, B(OH)2, PO3R3R4, SO2NR3R4, tetrazole, -COOR3, -CONR3R4, NR3COR4, or -COOCOR3).

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