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Ajinomoto Co.,Inc. Patents
Assignee:
Ajinomoto Co.,Inc.
Address:
Tokyo, JP
No. of patents:
1065
Patents:




Patent Number Title Of Patent Date Issued
RE38796 Process for producing 3-amino-2-oxo-1-halogenopropane derivatives September 13, 2005
Compounds formed by reacting a protected amino acid with an alkali metal enolate of an alkyl acetate are reacted with a halogenating agent for halogenation of the 2-position, or a protected amino acid is reacted with an alkali metal enolate of an alkyl halogenoacetate, to form a 4-am
RE38257 Piperdine derivatives and hypotensives containing the same September 23, 2003
A piperidine compound of the formula (I): ##STR1##wherein A is a fused aromatic ring; R is hydrogen, chloro or methoxy; X is (CH.sub.2).sub.n, which may be substituted, in which n is 0 or an integer of 1 to 10, --CH.ident.CH--, --C.ident.C--, --O--, --S--, --NH--, --N(COCH.sub.3)--,
RE37187 Aminopeptidase GX, and a method of hydrolyzing a protein with the same May 22, 2001
An aminopeptidase is provided which efficiently decomposes a low-molecular-weight peptide containing glutamic acid or aspartic acid in its sequence. A method of hydrolyzing a peptide or protein by use of the aminopeptidase is also provided. Aminopeptidase GX is derived from germinate
RE35609 Process for purifying 2',3'-dideoxynucleosides September 16, 1997
A biological process for producing a 2',3'-dideoxynucleoside from 2',3'-dideoxyuridine is disclosed. The 2',3'-dideoxynucleoside can be purified readily using a porous nonpolar resin absorbent.
RE34878 Hypoglycemic agent March 14, 1995
A compound of D-phenylalanine derivative for hypoglycemic use, represented by the general formula ##STR1## R.sup.1 is selected from hydrogen, alkyl of 1 to 5 carbon atoms, aryl of 6 to 12 carbon atoms, aralkyl of 6 to 12 carbon atoms, ##STR2## --CH.sub.2 CO.sub.2 R.sup.3, --C
7470524 Method for producing L-amino acids using bacteria of the Enterobacteriaceae family December 30, 2008
There is disclosed a method for producing an L-amino acid, for example L-threonine, L-lysine, L-histidine, L-phenylalanine, L-arginine, L-tryptophan or L-glutamic acid, using a bacterium of the Enterobacteriaceae family, wherein the bacterium has been modified to enhance an activity
7468262 Polynucleotides encoding useful polypeptides in corynebacterium glutamicum ssp. lactofermentum December 23, 2008
The present invention provides novel polypeptides and polynucleotides useful as biotechnological tools, specifically identified in a coryneform bacterium Corynebacterium glutamicum ssp. lactofermentum and methods of producing substances in organisms having enhanced or attenuated expr
7462630 Diarylalkene derivatives and novel diarylalkane derivatives December 9, 2008
The invention relates to a compound represented by the following general formula (1) or its analogue, which selectively inhibit N-type calcium channels or its analogue, and to a method for treating pain etc. comprising the compound represented by the following general formula (1) or
7459585 Benzene derivatives and pharmaceutical use thereof December 2, 2008
The present invention provides an AP-1 activation inhibitor, NF-kappa B activation inhibitor, inflammatory cytokine production inhibitor, matrix metalloprotease production inhibitor, inflammatory cell adhesion molecule expression inhibitor, anti-inflammatory agent, antirheumatic agent,
7459582 Methods for producing nateglinide crystals December 2, 2008
There is provided methods for producing nateglinide crystals, which comprises the steps of adding an acid(s) to a reaction mixture containing nateglinide to make it acidic, the reaction mixture being obtained by reacting trans-4-isopropylcyclohexylcarbonyl chloride with D-phenylalani
7455996 Soybean raffinose synthase and a method for producing raffinose November 25, 2008
Raffinose is produced by allowing a raffinose synthase having the following properties to act on sucrose and galactinol: (1) action and substrate specificity: produces raffinose from sucrose and galactinol; (2) optimum pH: about 6 to 8; (3) optimum temperature: about 35 to 40.degre
7452905 Phenylalanine derivatives November 18, 2008
Specific phenylalanine derivatives or pharmaceutically acceptable salts thereof have an antagonistic effect on the .alpha. 4 integrins and, therefore, are usable as therapeutic agents or preventive agents for diseases in which .alpha. 4 integrin-depending adhesion process participate
7449452 Method for estimating immunostimulant activity of a polysaccharide November 11, 2008
