Drug intelligence / Profile preview

aminophylline + sunitinib

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Aminophylline + sunitinib is a combination of two small molecule drugs with distinct mechanisms of action. Aminophylline is a bronchodilator composed of theophylline and ethylenediamine, primarily used to treat bronchospasm in conditions such as asthma, emphysema, and chronic bronchitis. Its mechanism involves inhibition of phosphodiesterase (PDE) enzymes, antagonism at adenosine receptors (A1 and A3), and activation of histone deacetylase 2, leading to bronchodilation and anti-inflammatory effects[1]. Sunitinib is an oral multikinase inhibitor approved for the treatment of cancers such as gastrointestinal stromal tumor (GIST) and advanced renal cell carcinoma. It targets multiple receptor tyrosine kinases including vascular endothelial growth factor receptors (VEGFRs), platelet-derived growth factor receptors (PDGFRs), stem cell factor receptor (c-KIT), FMS-like tyrosine kinase 3 (FLT3), colony-stimulating factor 1 receptor (CSF1R), and glial cell line-derived neurotrophic factor receptor. This results in inhibition of tumor angiogenesis and proliferation[4]. There is no evidence that this specific combination has been developed or approved for any indication.

02

Targets

ADORA1 (Adenosine receptor A1 subtype)ADORA3 (Adenosine A3 receptor)CSF1R (Macrophage colony-stimulating factor receptor)FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)PDE3A (Phosphodiesterase 3A)RET (Rearranged during transfection receptor tyrosine kinase)GFRA4 (GDNF family receptor alpha-4)HDAC2 (Histone deacetylase 2)VEGFR (VEGFR family)

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