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Design and synthesis of sulfonamide derivatives of pyrrolidine and piperidine as anti-diabetic agents.

European journal of medicinal chemistry (2014-12-02)
Radhika Sharma, Shubhangi S Soman
ABSTRACT

Type 2 diabetes (T2D) is a lifestyle disease affecting millions of people worldwide. Various therapies are available for the management of T2D and dipeptidyl peptidase-IV (DPP-IV) inhibition has emerged as a promising therapy for the treatment of type 2 diabetes (T2D). Here we report design, synthesis and in vitro efficacy of sulfonamide derivatives of pyrrolidine and piperidine as anti-diabetic agents. Amongst all the compounds synthesized in this series, 9a, is the most potent (IC50 = 41.17 nM).

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Metanolo, suitable for HPLC, ≥99.9%
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Metanolo, ACS reagent, ≥99.8%
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Dimetilsolfossido-d6, 99.9 atom % D
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Diclorometano, suitable for HPLC, ≥99.8%, contains amylene as stabilizer
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Etilacetato, ACS reagent, ≥99.5%
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Metanolo, suitable for HPLC, gradient grade, ≥99.9%
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Etilacetato, suitable for HPLC, ≥99.7%
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Diclorometano, contains 40-150 ppm amylene as stabilizer, ACS reagent, ≥99.5%
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Solfato di sodio, ACS reagent, ≥99.0%, anhydrous, granular
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Diclorometano, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%, contains 50-150 ppm amylene as stabilizer
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Solfato di sodio, ACS reagent, ≥99.0%, anhydrous, powder
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Metanolo, HPLC Plus, ≥99.9%
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Bromuro di potassio, ≥99% trace metals basis
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Dimetilsolfossido-d6, 99.9 atom % D, contains 0.03 % (v/v) TMS
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