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Daniel Jon Sall Patents
Inventor:
Sall; Daniel Jon
Address:
Greenwood, IN
No. of patents:
34
Patents:




Patent Number Title Of Patent Date Issued
7297706 Certain glycine derivatives as factor Xa inhibitors for use in the treatment of thrombotic disor November 20, 2007
Compounds of formula (I) ##STR00001## in which R, R.sup.1, R.sup.2, n and X.sup.1 have the meanings given in the specification are Factor Xa inhibitors useful in the treatment of thrombotic disorders.
7294627 Chemical compounds November 13, 2007
Compounds of formula (I) ##STR00001## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4, have the meanings given in the specification are Factor Xa inhibitors useful in the treatment of thrombotic disorders.
7265127 .beta..sub.3 adrenergic agonists September 4, 2007
The present invention relates to 2-imidazo[1,2-a]pyridine group containing .beta..sub.3 adrenergic receptor agonists or pharmaceutical salts thereof.
7265121 Chemical compounds September 4, 2007
Compounds of formula (I) ##STR00001## in which R.sup.1, R.sup.2 and X.sup.4 have the meanings given in the specification are Factor Xa inhibitors useful in the treatment of thrombotic disorders.
7253181 .beta..sub.3 adrenergic agonists August 7, 2007
The present invention relates to pyrrolopyridine-3-yl group containing .beta..sub.3 adrenergic receptor agonists or pharmaceutical salts thereof.
7241772 .beta..sub.3 adrenergic agonists July 10, 2007
The present invention relates to 2-imidazo[1,5-a]pyridine containing .beta..sub.3 adrenergic receptor agonists or pharmaceutical salts thereof.
7208505 .beta.3 adrenergic agonists April 24, 2007
The present invention relates to a .beta.3 adrenergic receptor agonist of formula (I); or a pharmaceutical salt thereof; which is capable of increasing lipolysis and energy expenditure in cells and, therefore, is useful, e.g., for treating Type 2 diabetes and/or obesity ##STR00001##
7205407 3-Substituted oxindole .beta.3 agonists April 17, 2007
The present invention relates to a .beta.3 adrenergic receptor agonist of Formula (I) or a pharmaceutical salt thereof; useful for treating Type II diabetes and/or obesity ##STR00001##
7160909 Cyclopenta[b]indole derivatives as sPLA.sub.2 inhibitors January 9, 2007
A novel class of tricyclic compounds of the following formula (I) is disclosed together with the use of such compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of Inflammatory Diseases such as septic shock.
7122680 3-Substituted oxindole .beta..sub.3 agonsists October 17, 2006
The present invention relates to a .beta..sub.3 adrenergic receptor agonist of formula I: ##STR00001## or a pharmaceutical salt thereof; which is useful for treating Type II diabetes and/or obesity.
7115609 Alanyl-piperidine heterocyclic derivatives useful against cardiovascular diseases October 3, 2006
Compounds of formula (I) ##STR00001## in which R.sup.1, R.sup.2, n and X.sup.1 have the meanings given in the specification are Factor Xa inhibitors useful in the treatment of thrombotic disorders.
7109231 Cyclohept[b]indole derivatives September 19, 2006
A novel class of tricyclic compounds of the following formula (I): (formula I); is disclosed together with the use of such compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of inflammatory diseases such as septic shock ##STR00001##
7087635 3-substituted oxindole .beta.3 agonists August 8, 2006
The present invention relates to a .beta.3 adrenergic receptor agonist of formula I: ##STR00001## or a pharmaceutical salt thereof; which is capable of increasing lipolysis and energy expenditure in cells and, therefore, is useful for treating Type 2 diabetes and/or obesity.
7078415 Certain glycine derivatives as factor Xa inhibitors for use in the treatment of thrombotic disor July 18, 2006
Compounds of formula (I) ##STR00001## in which R, R.sup.1, R.sup.2, n and X.sup.1 have the meanings given in the specification are Factor Xa inhibitors useful in the treatment of thrombotic disorders.
7071208 .beta..sub.3 Adrenergic agonists July 4, 2006
The present invention relates to a .beta..sub.3 adrenergic receptor agonist of formula (I) or a pharmaceutical salt thereof; useful for treating Type II diabetes and/or obesity.
6992100 sPLA.sub.2 inhibitors January 31, 2006
A novel class of tetracyclic compounds is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of Inflammatory Diseases such as septic shock.
6974831 sPLA2 inhibitors December 13, 2005
