1
Kevin Rodzinak
Armstrong Donna J, Hu Essa H, Kelly Michael J Iii, Layton Mark E, Li Yiwei, Liang Jun, Rodzinak Kevin J, Rossi Michael A, Sanderson Philip E, Wang Jiabing: Inhibitors of akt activity. Merck & Co, Armstrong Donna J, Hu Essa H, Kelly Michael J Iii, Layton Mark E, Li Yiwei, Liang Jun, Rodzinak Kevin J, Rossi Michael A, Sanderson Philip E, Wang Jiabing, MERCK 126 East Lincoln Avenue Rahway NJ 07065 0907, December 21, 2006: WO/2006/135627 (19 worldwide citation)

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt ...


2
Kevin Rodzinak
Arruda Jeannie M, Campbell Brian T, Cosford Nicholas D P, Hoffman Jacob M, Hu Essa H, Layton Mark E, Li Yiwei, Liang Jun, Rodzinak Kevin J, Siu Tony, Stearns Brian A, Tehrani Lida R: Inhibitors of akt activity. Merck & Co, Arruda Jeannie M, Campbell Brian T, Cosford Nicholas D P, Hoffman Jacob M, Hu Essa H, Layton Mark E, Li Yiwei, Liang Jun, Rodzinak Kevin J, Siu Tony, Stearns Brian A, Tehrani Lida R, MERCK 126 East Lincoln Avenue Rahway NJ 07065 0907, June 22, 2006: WO/2006/065601 (17 worldwide citation)

The present invention is directed to compounds which contain substituted naphthyridines which inhibit the activity of Akt, a serine/threonine protein kinase. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for treating cancer ...


3
Kevin Rodzinak
Layton Mark E, Rodzinak Kevin J, Kelly Michael J Iii, Sanderson Philip E: N-alkyl-azacycloalkyl nmda/nr2b antagonists. Merck & Co, Layton Mark E, Rodzinak Kevin J, Kelly Michael J Iii, Sanderson Philip E, MERCK 126 East Lincoln Avenue Rahway New Jersey 07065 0907, October 26, 2006: WO/2006/113471 (3 worldwide citation)

Compounds represented by Formula (I): and/or pharmaceutically acceptable salts, individual enantiomers and stereoisomers thereof, are effective as NMDA/NR2B antagonists useful for treating conditions such as pain, Parkinson’s disease, Alzheimer’s disease, epilepsy, depression, anxiety, ischemic brai ...


4
Kevin Rodzinak
Layton Mark E, Rodzinak Kevin J, Sanderson Philip E: Inhibitors of akt activity. Merck & Co, Layton Mark E, Rodzinak Kevin J, Sanderson Philip E, MERCK 126 East Lincoln Avenue Rahway New Jersey 07065 0907, June 12, 2008: WO/2008/070134 (3 worldwide citation)

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt ...


5
Kevin Rodzinak
Layton Mark E, Rodzinak Kevin J, Kelly Michael J Iii, Sanderson Philip E: 1,3-disubstituted heteroaryl nmda/nr2b antagonists. Merck & Co, Layton Mark E, Rodzinak Kevin J, Kelly Michael J Iii, Sanderson Philip E, MERCK 126 East Lincoln Avenue Rahway New Jersey 07065 0907, February 16, 2006: WO/2006/017409 (2 worldwide citation)

Compounds represented by Formula I: (wherein A, B, D, P, Q, R1, R2, R3, W and Y are described herein) or pharmaceutically acceptable salts thereof, are effective as NMDA/NR2B antagonists useful for treating neurological conditions such as, for example, pain, Parkinson’s disease, Alzheimer’s disease, ...


6
Kevin Rodzinak
Jeannie M Arruda, Brian T Campbell, Nicholas DP Cosford, Jacob M Hoffman, Essa H Hu, Mark E Layton, Yiwei Li, Jun Liang, Kevin J Rodzinak, Tony Siu, Brian A Stearns, Lida R Tehrani, Mark T Bilodeau, Peter J Manley: Inhibitors of Akt Activity. Merck And Co, November 20, 2008: US20080287457-A1

The present invention is directed to compounds which contain substituted naphthyridines which inhibit the activity of Akt, a serine/threonine protein kinase. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for treating cancer ...


7
Kevin Rodzinak
Mark E Layton, Kevin J Rodzinak, Michael J Kelly, Philip E Sanderson: 1,3-Disubstituted Heteroaryl Nmda/Nr2b Antagonists. Merck And Co, December 20, 2007: US20070293515-A1

Compounds represented by Formula I: (wherein A, B, D, P, Q, R1, R2, R3, W and Y are described herein) or pharmaceutically acceptable salts thereof, are effective as NMDA/NR2B antagonists useful for treating neurological conditions such as, for example, pain, Parkinson's disease, Alzheimer's disease, ...


8
Kevin Rodzinak
Donna J Armstrong, Essa H Hu, Michael J Kelly III, Mark E Layton, Yiwei Li, Jun Liang, Kevin J Rodzinak, Michael A Rossi, Philip E Sanderson, Jiabing Wang: Inhibitors of akt activtiy. Merck, September 2, 2010: US20100222321-A1

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt ...


9
Kevin Rodzinak
Mark E Layton, Kevin J Rodzinak, Philip E Sanderson: Inhibitors of akt activity. Merck And Co, January 28, 2010: US20100022573-A1

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt ...


10
Holloway M Katharine, Liverton Nigel J, Ludmerer Steven W, Mccauley John A, Olsen David B, Rudd Michael T, Vacca Joseph P: Hcv ns3 protease inhibitors. Merck & Co, Holloway M Katharine, Liverton Nigel J, Ludmerer Steven W, Mccauley John A, Olsen David B, Rudd Michael T, Vacca Joseph P, MERCK 126 East Lincoln Avenue Rahway NJ 07065 0907, November 9, 2006: WO/2006/119061 (105 worldwide citation)

The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections. I



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