Patents Examined by Mary C. Lee
-
Patent number: 5470974Abstract: A composition of polymer molecules effective to bind, with substantially uniform binding affinity, to a single-stranded polynucleotide containing a target sequence of bases. The polymer molecules are composed of a sequence of base-pairing moieties effective to hydrogen bond to corresponding, complementary bases in the target sequence, under selected binding conditions, and a predominantly uncharged, achiral backbone supporting the base-pairing moieties at positions and in orientations which allow hydrogen bonding between the pairing moieties of the polymer and the corresponding complementary bases in the target sequence. The composition has diagnostic uses, in a solid-support assay system, and therapeutic uses involving inhibition or inactivation of target polynucleotides.Type: GrantFiled: February 25, 1994Date of Patent: November 28, 1995Assignee: Neu-Gene Development GroupInventors: James Summerton, Dwight Weller, Eugene Stirchak
-
Patent number: 5451683Abstract: Methods and compositions are described for immobilizing anti-ligands, such as antibodies or antigens, hormones or hormone receptors, oligonucleotides, and polysaccharides on surfaces of solid substrates for various uses. The methods provide surfaces covered with caged binding members which comprise protecting groups capable of being removed upon application of a suitable energy source. Spatially addressed irradiation of predefined regions on the surface permits immobilization of anti-ligands at the activated regions on the surface. Cycles of irradiation on different regions of the surface and immobilization of different anti-ligands allows formation of an immobilized matrix of anti-ligands at defined sites on the surface. The immobilized matrix of anti-ligands permits simultaneous screenings of a liquid sample for ligands having high affinities for certain anti-ligands of the matrix. A preferred embodiment of the invention involves attaching photoactivatable biotin derivatives to a surface.Type: GrantFiled: April 23, 1993Date of Patent: September 19, 1995Assignee: Affymax Technologies N.V.Inventors: Ronald W. Barrett, Michael C. Pirrung, Lubert Stryer, Christopher P. Holmes, Steven A. Sundberg
-
Patent number: 5444165Abstract: An unsaturated imide compound represented by formula (1): ##STR1## wherein Q is an alicyclic structure-containing hydrocarbon group having 4-20 carbon atoms; each of R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.i and R.sub.j represents a hydrogen atom, a halogen atom, a hydrocarbon group having 1-6 carbon atoms or a halogen-containing hydrocarbon group having 1-6 carbon atoms; each of a, b, c, d, e and f represents an integer of 0 to 4 satisfying a+b.ltoreq.4, c+d.ltoreq.4 and e+f.ltoreq.4 and D represents a divalent organic group having 2-24 carbon atoms and an ethylenically unsaturated double bond, a process for producing the unsaturated imide compound of formula (1) and intermediates for producing the unsaturated imide compound of formula (1). The unsaturated imide compound of formula (1) is well soluble in organic solvents and can give cured products excellent in heat resistance, low water absorption and flexibility.Type: GrantFiled: February 25, 1994Date of Patent: August 22, 1995Assignee: Sumitomo Chemical Company, LimitedInventors: Yasuhiro Hirano, Yasuhiro Endo, Kazuo Takebe, Mitsuhiro Shibata, Shuichi Kanagawa, Yutaka Shiomi, Masatsugu Akiba, Shinichiro Kitayama
-
Patent number: 5441973Abstract: The invention is directed to N-acetyl-4-phenyl-pyrrolidin-2-ones, which, because of their pronounced cerebroprotective effect in human medicine, can be used for the prophylaxis and treatment of cerebral functional disorders. Pursuant to the invention, these compounds are synthesized by reacting 4-phenyl-pyrrolidin-2-ones with a reactive derivative of a carboxylic acid, or by cyclizing N-acylaminobutyric acid derivatives.Type: GrantFiled: January 13, 1994Date of Patent: August 15, 1995Assignee: Arzneimittelwerk Dresden G.m.b.H.Inventors: Lothar Zenker, Helmut Wunderlich, Dieter Lohmann, Angelika Rostock, Christine Siegemund, Artur V. Valdman, Tatjana A. Voronina, Ilmira C. Rachmankulova, Oleg M. Glozman, Taisija L. Garibova, Larisa M. Mescerjakova, Ljudmila A. Zmurenko, Sergej B. Seredenin, Grigorij G. Rozancev
