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Analysis

1 / 38,583
1.215148DNA SEQUENCE ENCODING NON-HUMAN ANIMAL INTERFERON, EXPRESSION VEHICLES AND TRANSFORMANTS
NZ - 31.08.1987
Int.Class C07H 21/04
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
21Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
04with deoxyribosyl as saccharide radical
 Appl.No 21514883 Applicant GENENTECH INC Inventor CAPON D J
2.212562CIS-2,3,3A,4,5,7A-HEXAHYDRO(1H)INDOL-2-YLCARBOXYLIC ACID DERIVATIVES
NZ - 29.05.1987
Int.Class C07D 209/00
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
209Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
 Appl.No 21256283 Applicant HOECHST AG Inventor URBACH H
3.238998PHARMACEUTICALS
NZ - 25.11.1993
Int.Class C07F 9/00
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
FACYCLIC, CARBOCYCLIC, OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
9Compounds containing elements of Groups 5 or 15 of the Periodic Table
 Appl.No 238998 Applicant BEECHAM GROUP p.l.c. Inventor Harnden, Michael Raymond
These are derivatives of the general formula and pharmaceutically acceptable salts thereof, wherein X is -CH2O- or -CH2-; R1 is -OH or -NH2, R2 is -OH or NH2; R3 is H, -CH2-OH or acyloxymethyl; and R4 is a group of the formula -P(O)(OR5)(OR6) wherein R5 and R6 are independently selected from hydrogen, C1-6alkyl and optionally substituted phenyl. Such derivatives are reported to possess antiviral activity particularly against DNA viruses and retroviruses.
4.239030A METHOD OF CODING A SAMPLED SPEECH SIGNAL VECTOR
NZ - 14.12.1993
Int.Class H03M 7/30
HELECTRICITY
03ELECTRONIC CIRCUITRY
MCODING, DECODING OR CODE CONVERSION, IN GENERAL
7Conversion of a code where information is represented by a given sequence or number of digits to a code where the same information is represented by a different sequence or number of digits
30Compression; Expansion; Suppression of unnecessary data, e.g. redundancy reduction
 Appl.No 239030 Applicant TELEFONAKTIEBOLAGET LM ERICSSON (publ) Inventor MINDE T B
A method of coding a sampled speech signal vector by selecting an optimal excitation vector in an adaptive code book 100 is disclosed. The optimal excitation vector is obtained by maximising the energy normalised square of the cross correlation between the convolution of the excitation vectors with the impulse response of a linear filter and the speech signal vector. Before the convolution the vectors of the code book are block normalised 200 with respect to its largest component and the speech signal vector is also normalised 202. Calculated values for the squared cross correlation CI and the energy EI and corresponding values CM, EM for the best excitation vector so far are divided into a mantissa and a sealing factor with a limited number of scaling levels. The number of levels can be different for C and E. During the calculation of the products CIEM and EICM for determining the optimal excitation vector, the respective mantissas are multiplied and a separate scaling factor calculation is performed...
5.239033OSMOTIC DEVICE WITH HYDROGEL DRIVING MEMBER
NZ - 27.04.1994
Int.Class A61K 31/44
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
31Medicinal preparations containing organic active ingredients
33Heterocyclic compounds
395having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
435having six-membered rings with one nitrogen as the only ring hetero atom
44Non-condensed pyridines; Hydrogenated derivatives thereof
 Appl.No 239033 Applicant ALZA CORPORATION Inventor Place, Virgil A
This osmotic device for the controlled systemic delivery of nicotine base through an oral mucosal membrane in an oral cavity over an extended delivery period, comprises a semipermeable wall surrounding and forming a compartment containing a nicotine salt which when reacted with an aqueous fluid forms nicotine base, the wall being formed of a material which is permeable to the passage of an aqueous fluid present in the oral cavity, and a passageway through the semipermeable wall for delivering the nicotine salt and the nicotine base formed in the compartment into the oral cavity, wherein the device when in operation in the oral cavity imbibes the aqueous fluid through the wall into the compartment, thereby initiating a chemical reaction between the nicotine salt and the aqueous fluid to produce nicotine base, wherein nicotine salt and nicotine base are delivered from the compartment through the passageway and into the oral cavity over time.
6.239108NO-SPILL FLUID SECURITY COUPLING
NZ - 11.06.1993
Int.Class F16L 37/36
FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
16ENGINEERING ELEMENTS OR UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
LPIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
37Couplings of the quick-acting type
28with fluid cut-off means
30with fluid cut-off means in each of two pipe-end fittings
36with two lift valves being actuated to initiate the flow through the coupling after the two coupling parts are locked against withdrawal
 Appl.No 239108 Applicant AEROQUIP AG Inventor MCCRACKEN D G
A fluid coupling has a first part 10 mounted to a receptacle 16 and a second part 12 mounted on a dispensing hose. Part 12 is forced down onto part 10 so that spring fingers 114 snap in behind shoulder 42. A valve sleeve 128 on the second part engages with a shoulder 54 on the first part and is lifted and unseated. A valve head 68 on the first part is lowered and unseated by a head 124 on the second part. This double unseating allows fluid to flow from receptacle 16 through parts 10 and 12. A check valve ball 84 prevents downward flow. When an alternative second part is used with a longer neck 120 valve head 68 is forced further downward thereby forcing a cage 56 and a piston 78 downward so that ball 84 contacts an abutment 96 allowing fluid to flow through parts 12 and 10 to receptacle 16. Such construction is stated to provide a ''no-spill'' security coupling.
