Synthesis, Antiproliferative and Anti-inflammatory Activities of Novel Simplified Imatinib Analogues

  • Sampaio T
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Abstract

We described the synthesis of carboxamide derivatives designed as novel simplified imatinib analogues and their antiproliferative and anti-inflammatory activities. Compound 2c showed a unique conformation determined by X-ray diffraction and by NMR 1 H and displayed antiproliferative potency in the same magnitude order than the standard imatinib. Compounds 6-10 were prepared by structural modification in carboxamide 2c, and with exception of derivative 10, they were inactive as antiproliferative agent. However, these compounds showed same anti-inflammatory potency than imatinib, standing out carboxamide 9 that was six time more potent as TNF-α inhibitor production.

Figures

  • Figure 1: Design conception of carboxamide derivatives (2a-c) through molecular simplification from imatinib.
  • Figure 2: ORTEP view of compounds 2a-c with the atom displacement ellipsoids drawn at 30% of probability level. A) compound 2a; B) compound 2b; C) compound 2c.
  • Table 1: Hydrogen-bonds and intermolecular interactions geometry (Å,°).
  • Figure 3: Design conception of carboxamide derivatives (6-10) from the prototype 2c.
  • Table 3: Effects of carboxamides 2c, 6-10, imatinib and acetylsalicylic acid (ASA) in leukocyte migration and TNF-α production induced by carrageenan injection into the subcutaneous air pouch.
  • Table 4: Crystal data and structure refinement details of compounds 2a-c.

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APA

Sampaio, T. S. (2014). Synthesis, Antiproliferative and Anti-inflammatory Activities of Novel Simplified Imatinib Analogues. Medicinal Chemistry, 4(11). https://doi.org/10.4172/2161-0444.1000226

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