Reddy, Andhra Pradesh
Adla Malla Reddy, Andhra Pradesh IN
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20110046111 | QUINAZOLINE LINKED PYRROLO[2,1-C][1, 4]BENZODIAZEPINE HYBRIDS AS POTENTIAL ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides a compound of general formula 5, useful as potential antitumour agents against human cancer cell lines. The present invention further provides a process for the preparation of pyrrolo[2,1-c][1,4]benzodiazepine hybrids of general formula (5): wherein n=3, 4, 5, 6, 8 and wherein R1 and R | 02-24-2011 |
20110201600 | CHALCONE LINKED PYRROLO[2,1-C][1, 4]BENZODIAZEPINE HYBRIDS AS POTENTIAL ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention relates to chalcone linked pyrrolo[2,1-c][1,4]benzodiazepine hybrids and a process for the preparation there of. More particularly it relates to 7-Methoxy-8-{n[4-1-(2 or 4-substituted phenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-one]alkyl}-oxy}-(11aS)-1,2,3,11a-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one and 7-Methoxy-8-{n[-3-(4-hydroxy-3-methoxyphenyl)-1-(2,4-alkyl-3-quinolyl)-2-propen-1-one]alkyl}-oxy-(11aS)-1,2,3,11a-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one with aliphatic chain length variations useful as anticancer (antitumour) agent. The general structural formula of these chalcone linked pyrrolo[2,1-c][1,4]benzodiazepines hybrids is given below. wherein R | 08-18-2011 |
Bandi Parthasarad-Hi Reddy, Andhra Pradesh IN
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20120225121 | BIOEQUIVALENT FORMULATION OF EFAVIRENZ - The present invention provides a suitable technique namely wet milling and the process for reducing the particle size of efavirenz and making a tablet or capsule formulation with desired bioavailability equivalent to the reference listed drug without loosing its characteristics. | 09-06-2012 |
Chandrakantha Reddy, Andhra Pradesh IN
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20110167488 | SYSTEMS AND METHODS FOR LOCATION AWARE ACCESS CONTROL MANAGEMENT - Described herein are systems and methods for access control management, these generally being directed towards location aware access control management. Embodiments of the invention have been particularly developed for providing additional functionalities in access control systems having disconnected devices, and the present disclosure is primarily focused accordingly. For example, embodiments include access control devices configured to operate in conjunction with a GPS receiver or other source of geographical positional information, and methods associated with the use of such devices. | 07-07-2011 |
Dontireddy Venkat Reddy, Andhra Pradesh IN
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20090012722 | METHOD FOR EVALUATION OF PERFORMANCE OF PERCOLATION TANKS USING ENVIRONMENTAL CHLORIDE AS A TRACER - Naturally present chloride concentration in natural water is utilized for the development of the technique to gauge the performance of percolation tanks in space and time. The chloride mass balance technique is simple, sensitive, reliable and yet powerful enough to resolve the temporal variation due to the effect of silting or climate factors. The percolation efficiency data of percolation tanks can aid in the formulation of guidelines for selection of suitable sites for future tanks with greater efficiency. Otherwise unscientific construction of percolation tanks in sites that yield poor percolation efficiency is uneconomical, and the very purpose of their construction will be forfeited. Thus the technique developed using chloride mass balance in tank water for evaluation of tank performance is highly economy oriented. | 01-08-2009 |
D. Sreedhar Reddy, Andhra Pradesh IN
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20140364595 | CONJUGATE-BASED ANTIFUNGAL AND ANTIBACTERIAL PRODRUGS - The invention provides conjugate-based antifungal or antibacterial prodrugs formed by coupling at least one anti-fungal agent or antibacterial agent with at least one linker and/or carrier. The prodrugs are of formula: (i) (AFA) | 12-11-2014 |
Dumbala Srinivas Reddy, Andhra Pradesh IN
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20110230403 | GLYCOSIDE DERIVATIVES AND USES THEREOF - The present invention relates to compounds of formula I | 09-22-2011 |
Goli Kamalakar Reddy, Andhra Pradesh IN
