Co-organizors  :

               南京人事局

Welcome to International Symposium on Organic Synthesis and Drug Development 2008

 

Keynote Speaker

                                                                              (Alphabetically)

 

    Aharon Jehuda Ciechanover was Nobel Winner in 2004. He was born in Haifa, Israel, he received his Master of Science in 1971 and his M.D. in 1974 from the Hadassah Medical School of the Hebrew University in Jerusalem. He received his doctorate in medicine in 1982 from the Technion (Israel Institute of Technology), in Haifa. He is currently a Professor in the Unit of Biochemistry and Director of the Rappaport Family Institute for Research in Medical Sciences at the Technion.

 

                        

 Ferenc Avraham Hershko was Nobel Winner in 2004. He was born in 1937, in Karcag, Hungary. He did his graduate work in 1967-69 at the Hadassah Medical School of the Hebrew University in Jerusalem, receiving a Ph. D. degree in 1969.In 1969-72, Hershko was a postdoctoral fellow at the University of California, San Francisco. He is a Distinguished Professor at the Unit of Biochemistry, the Rappaport Faculty of Medicine at the Technion (Israel Institute of Technology) in Haifa, Israel.             

 

 

    Karl Barry Sharpless was Nobel Winner in 2001. He was born in Philadelphia in April 28, 1941. He began his studies in Dartmouth College and earned his PhD from Stanford University in 1963. He continued post-doctoral work at Stanford University and Harvard  University. Sharpless became professor at the Massachusetts Institute of Technology, Stanford University, and the Scripps Research Institute, where he currently holds the W. M. Keck professorship in chemistry.
 

 

 

Confirmed Plenary Speakers

   

 (Alphabetically)

Burgess Kevin

Texas A&M University

USA

Libraries of Bivalent Peptidomimetics for Mimicking or Disrupting Protein-Protein Interactions

Chen  Li

Chief Scientific Officer, VP, Roche-China

Regulation of Signals through Protein-Protein Interaction: 15 years and counting

Futran Mauricio

Vice President of Process Research & Development, Bristol-Myers Squibb

Knowledge Creation in Pharmaceutical Process Development in the Context of Global Partnerships

Imwinkelried Rene

Vice President of Chemical and Physical Sciences, Schering-Plough, USA

TBA

Lin Guo-Qiang

Shanghai Institute of Org.Chem, CAS and NSFC, China

New Synthetic Methodologies and Their Utilities in the Synthesis of Bio-active Products

Lipshutz Bruce

University of California, Santa Barbara, USA

Green Chemistry Using "Designer" Surfactants. Just Add Water

Lu Xiyan

Shanghai Institute of Organic Chemistry, CAS, China

Paladium(II) catalyzed addition of arylboronic acids to carbon-heteroatom multiple bonds. An enantioselective, catalytic Grignard type reaction

Portoghese Philip S.

University of Minnesota, USA

Ligands that activate heterodimeric opioid receptors: functional and clinical relevance

Schiller Peter W.

Clinical Research Institute of Montreal, Canada

Use of Novel Amino Acid Analogues in the Development of Peptides as Drugs or Pharmacological Tools

Scypinski Stephen VP of Bristol-Myers Squibb Company Overview of the Drug Development Process: Assuring Product Quality and Efficacy

Volante Ralph P

Vice President of Process Research, Merck

TBA

 

Invited Speakers

 

 

Confirmed Invited Speakers

Part A Organic Synthesis

Part B Process Chemistry

Session 1:  Organic Chemistry and Process Chemistry

Session 2:  Chemistry Application in Pharmaceutical Industry

Session 3:  Outsourcing in Chemistry and Drug Development

Session 4:  Drug Development Process

 

Part CMedicinal Chemistry

Session 1:  General Medicinal Chemistry

Session 2:  Medicinal Chemistry Approaches to tackling Cardiovascular disease

Session 3:  Medicinal Chemistry Approaches to tackling inflammation disease

Session 4.: Medicinal Chemistry Approaches to Tackling Oncology Disease

Session 5 : Medicinal Chemistry Approaches to Tackling Metabolic Disease

  

Part A: Organic synthesis

Bogyo Matthew Stanford Univ.

