Total Synthesis Ltd.

Other

Gilead Sciences, Inc.

Cv Therapeutics, Inc.

The Endowment for Research in Human Biology, Inc.

Michael Organ

Debasis Mallik

Jeff A Zablocki

Elfatih O Elzein

Matthew Abelman

Wing Ming Keung

Guoxin Tao

Yaroslav Bilokin

Rao V Kalla

Thao Perry

Xiaofen Li

Tetsuya Kobayashi

Robert H Jiang

Scott Carson Miller

Stanislas Mayer

Jee Seong Kwak

Wenyao Zhang

Ivan Diamond

Zhan Jiang

Anthony Disanti

Peter Kernast

Christopher J O'Brien

Assam (Eric) B Kantchev

Maria Pia Arolfo

Peidong Fan

Lina Yao

A fluid diverting module includes a multi-position fluid diverting device comprising three-dimensional movable flow-paths with minimal tortuosity in the movable portion (the rotor) of the fluid diverting device. In some embodiments, the device is also equipped with a filtration module that is capable of filtering solid particulates from fluidic samples. The invention relates to an area of non-disruptive sampling from various sample sources including ones containing solids. The fluid diverting device maintains fluid communication between the sample source and a pressure creating device in all positions of the fluid diverting device, thus conserving the pressure inside the sample source during sampling. The sampling operation is controlled from a controller, which is equipped with a software for manual or intelligent control.

Fluid diverting module

A multidimensional chromatographic assembly includes a pump module, an injector, a path selector device, an array of chromatographic media, a loop selector device and a detector assembly for receiving at least a portion of an analyte stream and flowing the injected stream into the detector assembly via a chromatographic medium (the first dimension). At least a portion of the analyte of interest is then channeled into a chromatographic medium of interest (the second dimension) and re-circulated through the detector assembly. The iteration (multidimension) is continued until all aspects of the chromatogram and the peaks are judged to be analyzed. The entire process is controlled from a computer and the results are collected to make decisions on the analytical and the process controls.

Multidimensional peak purity analysis

A sampling module of a fluid processing apparatus includes at least one multi-configuration device connected to a filtration module. The invention relates to an area of non-disruptive sampling from any flow stream including the ones containing solids. The fluid processing apparatus remains in fluid communication with a sample processing module in all configurations of the sampling module and the parameters deemed critical for a chemical process remain unaffected during the sampling event. The entire event is controlled from a computer and the results are collected to make decisions on analytical and process controls.

Non-disruptive sampler for fluid processing apparatus

A fluid processing assembly includes a lumen for receiving at least one inlet stream and dispensing a primary product stream, and an energizing device for supplying energy to an energizable portion of the lumen. A primary product collection assembly is in fluid communication with the lumen for receiving the primary product stream. The energizable portion is positioned exterior to the primary product collection assembly. A pressurized gas source is downstream of the lumen. The pressurized gas source supplies pressurized gas to the primary product collection assembly for pressurizing at least a portion of the primary product collection assembly and the lumen.

Fluid processing apparatus

Disclosed are novel isoflavone derivatives having the structure of Formula I which are useful as ALDH-2 inhibitors for treating mammals for dependence upon drugs of addiction, for example addiction to dopamine-producing agent such as cocaine, morphine, amphetamines, nicotine, and alcohol.

ALDH-2 inhibitors in the treatment of addiction

Disclosed are novel quinazolinone derivatives of formula: wherein:

Quinazolinone derivatives as ALDH-2 inhibitors

Disclosed are syntheses suitable for large scale manufacture of novel compounds that are partial and full Aadenosine receptor agonists, useful for treating various disease states, in particular tachycardia and atrial flutter, angina, and myocardial infarction.

Partial and full agonists of A1 adenosine receptors

The present invention relates to catalysts of transition metal complexes of N-heterocyclic carbenes, their methods of preparation and their use in chemical synthesis. The synthesis, ease-of-use, and activity of the compounds of the present invention are substantial improvements over in situ catalyst generation. Further, the transition metal complexes of N-heterocyclic carbenes of the present invention may be used as precatalysts in metal-catalyzed cross-coupling reactions.

Transition metal complexes of N-heterocyclic carbenes, method of preparation and use in transition metal catalyzed organic transformations

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Burlington, Canada

Michael Organ