Optimization and preclinical development of FAAH inhibitors for smoking cessation
Optimization and preclinical development of FAAH inhibitors for smoking cessation
批准号:
8104786
负责人:
Daniele Piomelli
金额:
$76.5万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-30 至 2015-07-31
关键词:
Behavioral inhibitionDevelopmentEnzymesGoalsHumanInvestigational DrugsInvestigational New Drug ApplicationLaboratoriesLeadModelingMolecular TargetNew Drug ApprovalsNicotineNicotine DependenceRelapseResearchSafetySaimiriScientistSelf AdministrationTobacco DependenceTranslatingabstractinganandamidebasedesigndrug discoveryexperiencefatty acid amide hydrolasein vitro testingin vivoinhibitor/antagonistpre-clinicalpreventprogramsskillssmoking cessationtherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): We have shown that pharmacological inhibition of the anandamide-degrading enzyme, fatty acid amide hydrolase (FAAH), blocks nicotine self-administration and prevents nicotine-induced reinstatement in squirrel monkeys, a model of human nicotine addiction and relapse to nicotine use. Based on these results, which point to FAAH as a promising molecular target for tobacco dependence, we propose to undertake a drug discovery program aimed at the optimization and preclinical development of FAAH
inhibitors for smoking cessation. Our proposal has two primary goals: Specific Aim 1: Optimization of FAAH inhibitors and identification of a preclinical candidate for smoking cessation. We will conduct a lead optimization campaign starting from the compound
URB694, a potent FAAH inhibitor previously identified in our laboratory. Compounds will be synthesized and tested in vitro and in vivo, and information collected will be used to design new molecules until a preclinical candidate with suitable efficacy and safety profile is selected.
Specific Aim 2: Preclinical development of FAAH inhibitors for smoking cessation. We will (a) advance through preclinical development the candidate identified in Aim 1; (b) prepare and submit an Investigational New Drug (IND) application for the candidate with smoking cessation as therapeutic target; (c) seek private and/or public sponsors to support safety and proof-of-concept studies in humans after IND approval. To achieve these goals, we have assembled a multi-disciplinary consortium that unites scientific excellence with experience in industrial drug discovery and preclinical development. The team includes scientist and entrepreneur Daniele Piomelli (UCI), a leader in the field of FAAH inhibition; behavioral pharmacologist Steven Goldberg (NIDA-IRP), a pioneer in nicotine research; senior chemist Tiziano Bandiera (IIT); senior pharmacologist Angelo Reggiani (IIT); and preclinical development expert Edward Monaghan. Thus, o
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