Small molecule activity based probes for diagnostic imaging and drug discovery applications

Chen Wanzhi Department of Chemsitry
Zhejiang University

Highly Efficient Catalysts Supported by Multidentate N-Heterocyclic Carbenes for C-C Coupling Reactions

Debrabander Jef K. Univ. of Texas Southwestern Medical Center

Natural Products: An Inspirational platform for New Discoveries

Ding Kuiling

SIOC, CAS

Development of highly efficient chiral catalysts for asymmetric reactions: practical synthesis of chiral drug intermediates

Franzen Robert

Tampere University of Technology, Department of Chemistry and Bioengineering

Recent advances in the Suzuki cross-coupling reaction of different organoboron derivatives

Huang Feihe

Zhejiang Univ.

Threaded structures based on crown ether derivative hosts

Jiang Biao

SIOC, CAS

Synthesis of Chiral Gossypol and Their Dericatives and Evaluation of Their Anticancer Activity

Liu Lei Tsinghua Univ. TBA
Lutz F. Tietze Institut für Organische und Biomolekulare Chemie, Universität Göttingen. New Approaches for a Selective Treatment of Cancer Based on Prodrugs and Monoclonal Antibody-Enzyme Conjugates

Ma Dawei

SIOC, CAS

TBA

Shaw Robert Texas Tech University, USA  

Antibiotic Resistance in Bacteria: Novel Metalloenzyme Inhibitors

 

Shi  Zhangjie Peking Univ.

Transition-Metal Catalyzed C-H Activation

Snyder Scott Columbia University, USA  

Achieving Synthetic Control When Nature Abandons Selectivity

 

Wang Meixiang

Insitute of Chemsitry, CAS

TBA

Xi  Zhenfeng

Peking Univ.

Synthesis of Multiply Substituted Pyrrolopyridiens, Pyridines and Pyrroles

Yudin Andrei University of Toronto
Protecting Group-Free Synthesis of Complex Amines
 

Zhang Liming

Department of Chemistry, University of Nevada, Reno

Au-Catalyzed Cycloaddition Reactions

Zhu Chengjian

Nanjing Univ.

TBA

 

Part B: Process Organic Chemistry

Bhongle Nandu

Sepracor

TBA

Colacot Thomas

Johnson Matthey Catalyst

Highly Active, Air-Stable Pd Catalysts for Challenging Cross-Coupling Reactions
Discordia Robert  Bristol-Myers Squibb Company

The Process Development of an MMP Inhibitor: Development and Execution of a Crystallization Induced Dynamic Resolution

Guo Paul (Peng)

President, AstaTech, Inc (USA),

Process Technology Commercialization: From Target to Technology Development

Houpis Yannis

Johnson and Johnson PRD

Carboxylate Directed Pd-Catalyzed Cross Coupling Reactions in the Selective Synthesis of tri-Substituted Aromatics

Hong Yaping

Princeton GlobalSynthesis LLC

Introduction of Chemical Process R/D : Trends and Challenges

Huang Jason Bristol-Myers Squibb Company Analytical Role in Pharmaceutical Development and GMP Compliance

 

Liang Leon  

Bristol-Myers Squibb Company

 

TBA

Lu  Zhi-Hui

 

Boehringer-Ingelheim Pharmaceuticals

 

Practical Synthesis Of 2,3-Disubstituted And Polycyclic Indoles

Ruan Joan Bristol-Myers Squibb Company

Forced Degradation Strategy

Wang Jianji Bristol-Myers Squibb Company Pharmaceutical Process Research and Development

Yu Jurong

Nanjing Pharma.

My experience of doing Process R&D in China: the Story in Nanjing

 

Salvino Joseph M. Director, Hit to Lead Chemistry, Cephalon, Inc.

Practical Approaches toward Lead Finding and Lead Optimization Library Synthesis

Shi Xiongwei

United Pharmatech

Sundia's Strategies and Steps towards Meeting Client's Requirement for Outsourcing Services

Zhou Maotang VP of R&D, Chiral Quest (China)

 

Advances in Asymmetric Hydrogenation: From Innovative Ligands to Commercial Manufacture

 

 

Part C: Medicinal Chemistry

Cheng Jiefei Otsuka Maryland Medicinal Laboratories Inc, USA

TheYin andYang of theFattyAcid Oxidation Modulation

Chen Li

Hoffmann-La Roche, USA

Discovery of VLA4 Antagonists for the Treatment of Autoimmune Diseases

Cherney Robert J.