The ability of a polysaccharide to act as an immunostimulant may be assessed by comparing the degree of binding of a detection reagent, which contains a fluorescence-labeled version of the polysaccharide, with the binding of a reference reagent, which contains a fluorescence-labeled
7445921 Transglycosylation method and protein having transglycosylation activity November 4, 2008
The present invention provides a transglycosylation method and a protein catalyzing a transglycosylation reaction. A reaction of transferring a galactosyl.beta.1.fwdarw.3N-acetylgalactosaminyl group from a sugar donor containing a sugar chain having a galactosyl.beta.1.fwdarw.3N-acet
7439038 Method for producing L-amino acid using methylotroph October 21, 2008
A DNA encoding for a mutant of LysE protein, or a homologous protein thereof, of a coryneform bacterium, wherein the mutant, when introduced into a methanol-assimilating bacterium imparts resistance to L-lysine analogue. The DNA encoding for a mutant of LysE protein, or a homologous
7435560 Method for producing purine nucleoside by fermentation October 14, 2008
A microorganism which has a gene encoding an enzyme in which feedback inhibition is desensitized by substitution of one or two amino acids in PRPP amidotransferase encoded by purF of Escherichia coli, a gene encoding a protein which is an inactivated repressor of purine nucleotide bi
7432100 Variant aldolase and processes for producing an optically active IHOG and an optically active mo October 7, 2008
The present invention relates to variant aldolase enzymes that are modified so as to produce IHOG (4-(indol-3-ylmethyl)-4-hydroxy-2-oxoglutaric acid: IHOG), a process for producing an optically active IHOG using the same, and a process for producing an optically active monatin.
7432085 Method for producing L-amino acid October 7, 2008
In a method for producing an L-amino acid by culturing a microorganism having an ability to produce an L-amino acid in a medium to produce and accumulate the L-amino acid in the medium and collecting the L-amino acid from the medium, a Gram-negative bacterium having the Entner-Doudoroff
7427688 Production method of optically active diphenylalanine compounds September 23, 2008
The present invention provides a production method including reacting a diphenylmethylene halide compound represented by the following formula (1) with a malonic acid diester compound represented by the following formula (2) in an organic solvent selected from N-methyl-2-pyrrolidone,
7423019 Agent for inducing conversion of intestinal cells into insulin-producing cells and antidiabetic September 9, 2008
A partial peptide of a preproglucagon peptide comprising at least the amino acid sequence at positions 92-97 of a preproglucagon peptide is used as an effective ingredient of an antidiabetic drug.
7422880 Method for producing an l-amino acid using a bacterium of the enterobacteriaceae family having a September 9, 2008
There is provided a method for producing an L-amino acid using a bacterium of the Enterobacteriaceae family, particularly a bacterium belonging to the genus Escherichia or Pantoea, having the glycogen biosynthesis pathway disrupted.
7419810 Arginine repressor deficient strain of coryneform bacterium and method for producing L-arginine September 2, 2008
L-Arginine is produced by culturing a coryneform bacterium in which an arginine repressor involved in L-arginine biosynthesis is deleted by disrupting a gene coding for the repressor, and which has L-arginine producing ability in a medium to produce and accumulate L-arginine in the m
7416740 Dry granulated product containing L-lysine as main component August 26, 2008
Hydrochloric acid, sulfuric acid or an L-lysine solution having an equivalent ratio of anion/L-lysine higher than 0.95 is added to a raw material L-lysine solution having an equivalent ratio of anion/L-lysine lower than 0.68 to adjust the equivalent ratio of anion/L-lysine of the raw
7414075 Composition for lowering internal lipid content August 19, 2008
A composition for lowering internal lipid in a subject which contains a capsinoid substance represented by the following formula ##STR00001## wherein n is an integer from 0 to 10. Methods of using the compositions are disclosed and include administering to a subject in need of such t
7411089 Nateglinide crystals August 12, 2008
New nateglinide crystals, i.e. nateglinide A-type crystals (main peaks in powder X-ray diffraction: 4.4.degree., 5.2.degree., 15.7.degree., 18.5.degree.(2.theta.)), M-type crystals (main peaks in powder X-ray diffraction: 6.0.degree., 14.2.degree., 15.2.degree., 18.8.degree.(2.theta.
