| Patent Number |
Title Of Patent |
Date Issued |
| 7078040 |
Method of inhibiting the expression of inflammatory cytokines and chemokines |
July 18, 2006 |
| A method of inhibiting the expression of inflammatory cytokines and chemokines in an animal or man, is disclosed. The method comprises administration to said animal or man of at least one type of xanthophyll, e.g. astaxanthin, in an amount inhibiting the expression of inflammatory cy |
| 7064101 |
Stable astaxanthin-containing powdery compositions and process for producing the same |
June 20, 2006 |
| The present invention relates to a stable astaxanthin-containing powdery composition which is obtained by drying a suspension containing a ground Haematococcus alga containing astaxanthin, a surfactant, an antioxidant, an excipient and water and to a process for preparing the same.Accord |
| 6608103 |
Inhibitor for neovasculation, cell multiplication, lumen formation and FGF |
August 19, 2003 |
| This invention relates to an inhibitor having inhibitory activity against neovasculation, cell multiplication, lumen formation and fibroblast growth factor which comprises .beta.-, .gamma.- or .delta.-tocotrienol. |
| 6562372 |
Tocotrienol-containing powder, a process for preparing it and a tablet comprising compressed sai |
May 13, 2003 |
| A tocotrienol-containing powder prepared by a process wherein an oil containing a tocotrienol is treated with a lecithin, a cellulose and an emulsifying agent in water to form an emulsion, a powder substance is mixed with the formed emulsion to form a suspension and then the formed s |
| 6555137 |
Sucralfate-containing composition and process for the preparation thereof |
April 29, 2003 |
| A coated antacid comprising sucralfate and an antacid inhibits decline in the adhesion characteristics of sucralfate whereby the drug ingested can reliably show its effect in the stomach. This coated antacid not only shows the mucosa repairing effect of sucralfate itself, but also shows |
| 6395250 |
Lithium/nickel/cobalt composite oxide, process for preparing the same, and cathode active materi |
May 28, 2002 |
| There can be provided a positive electrode active material for a secondary battery which is excellent in the charging and discharging cycle characteristics so that it retains high battery capacity that is comparable to the hitherto known LiNiO.sub.2 even by increasing the number of c |
| 6325988 |
Process for preparing spinel type lithium manganese composite oxide and cathode active material |
December 4, 2001 |
| A process for preparing a spinel lithium manganese complex oxide having the general formula Li.sub.x Mn.sub.2-y Al.sub.y O.sub.4 (wherein 0.9.ltoreq.x.ltoreq.1.1, and 0.002.ltoreq.y.ltoreq.0.5) the process comprising the steps of reacting a manganese complex hydroxide represented by |
| 6248817 |
Infrared absorber and agricultural film |
June 19, 2001 |
| An infrared absorber which comprises containing as an effective ingredient a hydroxide complex salt represented by the formula(wherein M.sup.2+ is a divalent metal, A.sup.n- is an anion having a valence of n, and m, x and y are numbers respectively in the ranges of 0.ltoreq.m<5, 0.01. |
| 6201121 |
Process for the preparation of 3-dihalobenzyl-2,4-quinazolinedione derivatives |
March 13, 2001 |
| A process for preparing a 3-dihalobenzyl-2,4-quinazolinedione derivative represented by the formula (V): ##STR1##(whereinX.sup.1, X.sup.2, X.sup.3 are independently a halogen atom, andA is an alkylene group),which comprises:reacting a dihalobenzyl derivative represented by the formula (III): |
| 6045771 |
Lithium-nickel complex oxide, a process for preparing the same and a positive electrode active m |
April 4, 2000 |
| There is provided a novel lithium nickel complex oxide represented by the general formula:wherein M represents one selected from the group consisting of Al, Fe, Co, Mn and Mg, x=x.sub.1 +x.sub.2, O<x.sub.1 .ltoreq.0.2, O<x.sub.2 .ltoreq.0.5, 0<x.ltoreq.0.5, and 0.9.ltoreq.y.ltor |
| 5767179 |
Lithium-aluminum hydroxide complex with condensed silicate |
June 16, 1998 |
| A novel hydroxide complex with condensed silicate represented by the formula (I)wherein M.sup.2+ is a divalent metal, m, x and y are numbers respectively in the ranges of 0.ltoreq.m<5, 0.ltoreq.x<1 and 2.ltoreq.y.ltoreq.4, a process for preparing the same, an infrared absorber cont |
| 5648057 |
Process for producing LiM.sup.3+ O.sub.2 or LiMn.sub.2 O.sub.4 and LiNi.sup.+ O.sub.2 for use in |
July 15, 1997 |
| A process for producing a compound of the formula LiM.sup.3+ O.sub.2 (wherein M.sup.3+ Ni.sup.3+ is or/and Co.sup.3+) or LiMn.sub.2 O.sub.4 is provided which comprises the steps of reacting a basic metal salt represented by the formula M.sup.2+ (OH).sub.2-nx (A.sup.n-).sub.x .multid |
| 4068070 |
.alpha.-Cyanoamine compounds and a process for producing the same |
January 10, 1978 |
| .alpha.-Cyanoamine compounds represented by the following formula or an acid addition salt thereof ##STR1## WHEREIN R.sub.1 is a halogen atom or lower alkoxy group, R.sub.2 and R.sub.3 are a hydrogen atom or lower alkoxy group, R.sub.4 is a hydrogen atom or lower alkyl group, R.s |
| 4019982 |
Method for treatment of waste water containing organic pollutants |
April 26, 1977 |
| An aqueous solution containing aluminum is mixed with an aqueous solution containing calcium and/or an aqueous solution containing magnesium and, if necessary, further with an aqueous solution containing iron and the pH of the resulting mixture is adjusted to cause insolubilization of th |
| 3962247 |
Alpha-cyanoamine compounds and a process for producing the same |
June 8, 1976 |
| .alpha.-Cyanoamine compounds represented by the following formula or an acid addition salt thereof ##SPC1##Wherein R.sub.1 is a halogen atom or lower alkoxy group, R.sub.2 and R.sub.3 are a hydrogen atom or lower alkoxy group, R.sub.4 is a hydrogen atom or lower alkyl group, R.sub.5 |
| 3948899 |
.alpha.-Cyanobenzylpiperazines and a process for producing the same |
April 6, 1976 |
| .alpha.-Cyanobenzylpiperazines represented by the formula ##SPC1##Or an acid addition salt thereof, wherein R.sub.1 is a halogen or 1-3C lower alkoxy, R.sub.2 and R.sub.3 are each hydrogen or 1-3C lower alkoxy, R.sub.4 is 1-3C lower alkyl, and R.sub.5 is hydrogen or 1-3C lower alkyl, |
