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16 results about "PDE1" patented technology
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PDE1 (phosphodiesterase type 1) is a phosphodiesterase enzyme also known as calcium- and calmodulin-dependent phosphodiesterase. It is one of the 11 families of phosphodiesterase (PDE1-PDE11). PDE1 has three subtypes, PDE1A, PDE1B and PDE1C which divide further into various isoforms. The various isoforms exhibit different affinities for cAMP and cGMP.
The disclosure relates to the use of phosphodiesterase 1 (PDE1) inhibitors for preventing or treating chemobrain, e.g., inhibiting or mitigating one or more symptoms of chemobrain, e.g., feeling of mental fogginess, deficit in attention, disorganized behavior or thinking, confusion, impaired concentration, difficulty finding the right word, difficulty learning new skills, difficulty multitasking, memory impairment (e.g., short-term memory problems, long-term memory problems, impaired verbal memory, impaired visual memory), and / or fatigue.
The disclosure relates to the combination of phosphodiesterase 1 (PDE1) inhibitors, which is useful for treating certain cancers or tumors, such as colon cancer. In another form, the disclosure relates to the use of PDE1 inhibitors and an optional antitumor agent for treating certain cancers or tumors.
Please add the following heading and paragraph on a separate sheet, after the claims: The disclosure relates to the use of phosphodiesterase 1 (PDE1) inhibitors for the treatment of cancers and tumors, including for inhibiting tumor recruitment of macrophages and other cells to the tumor or cancer, for complementing and enhancing checkpoint inhibitor therapies, and for mitigating the side effects (i.e., inflammatory-related adverse events) associated with checkpoint inhibitor therapies.
The disclosure relates to the use of phosphodiesterase 1 (PDE1) inhibitors in combination with a Compound of Formula VIII or a Compound of Formula IX, as described herein, or in combination with an antiemetic agent, such as an antipsychotic agent, e.g., olanzapine, for preventing or treating nausea and / or vomiting, e.g., CINV (chemotherapy-induced nausea and vomiting). In some embodiments, the Compound of Formula VIII or the Compound of Formula IX is used as mono-therapy (i.e., without a PDE1 inhibitor).
The present application belongs to the technical field of biological medicine, and particularly relates to a pyridodihydrofuranone derivative, a preparation method and application thereof. The derivative shows good inhibitory effect on phosphodiesterase type 1 (PDE1), and can be applied as a phosphodiesterase type 1 inhibitor. According to the research on phosphodiesterase type 1 related diseases in the prior art, the pyridodihydrofuranone derivative can be further applied in the treatment of pulmonary arterial hypertension, idiopathic pulmonary fibrosis, liver fibrosis, vascular dementia, intestinal inflammation and other diseases related to phosphodiesterase type 1, more optional drugs are provided, and the pyridodihydrofuranone derivative has important medicinal value and clinical application prospect. Moreover, the pyridodihydrofuranone derivative has novel structure, the preparation method is simple, and is very suitable for large-scale industrial production and application.
The disclosure relates to the combination of inhibitors of phosphodiesterase 1 (PDE1) useful for the treatment of certain cancers or tumors, such as gliomas. In another embodiment, the disclosure relates to the combination of inhibitors of PDE1 and an antitumor agent for the treatment of certain cancers or tumors, such as gliomas.