Bristol-MyersSquibb,  Pharmaceutical Research Institute, USA

Discovery of Potent CCR2 Antagonists

Deng Jianghe

GlaxoSmithKline. Co

 

Encoded Library Technology: A New Methodology for Lead Discovery

Ge Min

CSO, Acesys Pharmatech

Medicinal Chemistry Outsourcing in Nanjing

He Yun

Medical Chemistry DepartmentRoche R&D Center (China) Ltd

TBA

Henry Jim

Eli Lilly and Company, USA

Type II Kinase Inhibitors for the Treatment of Cancer

Jadhav Prabhakar

Eli Lilly & Company,  USA

Orally bioavailable, nonsteroidal MR antagonist LY2180176 for the treament of hypertension

Kang Jiesheng

Sanofi Aventis, New Jercy, USA

 

HERG and the LQT Syndrome: Background, Regulations & Non-Clinical Strategy

Li Qun

Chief Scientific Officer, Egret Pharma, Shanghai, China

Design and Synthesis of Orally Bioavailable Akt Kinase (PKB) Inhibitors as Anticancer Agents

Liu Hong

The Novartis Research Foundation, San Diego, USA

 

Structure Based Design and Synthesis of Noncovalent Inhibitors of Cathepsin S and Their Applications in Treating Neuropathic Pain

 

Long Ya-Qiu

Shanghai Institute of Materia Medica Chinese Academy of Sciences

1,6-naphthyridine-7-carboxamide Templated Active Compounds: Switching From hiv-1 Integrase Inhibitors to Anti-tumor Agents

Pinto Donald

Bristol-Myers Squibb Company, Princeton, NJ 08543, USA

A Next Generation Oral Anticoagulant: The Discovery of Apixaban, a Potent, Selective and Orally Bioavailable Factor Xa Inhibitor

Procter Martin

Prosidion, UK

Design and Synthesis of Orally Bioavailable Glucokinase Activators

Qian Shawn Associate Director, Meidcinal Chemistry, Cytokinetics, Inc Discovery of Mitotic Kinesin Inhibitors as Novel Anticancer Agents

Shao Feng

Pepper Hamilton LLP

Philadelphia, PA, USA

Navigation Through Patentability and Freedom to Operate - An Introduction to the U.S. Patent Law

Shih Joe

Eli Lilly and Company, USA

The Evolution of Lilly Oncology: From Cytotoxic Agents (Discovery and Development of ALIMTAÒ) to Kinase Inhibitors

Wang Yonghui

GlaxoSmithKline

7TM Receptor Antagonists: Lead Discovery Strategy and Case Studies

Wei Xudong

Boehringer-Ingelheim Pharmaceuticals

Practical Large Scale Synthesis of Macrocyclic HCV Protease Inhibitors

Xing  Bengang

School of Physical & Mathematical Sciences Nanyang Technological University

TBA

Xu Weizheng    (William)

MGI Pharmaceutical, USA

 

Design, Synthesis and Biological Evaluation of PARP Inhibitors as Chemosensitizers

Xu Yaohua

Novartis AG

Serotonin Antagonist And Its Application In Smoking Cessation and Anti-depression

Yao Wenqing

Incyte Corporation, USA

Discovery of Potent and Selective 11ßHSD1 Inhibitors: Scaffold Hopping Approach for Novel Lead Generation Based on Medchem Intuition

Yao Yiming

 

EnzMed (nanjing) Co., Ltd Enzymatic synthesis in pharmaceutical development

Zhang Frank

CEO, Genscript Corporation

Accelerate your drug discovery by outsourcing your biology

Zhao Gang

Abbott, USA

AMPK Activators

 

Zhou Maotang VP of R&D, Chiral Quest (China)

Advances in Asymmetric Hydrogenation: From Innovative Ligands to Commercial Manufacture

Zhu Guidong Abbott Laboratories

ABT-888 and Back Up, Orally Efficacious
Inhibitors of Poly(ADP-ribose) Polymerase (PARP) for the Treatment of Cancer

 

 

 

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