-
Patent number: 5442088Abstract: Process for the preparation of phosphorus-containing L-amino acids, their derivatives and intermediates for this processL-amino acids of the formula I and salts thereof, ##STR1## in which R.sup.1 to R.sup.5 are defined as in claim 1 and n is 0 or 1, are obtained according to the invention bya) reacting an optically active S-homoserine lactone of the formula II, ##STR2## with hydrogen chloride in the presence of an alcohol of the formula R.sup.5 --OH to give novel compounds of the formula III, ##STR3## in which R.sup.3, R.sup.4 and R.sup.5 are defined as in formula I, except that R.sup.5 =H, andb) reacting the resulting compound of formula III with a compound of formula IV,R.sup.1 (O).sub.n -R(OR.sup.2).sub.2 (IV)and if desired, hydrolyzing the product to give a compound of formula I, in which R.sup.5 =H.Type: GrantFiled: July 7, 1994Date of Patent: August 15, 1995Assignee: Hoechst AktiengesellschaftInventor: Michael Hoffmann
-
Patent number: 5438137Abstract: An asymmetric dioxazine compound of the following formula in the free acid form, ##STR1## wherein R is hydrogen, halogen, sulfo or alkoxy, R.sub.1, R.sub.2 and R.sub.3 are each hydrogen or alkyl, X.sub.1 and X.sub.2 are each hydrogen, halogen, alkyl, alkoxy or phenoxy, Y is alkylene, phenylene or naphthylene, Z is --SO.sub.2 CH.dbd.CH.sub.2, --SO.sub.2 CH.sub.2 CH.sub.2 OSO.sub.3 H or the like, V is hydrogen, alkyl, acyl or substituted triazinyl, and Q is halogen, alkoxy, amino or a group similar to that of ##STR2## provided that R is hydrogen, and Q is amino or a group similar to that of ##STR3## when V is substituted triazinyl, which is useful for dyeing or printing fiber materials to give dyed or printed products of a brilliant blue color superior in fastness properties, particularly those such as chlorine fastness with superior build-up property.Type: GrantFiled: September 30, 1993Date of Patent: August 1, 1995Assignee: Sumitomo Chemical Company, LimitedInventors: Tetsuya Miyamoto, Miyao Takahashi, Takahiko Fujisaki, Shinei Ikeou, Takashi Omura, Naoki Harada
-
Patent number: 5436324Abstract: Improved reactive dyestuffs of the following formula (I) ##STR1## in which the substituents have the meaning given in the description. The improved reactive dyestuffs are highly suitable for the dyeing and printing of natural or synthetic OH-- and/or amido-containing materials, in particular, those made of cellulose and polyamides.Type: GrantFiled: July 23, 1992Date of Patent: July 25, 1995Assignee: Bayer AktiengesellschaftInventors: Wolfram Reddig, Karl-Josef Herd
-
Patent number: 5436362Abstract: In a method of producing dialkylcarbonate, alcoholic compound and cyclo-carbonate are subjected to a catalytic reaction each other at a reaction temperature of 20.degree. to 200.degree. C. and under a pressure of 0 to 40 kg/cm.sup.2 G, which keeps the reaction system liquid, in the presence of ion exchanged zeolite which is ion-exchanged with alkali metal ion and/or alkaline earth metal ion.Type: GrantFiled: December 16, 1993Date of Patent: July 25, 1995Assignee: Chiyoda CorporationInventors: Tadami Kondoh, Yoshimi Okada, Fumiaki Tanaka, Sachio Asaoka, Susumu Yamamoto
-
