The Synaptic Vesicular Amine Transporter pipeline drugs market research report outlays comprehensive information on the Synaptic Vesicular Amine Transporter targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Synaptic Vesicular Amine Transporter pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
The report also covers products from therapy areas such as Central Nervous System which include the indications Tardive Dyskinesia, and Huntington Disease. It also reviews key players involved in Synaptic Vesicular Amine Transporter targeted therapeutics development with respective active and dormant or discontinued products.
The Synaptic Vesicular Amine Transporter pipeline targets constitutes close to eight molecules. Out of which, approximately eight molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase II, Phase I, and Preclinical stages are 1, 3, 1, and 3 respectively.
Synaptic Vesicular Amine Transporter overview
Synaptic vesicular amine transporter (SLC18A2) acts as an ATP-dependent transporter of monoamines, such as dopamine, norepinephrine, serotonin, and histamine. SLC18A2 exchanges one cationic monoamine with two intravesicular protons across the membrane of secretory and synaptic vesicles. Also, uses the electrochemical proton gradient established by the V-type proton-pump ATPase to accumulate high concentrations of monoamines inside the vesicles prior to their release via exocytosis.
For a complete picture of Synaptic Vesicular Amine Transporter’s drug pipeline, buy the report here.
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