Ahmed, IN
Asma Ahmed, Secunderabad IN
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20150017687 | METHOD FOR OBTAINING A GLYCOPROTEIN COMPOSITION - Provided is a method for producing glycoprotein with a specific glycoform compostion. The desired glycoform profile is brought about Iby altering the culture conditions on the basis of IVCC rather than the age of the culture. Further, the method renders a high product yield. | 01-15-2015 |
Hussam Ahmed, Calicut IN
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20150293045 | MEASURING ELECTRODE IMPEDANCE IN AN IMPEDANCE MEASUREMENT CIRCUIT - The disclosure provides a circuit for impedance measurement. The circuit includes an excitation source coupled between a first set of input switches. An impedance network is coupled between the first set of input switches and a first set of output switches. The impedance network includes a body impedance and a plurality of electrode impedances. A sense circuit is coupled to the first set of output switches. The sense circuit measures the body impedance and at least one electrode impedance of the plurality of electrode impedances. | 10-15-2015 |
20150305648 | IMPEDANCE MEASUREMENT CIRCUIT - The disclosure provides a circuit for impedance measurement. The circuit includes an excitation source that generates an excitation signal. A switched resistor network is coupled to the excitation source, and generates an output signal in response to the excitation signal. A sense circuit is coupled to the switched resistor network, and generates a sense signal in response to the output signal. A comparator is coupled to the sense circuit, and generates a clock signal in response to the sense signal. A mixer is coupled to the sense circuit, and multiplies the sense signal and the clock signal to generate a rectified signal. A low pass filter is coupled to the mixer and filters the rectified signal to generate an averaged signal. A processor is coupled to the low pass filter and measures a body impedance from the averaged signal. | 10-29-2015 |
Israr Ahmed, Kolkata IN
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20140155331 | NOVEL HIGH AFFINITY BIVALENT HELICALLY CONSTRAINED PEPTIDE AGAINST CANCER - The present invention describes a novel bivalent helically constrained peptide targeted against S100B that is an effective anti-cancer drug against cancers that over-express S100B. This helix mimetic targeted against S100B induces rapid apoptosis in cancer cells that over-express a calcium binding protein S100B through simultaneous inhibition of key growth pathways including activation of p53. | 06-05-2014 |
Kamal Ahmed, Andhra Pradesh IN
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20110166346 | NOVEL NAPTHALIMIDE-BENZIMIDAZOLE HYBRIDS AS POTENTIAL ANTITUMOR AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides the compounds of general formula 5 and 9 useful as potential antitumour agents against human cancer cell lines. The present invention further provides the process for preparation of napthalimide-benzimidazole hybrids of general formula 5 and 9, n-1-2, R=n-methylpiperazine or morpholine (Formula 9), wherein: n=2-3, m=2-3 and R=n-methylpiperazine or morpholine. | 07-07-2011 |
Kamal Ahmed, Hydergabad IN
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20090036657 | PYRROLO[2, 1-C][1, 4]BENZODIAZEPINE-GLYCOSIDE PRODRUG USEFUL AS A SELECTIVE ANTI TUMOR AGENT - The present invention provides novel pyrrolo[2,1-c][1,4]benzodiazepine-glycoside prodrug of general formula 1a-b, useful as selective anticancer agents. The present invention also provides a process for the preparation of novel pyrrolo[2,1-c][1,4]benzodiazepine-glycoside prodrugs of general formula 1a-b. This invention also provides activation of these produgs by | 02-05-2009 |
Kamal Ahmed, Hyderabad IN
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20080275248 | NOVEL 4BETA-AMINO PODOPHYLLOTOXIN CONGENERS AS POTENTIAL ANTICANCER AGENTS AND A PROCESS FOR THE PREPARATION THEREOF - The present invention provides new class of 4β-[4″-(1″,3″-benzothiazole-2″-yl)anilino]podophyllotoxin analogues having the structural formula as follows (4). | 11-06-2008 |
20110118237 | Isoxazoline linked pyrrolo[2,1-c][1,4]benzodiazepine hybrids as potential anticancer agents and the process for preparation thereof - The present invention provides compounds of general formula (5a-d) and (9a-h) useful as potential antitumour agents against human cancer cell lines. The present invention also provides a process for the preparation of pyrrolo [2,1-c][1,4]benzodiazepine hybrids of general formula (5a-d) and (9a-h). | 05-19-2011 |