Patent number: 5436346Abstract: The process for the preparation of benzothiazolyl-2-sulphenamides, by reacting a 2-mercaptobenzothiazole or dibenzothiazolyl 2,2'-disulphide with a primary or secondary aliphatic or cycloaliphatic amine in the presence of hydrogen peroxide as oxidizing agent in an aqueous medium is distinguished in that an aqueous hydrogen peroxide solution is metered at a temperature in the range from 30.degree. to 70.degree. C. into an aqueous suspension of the respective amine and the 2-mercaptobenzothiazole or dibenzothiazolyl 2,2'-disulphide in a ratio in the range between 1.0 and 1.5 mol of amine per mole of 2-mercaptobenzothiazole or per equivalent of dibenzothiazolyl 2,2'-disulphide, preferably in a quantity of below 1.35 mol per mole of 2-mercaptobenzothiazole or per equivalent of dibenzothiazolyl 2,2'-disulphide over a period of at least 60 minutes. The total quantity of water in the reaction mixture should not exceed 1500 g per mole of 2-mercaptobenzothiazole.Type: GrantFiled: June 21, 1994Date of Patent: July 25, 1995Assignee: Akzo Nobel N.V.Inventors: Ludwig Eisenhuth, Manfred Bergfeld
-
Patent number: 5434269Abstract: A process for the asymmetric hydrogenation of furoimidazole derivatives of the general formula: ##STR1## with hydrogen in the presence of a homogeneous catalyst to give the corresponding diastereomeric dihydrofuroimidazole derivatives of the general formula: ##STR2## R.sub.1 and R.sub.2 are protective groups, although R.sub.2 can be hydrogen. The dihydrofuroimidazole derivatives of the general formula II are intermediates for the preparation of (+)-biotin.Type: GrantFiled: August 3, 1994Date of Patent: July 18, 1995Assignee: Lonza Ltd.Inventors: Martin Eyer, Ronald E. Merrill
-
Patent number: 5434251Abstract: Symmetric azo dyestuffs of the formula ##STR1## wherein the substituents have the meaning given in the description, produce improved dyeings or prints on wool and cellulose materials.Type: GrantFiled: April 2, 1993Date of Patent: July 18, 1995Assignee: Bayer AktiengesellschaftInventor: Karl-Josef Herd
-
Patent number: 5434252Abstract: Reactive dyes of the formula ##STR1## in which D, R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are as defined in claim 1, are particularly suitable for dyeing or printing cellulosic fiber materials or naturally occurring or synthetic polyamide fiber materials with a high tinctorial yield, and produce dyeings and prints having good fastness properties.Type: GrantFiled: October 25, 1994Date of Patent: July 18, 1995Assignee: Ciba-Geigy CorporationInventors: Paul Herzig, Athanassios Tzikas, Anton Andreoli, Claudia Carisch
-
Patent number: 5434143Abstract: The phosphite-borane compounds of the present invention correspond to the formula ##STR1## where R.sub.1 is independently selected from H, C.sub.1 -C.sub.20 alkyl, alkylaryl, aryl, trialkylsilyl, with the proviso that both R.sub.1 groups cannot simultaneously be H.sub.1, andR.sub.2 is selected from H, a monovalent cation such as Li.sup.+, Na.sup.+, K.sup.+, NH.sub.4.sup.+, N(R.sub.3.sup.+).sub.4, where R.sub.3 is independently selected from H, C.sub.1 -C.sub.20 alkyl.The phosphite-borane compounds of the present invention are bioactive in character, variously exhibiting anti-tumor, anti-inflammatory, and hypolipidemic activity. Also disclosed are various synthetic methods for making such phosphite-borane compounds, and for formulating same in unit dosage forms as well as other pharmaceutically and pharmacologically acceptable formulations.Type: GrantFiled: October 19, 1994Date of Patent: July 18, 1995Assignee: Boron Biologicals, Inc.Inventors: Bernard F. Spielvogel, Anup Sood
-
Patent number: 5432288Abstract: Novel O.sub.10eq -derivatives of ryanodine and dehydroryanodine characterized as binding strongly to ryanodine receptor, useful in affecting Ca.sup.++ efflux in tissue and also in isolating ryanodine receptor from sarcoplasmic reticulum. Also described are novel radio-iodinated alanine derivatives useful to radio label ryanodine and dehydroryanodine derivatives.Type: GrantFiled: March 2, 1993Date of Patent: July 11, 1995Assignee: Indiana University FoundationInventors: Koert Gerzon, Rod A. Humerickhouse, Henry R. Bensch, Jr., Keshore R. Bidasee
-