A novel class of cycloalkyl fused indole compounds is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of Inflammatory Diseases such as septic shock.
6930123 sPLA2 inhibitors August 16, 2005
A novel class of benz[f]indole compounds is disclosed together with the use of such compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of Inflammatory Diseases such as septic shock.
6916840 Spla2 inhibitors July 12, 2005
A novel class of benz[g]indole compounds is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of Inflammatory Diseases such as septic shock.
6911463 3-substituted oxindole .beta.-3 agonists June 28, 2005
The present invention relates to a .beta.3 adrenergic receptor agonist of formula (I); or a pharmaceutical salt thereof; which is capable of increasing lipolysis and energy expenditure in cells and, therefore, is useful for treating Type 2 diabetes and/or obesity.
6872743 sPLA2 inhibitors March 29, 2005
A novel class of tetracyclic compounds represented by the formula I ##STR1##wherein R1, R2, R3, R4, R5, R6, R7, A, B, C, D, E, and n are as defined is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of Inflammatory Dise
6825220 3-Substituted oxindole .beta. 3 agonists November 30, 2004
The present invention relates to a .beta.;3 adrenergic receptor agonist of formula I: (1); or a pharmaceutical salt thereof; which is useful for treating Type II diabetes and/or obesity.
6730792 .beta.3 adrenergic agonists May 4, 2004
The present invention relates to a .beta..sub.3 adrenergic receptor agonist of formula (I) or a pharmaceutical salt thereof, which is capable of increasing lipolysis and energy expenditure in cells and, therefore, is useful for treating Type II diabetes and/or obesity. The compound can a
6713645 Substituted tricyclics March 30, 2004
A class of novel tricyclics is disclosed together with the use of such compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of conditions such as septic shock.
6620837 Antithrombotic agents September 16, 2003
This application relates to novel compounds of formula (I) (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula (I), and the use of defined compounds
6448284 Substituted tricyclics September 10, 2002
A class of tricycles is disclosed together with the use of such for inhibiting Spla.sub.2 mediated release of fatty acids for the treatment of conditions such as septic shock.
6359136 Antithrombotic agents March 19, 2002
This application relates to novel compounds of formula I (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula I, and the use of the compounds of formu
6274578 sPLA2 inhibitor ester August 14, 2001
The compound, ((3(2-amino-1,2-dioxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-4-yl)oxy)ac etic acid N-morpholino ester, is disclosed together with its use as a highly bioavailable indole sPLA.sub.2 inhibitor compound.
6265416 Antithrombotic agents July 24, 2001
This application relates to novel compounds of formula I (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula I, and the use of the compounds of formu
6251921 Antithrombotic diamines June 26, 2001
This application relates to the use as thrombin inhibitors, coagulation inhibitors and thromboembolic disorder agents of diamines of formula I as defined herein. It also provides novel compounds of formula I, processes and intermediates for their preparation, and pharmaceutical formulati
6177440 Substituted tricyclics January 23, 2001
A class of novel tricyclics is disclosed together with the use of such compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of conditions such as septic shock.
6140327 Morpholino-n-ethyl ester derivative of an indole sPLA.sub.2 inhibitor October 31, 2000
The compound, ((3-(2-amino-1,2-dioxoethyl)-2-ethyl-1-(phenylmethyl)-1H-indol-4-yl)oxy)ac etic acid morpholino-N-ethyl ester, is disclosed together with its use as a highly bioavailable indole compound for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of condition
6133262 Antithrombotic agents October 17, 2000
This application relates to novel compounds of formula I (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula I, and the use of the compounds of formu
6025382 Antithrombotic diamines February 15, 2000
This application relates to the use as thrombin inhibitors, coagulation inhibitors and thromboembolic disorder agents of diamines of formula I as defined herein. It also provides novel compounds of formula I, processes and intermediates for their preparation, and pharmaceutical formulati


 
 
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