20110207924 | NEW PHENANTHRYLPHENOL LINKED PYRROLO [2, L-C] [L, 4] BENZODIAZEPINE HYBRIDS AS POTENTIAL ANTITUMOUR AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides a compounds of general formula (6), 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 (6). | 08-25-2011 |
20120095213 | CINNAMIDO-PYRROLO[2,1-C][1,4]BENZODIAZEPINES AS POTENTIAL ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides a compound of general formulae (8a-i), (11a-i), (14a-i), and (17a-i), useful as potential antitumour agents against human cancer cell lines. The present invention further provides a process for the preparation of Cinnamido-pyrrolo[2,1-c][1,4]benzodiazepines of general formulae (8a-i), (11a-i), (14a-i), and (17a-i). | 04-19-2012 |
20120095214 | QUINAZOLINONE 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 formulae 5a-r, 9a-i to 13a-i and 17a-i to 22a-i, 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 formulae 5a-r, 9a-i to 13a-i and 17a-i to 22a-i. | 04-19-2012 |
20120101270 | NOVEL PYRROLO[2,1-C][1,4] BENZODIAZEPINE DERIVATIVES WITH DITHIOCARBAMATE SIDE CHAINS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides synthesis and in vitro anticancer activity of novel pyrrolo[2,1-c][1,4]benzodiazepine derivatives with dithiocarbamate side chains. The present invention also relates to a process for the preparation of new pyrrolo[2,1-c][1,4]benzodiazepine derivatives with dithiocarbamate side chains of general formula (A) and a process for the preparation thereof. | 04-26-2012 |
20120316335 | PYRROLO[2,L-C][L,4]BENZODIAZEPINE-BENZOTHIAZOLE OR BENZOXAZOLE CONJUGATES LINKED THROUGH PIPERAZINE MOIETY AND PROCESS FOR THE PREPARATION THEREOF - A compound of general formula 9, useful as potential antitumour agents against human cancer cell line and a process for the preparation of Pyrrolo[2,1-c] [1,4]benzodiazepine-benzothiazole or benzoxazole conjugates linked through piperazine of general formula 9 wherein: R, R | 12-13-2012 |
20130066081 | IMIDAZOLONE-CHALCONE DERIVATIVES AS POTENTIAL ANTICANCER AGENT AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides Chalcone linked Imidazolone compounds of formula A as anti cancer agent against fifty three human cancer cell lines. | 03-14-2013 |
20130225672 | SUBSTITUTED 4-BETA-ACRYLAMIDOPODOPHYLLOTOXIN CONGENERS AS ANTITUMOUR ANTIBIOTICS AND THE PROCESS FOR PREPARATION THEREOF - The present invention provides compounds of general formula (3) as useful potential antitumour agents against human cancer cell lines. The present invention further provides a process for the synthesis of 4β-acrylamidopodophyllotoxin congeners of general formula (3), wherein R and R1 are an aryl group and R is selected from 3,4,5-trimethoxyphenyl or 2-methoxy phenyl and R1 is selected from the group consisting of 4-hydroxy-3-methoxyphenyl, 3-hydroxy-4-methoxyphenyl, 4-fluoro-3-methoxyphenyl, 3-fluoro-4-methoxyphenyl, 2-fluoro-5-methoxyphenyl, 2-fluoro-4-methoxyphenyl, 4-hydroxy-3-nitrophenyl, 4-methoxy-3-nitrophenyl, 4-nitrophenyl, 3-nitrophenyl, 2-nitro phenyl, 4-methoxyphenyl, 3-methoxyphenyl and 4-hydroxyphenyl. | 08-29-2013 |
20130245048 | 4-AZA-2, 3-DIDEHYDROPODOPHYLLOTOXIN COMPOUNDS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides 4-Aza-2,3-didehydropodophyllotoxin compound of general formula A (4a-4z and 4aa-4ae) as useful potential antitumour agents against human cancer cell lines. The present invention further provides a process for the synthesis of 4-Aza-2,3-didehydropodophyllotoxin compounds (4a-4z and 4aa-4ae). | 09-19-2013 |
20130317231 | Amidobenzothiazoles And Process For The Preparation Thereof - The present invention provides a compound of general formulae A useful as potential anti-cancer agents against human cancer cell lines and a process for the preparation thereof. Where in R, R | 11-28-2013 |
20150141657 | 2-PHENYL BENZOTHIAZOLE LINKED IMIDAZOLE COMPOUNDS AS POTENTIAL ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides 2-phenyl benzothiazole linked imidazole compounds of formula A as anti cancer agent against fifty three human cancer cell lines. | 05-21-2015 |
20150322009 | NOVEL 3,4,5-TRIMETHOXYSTYRYLARYLAMINOPROPENONES AS POTENTIAL ANTICANCER AGENTS - The present invention relate to compounds of general formula A. The invention also provides the synthesis of 3,4,5-trimethoxystyrylarylaminopropenones useful as potential antitumor agents against human cancer cell lines and a process for the preparation thereof. | 11-12-2015 |
