2014
DOI: 10.1155/2014/249780
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Synthesis and Evaluation of Novel Pyrroles and Pyrrolopyrimidines as Anti-Hyperglycemic Agents

Abstract: A series of pyrrole and pyrrolopyrimidine derivatives were examined for their in vivo antihyperglycemic activity. Compounds Ia–c,e, and IVg showed promising antihyperglycemic activity equivalent to a well-known standard antihyperglycemic drug, Glimepiride (Amaryl, 4 mg/kg). In this paper, we examine and discuss the structure-activity relationships and antihyperglycemic activity of these compounds.

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Cited by 21 publications
(17 citation statements)
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“…The synthesis of the target compounds is summarized in Scheme 1 . To synthesize compounds 3a – l and 4a – l , several 2-aminopyrrole-3-carbonitriles 1a – f were prepared by condensing malononitrile with the two intermediates I or II , respectively, in strong basic medium [ 38 , 39 , 40 , 41 ]. The 2-arylidene malononitriles 2a , b were prepared by condensation of malononitrile with the aromatic aldehydes benzaldhyde or anisaldehyde [ 42 , 43 , 44 ].…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of the target compounds is summarized in Scheme 1 . To synthesize compounds 3a – l and 4a – l , several 2-aminopyrrole-3-carbonitriles 1a – f were prepared by condensing malononitrile with the two intermediates I or II , respectively, in strong basic medium [ 38 , 39 , 40 , 41 ]. The 2-arylidene malononitriles 2a , b were prepared by condensation of malononitrile with the aromatic aldehydes benzaldhyde or anisaldehyde [ 42 , 43 , 44 ].…”
Section: Resultsmentioning
confidence: 99%
“…The Fock matrix analysis with the stabilization energy E (2) greater than 2 Kcal mol -1 was shown in Table 2. The larger stabilization intramolecular interaction was observed between LP(N1) to π*(C2-C3) and π*(C4-C5) orbitals with stabilization energy of 39.84 Kcal mol -1 .…”
Section: Nbo Analysismentioning
confidence: 99%
“…Pyrrole derivatives have potent biological activities such as antimicrobial, antiviral, anti-inflammatory and antitumor agents [1,2]. The different applications of the pyrrole compounds have attracted to study the spectroscopic and vibrational studies of its derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the importance of this ring system, 39 we prepared some fused o-aminocyano tetrahydrobenzo[b]pyrrole derivatives as an essential propagation step in our search for new pyrrole and pyrrolopyrimidine derivatives, [40][41][42][43] and evaluated them for the anti-inflammatory activities. In addition, a molecular docking study has been done to explain the activity of the biologically active compounds.…”
Section: Introductionmentioning
confidence: 99%