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Assignee: Tanabe Seiyaku Co., Ltd.


Location: Osaka, JP
No. of patents: 302

1                
NumberTitleIssue Date
8012731Phosphodiesterase and gene thereof
The present invention is to provide a novel phosphodiesterase and a gene thereof, specifically, Type 11 phosphodiesterase (PDE11) and a gene thereof, more specifically, a phosphodiesterase selected from (A) a protein having an amino acid sequenced shown by SEQ.ID.NO...
09/06/2011
7799929Biotin intermediate and process for preparing the same
The present invention is to provide a process for preparing a synthetic intermediate of biotin which is industrially advantageous, and discloses a process for preparing a compound represented by the formula (I): 1 wherein R1 and R2 may be the s...
09/21/2010
7385083Potassium channel opener
A potassium channel opener comprising a compound (e.g., pimaric acid) represented by the formula [I]: wherein R1, R2, R3, R4, R5, R6
06/10/2008
7332487Nitrogen-containing 5-membered ring compound
The present invention is to provide an aliphatic nitrogen-containing 5-membered ring compound represented by the formula [I]: wherein symbols in the formula have the following meanings; ...
02/19/2008
7332317Phosphodiesterase and genes thereof
The present invention is to provide a novel phosphodiesterase and a gene thereof, specifically, Type 11 phosphodiesterase (PDE11) and a gene thereof, more specifically, a phosphodiesterase selected from (A) a protein having an amino acid sequenced shown by SEQ.ID.NO...
02/19/2008
7323337Gene transfer into primate embryonic stem cells using VSV-G pseudotyped simian immunodeficiency virus vectors
Highly efficient gene transfer into primate-derived embryonic stem (ES) cells has successfully been achieved by using a simian immunodeficiency virus vector (SIV) pseudotyped with VSV-G protein, which is a surface glycoprotein of vesicular stomatitis virus (VSV) The...
01/29/2008
7273868Pyrazine derivatives
1. A cyclic compound of the formula (I) or a pharmacologically acceptable salt thereof, wherein X is ═CH— or ═N—, Y is —NH—, —NR4—, —S—, ...
09/25/2007
7220736Pyrimidine compounds
A cyclic compound of the formula (I) or a pharmacologically acceptable salt thereof, wherein X is ═CH— or ═N—, Y is —NH—, —NR4—, —S—, —O—, —CH═N—,...
05/22/2007
7220430Sustained-release preparation and process for producing the same
The present invention is to provide a sustained release preparation comprising a drug-containing core substance and a multilayered coating layer covering the core substance, wherein all adjacent layers in the multilayered coating layer contain mutually different hyd...
05/22/2007
7160877Aliphatic nitrogen-containing 5-membered ring compound
The present invention is to provide an aliphatic nitrogen-containing 5-membered ring compound represented by the formula [I]: wherein A represents —CH2— or —S—, ...
01/09/2007
7153886Method for treatment of peripheral inflammation of a loop ileal artificial anus
The present invention provides a novel agent for prophylaxis or treatment of inflammatory bowel diseases for oral administration or intra-intestinal infusion, which comprises as an active ingredient a compound of the formula (I):
12/26/2006
7153859Condensed polycyclic compounds
The present invention provides a novel a condensed polycyclic compound useful as a phosphodiesterase 4 inhibitor, which is shown by the formula [I]: or a pharmaceutically acceptable salt thereof and a pharmaceuti...
12/26/2006
7138397Nitrogenous 5-membered ring compounds
The present invention is to provide an aliphatic nitrogen-containing 5-membered ring compound represented by the formula [I]: wherein symbols in the formula have the following meanings;
11/21/2006
7083977Monkey-origin embryonic stem cells
A method for producing a monkey-derived embryonic stem cell comprising the steps of carrying out fertilization by insemination by in vitro fertilization or intracytoplasmic sperm injection using a monkey ovum and monkey sperms, thereby giving a fertilized ovum, allo...
08/01/2006
7078522Pyridopyrimidine or naphthyridine derivative
A pyridopyrimidine or a naphthyridine derivative of the formula (I): wherein R1 is an optionally substituted nitrogen-containing heterocyclic group, etc.; R2 is H or a lower alkyl group; R
07/18/2006
7070946Bone metabolism related protein and gene thereof
The present invention is directed to a novel method of detecting a function or activity of a polypeptide which is related to bone metabolism, in particular, differentiation (maturation) of osteoblast or morphological change (retraction), specifically relating to a p...
07/04/2006
70675355-Phenylbenzylamine compounds, process for their production and intermediates for their synthesis
The present invention relates to a 5-phenylbenzylamine compound represented by the formula [1]: wherein Ring A represents a phenyl group having a substituent(s), Ra
06/27/2006
7060832Nitrogen-containing fused heterocyclic carboxylic acids having an absolute configuration of “R”
Nitrogen-containing fused heterocyclic carboxylic acid having an absolute configuration of “R” of the formula [XIX]: wherein Y is substituted or unsubstituted arylsulfonyl group or an alkylsulfonyl group, and...
06/13/2006
7045298Method for identifying or screening agonist and antagonist to PPAR
A method for identifying or screening an agonist for or antagonist to a peroxisome proliferator activated receptor (PPAR) which comprises allowing a test cell and a substance to be tested to coexist, and detecting a change in a ligand-dependent interaction between t...
05/16/2006
7026501Inhibitors of α4 mediated cell adhesion
The present invention relates to a phenylalanine derivative of Formula (I) wherein X1 is a halogen atom, X2 is a halogen atom, Q is a CH2R— is a carboxyl group which may be esterified; or a pharmaceutically acceptable salt thereof....