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20120225121 | BIOEQUIVALENT FORMULATION OF EFAVIRENZ - The present invention provides a suitable technique namely wet milling and the process for reducing the particle size of efavirenz and making a tablet or capsule formulation with desired bioavailability equivalent to the reference listed drug without loosing its characteristics. | 09-06-2012 |
20150045400 | RITONAVIR COMPOSITIONS - The present invention relates to pharmaceutical compositions comprising ritonavir premix, a water soluble polymer and a surfactant and process for preparing the same. More particularly, the present invention relates to hot-melt extrusion process for preparing solid oral compositions of ritonavir premix. | 02-12-2015 |
Karamala Ramasubba Reddy, Andhra Pradesh IN
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20090171092 | Process for the Preparation of Montelukast and Its Pharmaceutically Acceptable Salts - An improved process for the preparation of Montelukast and its pharmaceutically acceptable salts comprises of reacting (S) Benzenepropanol α-[3-[2-(7-chloro2-quinolinyl)ethenyl]phenyl]-2-(1-hydroxy-1-methyl ethyl)-α-methane sulfonate compound of formula (II) with | 07-02-2009 |
Manne Satyanarayana Reddy, Andhra Pradesh IN
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20090012315 | Process for Pure Duloxetine Hydrochloride - A process for the preparation of pure Duloxetine hydrochloride comprises the steps of: a) reacting 1-(thiophen-2-yl)ethanone with dimethylamine hydrochloride, b) purifying the component in a solvent, c) reducing the component with an alkali metal borohydride, d) resolving the compound with a chiral acid, and treating the obtained compound with weak inorganic base, e) reacting the compound to give Duloxetine oxalate salt and f) converting the Duloxetine salt into its hydrochloride salt. Further the purifications of the obtained compound and of two intermediate products are described. | 01-08-2009 |
20090048441 | Process for the Preparation of Ezetimibe - The present invention relates to a cost effective and industrially advantageous process for the preparation of (3R,4S)-1-(4-Fluorophenyl)-3-[3(S)-3-(4-fluorophenyl)-3-hydroxypropyl)]-4-(4-hydroxyphenyl)-2-azetidinone, referred to here as Ezetimibe, it is represented as formula (1). | 02-19-2009 |
20090171092 | Process for the Preparation of Montelukast and Its Pharmaceutically Acceptable Salts - An improved process for the preparation of Montelukast and its pharmaceutically acceptable salts comprises of reacting (S) Benzenepropanol α-[3-[2-(7-chloro2-quinolinyl)ethenyl]phenyl]-2-(1-hydroxy-1-methyl ethyl)-α-methane sulfonate compound of formula (II) with | 07-02-2009 |
20090275752 | Novel Process for Statins and its Pharmaceutically Acceptable Salts Thereof - Novel process for statins and its pharmaceutically acceptable salts thereof represented by general formula (I). | 11-05-2009 |
20110263854 | Improved Process For The Preparation Of Endothelin Receptor Antagonists - The present invention relates to improved processes for the preparation of Endothelin receptor antagonists, their salts and intermediates. | 10-27-2011 |
20120016129 | Process for Preparing Pitavastatin, Intermediates and Pharmaceuctically Acceptable Salts Thereof - Processes for preparing pravastatin, intermediates and pharmaceutically acceptable salts thereof are provided Crystalline forms of pravastatin, intermediates and pharmaceutically acceptable salts thereof are also disclosed. | 01-19-2012 |
20120323005 | Process For The Preparation Of Amide Intermediates And Their Use Thereof - The present invention relates to an improved process for the preparation of amide intermediates useful in the preparation of cholesterol reducing agents. | 12-20-2012 |
Maramreddy Sahadeva Reddy, Andhra Pradesh IN
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20090275752 | Novel Process for Statins and its Pharmaceutically Acceptable Salts Thereof - Novel process for statins and its pharmaceutically acceptable salts thereof represented by general formula (I). | 11-05-2009 |
20120016129 | Process for Preparing Pitavastatin, Intermediates and Pharmaceuctically Acceptable Salts Thereof - Processes for preparing pravastatin, intermediates and pharmaceutically acceptable salts thereof are provided Crystalline forms of pravastatin, intermediates and pharmaceutically acceptable salts thereof are also disclosed. | 01-19-2012 |
20120323005 | Process For The Preparation Of Amide Intermediates And Their Use Thereof - The present invention relates to an improved process for the preparation of amide intermediates useful in the preparation of cholesterol reducing agents. | 12-20-2012 |
Narayan Sripathi Reddy, Andhra Pradesh IN
