Mohammad R. Marzabadi - Ridgewood NJ Stewart A. Noble - Upper Saddle River NJ Mahesh N. Desai - Clifton NJ
Assignee:
Synaptic Pharmaceutical Corporation - Paramus NJ
International Classification:
C07D25150
US Classification:
514245, 544197, 544198, 544208, 544209
Abstract:
This invention is directed to triazine derivatives which are selective antagonists for a NPY (Y5) receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of the compound of this invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier.
Mohammad R. Marzabadi - Ridgewood NJ Stewart A. Noble - Upper Saddle River NJ Mahesh N. Desai - Clifton NJ
Assignee:
Synaptic Pharmaceutical Corporation - Paramus NJ
International Classification:
C07D25150
US Classification:
514245, 544197, 544198, 544208, 544209
Abstract:
This invention is directed to triazine derivatives which are selective antagonists for a NPY (Y5) receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of the compound of this invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier.
Compounds Specific For The Human 1D Adrenergic Receptor And Uses Thereof
Michael Konkel - Garfield NJ John M. Wetzel - Fair Lawn NJ Stewart A. Noble - Wheeling IL Charles Gluchowski - Danville CA Douglas A. Craig - Emerson NJ
Assignee:
Synaptic Pharmaceutical Corporation - Paramus NJ
International Classification:
A61P 4300
US Classification:
51425311, 51425312, 544360, 544365
Abstract:
This invention is directed towards a method of inhibiting activation of a human adrenergic receptor which comprises contacting the receptor with a compound so as to inhibit activation of the receptor, wherein the compound binds selectively to a human adrenergic receptor. This invention provides for a compound which binds selectively to a human adrenergic receptor. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier. This invention further provides for a method of treating a subject afflicted with a disease which is susceptible to treatment by antagonism of the human adrenergic receptor which comprises administering to the subject an amount of the above defined compounds effective to treat the disease.
Selective Melanin Concentrating Hormone-1 (Mch1) Receptor Antagonists And Uses Thereof
Mohammad R. Marzabadi - Ridgewood NJ John Wetzel - Fairlawn NJ John E. DeLeon - North Bergen NJ Bharat Lagu - Belle Mead NJ Charles Gluchowski - Danville CA Stewart Noble - Lake Forest IL Dhanapalan Nagarathnam - Bethany CT
Assignee:
Synaptic Pharmaceutical Corporation - Paramus NJ
International Classification:
C07D23932
US Classification:
51425214, 514274, 544316
Abstract:
This invention is directed to compounds which are selective antagonists for melanin concentrating hormone-1 (MCH1) receptors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of the compound of this invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of the compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of modifying feeding behavior of a subject which comprises administering to the subject an amount of a compound of the invention effective to decrease the consumption of food by the subject. This invention further provides a method of treating a feeding disorder in a subject which comprises administering to the subject an amount of a compound of the invention effective to decrease the consumption of food by the subject. In an embodiment of the invention, the feeding disorder is bulimia, bulimia nervosa or obesity.
Mohammad R. Marzabadi - Ridgewood NJ, US Wai C. Wong - Hamden CT, US Stewart A. Noble - Wheeling IL, US Manesh N. Desai - Nutley NJ, US
Assignee:
H. Lundbick A/S - Volby-Copenhagen
International Classification:
C07D 513/04 C07D 513/22 A61K 31/381 A61P 3/04
US Classification:
51421111, 540548, 548151, 514366
Abstract:
This invention is directed to triazine derivatives, bicyclic compounds and tricyclic compounds which are selective antagonists for a NPY (Y5) receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of this invention and a pharmaceutically acceptable carrier. This invention provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The invention further provides the use of a compound of the invention for the preparation of a pharmaceutical composition for treating an abnormality, wherein the abnormality is alleviated by decreasing the activity of a human Y5 receptor.
Mohammad R. Marzabadi - Ridgewood NJ, US Stewart A. Noble - San Diego CA, US Mahesh N. Desai - Nutley NJ, US
Assignee:
H. Lundbeck A/S - Valby-Copenhagen
International Classification:
C07D 251/50 C07D 251/70 A61K 31/53 A61P 3/04
US Classification:
514245, 544197, 544198, 544208, 544209
Abstract:
This invention is directed to triazine derivatives, bicyclic compounds and tricyclic compounds which are selective antagonists for a NPY (Y5) receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of this invention and a pharmaceutically acceptable carrier. This invention provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The invention further provides the use of a compound of the invention for the preparation of a pharmaceutical composition for treating an abnormality, wherein the abnormality is alleviated by decreasing the activity of a human Y5 receptor.
