New pyridothiazepines with blocking activity of the mitochondrial sodium/calcium exchanger and their use for applications on Nervous System Pathologies

Desarrollado por: IIS del Hospital Universitario de La Princesa

Descripción

Mitochondria are the energy-producing factory of eukaryotic cells. In addition, they play a fundamental role in the clearance of the cytosolic Ca2+ Upon cell stimulation, mitochondria are capable of accumulating vast amounts of Ca2+ in their matrix through the Ca2+ uniporter that uses the driving force of the electrical potential across the mitochondrial membrane. After cell stimulation ceases, the Ca2+ accumulated in the mitochondrial matrix is then released back into the cytosol through antiporters like the Na+/Ca2+ exchanger (mNCX).

The Ca2+ set-point hypothesis implies that a minimal cytosolic Ca2+ level is required to maintain neuronal viability; when this Ca2+ moves below or above this set-point, apoptosis is rapidly induced and the death of neurons occurs. We explored the possibility that the mitigation of the rate of mitochondrial Ca2+ efflux to the cytosol by the mNCX blocker CGP37157 could afford neuroprotection against neurotoxicity elicited by cell Ca2+ overload. In addition, the study of CGP37157 derivatives with blocking activity of mNCX has been also of interest for other pathologies, such as diabetes.

However, CGP37157 also blocks voltage-gated Na+ channels, voltage-gated Ca2+ channel, the plasmalemmal NCX, and the recently discovered channel Ca2+ homeostasis modulator 1 (CALHM1), among other targets. Given the high relevance of the mNCX as a potential target to develop new neuroprotective agents, among other pathologies, we hypothesized that newly synthesized compounds to target mNCX with more selectivity and potency could find therapeutic potential in neurodegenerative diseases, stroke, diabetes, or any other pathologies where the function of mNCX was compromised. We have recently reported a family of CGP37157 derivatives, finding an improvement in the neuroprotective properties together with an slight enhancement of the blockade of mNCX.

Attempting to optimize the pharmacokinetic profile of potential new drugs based on CGP37157, we paid attention to the recognized liposolubility of this type of 4,1- benzothiazepines, what would be beneficial for crossing the blood-brain barrier, but detrimental for a correct water solubility in a living organism. Prediction of log P indicated that its values would be close to the highest limit upon the Lipinski’s rules to predict drugability of chemical compounds. This fact prompted us to search for structural alternatives to improve water solubility and reducing log P values. Hence, we consider to replace the benzene-fused ring by pyridine, which would increase in polarity, as well as the possibility to prepare, for instance, their hydrochloride salts. Similar computational prediction confirmed that such a replacement to a significant reduction in the log P to about 3.

For this reason, we have proposed the design and preparation of small-sized drugs that block mNCX selectively, not only to develop new medicines, but also to clarify the role of mNCX in the physiological and pathological processes where they have been implicated.

Aplicaciones

Due to the key role of the control of the cell Ca2+ levels in neurons and other cells, these compounds can regulate the Ca2+ overload described in several pathologies of the nervous system, such as neurodegenerative (Alzheimer’s, Parkingson’s, Amyotrophyc Lateral Esclerosis), stroke, pain, and epilepsy, but also in diabetes, cardiovascular diseases, etc. Moreover, due to the lack of selectivity and potency of CGP37157 to block mNCX, the new compounds can serve as pharmacological tools to explore the role of mNCX in physiological and pathological processes, in a more accurate fashion than when using CGP37157

Estado de protección

P201500509 PRIORITY DATE: 07/10/2015 

Cooperación que se desea

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Estado:
En busca de codesarrolladores, En desarrollo, Transferible
Tecnología sanitaria:
Medicamentos - Farma