7410790 Method for producing .gamma.-glutamylcysteine August 12, 2008
The yeast which has .gamma.-glutamylcysteine-producing ability and is auxotrophic for pantothenic acid is proliferated in a medium containing a sufficient amount of pantothenic acid, and then it is cultured in a medium containing a limited amount of pantothenic acid to increase the .
7405346 Gene capable of imparting salt stress resistance July 29, 2008
This invention provides a novel gene that can impart salt stress tolerance to plants for a long period of time and salt stress tolerant transgenic plants to which such gene has been introduced. Such novel gene encodes the following protein (a), (b), or (c), and such salt stress tolerant
7405315 Mesoporous silica and process for producing the same July 29, 2008
(A) An anionic surfactant, (B) a silicate monomer and (C) a basic silane are mixed in water or a mixed solvent of a water-miscible organic solvent and water to obtain a mesoporous silica complex having mesopores with a uniform size, the anionic surfactant Component (A) is removed by wash
7402696 Benzene compounds July 22, 2008
The present invention provides novel benzene compounds presented by the following formulas, and analogs thereof, that exert an ACC activity-inhibiting effect that is effective in the treatment of obesity, hyperlipemia, fatty liver, hyperglycemia, impaired glucose tolerance, diabetes,
7402412 Mutated D-aminotransferase and method for producing optically active glutamic acid derivatives u July 22, 2008
A D-aminotransferase can be modified so as to efficiently produce (2R, 4R)-monatin having high sweetness intensity from 4-(indol-3-ylmethyl)-4-hydroxy-2-oxoglutaric acid by substituting an amino acid at least at one of positions (positions 100, 180 to 183, 243 and 244) involved in ef
7399618 Method for producing L-histidine using bacteria of Enterobacteriaceae family July 15, 2008
A method is provided for producing L-histidine using bacterium of the Enterobacteriaceae family, wherein the L-amino acid productivity of the bacterium is enhanced by enhancing an activity of the transaldolase encoded by the talB gene.
7399617 Method for producing an L-amino acid in an Escherichia bacterium via altering expression levels July 15, 2008
A bacterium belonging to the genus Escherichia which has an ability to produce an L-amino acid, wherein the ability to produce the L-amino acid is increased by increasing expression of an L-amino acid excretion protein is described. A method for producing the L-amino acid using the b
7396941 Method for producing monatin July 8, 2008
By simultaneously carrying out an isomerization reaction at position 2 of monatin in different configurations at positions 2 and 4 in the presence of an aldehyde under a condition of pH 4 to 11 in a mixture solvent of water and an organic solvent, and the crystallization of monatin in th
7396844 Benzamidine derivatives July 8, 2008
Benzamidine derivatives of the following formulae or analogs thereof, i.e., pharmaceutically acceptable salts thereof, are provided. These compounds or salts thereof have a blood-coagulation inhibiting effect based on an excellent effect of inhibiting the action of activated blood co
7390909 Processes of producing glutamic acid compounds and production intermediates therefore and novel June 24, 2008
The present invention relates to processes of producing glutamic acid compounds, for example, monatin, which are useful as, for example, production intermediates for sweetener or pharmaceutical products.
7388030 Suppressors of anemia and appetite suppressors and methods for suppressing anemia and suppressin June 17, 2008
The present invention provides a method for suppressing hemolytic anemia by selectively ameliorating reticulocyte increase and iron deposition on spleen caused as the side effects of methionine. The present invention also provides an appetite suppressor with reduced such side effects,
7385080 Method for producing optically active .beta.-phenylalanine compounds June 10, 2008
Optically active .beta.-phenylalanine compound may be prepared in an industrially advantageous manner by reacting an N-acyl-.beta.-phenylalanine compound with a specific optically resolving agent to effect an optical resolution by formation of diastereomer salts, and removing the opt
7381548 Method for producing L-amino acid using bacterium of Enterobacteriaceae family having expression June 3, 2008
The present invention provides a method for producing an L-amino acid using a bacterium of the Enterobacteriaceae family, particularly a bacterium belonging to genus Escherichia or Pantoea, which has been modified to attenuate expression of the yafA gene.
