Easy To Use Patents Search & Patent Lawyer Directory

At Patents you can conduct a Patent Search, File a Patent Application, find a Patent Attorney, or search available technology through our Patent Exchange. Patents are available using simple keyword or date criteria. If you are looking to hire a patent attorney, you've come to the right place. Protect your idea and hire a patent lawyer.

Searching:





Search by keyword, patent number, inventor, assignee, city or state:




Patent # Description
US-9,475,862 Neutralizing GP41 antibodies and their use
Monoclonal neutralizing antibodies are disclosed that specifically bind to the HIV-1 gp41 membrane-proximal external region (MPER). Also disclosed are...
US-9,475,861 Binding molecule having influenza A virus-neutralizing activity produced from human B cell
The present invention relates to a binding molecule having influenza A virus-neutralizing activity derived from a human B cell, and the binding molecule having...
US-9,475,860 Process for obtaining immunoglobulins from colostral milk
Suggested is a process for obtaining immunoglobulins, wherein (a) colostral milk from days 0 to 7 is subjected to thermal treatment, skimming the cream, (b) the...
US-9,475,859 Polynucleotides encoding rodent antibodies with human idiotypes and animals comprising same
The invention relates to polynucleotides, particularly chimeric polynucleotides useful for optimal production of functional immunoglobulins with human idiotypes...
US-9,475,858 Cell culture process
A method for producing recombinant polypeptides, including antibodies, having targeted levels of carboxyl terminal (C-terminal) lysine or arginine residues is...
US-9,475,857 Methods and compositions using a Klotho-FGF23 fusion polypeptide
The present invention is directed to methods, kits and compositions for preventing or treating age-related conditions or metabolic disorders. The Klotho fusion...
US-9,475,856 Chimeric FGF21 proteins with enhanced binding affinity for .beta.-klotho for the treatment of type II diabetes,...
The present invention relates to chimeric proteins that include an N-terminus coupled to a C-terminus, where the N-terminus includes an N-terminal portion of...
US-9,475,855 Human Notch3 based fusion proteins as decoy inhibitors of Notch3 signaling
This invention provides a fusion protein comprising a signal peptide, EGF repeats 1-X of the extracellular domain of human Notch3 receptor protein wherein X is...
US-9,475,854 Lead compound for otoprotection: targeting HGF signaling with dihexa
A novel method of preventing or reducing ototoxicity in vertebrates undergoing treatment with therapeutically effective amounts of platinum-based...
US-9,475,853 Fusion protein for enhancing immunogenicity of bacterial antigen/immunogen
Establishment of an effective and uniform vaccine development strategy is key to conquering current and emerging infectious diseases. Despite successes against...
US-9,475,852 Method for producing web protein, a fused protein, recombinant DNA, an expression vector, a host cell and...
The invention relates to the field of biotechnology and provides a method for producing recombinant proteins from the orb-weaving spider silk in yeast cells....
US-9,475,851 High MAST2-affinity polypeptides and uses thereof
The invention relates to polypeptides containing a cytoplasmic domain ending with a MAST-2 binding domain, from 11 to 13 residues, the first two residues of...
US-9,475,850 Methods for treatment of nephrotic syndrome and related conditions
The present disclosure provides a method for treating and/or preventing a condition characterized as a nephrotic syndrome, such as but not limited to minimal...
US-9,475,849 Brassica plant comprising a mutant INDEHISCENT allele
This invention relates to crop plants of which the fruit dehiscence properties are modulated. More specifically the invention relates to improved methods and...
US-9,475,848 Fermentation process for producing a virulence factor from bordetella
A process for fermenting Bordetella species comprising incubating a sample of bacteria of a Bordetella species in a first environment under at least one bvg...
US-9,475,847 Insecticidal proteins and methods for their use
