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Reijo Backstrom Patents
Inventor:
Backstrom; Reijo
Address:
Helsinki, FI
No. of patents:
16
Patents:




Patent Number Title Of Patent Date Issued
6943164 Pharmaceutical solutions of levosimendan September 13, 2005
Levosimendan solutions for pharmaceutical use, and particularly for intravenous administration. The solutions of the invention have enhanced stability and they are particularly useful as infusion or injection solutions or infusion concentrates. Levosimendan is useful in the treatment
6903114 Derivatives of naphthalene with COMT inhibiting activity June 7, 2005
Compounds of formula (I'), wherein A, R.sub.1 to R.sub.3 and t are as defined in the disclosure, exhibit COMT enzyme inhibiting activity so that they are useful as COMT inhibitors.
6730673 Pharmaceutical solutions of levosimendan May 4, 2004
Levosimendan solutions for pharmaceutical use, and particularly for intravenous administration. The solutions of the invention have enhanced stability and they are particularly useful as infusion or injection solutions or infusion concentrates. Levosimendan is useful in the treatment
6699868 Pyridazinyl phenyl hydrazones useful against congestive heart failure March 2, 2004
Therapeutically active compounds of formula (I): ##STR1## in which R.sub.1 to R.sub.4 means hydrogen, alkyl, alkenyl, aryl, arylalkyl, carboxyalkyl, hydroxyalkyl or halogenalkyl, or R.sub.2 and R.sub.3 form a ring of 5-7 carbon atoms, R.sub.5 to R.sub.9 means hydrogen, alkyl, alke
6340764 Reference compound for use in the analysis of levosimendan batches January 22, 2002
A pyridazinyl derivative (I) and its use as a reference compound in the determination of potentially genotoxic impurities in levosimendan samples. An analytic method for the determination of potentially genotoxic impurities in levosimendan samples wherein (I) is used as a reference c
6201027 Substituted .beta. diketones and their use March 13, 2001
The invention relates to the compounds of formula I: ##STR1##wherein one of X.sub.1 and X.sub.2 is MeSO.sub.2 and the other one is hydrogen or halogen and X.sub.3 is hydrogen or halogen. These compounds have been found to be useful in the prevention and the treatment of respiratory d
6180789 Method for obtaining pure enantiomers of a pyridazinone derivative January 30, 2001
The present invention relates to a method for preparing optically active enantiomers of [[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-hydrazono]pro panedinitrile (I), particularly (-) enantiomer of (I). Furthermore, the invention relates to a novel crystalline polymorph
6121303 Pharmacologically active catechol derivatives September 19, 2000
A compound of formula I ##STR1## wherein R.sub.1 is nitro, halogeno or cyano group and R.sub.2 is a group selected from ##STR2## wherein Y and Z are independently oxygen, sulfur or NR, wherein R is hydrogen, straight or branched C.sub.1-8 alkyl, C.sub.5-7 cycloalkyl, phen
5889037 Pharmacologically active catechol derivatives March 30, 1999
5614541 Pharmacologically active catechol derivatives March 25, 1997
New catechol derivatives and pharmaceutically acceptable salts and esters thereof useful as pharmaceutical antioxidants are disclosed. Cellular damage by oxygen derived radicals is a significant factor in heart disease, rheumatoid arthritis, cancer, inflammatory disease, transplant r
5569657 (-)-[[4-(1,4,5,6-tetrahydro-4-m ethyl-6-oxo-3-pyridazinyl)phenyl]-hydrazono]propanedinitrile October 29, 1996
The compound (-)-[[4-(1,4,5,6 tetrahydro-4-methyl-6-oxo-3 pyridazinyl) phenyl]-hydrazono] propane dinitrile and its salts are prepared and used for treating congestive heart failure.
5512571 (-) [[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-hydra-zono] propanedinitrile April 30, 1996
Diastereomeric intermediate salts of formulae (IIIa) or (IIIb) ##STR1## are prepared.
5424428 ( -)-[[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-hydrazono]p r June 13, 1995
Optically substantially pure (-) enantiomer of [[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]hydrazono)prop anedinitrile or pharmaceutically acceptable salt thereof, intermediates and a process for the preparation are described. The product is useful as a cardiotonic age
5362733 Pharmacologically active catechol derivatives November 8, 1994
Compounds of formula(I) ##STR1## wherein R.sub.1 is nitro, halo, cyano and R.sub.2 is a group selected from ##STR2## wherein Y is oxygen or sulfur; X.sub.1 is NR wherein R is hydrogen, C.sub.1-8 alkyl or phenyl and pharmaceutically acceptable salts thereof are useful in the p
5356923 1-hydroxy-4(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone and anti-hypertensive use thereof October 18, 1994
5112861 Method of treating Parkinson's Disease using pentanedione derivatives May 12, 1992
The invention concerns a method for the treatment of Parkinson's Disease. The method comprises administering a catechol-O-methyl-transferase inhibiting amount of a compound having the formula I ##STR1## wherein R.sub.1 and R.sub.2 independently represent hydrogen, alkylcarbamoyl


 
 
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