S. Gullapalli

发表

Design, Synthesis, and Pharmacological Evaluation of 5,6-Disubstituted Pyridin-2(1H)-one Derivatives as Phosphodiesterase 10A (PDE10A) Antagonists.

V. S. Lingam, Dnyaneshwar H. Dahale, Vijayesh Rathi, 2015, Journal of medicinal chemistry.

Characterization of active and inactive states of CB1 receptor and the differential binding state modulation by cannabinoid agonists, antagonists and inverse agonists

S. Gullapalli, V. Karande, M. R. Kandadi, 2010, Neuropharmacology.

GRC-6211, a new oral specific TRPV1 antagonist, decreases bladder overactivity and noxious bladder input in cystitis animal models.

S. Gullapalli, S. Narayanan, L. Gharat, 2009, The Journal of urology.

Role of L-type Ca2+ channels in attenuated morphine antinociception in streptozotocin-diabetic rats.

S. Gullapalli, P. Ramarao, C. Kaul, 2002, European journal of pharmacology.

Imidazopyridazinones as novel PDE7 inhibitors: SAR and in vivo studies in Parkinson's disease model.

Mahesh Y. Pawar, Neelima Khairatkar-Joshi, M. Bajpai, 2012, Bioorganic & medicinal chemistry letters.

L-type Ca2+ channel modulation by dihydropyridines potentiates κ-opioid receptor agonist induced acute analgesia and inhibits development of tolerance in rats

S. Gullapalli, P. Ramarao, 2002, Neuropharmacology.

Isothiazole and isoxazole fused pyrimidones as PDE7 inhibitors: SAR and pharmacokinetic evaluation.

M. Bajpai, S. Gullapalli, G. Gudi, 2012, Bioorganic & medicinal chemistry letters.

Regulation of Opioid Receptors by Their Endogenous Opioid Peptides

S. Gullapalli, J. Pintar, L. Devi, 2021, Cellular and molecular neurobiology.

Abstract 1701: EPL-1410, a novel fused heterocycle based orally active dual inhibitor of IDO1/TDO2, as a potential immune-oncology therapeutic

P. Singh, S. Gullapalli, M. K. Gurjar, 2018, Immunology.

Regulation of dihydropyridine-sensitive Ca(2+) channels during naloxone-induced opioid supersensitivity in rats.

S. Gullapalli, P. Ramarao, 2002, European journal of pharmacology.

Modulation of Opiate-Related Signaling Molecules in Morphine-Dependent Conditioned Behavior: Conditioned Place Preference to Morphine Induces CREB Phosphorylation

S. Gullapalli, L. Devi, J. Morón, 2010, Neuropsychopharmacology.

Role of Ca2+ channels on the hypothermic response produced by activation of κ-opioid receptors

S. Gullapalli, P. Ramarao, K. Nemmani, 2002, Pharmacology Biochemistry and Behavior.

Role of L-type Ca2+ channels in pertussis toxin induced antagonism of U50,488H analgesia and hypothermia

S. Gullapalli, P. Ramarao, 2002, Brain Research.

Regulation of Opioid Receptors by Their Endogenous Opioid Peptides

S. Gullapalli, J. Pintar, L. Devi, 2021, Cellular and Molecular Neurobiology.

Discovery of benzo[d]imidazo[5,1-b]thiazole as a new class of phosphodiesterase 10A inhibitors.

Neelima Khairatkar-Joshi, M. Bajpai, S. Gullapalli, 2013, Bioorganic & medicinal chemistry letters.

Drug Target Identification and Validation

Srinivas Gullapalli, S. Gullapalli, 2021, Drug Discovery and Development.

Potentiation of κ-opioid receptor agonist-induced analgesia and hypothermia by fluoxetine

S. Gullapalli, P. Ramarao, K. Nemmani, 2001, Pharmacology, Biochemistry and Behavior.

Imidazopyridazinones as novel PDE7 inhibitors: SAR and in vivo studies in Parkinson's disease model.

Mahesh Y. Pawar, Neelima Khairatkar-Joshi, M. Bajpai, 2012, Bioorganic & medicinal chemistry letters.