20160002214 | ANTICANCER AGENT AND PROCESS FOR THE PREPARATION THEREOF - The present invention provides a compound of general formula A for use as a potential anticancer agent against human cancer cell lines and a process for the preparation thereof. | 01-07-2016 |
Kamal Ahmed, Andra Pradesh IN
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20110213165 | NOVEL 4BETA-AMINO PODOPHYLLOTOXIN CONGENERS AS ANTI TUMOUR ANTIBIOTICS A PROCESS FOR THE PREPARATION THEREOF - The present invention provides novel β-amino podophyllotoxin congeners of general formula (A); R═CH | 09-01-2011 |
Monsur Borbhuiya Ahmed, Mumbai IN
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20090035815 | Synthetic Gene for Enhanced Expression in E. Coli - A novel nesiritide synthetic cDNA chimera encoding human b-type natriuretic peptide (hBNP) or nesiritide and a process for the preparation of the said novel chimera. Further, the inventors disclose the use of nesiritide synthetic cDNA chimera to obtain an expressible construct to produce mature nesiritide. Particularly, the inventors disclose an application of recombinant cloning method to prepare an ORF of a nesiritide chimeric construct, which is simultaneously codon optimized for | 02-05-2009 |
Mubashshir Ahmed, Bharuch IN
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20150051400 | A PROCESS FOR THE PREPARATION OF METHYLPHENIDATE HYDROCHLORIDE AND ITS INTERMEDIATES THEREOF - The present invention relates to an industrially feasible and economically viable process for the preparation of methylphenidate hydrochloride of formula I and its intermediates thereof. | 02-19-2015 |
Mumshad Faraz Ahmed, Bangalore, Karnataka IN
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20160082781 | METHOD AND SYSTEM FOR INDICATING WEAR OF TYRE IN A VEHICLE AND A TYRE THEROF - A tyre of a vehicle is disclosed in the present disclosure comprising at least one sensor, a control module and one or more indicators. The at least one sensor is located at a re-threading level of the tyre to sense contact with ground surface. Upon contact with the ground surface, the at least one sensor generates data. The control module receives the data from the at least one sensor through one or more connectors. Upon receiving the data, the control module determines a predefined condition. The control module transmits the data to a dashboard upon determining the predefined condition. The transmitted data is displayed on the dashboard which is communicatively connected to the control module for indicating wearing of the tyre. In an embodiment, the dashboard provides signal relating to the displayed data. The one or more indicators is communicatively connected to the dashboard to receive signal relating to the data for indicating wearing of the tyre. | 03-24-2016 |
Nasimuddin Ahmed, Kolkata IN
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20150257014 | COMPUTER IMPLEMENTED SYSTEM AND METHOD FOR WI-FI BASED INDOOR LOCALIZATION - The present disclosure envisages a computer implemented system and method for Wi-Fi based indoor localization. The system includes a repository for storing attributes of the floor plan of an indoor area with respect to the zones on the floor plan. A communicating module receives a threshold number of data points from user devices located in the area. These data points include a plurality of Received Signal Strength Indicators (RSSI) captured from the access points positioned in the area. A k-means clustering is then performed on the data points for grouping the data points into ‘k’ number of clusters and a decision tree is built by following a condition based approach. Distance values are then calculated pertaining to the RSSIs stored at the decision tree, and zone circles are plotted. Zone of user presence is then determined by correlating the plotted zone circles upon the floor plan using maximum overlap property. | 09-10-2015 |
Nizam Ahmed, Hyderabad-Idc IN
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20130139113 | QUICK ACTION FOR PERFORMING FREQUENT TASKS ON A MOBILE DEVICE - A shortcut is created that groups and sequences actions to perform a task. A user may record actions both within an application and outside of an application to perform the task. For example, a user may record launching an application, accessing an item within the application, and performing one or more actions that involve the item. An Application Programming Interface (API) may be used by one or more applications to specify recordable actions that are associated with the application. For example, an application may specify that configuration settings for the application are not recordable while other user actions are recordable. After recording the actions for the task, a shortcut is created. The shortcut may be accessible from a home display of a mobile device (e.g. a start screen of a smart phone) and/or some other accessible location. | 05-30-2013 |