Compositions and methods for controlling pests are provided. The methods involve transforming organisms with a nucleic acid sequence encoding an insecticidal...
US-9,475,846 Conjugated Vi saccharides
Two Vi conjugates have been prepared by carbodiimide-mediated synthesis, using adipic acid dihydrazide derivatized CRM.sub.197 (a non-toxic variant of...
US-9,475,845 Modified virus vectors and methods of making and using the same
The present invention provides AAV capsid proteins (VP1, VP2 and/or VP3) comprising a modification in the amino acid sequence in the three-fold axis loop 4 and...
US-9,475,844 Method for producing bio-active agent for the prevention of disease caused by White Spot Syndrome Baculovirus...
A method of producing an agent capable of eliciting immune response against White Spot Syndrome Baculovirus complex in crustaceans of Penaeidae family upon...
US-9,475,843 Antimicrobial peptide WY-21 and application thereof
An antimicrobial peptide WY-21 has amino acid sequence of Val-Lys-Phe-Phe-Arg-Lys-Leu-Lys-Lys-Ser-Val-Lys-Glu-Lys-Ile-Gly-Lys-Glu-P- he-Lys-Arg (SEQ ID NO: 1)....
US-9,475,842 Hexadepsipeptide analogues as anticancer compounds
This invention relates to an isolated compound of Formula (1) ##STR00001## or derivatives or pharmaceutically acceptable salts thereof. The invention also...
US-9,475,841 Melanoma antigen peptide and uses thereof
The present invention relates to a melanoma antigen peptide comprising the amino acids sequence selected in the group consisting of SEQ ID NO: 10, SEQ ID NO:...
US-9,475,840 Protease-resistant compounds useful as shuttles through the blood-brain barrier and shuttle-cargo constructs
The peptides of formula (I) where: R.sub.1 is the group attached to the N-terminal of the first amino acid of the sequence P, optionally via the ligand X, and...
US-9,475,839 Peptide-based inhibitor of interleukin-10 or interferon-gamma signaling
A peptide or peptidomimetic comprising an amino acid sequence based on conserved regions of IL10 or IFN-gamma receptor sequences, and related compounds and...
US-9,475,838 Process for purification of a fatty acid binding protein
A process for purification of a fatty acid binding proteins such as, e.g., Sm14 of Pichia pastoris or type-3 FABP protein of Fasciola hepatica. The process...
US-9,475,837 Process for the synthesis of therapeutic peptides
The present invention relates to a process for the large-scale synthesis of therapeutic peptides using a Sieber Amide resin, which comprises solid-phase...
US-9,475,836 Protopanoxadiol derivative, preparation method thereof and application thereof
The present invention provides a protopanoxadiol derivative of structural formula I or II, a preparation method and an application thereof. The present...
US-9,475,835 Synthetic intermediate of 1-(2-deoxy-2-fluoro-4-thio-.beta.-D-arabinofuranosyl) cytosine, synthetic ...
A compound represented by a formula [1D] as shown below (wherein R.sup.1A, R.sup.1B, R.sup.2A, R.sup.2B, R.sup.3A and R.sup.3B represent a hydrogen atom, an...
US-9,475,834 Anticancer agents of the anthracyclin family
Anthracyclin compounds of the general structure: ##STR00001## are disclosed. In these compounds R.sup.1 is methyl, acetyl or hydroxyacetyl; R.sup.2--R.sup.5...
US-9,475,833 Method for lignin separation from black liquor comprising removal of sulfur compounds from formed water effluent
The method is for separation of lignin from original black liquor (BL.sub.IN) having a first precipitation phase (PR1/PR2) for precipitation of lignin by a...
US-9,475,832 Phosphonates with reduced toxicity for treatment of viral infections
There are provided, inter alia, acyclic nucleoside phosphonate compounds having reduced toxicity and enhanced antiviral activity, and pharmaceutically accepted...
US-9,475,831 Formylpyrrole-based heterocycles for nucleic acid attachment to supports
A compound has Formula I: ##STR00001## A, B, C, D, W, X, Y, and Z are independently selected from hydrogen, optionally substituted C.sub.1-C.sub.6 alkyl,...
US-9,475,830 Concentrated therapeutic phospholipid compositions
The invention relates to concentrated therapeutic phospholipid compositions; methods for treating or preventing diseases associated with cardiovascular disease,...
US-9,475,829 Method for the hydrosilylation of a siloxane photocatalysed by a polyoxometalate compound
