Design and synthesis of novel xanthine derivatives as potent and selective A(2B) adenosine receptor antagonists for the treatment of chronic inflammatory airway diseases

• Published in: European journal of medicinal chemistry Vol. 134; pp. 218 - 229
• Main Authors: Basu, Sujay, Barawkar, Dinesh A., Ramdas, Vidya, Patel, Meena, Waman, Yogesh, Panmand, Anil, Kumar, Santosh, Thorat, Sachin, Naykodi, Minakshi, Goswami, Arnab, Reddy, B. Srinivasa, Prasad, Vandna, Chaturvedi, Sandhya, Quraishi, Azfar, Menon, Suraj, Paliwal, Shalini, Kulkarni, Abhay, Karande, Vikas, Ghosh, Indraneel, Mustafa, Syed, De, Siddhartha, Jain, Vaibhav, Banerjee, Ena Ray, Rouduri, Sreekanth R., Palle, Venkata P., Chugh, Anita, Mookhtiar, Kasim A.
• Format: Journal Article
• Language: English
• Published: PARIS Elsevier 07.07.2017
• Subjects: Chemistry, Medicinal; Life Sciences & Biomedicine; Pharmacology & Pharmacy; Science & Technology; FIBROSIS; Propargyl; Adenosine; HIGH-AFFINITY; Bioavailability; THEOPHYLLINE; cAMP; AGONISTS; LIGANDS; INCREASE; Heteroaryl; BIOLOGICAL EVALUATION; Human liver microsomes; ASTHMA; SMOOTH-MUSCLE-CELLS; HIGHLY POTENT
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2017.04.014

Adenosine induces bronchial hyperresponsiveness and inflammation in asthmatics through activation of A(2B) adenosine receptor (A(2B)AdoR). Selective antagonists have been shown to attenuate airway reactivity and improve inflammatory conditions in pre-clinical studies. Hence, the identification of novel, potent and selective A2BAdoR antagonist may be beneficial for the potential treatment of asthma and Chronic Obstructive Pulmonary Disease (COPD). Towards this effort, we explored several prop-2-ynylated C8-aryl or heteroaryl substitutions on xanthine chemotype and found that 1-prop-2-ynyl-1H-pyrazol-4-yl moiety was better tolerated at the C8 position. Compound 59, exhibited binding affinity (K-i) of 62 nM but was non-selective for A(2B)AdoR over other AdoRs. Incorporation of substituted phenyl on the terminal acetylene increased the binding affinity (KO significantly to <10 nM. Various substitutions on terminal phenyl group and different alkyl substitutions on N-1 and N-3 were explored to improve the potency, selectivity for A(2B)AdoR and the solubility. In general, compounds with meta-substituted phenyl provided better selectivity for A(2B)AdoR compared to that of para-substituted analogs. Substitutions such as basic amines like pyrrolidine, piperidine, piperazine or cycloalkyls with polar group were tried on terminal acetylene, keeping in mind the poor solubility of xanthine analogs in general. However, these substitutions led to a decrease in affinity compared to compound 59. Subsequent SAR optimization resulted in identification of compound 46 with high human A2BAdoR affinity (K-i = 13 nM), selectivity against other AdoR subtypes and with good pharmacokinetic properties. It was found to be a potent functional A(2B)AdoR antagonist with a K-i; of 8 nM in cAMP assay in hA(2B)-HEK293 cells and an IC50 of 107 nM in IL-6 assay in NIH-3T3 cells. Docking study was performed to rationalize the observed affinity data. Structure activity relationship (SAR) studies also led to identification of compound 36 as a potent A(2B)AdoR antagonist with K; of 1.8 nM in CAMP assay and good aqueous solubility of 529 mu M at neutral pH. Compound 46 was further tested for in vivo efficacy and found to be efficacious in ovalbumin-induced allergic asthma model in mice. (C) 2017 Elsevier Masson SAS. All rights reserved.