Rizwan Ahmed, Vizianagaram IN
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20150284421 | FORMULATION OF 5-AZACYTIDINE - The present invention relates to lyophilized formulations comprising crystalline 5-azacytidine and process for preparing lyophilized formulations comprising crystalline 5-azacytidine. | 10-08-2015 |
Saeed Ahmed, Faridabad IN
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20130197251 | PROCESS FOR REMOVAL OF METALS FROM OILS/FATS - The invention describes process for demetallation of vegetable oils and animal fats to reduce metal content below 1 ppm to make them suitable for hydroprocessing feedstocks. The process comprises acid treatment with very low concentration of acids, utilizing synergistic effect of phosphoric acid and citric acid, followed by counter-current treatment with clay without intermediate step of water washing and treatment with ion exchange resin. | 08-01-2013 |
20140231271 | PROCESS FOR METAL REDUCTION OF HYDROCARBON OIL - A novel process for metal content reduction of hydrocarbon oil is disclosed, which is primarily aimed at reduction of vanadium and nickel. The process uses electricity to accelerate the demetallation process, but only the flow of electrons of the electric current is used to expedite the reaction, instead of the electrolysis effect of the electric current. The process is carried out by adding inter-phase surface active reagent and phase transfer catalyst at a relatively low temperature range of 80 to 200° C. and achieves metal content reduction for vanadium and nickel. Aqueous phase alcoholic derivatives of amine solution is treated with hydrogen sulfide, carbon dioxide, etc. by additive reaction to render it more suitable for carrying more electric current and make them more active for metal reduction. | 08-21-2014 |
Saiyed Akeel Ahmed Shakeel Ahmed, Vadodara IN
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20160115198 | METHODS OF MAKING CARFILZOMIB AND INTERMEDIATES THEREOF - Racemization-free methods are disclosed for the synthesis of carfilzomib. Novel intermediates and methods of making carfilzomib employing fragment condensation using the novel intermediates are disclosed. Amorphous carfilzomib and methods of making same are disclosed. | 04-28-2016 |
Sayed Ahmed, Karnataka IN
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20140035240 | SLIDING SEAL FOR SEALING A JOINT IN A TURBINE CASING AND METHOD FOR SEALING - A seal and slot assembly for sealing joints between casings of a turbomachine including: a first slot in a first casing flange; a second slot in a second casing flange, wherein a joint is formed between the first casing flange and second casing flange and the first slot overlaps with the second slot; a chamber formed by the first slot and second slot, and a seal in the chamber and configured to slide with respect to at least one surface of the first slot and the second slot due to gas pressure in the chamber. | 02-06-2014 |
Sayed Murtuza Ahmed, Amravati IN
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20090285675 | Systems and Methods for Modifying Modal Vibration Associated with a Turbine - Shroud assemblies and methods for modifying modal vibrations associated with a turbine are described. A shroud assembly includes an inner shroud and an outer shroud. The inner shroud includes a body with a first end portion, a second end portion opposite to the first end portion, an upper surface and a lower surface, wherein the lower surface is adjacent to a plurality of rotating turbine blades. The inner shroud further includes at least two rails formed on the upper surface and extending between the first end portion and the second end portion, wherein an impingement cooling area is defined between the at least two rails. Additionally, the inner shroud includes at least one cross-member formed on the upper surface in a direction transverse to the at least two rails. | 11-19-2009 |
Shafeeq Ahmed, Gulbarga IN
