Search Results - Freidinger, R O

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  1. 1
    De novo design of a novel oxazolidinone analogue as a potent and selective alpha1A adrenergic receptor antagonist with high oral bioavailability

    De novo design of a novel oxazolidinone analogue as a potent and selective alpha1A adrenergic receptor antagonist with high oral bioavailability by Lagu, B, Tian, D, Jeon, Y, Li, C, Wetzel, J M, Nagarathnam, D, Shen, Q, Forray, C, Chang, R S, Broten, T P, Ransom, R W, Chan, T B, O'Malley, S S, Schorn, T W, Rodrigues, A D, Kassahun, K, Pettibone, D J, Freidinger, R O, Gluchowski, C

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  2. 2
    Discovery of a Potent, Non-peptide Bradykinin B1 Receptor Antagonist

    Discovery of a Potent, Non-peptide Bradykinin B1 Receptor Antagonist by Su, Dai-Shi, Markowitz, M. Kristine, DiPardo, Robert M, Murphy, Kathy L, Harrell, C. Meacham, O'Malley, Stacy S, Ransom, Richard W, Chang, Raymond S. L, Ha, Sookhee, Hess, Fred J, Pettibone, Douglas J, Mason, Glenn S, Boyce, Susan, Freidinger, Roger M, Bock, Mark G

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  3. 3
    Development of an efficient and selective radioligand for bradykinin B1 receptor occupancy studies

    Development of an efficient and selective radioligand for bradykinin B1 receptor occupancy studies by SU, Dai-Shi, MARKOWITZ, M. Kristine, WALLACE, Michael A, RAAB, Conrad E, DEAN, Dennis C, PETTIBONE, Douglas J, FREIDINGER, Roger M, BOCK, Mark G, MURPHY, Kathy L, WAN, Bang-Lin, ZRADA, Matthew M, HARRELL, C. Meacham, O'MALLEY, Stacy S, HESS, J. Fred, RANSOM, Rick W, CHANG, Ray S

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  4. 4
    Benzodiazepines as Potent and Selective Bradykinin B1 Antagonists

    Benzodiazepines as Potent and Selective Bradykinin B1 Antagonists by Wood, Michael R, Kim, June J, Han, Wei, Dorsey, Bruce D, Homnick, Carl F, DiPardo, Robert M, Kuduk, Scott D, MacNeil, Tanya, Murphy, Kathy L, Lis, Edward V, Ransom, Richard W, Stump, Gary L, Lynch, Joseph J, O'Malley, Stacey S, Miller, Patricia J, Chen, Tsing-Bau, Harrell, Charles M, Chang, Raymond S. L, Sandhu, Punam, Ellis, Joan D, Bondiskey, Peter J, Pettibone, Douglas J, Freidinger, Roger M, Bock, Mark G

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  5. 5
    Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 2. Approaches To Eliminate Opioid Agonist Metabolites via Modification of Linker and 4-Methoxycarbonyl-4-phenylpiperidine Moiety

    Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 2. Approaches To Eliminate Opioid Agonist Metabolites via Modification of Linker and 4-Methoxycarbonyl-4-phen... by Murali Dhar, T. G, Nagarathnam, Dhanapalan, Marzabadi, Mohammad R, Lagu, Bharat, Wong, Wai C, Chiu, George, Tyagarajan, Sriram, Miao, Shou Wu, Zhang, Fengqi, Sun, Wanying, Tian, Dake, Shen, Quanrong, Zhang, Jack, Wetzel, John M, Forray, Carlos, Chang, Raymond S. L, Broten, Theodore P, Schorn, Terry W, Chen, Tsing Bao, O'Malley, Stacy, Ransom, Richard, Schneck, Kathryn, Bendesky, Robert, Harrell, Charles M, Vyas, Kamlesh P, Zhang, Kanyin, Gilbert, John, Pettibone, Douglas J, Patane, Michael A, Bock, Mark G, Freidinger, Roger M, Gluchowski, Charles

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