Patents Represented by Attorney, Agent or Law Firm George E. Heibel
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Patent number: 7566782Abstract: The present invention relates to a process for the preparation of rosuvastatin calcium, a promising new HMG-CoA reductase inhibitor.Type: GrantFiled: December 10, 2002Date of Patent: July 28, 2009Assignee: Ranbaxy Laboratories LimitedInventors: Yatendra Kumar, Hashim Nizar Poovanathil Nagoor Meeran, Shantanu De, Mohammad Rafeeq, Swargam Sathyanarayana
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Patent number: 7544708Abstract: This invention generally relates to muscarinic receptor antagonists which are useful, among other uses, for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through muscarinic receptors. Specifically, the invention relates to derivatives of azabicyclo compounds, including, for example, 6-substituted azabicyclo[3.1.0] hexanes, and 2,4,6-trisubstituted derivatives. The invention also relates to pharmaceutical compositions containing the compounds and the methods of treating the diseases mediated through muscarinic receptors.Type: GrantFiled: April 11, 2003Date of Patent: June 9, 2009Assignee: Ranbaxy Laboratories LimitedInventors: Mohammad Salman, Anita Mehta, Pakala Kumara Savithru Sarma, Shankar Jayram Shetty, Sankaranarayanan Dharmarajan, Naresh Kumar, Arundutt Vishwanatham Silamkoti, Anita Chugh
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Patent number: 7288562Abstract: This invention generally relates to the derivatives of novel 3,6 disubstituted azabicyclo[3.1.0] hexane's. The compounds of this invention are MUSCARINIC receptor antagonists which are useful, inter-ail for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through MUSCARINIC receptors. The invention also relates to processes for the preparation of the compounds of the invention, pharmaceutical compositions containing the compounds of the present invention and the methods of treating the diseases mediated through MUSCARINIC receptors.Type: GrantFiled: August 23, 2002Date of Patent: October 30, 2007Assignee: Ranbaxy Laboratories LimitedInventors: Anita Mehta, Jang Bahadur Gupta
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Patent number: 6833452Abstract: A process for the preparation of highly pure crystalline form of cefuroxime-1-acetoxyethyl ester (cefuroxime axetil) from cefuroxime by reacting an amine salt of cefuroxime with an esterifying reagent.Type: GrantFiled: July 16, 2001Date of Patent: December 21, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Om Dutt Tyagi, Gyan Chand Yadav, Vijay Kumar Handa
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Patent number: 6822119Abstract: The present invention relates to a cost effective and industrially advantageous process for the preparation of tolterodine and pharmaceutically acceptable salts thereof.Type: GrantFiled: May 18, 2004Date of Patent: November 23, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Yatendra Kumar, Mohan Prasad, Praveen Kumar Neela, Satyananda Misra
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Patent number: 6803468Abstract: The present invention relates to an improved and industrially advantageous process for the preparation of N-(5-methylnicotinoyl)-4-hydroxypiperidine of Formula I, as shown in the accompanied drawings. This compound is a key intermediate for the synthesis of rupatadine, a potent dual antagonist of histamine and platelet-activating factor (PAF).Type: GrantFiled: June 20, 2003Date of Patent: October 12, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Yatendra Kumar, Mohan Prasad, Shallendra Kumar Singh
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Patent number: 6734307Abstract: The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria such as multiply-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms such as Bacterioides spp. and Clostridia spp. species, and acid fast organisms such as Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.Type: GrantFiled: July 16, 2001Date of Patent: May 11, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Anita Mehta, Arora K. Sudershan, Biswajit Das, Abhijit Ray, Sonali Rudra, Ashok Rattan
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Patent number: 6710049Abstract: The present invention relates to the derivatives of specially substituted azole compounds which have improved antifungal activity as compared with presently available agents in this class and the processes for the preparation thereof. This invention also relates to pharmaceutical preparations containing the compounds of the present invention and their use in treating and/or preventing the fungal infections in mammals, preferably humans.Type: GrantFiled: December 21, 2001Date of Patent: March 23, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Mohammed Salman, Rita Katoch, Ashwani Kumar Verma, Jitendra Sattigeri, Ashok Rattan
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Patent number: 6686497Abstract: The present invention relates to a new and industrially advantageous process for the preparation of 3-ethoxy-4-ethoxy-carbonyl-phenyl acetic acid. This compound is a key intermediate for the synthesis of Repaglinide, an oral hypoglycemic agent.Type: GrantFiled: September 20, 2002Date of Patent: February 3, 2004Assignee: Banbaxy Laboratories LimitedInventors: Mohammad Salman, J. Suresh Babu, Purna C. Ray, Sujay Biswas, Naresh Kumar
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Patent number: 6677485Abstract: An improved and industrially advantageous process for the preparation of the antidepressant fluoxetine and its pharmaceutically acceptable salts, preferably hydrochloride.Type: GrantFiled: August 9, 2002Date of Patent: January 13, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Naresh Kumar, Bakthavathsalan Vijayaraghavan, Kinali Venkata Ramana, Swargam Sathyanarayana
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Patent number: 6673369Abstract: The present invention relates to a controlled release pharmaceutical composition comprising amounts ranging from about 0.1 to about 4.5% w/w, of one or more of rate controlling cellulosic ether polymers.Type: GrantFiled: January 22, 2002Date of Patent: January 6, 2004Assignee: Ranbaxy Laboratories LimitedInventors: Ashok Rampal, Rajeev S. Raghuvanshi, Manoj Kumar
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Patent number: 6670363Abstract: The present invention relates to the derivatives of specially substituted azole compounds which have improved antifungal activity as compared to known compounds such as fluconazole and itraconazole and the processes for the preparation thereof. This invention also relates to pharmaceutical compositions containing the compounds of the present invention and their use in treating and/or preventing fungal infections in mammals, preferably humans.Type: GrantFiled: May 22, 2000Date of Patent: December 30, 2003Assignee: Ranbaxy Laboratories LimitedInventors: Ashwani Kumar Verma, Sudershan K. Arora, Jasbir Singh Arora, Ashok Rattan
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Patent number: 6590085Abstract: This invention relates generally to compounds and processes for synthesizing derivatives of 2-3-O-isopropylidene-&agr;-L-xylo-2-hexulofuranosonic acid. The compounds of this invention are useful, inter-alia, for the inhibition and prevention of cell adhesion and cell adhesion-mediated pathologies, including inflammatory and autoimmune diseases, such as bronchial asthma, rheumatoid arthritis, type I diabetes, multiple sclerosis, allograft rejection and psoriasis. This invention also relates to pharmacological compositions containing derivatives of 2-3-O-isopropylidene-&agr;-L-xylo-2-hexulofuranosonic acid and the methods of treating such pathologies as listed above.Type: GrantFiled: March 25, 1999Date of Patent: July 8, 2003Assignee: Ranbaxy Laboratories LimitedInventors: Sudershan K Arora, Nawal Kishore, Jang Bahadur Gupta, Vishwas D Joshi
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Patent number: 6586005Abstract: A sustained release formulation of etodolac for once daily administration is described.Type: GrantFiled: August 25, 2000Date of Patent: July 1, 2003Assignee: Ranbaxy Laboratories LimitedInventors: Rajeev S. Raghuvanshi, Ashok Rampal, Himadri Sen