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20130139269 | CONTEXTUAL USE AND EXPIRATION OF DIGITAL CONTENT - Technologies related to contextual use and expiration of digital content are generally described. In some examples, a receiving device may connect with a sponsoring device having the digital content. A relationship property defines a relationship context between the receiving device and the sponsoring device. The receiving device may receive the digital content from the sponsoring device and use the digital content so long as allowed, as determined with reference to the relationship property. | 05-30-2013 |
20150199499 | CONTEXTUAL USE AND EXPIRATION OF DIGITAL CONTENT - Technologies related to contextual use and expiration of digital content are generally described. In some examples, a receiving device may connect with a sponsoring device having the digital content. A relationship property defines a relationship context between the receiving device and the sponsoring device. The receiving device may receive the digital content from the sponsoring device and use the digital content so long as allowed, as determined with reference to the relationship property. | 07-16-2015 |
Shahadal Ahmed, Haryana IN
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20100286211 | OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS - 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, for example, multiple-resistant | 11-11-2010 |
Shahadat Ahmed, Gurgaon IN
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20080300251 | Derivatives of 3-Azabicyclo[3.1.0] Hexane as Dipeptidyl Peptidase-IV Inhibitors - The present invention relates to novel 3-azabicyclo[3.1.0]hexane derivatives as dipeptidyl peptidase-IV inhibitors and the processes for the synthesis of the said compounds. This invention also relates to pharmacological compositions containing the compounds of the present invention, and methods of treating diabetes, especially type 2 diabetes, as well as prediabetes, diabetic dyslipidemia, metabolic acidosis, ketosis, satiety disorders, and obesity. These inhibitors can also be used to treat conditions manifested by a variety of metabolic, neurological, anti-inflammatory, and autoimmune disorders like inflammatory disease, multiple sclerosis, rheumatoid arthritis; viral, cancer and gastrointestinal disorders. The compounds of this invention can also be used for treatment of infertility arising due to polycystic ovary syndrome. | 12-04-2008 |
20090156465 | DERIVATIVES OF BETA-AMINO ACID AS DIPEPTIDYL PEPTIDASE-IV INHIBITORS - The present invention relates to β-amino acid derivatives as dipeptidyl peptidase-IV inhibitors and the processes for the synthesis of the same. This invention also relates to pharmacological compositions containing the compounds of the present invention, and methods of treating diabetes, especially type 2 diabetes, as well as prediabetes, diabetic dyslipidemia, metabolic acidosis, ketosis, satiety disorders, and obesity. These inhibitors can also be used to treat conditions manifested by a variety of metabolic, neurological, anti-inflammatory, and autoimmune disorders like inflammatory disease, multiple sclerosis, rheumatoid arthritis; viral, cancer and gastrointestinal disorders. The compounds of this invention can also be used for treatment of infertility arising due to polycystic ovary syndrome. | 06-18-2009 |
Shahadat Ahmed, Haryana IN
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20090215764 | Antimicrobial agents - Provided herein are substituted aromatic compounds, which are tRNA synthetase inhibitors, and hence can be used as antimicrobial agents. Compounds described herein can be used for the treatment or prevention of a condition caused by or contributed to by gram positive, gram negative, anaerobic bacteria or fungal organisms, more particularly against bacterium, for example, | 08-27-2009 |
Shahadat Ahmed, Karimganj IN
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20120108565 | PYRROLE CARBOXYLIC ACID DERIVATIVES AS ANTIBACTERIAL AGENTS - The present invention provides DNA Gyrase and/or Topo IV inhibitors of Formula (I), which can be used as antibacterial agents. Compounds disclosed herein can be used for treating or preventing conditions caused by or contributed by gram positive, gram negative and anaerobic bacteria, more particularly against, for example, | 05-03-2012 |
Shubbir Ahmed, Hewrah IN