04/11/2006
7011776Method and apparatus for preparing microspheres
An improved method for the preparation of a microsphere from an emulsion wherein an organic phase containing an organic solvent having a boiling point lower than that of water and a hardly-water-soluble polymer is emulsified in an aqueous phase by an in-water drying...
03/14/2006
6897225Inhibitors of αLβ2 mediated cell adhesion
The present invention relates to a compound of the following formula: or a pharmaceutically acceptable salt thereof. Also disclosed are compositions containing the compound and methods of preparing and using the compou...
05/24/2005
6855843Inhibitors of α4 mediated cell adhesion
The present invention relates to a pharmaceutical composition comprising as an active ingredient a compound of formula (I), wherein Ring A is an aromatic or a heterocyclic ring; Q is a bond, carbonyl, lower alkylene, lower alkenylene, —O— -(lower alkylene)-, etc...
02/15/2005
6849622Aliphatic nitrogenous five-membered ring compounds
The present invention is to provide an aliphatic nitrogen-containing 5-membered ring compound represented by the formula [I]: wherein A represents —CH2— or —S—,
02/01/2005
6797709Aromatic nitrogen-containing 6-membered cyclic compounds
An aromatic nitrogen-containing 6-membered cyclic compound of the formula (I): wherein Ring A is a substituted or unsubstituted nitrogen-containing heterocyclic group; R1 is a substituted or unsubstituted lowe...
09/28/2004
6794154Remedies for kidney diseases and method for screening the same
The present invention provides a method for screening or identifying therapeutic or prophylactic agents for renal diseases, which comprises assaying a test substance for the activity of up-regulating the expression of fatty acid-binding protein (FABP), and novel mou...
09/21/2004
6780877Acid addition salt of optically active piperidine compound and process for preparing the same
The present invention is to provide a benzenesulfonic acid salt and a benzoic acid salt of (S)-4-[4-[(4-chlorophenyl)(2-pyridyl)methoxy]piperidino]butanoic acid represented by the formula (I): wherein * represents an asy...
08/24/2004
6730702Therapeutic agents for inflammatory diseases of intestine
The present invention provides a novel agent for prophylaxis or treatment of inflammatory bowel diseases for oral administration or intra-intestinal infusion, which comprises as an active ingredient a compound of the formula (I):
05/04/2004
6716983S type 2-substituted hydroxy-2-indolidinylbutyric ester compounds and process for preparation thereof
A process for preparing S type 2-substituted hydroxy-2-indolidinylbutyric ester compound [II]: wherein Ro is residue of nitrogen-containing fused heterocyclic carboxylic acid having absolute configuration of ...
04/06/2004
6699888Inhibitors of ଱L댢 mediated cell adhesion
The present invention relates to small molecules according to formula (I) that are potent inhibitors of ଱Lଲ.sub.2 mediated cell adhesion and which could be useful for the treatment of inflammatory diseases: ##STR1##...
03/02/2004
6692769Sustained-release particles
The present invention discloses sustained release particles having a mean particle size of 300 μm, or less, comprising a drug-containing core substance coated with a mixed coating of a hydrophobic organic compound-water-insoluble polymer, which prevents ...
02/17/2004
6692768Preparation method of drug-containing spherical fine particles
The present invention discloses an efficient preparation method of spherical fine particles containing a drug for an easily-swallowed, controlled-release preparation comprising the production of drug-containing spherical fine particles (mean particle size...
02/17/2004
6685617Inhibitors of 댔댡 mediated cell adhesion
The present invention relates to compound of formula (I), that are potent inhibitors of 댔ଲ.sub.1 mediated adhesion to either VCAM or CS-1 and which could be useful for the treatment of inflammatory diseases. Specifically, the molec...
02/03/2004
6656935Aromatic nitrogen-containing 6-membered cyclic compounds
An aromatic nitrogen-containing 6-membered cyclic compound of the formula (I): ##STR1## wherein Ring A is a substituted or unsubstituted nitrogen-containing heterocyclic group; R1 is a substituted or unsubstituted lower alkyl group, --NH--...
12/02/2003
6638534Preparation capable of releasing drug at target site in intestine
A preparation capable of releasing a medicinal substance at a targeted site in the intestine, wherein the preparation dose not releases medicinal substance in endogastri at all, but can quickly release a medicinal substance when it reaches the desired sit...
10/28/2003
6617456Camptothecin derivatives
A camptothecin derivative comprising a compound of the formula [I]: ##STR1## wherein R1, R2, R3, R4 and R5 are (A) adjacent two groups combine to form alkylene, or both are H, and one of the remaining ...
09/09/2003
6596752Inhibitors of 댔댡 mediated cell adhesion
The present invention relates to small molecules according to the formula [I]: ##STR1## which are potent inhibitors of 댔ଲ.sub.1 mediated adhesion to either VCAM or CS-1 and which can be used for treating or preventing ଱
07/22/2003
6579679Method for examining central nervous system diseases and method for screening remedies
The present invention relates to a method for screening and identifying therapeutic agents or preventive agents for central nervous system diseases which comprises assaying a suppressing effect of a test substance on an expression of a splicing variant tr...
06/17/2003
6521666Inhibitors of 댔 mediated cell adhesion
##STR1## The present invention relates to a pharmaceutical composition comprising as an active ingredient a compound of formula (I), wherein Ring A is an aromatic or a heterocyclic ring; Q is a bond, carbonyl, lower alkylene, lower alkenylene, --O-(lower ...
02/18/2003
6512118Camptothecin derivatives
A camptothecin derivative comprising a compound of the formula [I] is disclosed: ##STR1## wherein R1, R2, R3, R4 and R5 are (A) adjacent two groups combine to form alkylene, or both are H, and one of ...
01/28/2003
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