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However, the structure of 5-azacitidine is very unstable and easily hydrolyzed and deaminated

Synthesis, biological evaluation and 3D-QSAR studies of 1,2,4-triazole-5-substituted carboxylic acid bioisosteres as uric acid transporter 1 (URAT1) inhibitors for the treatment of hyperuricemia associated with gout

Experimental models demonstrate that AOD 9604 modulates lipolysis through 3-adrenergic receptormediated pathways, which are central to triglyceride breakdown in adipocytes

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doi: 10.1016/j.clnu.2016.08.015

For clarification, oral administration of glucocorticoids also includes oromucosal, buccal, gingival and sublingual routes