7378387 Method of suppressing immune response by reducing intracellular content of glutathione in macrop May 27, 2008
A method of suppressing immune responses, comprising administering to a patient in need thereof an effective amount of a composition comprising a substance capable of reducing the content of reductive glutathione in macrophages.
7375085 Melanocyte-stimulating hormone inhibitors May 20, 2008
In the present specification is disclosed a melanocyte-stimulating hormone inhibitory composition which comprises, as the active ingredient, a di- or tripeptide derivative having a certain naphthyl group or the salts thereof, or a melanocyte-stimulating hormone inhibitory compound having
7371549 Aldolase, and method for producing optically active IHOG and monatin May 13, 2008
The present invention relates to a method for producing optically active IHOG, which can in turn be used for the production of monatin. The present invention further relates to a method for producing optically active monatin, and aldolase used for these methods. As such, the present
7365161 Mutant tyrosine repressor which does not require tyrosine to induce expression of the tyrosine p April 29, 2008
A mutant tyrosine repressor that does not require tyrosine to induce expression of tyrosine phenol-lyase gene is obtained by introducing a mutation into a tyrosine repressor (tyrR), isolated from Pantoea agglomerans, or a tyrosine repressor (tyrR) which is encoded by SEQ ID NO. 1 and
7361490 DNA encoding hydantoinase, DNA encoding N-carbamyl-L-amino acid hydrolase, recombinant DNA, tran April 22, 2008
The present invention provides a method of producing optically active amino acids from 5-substituted hydantoin by isolating a hydantoinase gene and an N-carbamyl-L-amino acid hydrolase gene involved in an ability to convert 5-substituted hydantoin or N-carbamylamino acid into optically
7361458 Method for producing .alpha.-L-aspartyl-L-phenylalanine-.beta.-ester and method for producing .a April 22, 2008
A method for producing an .alpha.-L-aspartyl-L-phenylalanine-.beta.-ester (also named .alpha.-L-(.beta.-o-substituted aspartyl)-L-phenylalanine), which is an intermediate of an .alpha.-L-aspartyl-L-phenylalanine-.alpha.-methyl ester (also named .alpha.-L-aspartyl-L-phenylalanine meth
7358368 Azlactone compound and method for preparation thereof April 15, 2008
Compounds represented by formula (II): ##STR00001## wherein M is a hydrogen atom, sodium, potassium, or lithium; P is a hydrogen atom, an alkyl group, and the like; and the wavy line indicates a cis form, a trans form, or a mixture thereof for the double bond to which it is attached
7357951 Composition for preventing atherosclerosis April 15, 2008
The present invention provides a composition obtained by organic solvent extraction of defatted plant seed which is an atherosclerosis preventative agent. The present invention further provides a food and a pharmaceutical composition containing the composition, as well as a method of
7357280 Foodstuff feeding apparatus and feeding method April 15, 2008
A foodstuff feeding apparatus to convey foodstuff to a metering unit from a hopper without masking or kneading the foodstuff. The apparatus includes a piston pump provided between a lower portion of a hopper and an end of a first pipe to draw foodstuff from the hopper and to press out
7354746 Method for producing optically active IHOG and monatin April 8, 2008
The present invention relates to a method for producing optically active IHOG, which can in turn be used for the production of monatin. The present invention further relates to a method for producing optically active monatin, and an aldolase which can be used in these methods. As suc
7354744 Process for producing L-glutamic acid April 8, 2008
L-glutamic acid is produced by culturing in a liquid medium containing L-glutamic acid at a saturation concentration and the carbon source a microorganism that can metabolize a carbon source at a specific pH, and wherein said microorganism has an ability to accumulate L-glutamic acid
7354615 Method for producing mixed crystal of disodium 5'-guanylate and disodium 5'-inosinate April 8, 2008
Disclosed herein are a process for producing mixed crystals of disodium 5'-guanylate and disodium 5'-inosinate which comprises precipitating mixed crystals of disodium 5'-guanylate and disodium 5'-inosinate (I+G mixed crystals) by adding an aqueous mixed solution of disodium 5'-guany

 
 
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