Patent number: 5430170Abstract: A industrially advantageous process for preparing dialkyl carbonates is provided. The process is characterized in that an alkylene carbonate and an alcohol are subjected to an transesterification in the presence of a catalyst which contains, as the catalytically active component, at least one rare-earth oxide. According to this process, the transesterification progresses rapidly due to the excellent activity of the catalyst, and the catalyst can be readily separated after termination of the reaction, allowing high efficiency isolation and purification of dialkyl carbonate.Type: GrantFiled: November 23, 1993Date of Patent: July 4, 1995Assignee: Nippon Shokubai Co., Ltd.Inventors: Yoshiaki Urano, Masaru Kirishiki, Yoshiyuki Onda, Hideaki Tsuneki
-
Patent number: 5430169Abstract: The present invention provides a series of non-toxic compounds which function to inhibit the activity of S-1-P aldolase in respect to its cleavage of S-1-P. These inhibitors are described by the compounds of formula I ##STR1## wherein R is a radical containing 1 to 15 carbon atoms, a halogen, or hydrocarbon, R' is an organic radical or hydrogen, and R" is --NH.sub.3.sup.+ or --NH--NH .sup.+, with the proviso that, when R is CH.sub.3 (CH).sub.12 (CH.dbd.CH) and R' is hydrogen, R" is --NH--NH.sub.3.sup.+.A method for preparing such compounds, which may generally be described as 1-phosphate derivatives of compounds which include a 2-amino-1,3-alcohol radical is also disclosed.Type: GrantFiled: February 14, 1994Date of Patent: July 4, 1995Assignee: The United States of America represented by the Department of Health and Human ServicesInventors: Ahcene Boumendjel, Stephen P. F. Miller
-
Patent number: 5428140Abstract: Reactive dyes of the formula ##STR1## where n is 0 or 1R.sup.1, R.sup.2 and R.sup.3 are in each case hydrogen, C.sub.1 -C.sub.4 -alkyl or phenyl,R.sup.4 is fluorine, chlorine, bromine, C.sub.1 -C.sub.4 -alkylsulfonyl, phenylsulfonyl or a radical of the formula ##STR2## L is a bridge member, A is unsubstitued or substituted C.sub.2 -C.sub.8 -alkylene,Y is vinyl or a radical of the formula --CH.sub.2 --CH.sub.2 --Q, Q being a group which can be removed under alkaline reaction conditions, andD is phenyl or naphthyl, it being possible for these radicals to be substituted,and a process for preparing reactive dyes by oxidation of the abovementioned compounds are described.Type: GrantFiled: June 6, 1994Date of Patent: June 27, 1995Assignee: BASF AktiengesellschaftInventors: Matthias Wiesenfeldt, Bernd Siegel, Manfred Patsch
-
Patent number: 5428163Abstract: A broad class of pharmaceutical agents which react directly with electron carriers or with reactive species produced by electron transport to release a pharmacologically active molecule to effect a therapeutic functional change in the organism by a receptor or nonrecepter mediated action.Type: GrantFiled: December 4, 1989Date of Patent: June 27, 1995Inventor: Randell L. Mills
-
Patent number: 5428138Abstract: The azo dyes of the formula I ##STR1## where X.sup.1 is for example hydrogen or (C.sub.1 to C.sub.6)alkyl,X.sup.2 is cyano or nitro,X.sup.3 is for example hydrogen or (C.sub.1 to C.sub.4)alkoxy,X.sup.4 is for example (C.sub.1 to C.sub.4)alkoxy, chlorine or hydrogen,R.sup.1 is hydrogen or (C.sub.1 to C.sub.6)alkyl,R.sup.2 is hydrogen or (C.sub.1 to C.sub.6)alkyl andR.sup.3 is for example (C.sub.1 to C.sub.8)alkyl,are highly suitable for dyeing and printing hydrophobic fiber materials.Type: GrantFiled: February 8, 1993Date of Patent: June 27, 1995Assignee: Cassella AGInventors: Ulrich Buhler, Margareta Boos, Reinhard Kuhn
-
Patent number: RE35009Abstract: Organic pigments selected from the diketopyrrolopyrrole, azo, isoindolinone and isoindoline series, which pigments consist of .Iadd.at least .Iaddend.50% by weight of platelets which are from 5 to 50 .mu.m long, 2 to 50 .mu.m wide and 0.01 to 5 .mu.m thick, with the proviso that the ratios of length:thickness and width:thickness must be at least 3.The pigments in platelet form are excellently suited to producing effect colorations in high molecular weight organic material and in cosmetic products.Type: GrantFiled: October 28, 1993Date of Patent: August 1, 1995Assignee: Ciba-Geigy CorporationInventors: Philippe Bugnon, Fritz Herren, Bernhard Medinger