The invention concerns a method of hydrosilylation between a siloxane compound (A) comprising at least one hydrogen atom bonded to a silicon atom and an...
US-9,475,828 Organopolysiloxane and use thereof as surfactant, powder treatment agent, thickening agent of oil-based raw...
The present invention provides a co-modified organopolysiloxane having a specified chemical structure in which a sugar alcohol-modified group and a silylalkyl...
US-9,475,827 Tris(trimethyl siloxyl)silane vinylic monomers and uses thereof
The invention provides a TRIS-containing vinylic monomer which comprises one sole (meth)acryloyloxy group and a tris(trimethylsiloxy)silyl group covalently...
US-9,475,826 Fluorine-containing nano composite particles and method for producing the same
Fluorine-containing nano composite particles comprising a condensate of a fluorine-containing alcohol represented by the general formula: R.sub.F-A-OH [I]...
US-9,475,825 3-(3H-imidazo[4,5-C]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridine and therapeutic uses thereof
Azaindazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present invention concerns the use of an azaindazole...
US-9,475,824 Fused pyrimidines as inhibitors of p97 complex
Disclosed are fused pyrimidine compounds having scaffolds composed of left and right rings, the left ring being a saturated carbocyclic or heterocyclic ring and...
US-9,475,823 Methods for the preparation of hydromorphone
The present application relates to methods for the preparation of morphine derivatives. In particular, the present application relates to methods for the...
US-9,475,822 Substituted 2- amidoquinazol-4-ones as matrix metalloproteinase-13 inhibitors
The present invention provides a novel amide derivative having a matrix metalloproteinase inhibitory activity, and useful as a pharmaceutical agent, which is a...
US-9,475,821 Process for preparation of Darunavir
Provided are a process for preparation of darunavir or solvates or a pharmaceutically acceptable salt thereof substantially free of bisfuranyl impurities and a...
US-9,475,820 Substituted imidazo[1,2-a]pyrazines as TNF activity modulators
A series of imidazo[1,2-a]pyrazine derivatives, being potent modulators of human TNF.alpha. activity, are accordingly of benefit in the treatment and/or...
US-9,475,819 Substituted 7-azabicycles and their use as orexin receptor modulators
The present invention is directed to compounds of Formula I: ##STR00001## wherein ring A is phenyl, naphthalenyl, pyridyl, quinolinyl, isoquinolinyl,...
US-9,475,818 Selective PI3K delta inhibitors
The present invention relates to selective inhibitors of PI3K delta protein kinases, methods of preparing them, pharmaceutical compositions containing them and...
US-9,475,817 Pyrazole substituted imidazopyrazines as casein kinase 1 d/e inhibitors
The invention provides compounds of Formula (I) and pharmaceutically acceptable salts thereof. The compounds of Formula (I) inhibit protein kinase activity...
US-9,475,816 Substituted-1,4-dihydropyrazolo[4,3-b]indoles
Disclosed are compounds of Formula 1, ##STR00001## and pharmaceutically acceptable salts thereof, wherein L, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5,...
US-9,475,815 Substituted benzothienyl-pyrrolotriazines and uses thereof
This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives having protein tyrosine kinase inhibitory...
US-9,475,814 Chiral N-acyl-5,6,7(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazi- nes as selective NK-3 receptor...
The present invention relates to novel compounds of Formula I and their use in therapeutic treatments. The invention further relates to a novel chiral synthesis...
US-9,475,813 Tricyclic pyrrolopyridine compound, and JAK inhibitor
To provide a novel tricyclic pyrrolopyridine compound having a JAK inhibitory activity and useful for prevention, treatment and/or improvement of particularly...
← Previous | 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 | Next →

File A Patent Application

  • Protect your idea -- Don't let someone else file first. Learn more.

  • 3 Easy Steps -- Complete Form, application Review, and File. See our process.

  • Attorney Review -- Have your application reviewed by a Patent Attorney. See what's included.