Carbonyl Compounds As Inhibitors Of Histone Deacetylase For The Treatment Of Disease
Paul L. Wash - San Diego CA, US Brandon M. Wiley - Encinitas CA, US Christian Hassig - San Diego CA, US James W. Malecha - Libertyville IL, US Stewart A. Noble - San Diego CA, US
Assignee:
Kalypsys, Inc. - San Diego CA
International Classification:
A61K 31/18 C07C 303/00
US Classification:
514602, 564 84, 564 88
Abstract:
Disclosed herein are carbonyl compounds of Formula I, II, or III, and others as described herein. Also disclosed are methods of treating disease, such as cancer, neurological disorders, including polyglutamine-repeat disorders, anemias, thalassemias, inflammatory conditions, autoimmune diseases and cardiovascular conditions, using the compounds of the invention. In addition, methods of modulating the activity of histone deacetylase (HDAC) are also disclosed.
Mohammad R. Marzabadi - Ridgewood NJ, US Wai C. Wong - Hamden CT, US Stewart A. Noble - San Diego CA, US Yasuchika Yamaguchi - Guilford CT, US
Assignee:
H. Lunbeck A/S - Copenhagen-Valby Novartis AG - Basel
International Classification:
A61K 31/426
US Classification:
514370
Abstract:
This invention is directed to bicyclic and tricyclic compounds which are selective antagonists for NPY (Y5) receptors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of this invention and a pharmaceutically acceptable carrier. The invention provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides the use of a compound of the invention for the preparation of a pharmaceutical composition for treating an abnormality, wherein the abnormality is alleviated by decreasing the activity of a human Y5 receptor.
Public Utilities
Supervisor - Construction Inspection Cross Connection Control Underground Infrastructure Locating
City of Riverside Public Utilities 2003 - 2011
Construction Inspector - Water
Skills:
Water Supervisory Skills Inspection Contract Management Construction Management Project Planning Civil Engineering Construction Budgets Government Municipalities Project Management Stormwater Management Water Resources Sustainability Emergency Management Policy Risk Assessment Environmental Awareness Cross Connection Control Water Resource Management Public Policy Budgeting
Certifications:
Water Distibution Operator Grade Iv Water Treatment Operator Grade Ii State of California Contractors License - C34 Pipeline Backflow Prevention Device Tester Building Inspector State Water Resources Control Board California State Dept of Corp County of Orange International Code Council
Vice President, Chemistry, Manufacturing And Controls
Civi Biopharma, Inc.
Vice President, Chemistry, Manufacturing and Controls
Noble R&D Consulting
Pharmaceutical R and D Consultant
Kalypsys 2003 - Dec 2013
President and Chief Executive Officer
Micell Technologies 2004 - 2009
Board Member
Pfizer 1999 - 2003
Senior Director, Chemistry
Education:
Kellogg School of Management 2011
Northwestern University - Kellogg School of Management 2009 - 2011
Master of Business Administration, Masters, Finance
University of Colorado Boulder 1981 - 1983
University of Birmingham 1975 - 1980
Doctorates, Bachelors, Doctor of Philosophy, Bachelor of Science, Chemistry
University of Birmingham 1978
Archbishop Holgates Grammar School 1975
The University of Birmingham
Skills:
Drug Discovery Biotechnology Chemistry Drug Development Pharmaceutical Industry Biopharmaceuticals Pharmacology R&D Technology Transfer Regulatory Affairs Clinical Trials Research and Development Cro Glp
For my friend Yvonnes 50th Birthday Party x 17th November 2012.
Duration:
2m 50s
Stewart Noble, Guide Glasgow
Duration:
2m 25s
Scottish Clans: The story behind Clan Stewart
Today the Red Stuart tartan is the most popular of any a fashion state...
Duration:
3m 21s
Full interview: Jon Stewart
In this episode of "Person to Person with Norah O'Donnell," O'Donnell ...
Duration:
21m 29s
Nobility in the Age of Destruction | Lori Ste...
Has anyone ever told you that you are a noble being? Lori Stewart remi...
Duration:
16m 56s
Across the Universe - The Beatles (Cover)
Catriona Blair Noble and her dad, Stewart Noble at Yvonnes 50th Birthd...
Duration:
2m 21s
Googleplus
Stewart Noble
About:
Sick of reading wine reviews that fail to sell me on the product itself my aim is to breath some much needed normality to an industry neck deep in bullshit speak and wine wank terminology. My aim is n...
Tagline:
The unqualified hack behind Wine without BS and No BS Events.