Beigene
Associate Director
Astex Pharmaceuticals Jun 2017 - Jun 2018
Associate Director
Amgen Jan 2013 - Jun 2017
Biostatistical Programming, Senior Manager
Genentech Aug 2008 - Jan 2013
Senior Statistical Programmer Analyst
Amylin Pharmaceuticals Dec 2006 - Aug 2008
Principal Statistical Analyst
Education:
University of California, Berkeley 1994 - 1997
Masters, Master of Arts
University of California
Skills:
Sas Cdisc Clinical Trials Sas Programming Oncology Data Analysis Clinical Development Pharmaceutical Industry Sdtm Biostatistics Biotechnology Survival Analysis Cro Clinical Data Management Data Management Statistical Programming Edc Gcp Clinical Research Drug Development 21 Cfr Part 11 Oracle Clinical Therapeutic Areas Validation Regulatory Submissions Statistics Time Series Analysis Unix Fda R Regulatory Affairs Life Sciences Programming Lifesciences Ctms Drug Discovery Medical Writing Genomics Logistic Regression Sop Cro Management Cdisc Standards Good Clinical Practice
Song Liu - Cincinnati OH David Edward Portlock - Maineville OH Schwe Fang Pong - West Chester OH
Assignee:
The Procter Gamble Company - Cincinnati OH
International Classification:
A61K 3155
US Classification:
51421402, 540579
Abstract:
The subject invention involves compounds having the structure: wherein the C âN , C -C , and C -C bonds are each single or double bonds, except that both C -C , and C -C are double bonds; R1 is selected from hydrogen, alkyl, aryl, and heterocycle; R2-R15 are independently selected from hydrogen and other substituents; and pharmaceutically-acceptable forms thereof. The subject invention also involves pharmaceutical compositions containing such compounds, and methods for treating or preventing diseases and disorders using such compounds.
Methods For Synthesis Of Amino-Tetrahydroisoquinoline-Sulfonamide Hydroxamic Acids
Song Liu - San Diego CA William Martin Rennells - Schenectady NY
Assignee:
The Procter Gamble Co. - Cincinatti OH
International Classification:
C07D21702
US Classification:
546141, 546139
Abstract:
Methods of preparing an amino-substituted-tetrahydroisoquinoline-sulfonamide hydroxamic acid include the steps of providing an amino-substituted-tetrahydroisoquinoline-carboxylate attached to a solid support; reacting the ring nitrogen of the amino-tetrahydroisoquinoline-carboxylate with a sulfonyl chloride; and cleaving the intermediate from the solid support to form an amino-tetrahydroisoquinoline-sulfonamide hydroxamic acid.
Imidazo-Containing Heterocyclic Compounds, Their Compositions And Uses
Song Liu - San Diego CA David Edward Portlock - Maineville OH Schwe Fang Pong - West Chester OH
Assignee:
The Procter Gamble Co. - Cincinnati OH
International Classification:
A61K 314745
US Classification:
514292, 51421205, 514821, 514825, 546 84, 540579
Abstract:
The subject invention involves compounds having the structure: wherein each R1 is independently alkyl, aryl, or heterocycle; each R2-R7 is independently hydrogen or other substituent; B is nil and n is 0-3, or B is ethenyl and n is 0-1; and pharmaceutically acceptable forms thereof. The subject invention also involves pharmaceutical compositions containing such compounds, and methods for treating or preventing diseases or disorders using such compounds.
N-(1-Phenylethyl)-5-Phenyl-Imidazole-2-Amine Compounds, Their Compositions And Uses
Song Liu - Cincinnati OH Benjamin Eric Blass - Cincinnati OH David Edward Portlock - Maineville OH
Assignee:
The Procter Gamble Company - Cincinnati OH
International Classification:
C07D23354
US Classification:
514341, 514398, 5483315, 5483215, 5462741
Abstract:
The subject invention involves compounds having structure (I): wherein each R1 is independently alkyl, aryl, or heterocycle; each R2, R4, R7, and R8 is independently hydrogen or other substituent; A is aryl or heterocycle; and pharmaceutically acceptable forms thereof. The subject invention also involves pharmaceutical compositions containing such compounds, and methods for treating or preventing diseases or disorders using such compounds.
Methods For Synthesis Of Amino-Tetrahydroisoquinoline Ring Compounds
Song Liu - San Diego CA William Martin Rennells - Schenectady NY
Assignee:
The Procter Gamble Company - Cincinnati OH
International Classification:
C07D21712
US Classification:
540555, 540559, 546 62, 546 81, 546 84
Abstract:
Methods of preparing amino-substituted-tetrahydroisoquinoline ring compounds include the steps of providing a support-bound amino-substituted-tetrahydroisoquinoline compound; forming an intermediate by reacting the support-bound amino-substituted-tetrahydroisoquinoline compound with a reagent; and cyclizatively cleaving the support-bound amino-substituted-tetrahydroisoquinoline compound to form the amino-substituted-tetrahydroisoquinoline ring compound.
Liming Huang - San Diego CA, US Song Liu - San Diego CA, US Elizabeth A. Lunney - San Diego CA, US Simon P. Planken - San Diego CA, US
Assignee:
Pfizer Inc. - Madison NJ
International Classification:
A61K 31/472
US Classification:
514310, 546143
Abstract:
The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein: R, R, Z, t, and ring A are as defined in the specification. The invention also relates to pharmaceutical compositions comprising the compounds of formula (I) and methods of treating a condition that is mediated by the modulation of JNK, such as diabetes, the method comprising administering to a mammal an effective amount of a compound of formula (I).
Methods For Synthesis Of Amino-Tetrahydroisoquinoline-Carboxylic Acids
Song Liu - San Diego CA, US William Rennells - Schenectady NY, US
International Classification:
C07D215/00
US Classification:
546/152000
Abstract:
Methods of preparing an amino-substituted-tetrahydroisoquinoline-carboxylic acid include the steps of providing a support-bound amino-substituted-tetrahydroisoquinoline-carboxylate wherein the ring nitrogen has a protecting group; attaching a first moiety to the amino-substituted group of the support-bound amino-substituted-tetrahydroisoquinoline-carboxylate; de-protecting the ring nitrogen; attaching a second moiety to the ring nitrogen to form a support-bound intermediate; and cleaving the support-bound intermediate from the solid support to form the carboxylic acid.
The present invention relates to compounds of formula (I),or a pharmaceutically acceptable salt or solvate thereof, wherein: R, R, Z, t, and ring A are as defined in the specification. The invention also relates to pharmaceutical compositions comprising the compounds of formula (I) and methods of treating a condition that is mediated by the modulation of JNK, such as diabetes, the method comprising administering to a mammal an effective amount of a compound of formula (I).