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Teva Gyogyszergyar Zartkoruen Mukodo Reszvenytarsasag Patents
Assignee:
Teva Gyogyszergyar Zartkoruen Mukodo Reszvenytarsasag
Address:
Debrecen, HU
No. of patents:
12
Patents:












Patent Number Title Of Patent Date Issued
7700752 Process for constructing strain having compactin hydroxylation ability April 20, 2010
The present invention is directed to methods and compositions for microbial based production of pravastatin. The compositions of the invention include novel strains of microorganisms that are capable of efficiently hydroxylating compactin (ML-236 B) resulting in production of pravast
7700337 Process for constructing strain having compactin hydroxylation ability April 20, 2010
The present invention is directed to methods and compositions for microbial based production of pravastatin. The compositions of the invention include novel strains of microorganisms that are capable of efficiently hydroxylating compactin (ML-236 B) resulting in production of pravast
7589128 Process for preparation of amorphous form of a drug September 15, 2009
Provided is a process for preparation of amorphous form of an active pharmaceutical ingredient.
7452991 Aztreonam .beta. polymorph with very low residual solvent content November 18, 2008
The invention relates to the .beta. polymorph of Aztreonam, which contains less than 2.5% by weight residual solvent and to a process of making said polymorph. In the process of the invention, a polymorph of Aztreonam is dissolved in an absolute C.sub.1-6 alcohol in the presence of a bas
7452692 Method for extracting a macrolide from biomatter November 18, 2008
Provided is a method for obtaining a macrolide, especially tacrolimus, ascomycin, pimecrolimus, sirolimus, or everolimus, from biomatter.
7432074 Method for extracting a macrolide from biomatter October 7, 2008
Provided is a method for obtaining a macrolide, especially tacrolimus, from biomatter.
7358247 Mycophenolate mofetil impurity April 15, 2008
Provided is an impurity of mycophenolate mofetil, processes for its preparation and its use as a reference.
7335772 1H-imidazo [4,5-c] quinolin-4-cyano and 1H-imidazo [4,5-c] quinolin-4-carboxamide intermediates February 26, 2008
The invention relates to a process for the synthesis of 1H-imidazo[4,5-c]quinoline 4-cyano and 1H-imidazo[4,5-c]quinoline 4-carboxamide intermediates useful in preparing 1H-imidazo[4,5-C]quinoline 4-amines, a process for preparing 1H-imidazo[4,5-C]quinoline 4-amines using such interm
7279571 Methods of preparing pimecrolimus October 9, 2007
The present invention provides a process for the preparation of pimecrolimus from ascomycin in which ascomycin is reacted with a conversion reagent that converts ascomycin to its activated derivative at C-32. The activated ascomycin is then reacted with chloride ion. The process of t
7153967 Preparation of 1H-imidazo [4,5-C] quinolin-4-amines via 1H-imidazo [4,5-C] quinolin-4-phthalimid December 26, 2006
The invention provides 1H-imidazo(4,5-C)quinolin-4-phthalimide intermediates useful in the synthesis of 1H-imidazo(4,5-C)quinoline-4-amines, particularly Imiquimod. The invention further provides a method for making the intermediates and a method for making 1H-imidazo(4,5-C)quinoline
7102026 Process for preparing and isolating rac-bicalutamide and its intermediates September 5, 2006
The present invention relates to a new process for the synthesis of racemic and optically active bicalutamide starting from ethyl pyruvate and methyl methacrylate. The present invention discloses processes of preparing bicalutamide intermediates including ethyl-[2-{4-fluorophenyl sul
7078223 Process for the preparation of pseudomonic acid a antibiotic by microbiological method July 18, 2006
A procedure for the preparation of pseudomonic acid A comprising submerged cultivation of a Pseudomonas bacterium strain capable of biosynthesis of the substantially pure pseudomonic acid A in aerated conditions via fermentation; and isolation of the desired compound is disclosed. In

 
 
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