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The Journal of Pharmacology and Experimental Therapeutics|September 1, 1984
Pharmacologic profile of a novel potent direct-acting dopamine agonist, (+)-4-propyl-9-hydroxynaphthoxazine [(+)-PHNO]G E Martin, M Williams, D J Pettibone, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1985
Selectivity of (+)-4-propyl-9-hydroxynaphthoxazine [(+)-PHNO] for dopamine receptors in vitro and in vivoG E Martin, M Williams, D J Pettibone, et al.
Life Sciences|January 1, 1989
[3H]L-657,743 (MK-912): a new, high affinity, selective radioligand for brain alpha 2-adrenoceptorsD J Pettibone, S D Flagg, J A Totaro, et al.
Biological Chemistry|March 22, 2001
Molecular cloning and pharmacological characterization of the canine B1 and B2 bradykinin receptorsJ F Hess, P J Hey, T B Chen, et al.
Toxicologic Pathology|March 1, 1995
The role of drug metabolism in drug discovery: a case study in the selection of an oxytocin receptor antagonist for developmentS H Chiu, K A Thompson, S H Vincent, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1986
L-654,284 a new potent and selective alpha 2-adrenoceptor antagonistD J Pettibone, B V Clineschmidt, V J Lotti, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|August 1, 1987
Pharmacological profile of a new potent and specific alpha 2-adrenoceptor antagonist, L-657,743D J Pettibone, B V Clineschmidt, V J Lotti, et al.
Life Sciences|January 1, 1992
Radioligand binding studies reveal marked species differences in the vasopressin V1 receptor of rat, rhesus and human tissuesD J Pettibone, M T Kishel, C J Woyden, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1988
A peripherally acting alpha-2 adrenoceptor antagonist: L-659,066B V Clineschmidt, D J Pettibone, V J Lotti, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1991
Antagonism of oxytocin in rats and pregnant rhesus monkeys by the novel cyclic hexapeptides, L-366,682 and L-366,948B V Clineschmidt, D J Pettibone, D R Reiss, et al.
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