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20080300843 | RECOMBINANT MESO-ACTIVE THERMOSTABLE PROTEINS AND PROCESSES OF DESIGN AND BIOSYNTHESIS THEREOF - The present invention deals with examination of the alterability of part, or whole, of the surfaces of beta sheet-based protein structures, focusing especially on enzymes. The alteration is done by supplanting/transplanting a part, or whole, of the surface of one protein onto the surface of a homologous protein of superimposable polypeptide backbone, by exploiting the structural features of beta sheets to alter only the regions of the surface involved in substrate/ligand binding and catalysis. The transplantation involves replacement of a selected set of non-contiguous residues constituting the surface regions desired to be altered in one enzyme/protein, by a set of non-contiguous residues located at analogous positions in the other enzyme/protein, in a manner that is likely to facilitate folding and function of the new protein formed by combining residues from both enzymes/proteins. The present invention also deals with using this surface engineering approach to selectively combine enzyme/protein characteristics from different domains of life that are not ordinarily combined by natural evolution, such as the creation of novel proteins that retains the bulk of the thermostable scaffold of a thermophile enzyme onto which the active surface of a mesophile homolog is transplanted, so as to create a thermo-stable protein with meso-active functional characteristics of pH and temperature of optimal function. | 12-04-2008 |
20150322418 | RECOMBINANT MESO-ACTIVE THERMO-STABLE PROTEIN AND PROCESSES OF DESIGN AND BIOSYNTHESIS THEREOF - The present invention deals with examination of the alterability of part, or whole, of the surfaces of beta sheet-based protein structures, focusing especially on enzymes. The alteration is done by supplanting/transplanting a part, or whole, of the surface of one protein onto the surface of a homologous protein of superimposable polypeptide backbone, by exploiting the structural features of beta sheets to alter only the regions of the surface involved in substrate/ligand binding and catalysis. The transplantation involves replacement of a selected set of non-contiguous residues constituting the surface regions desired to be altered in one enzyme/protein, by a set of non-contiguous residues located at analogous positions in the other enzyme/protein, in a manner that is likely to facilitate folding and function of the new protein formed by combining residues from both enzymes/proteins. The present invention also deals with using this surface engineering approach to selectively combine enzyme/protein characteristics from different domains of life that are not ordinarily combined by natural evolution, such as the creation of novel proteins that retains the bulk of the thermostable scaffold of a thermophile enzyme onto which the active surface of a mesophile homolog is transplanted, so as to create a thermo-stable protein with meso-active functional characteristics of pH and temperature of optimal function. | 11-12-2015 |
Syed K. Ahmed, Hyderabad IN
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20130343994 | Cholinesterase Inhibitors - The invention provides compounds that inhibit cholinesterases, such as acetylcholinesterase and butyrylcholinesterase. Such compounds are useful to prevent or treat exposure of a patient (e.g., a human) to an organophosphoric nerve agent (e.g., sarin and VX) or to treat a patient suffering from a neurodegenerative disorder such as Alzheimer's Disease or Lewy Body Dementia. The compounds are further useful as diagnostic tools for use in medical or research radiography (e.g., positron emission tomography) when synthesized with a radionuclide (e.g., [18F]. Synthetic schemes to produce such compounds are also provided. | 12-26-2013 |
20150023878 | Novel Aspartylamide Inhibitors of Excitatory Amino Acid Transporters - The compounds of the invention are inhibitors of excitatory amino acid transporters (EAAT) that penetrate the blood-brain barrier to access the central nervous system. The compounds of the invention follow the structural formula: | 01-22-2015 |
Syed Mushtag Ahmed, Banagalore IN
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20130120168 | SYSTEMS AND METHODS FOR LOAD BALANCING AND VIRTUAL PRIVATE NETWORKING FOR SMS CENTER - The present disclosure is directed towards systems and methods for compressing messages, such as Short Message Service (SMS) or text messages between fixed or mobile devices through communications networks. The data of, for example, SMS messages is compressed and forwarded through a communication network to an appliance having a processing unit. The appliance decompresses the message and controls its delivery through network communication devices, where the decompressed SMS message is forwarded to its destination. | 05-16-2013 |