7.239064ELECTROSTATICALLY DISSIPATIVE FUEL FILTER
NZ - 25.11.1993
Int.Class B01D 27/08
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
DSEPARATION
27Cartridge filters of the throw-away type
08Construction of the casing
 Appl.No 239064 Applicant ALLIEDSIGNAL INC. Inventor DANOWSKI, D R
A build-up of electrostatic charges, which may cause breakdown and leakage of a filter housing 12 for a motor vehicle fuel line, is prevented by providing an electrically conductive path through the primarily non-conductive housing between the fuel within and an earth potential of the motor vehicle 38. The conductive path is provided by embedding an electrically conductive material, e.g. stainless steel fibres, within the non-conductive housing material which is preferably a polymer, e.g. nylon. The fibres may account for 3-9% by weight of the composite material and have a minimum length of 4mm.
8.239161SUBSTITUTED [1H-IMIDAZOL-5-YL]ALKANOIC ACIDS
NZ - 26.01.1994
Int.Class C07D 233/00
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
233Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
 Appl.No 239161 Applicant GlaxoSmithKline LLC Inventor GIRARD, G R
Angiotensin II receptor antagonists have the formula: or a pharmaceutically acceptable salt thereof. R1 is adamantylmethyl, phenyl, biphenyl, or naphthyl, with each aryl group being optionally substituted by 1 to 3 substituents selected from Cl, Br, F, I, C1-6alkyl, nitro, CO2R8, tetrazol-5-yl, C1-6alkoxy, hydroxy, SC1-4alkyl, SO2NHR8, NHSO2R8, SO3H, CONR8R8, CN, SO2C1-4alkyl, and CnF2n+1', n is 1,2, or 3. R2 is C2-10alkyl, C3-10alkenyl, C3-10alkynyl, C3-6cycloalkyl, or (CH2)0-8phenyl optionally substituted by 1 to 3 substituents selected from C1-6alkyl, nitro, Cl, Br, F, I, hydroxy, C1-6alkoxy, NR8R8, CO2R8, CN, and CONR8R8. X is a single bond, S, or O. R3 is H, Cl, Br, F, I, CHO, hydroxymethyl, CO2R8, CONR8R8, NO2, or CnF2n+1. q is 0,1,2,3, or 4. m is 0, 1, or 2. R4 is H or C1-6alkyl. z is 0 or 1. R5 is C3-6alkyl, C3-6alkenyl, phenyl-Y-, 2- or 3-thienyl-Y-, 2- or 3-furyl-Y-, 2-, 3-, or 4-pyridyl-Y-, tetrazolyl-Y-, triazolyl-Y-, imidazolyl-Y-, pyrazolyl-Y-, thiazolyl-Y-, pyrrolyl-Y-, or oxazolyl-Y-, with each aryl ring being optionally substituted by C1-6alkyl, Cl, Br, F, I, C1-6alkoxy, NR8R8, CO2R8, or CONR8R8. Y is a single bond or C1-6alkyl which is branched or unbranched. R6 is CO2R8, CONR8R8, or tetrazol-5-yl. R7 is H, CO2R8, or C1-6alkyl. Each R8 independently is H, C1-6alkyl, or (CH2)0-4phenyl.
9.239297GRAM-NEGATIVE ALKALIPHILIC MICROORGANISMS
NZ - 26.07.1994
Int.Class C12P 21/00
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
21Preparation of peptides or proteins
 Appl.No 239297 Applicant GENENCOR INTERNATIONAL, INCORPORATED Inventor Jones, Brian Edward
10.239350CELLULOSE BASED PRODUCTS AND METHODS OF MAKING THEM
NZ - 26.01.1994
Int.Class D21H 19/52
DTEXTILES; PAPER
21PAPER-MAKING; PRODUCTION OF CELLULOSE
HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C, D21D84; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G97; PAPER NOT OTHERWISE PROVIDED FOR
19Coated paper; Coating material
36Coatings with pigments
44characterised by the other ingredients, e.g. the binder or dispersing agent
52Cellulose; Derivatives thereof
 Appl.No 239350 Applicant ALKO GROUP LTD Inventor
The claims are expressed in these independent ways: 1. A paper product is treated with a composition comprising a mixture of cellulose derivative hydrolysates derived from degradation of a cellulose derivative that has one or more substituents, the mixture having an average degree of polymerisation of from 5 to 70. 2. A paper product is treated with a degradation product of a cellulose derivative comprising a mixture of oligomers of the cellulose derivative comprising a mixture of oligomers of the cellulose derivative, a majority of the oligomers having a degree of polymerisation such that the oligomer conforms to a rod-like configuration. 3. A paper product is treated with a degradation product of a cellulose derivative comprising a mixture of oligomers of the cellulose derivative the majority of which have a Mark-Houwink exponent of at least 1.2 at an NaCl concentration of 0.005 N to 0.5 N. 4. A paper product is treated with a degradation product of a cellulose derivative comprising a mixture of oligomers, the majority of which have a degree of polymerisation in the range of 3 to 500. This may increase the dewatering properties of paper. The paper product may be a pulp, a finished paper product, a textile, or structural material.
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