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20110201495 | PROCESS FOR THE PREPARATION OF 1,1,1,2-TETRAFLUOROETHANE - The present invention relates to a process for preparing a co-precipated Cr | 08-18-2011 |
Naveen Reddy, Andhra Pradesh IN
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20120082158 | IP ADDRESS VERSION INTERWORKING IN COMMUNICATION NETWORKS - Systems and methods are provided for supporting IPv4-IPv6 interworking of SIP messages in wireless networks and IMS networks. The interworking can be provided to smooth migration to an all-IPv6 IMS network by allowing the use and support of existing legacy IPv4 infrastructure. This functionality may be provided by a call session control function (CSCF) interposed between a user equipment (UE) and an IMS core network with interworking functionality or an interworking module. This device serves as a back-to-back user agent (B2BUA), allocates IP addresses from a pool, performs next-hop route protocol discovery, and maintains and stores information within the gateway as well as interworking and rewriting IP addresses within network messages, while proxying and maintaining sessions between the UE and the IMS core network. This allows for faster call setup, reduced capex/opex, improved debuggability, increased capacity and subscriber density by call processing distribution, and better user experience. | 04-05-2012 |
Ramesh Reddy, Andhra Pradesh IN
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20110099562 | Method and System on Chip (SoC) for Adapting a Reconfigurable Hardware for an Application at Runtime - A method and System on Chip (SoC) for adapting a reconfigurable hardware for an application at run time is provided. The method includes obtaining a plurality of application substructures corresponding to the application. An application substructure performs one or more of a plurality of functions of the application. The method further includes retrieving compute metadata and transport metadata corresponding to each application substructure. Compute metadata specifies functionality of an application substructure and transport metadata specifies data flow path of an application substructure. Thereafter, the method maps each application substructure to a corresponding set of tiles in the hardware. The set of tiles includes one or more tiles and a tile performs one or more of a plurality of functions of the application. | 04-28-2011 |
20110134996 | Method and System on Chip (SoC) For Adapting a Runtime Reconfigurable Hardware to Decode a Video Stream - A method and System on Chip (SoC) for adapting a runtime reconfigurable hardware to decode a video stream, wherein the video stream is of one of a plurality of video types is disclosed. The method includes determining a video type of the video stream and identifying at least one functional block of a set of functional blocks in the runtime reconfigurable hardware in response to determining the video type. A functional block of the set of functional blocks corresponds to a decoding sub function of the video type. Thereafter, the method configures the one or more functional block based on a plurality of configuration parameters of the video type. Further, the method decodes the video stream using the one or more functional blocks in response of configuring the one or more functional block. | 06-09-2011 |
Ravisekhara P. Reddy, Andhra Pradesh IN
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20140005231 | FUNGICIDAL HETEROCYCLIC CARBOXAMIDES | 01-02-2014 |
Vummadi Venkat Reddy, Andhra Pradesh IN
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20100081084 | NOVEL DIAZONAPHTHOQUINONESULFONIC ACID BISPHENOL DERIVATIVE USEFUL IN PHOTO LITHOGRAPHIC SUB MICRON PATTERNING AND A PROCESS FOR PREPARATION THEREOF - The present invention provides novel diazonaphthoquinonesulfonic acid bisphenol derivatives. More particularly, the present invention relates to photo restive coating comprising alkali-soluble resin, a photoactive compound and a surfactant. The photoresist film prepared has less then one micron. The photoactive compound is soluble or swellable in aqueous alkaline solutions and is diazonaphthoquinonesulfonic bisphenol esters of the general formula (A), wherein DNQ represents a 2-Diazo-1-naphthoquinone-4-sulfonyl, 2-Diazo-1-naphthoquinone-5-sulfonyl, 1-Diazo-2-naphthoquinone-4-sulfonyl groups and R1 R1 represents an alkyl, aryl and substituted aryl groups. The invention also provides a process for coating and imaging the light-sensitive composition. | 04-01-2010 |