20140349691 | SYSTEMS AND METHODS FOR LOAD BALANCING AND VIRTUAL PRIVATE NETWORKING FOR SMS CENTER - The present disclosure is directed towards systems and methods for compressing messages, such as Short Message Service (SMS) or text messages between fixed or mobile devices through communications networks. The data of, for example, SMS messages is compressed and forwarded through a communication network to an appliance having a processing unit. The appliance decompresses the message and controls its delivery through network communication devices, where the decompressed SMS message is forwarded to its destination. | 11-27-2014 |
Tauheed Ahmed, Haryana IN
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20160142933 | Fair Distribution of Radio Resources Between Guaranteed Bit Rate (GBR) and non-GBR Data Bearers - User equipments (UEs) may be scheduled by, in a cell, determining relative priorities of data radio bearers (DRBs), each DRB associated with an active UE. A limit is established dividing radio resources available for allocation in the cell during a scheduling period into at least a first limited portion and a second remaining portion. According to the determined relative priorities: a) up to the first limited portion of the radio resources are allocated to only the DRBs that have a guaranteed bit rate (GBR), and thereafter b) the second remaining portion of the radio resources are allocated to only the DRBs which have not been fully allocated from the first limited portion. In carrier aggregation the radio resources are allocated in turn in each different cell per step a) and thereafter in turn in each different cell per step b). | 05-19-2016 |
20160143046 | Maximization of Radio Resource Allocation For A Carrier Aggregated User Equipment - To schedule user equipments (UEs) in a scheduling period, for each of X cells in a carrier aggregation (CA) system relative priorities of data bearers are determined. Each data bearer is associated with a respective UE having buffered data and at least one of the UEs is a CA-UE that is allowed radio resource allocation to its associated data bearers in at least two of the cells. For each CA-UE, the buffered data of the CA-UE is distributed across those cells in which the CA-UE and its associated bearers are allowed resource allocation using a measure of total data throughput for each of those cells. For each of the X cells resources are allocated to the data bearers according to the relative priorities such that for each CA-UE the resources allocated to its associated data bearers across those cells are sufficient to carry the buffered data as distributed. | 05-19-2016 |
Zakir Ahmed, Kamataka IN
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20100110469 | METHOD FOR PRINTING ON AN IMAGING DEVICE - A method for printing a print ready file transmitted by a print client on an imaging device includes creating a print data file associated with the print ready file, where the print data file includes information pertaining to the print ready file and the imaging device. In the method, the print data file is encrypted and transmitted to the imaging device. In addition, the print data file is authenticated in the imaging device and printing of the print ready file is enabled if the print data file is determined to be authentic and the print ready file is invalidated if the print data file is determined to be inauthentic. Also disclosed is an imaging device configured to perform the aforementioned method. | 05-06-2010 |
Z. Shameel Ahmed, Chennai IN
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20150341292 | SYSTEM AND METHOD OF DATA AND COMMAND REQUEST PROCESSING - Methods and systems are disclosed for processing data and command requests. In one aspect, a method for processing a data and command request is disclosed that includes receiving, at a server, a first electronic mail message from a requesting electronic mail address, the first electronic mail message including information that identifies an application. The method may also include transmitting, by the server, a query to an application data source associated with the application, the application data source being selected from a plurality of data sources associated with a plurality of applications and receiving, at the server, application data from the application data source. In addition, the method may also include transmitting, by the server, a second electronic mail message that includes at least some of the application data as a reply to the first electronic mail message. Systems and computer-readable media are also disclosed for implementing the above-described method. | 11-26-2015 |