Gullapalli S - Search Results

1

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

Banerjee A, Patil S, Pawar MY, Gullapalli S, Gupta PK, Gandhi MN, Bhateja DK, Bajpai M, Sangana RR, Gudi GS, Khairatkar-Joshi N, Gharat LA. Banerjee A, et al. Among authors: gullapalli s. Bioorg Med Chem Lett. 2012 Oct 1;22(19):6286-91. doi: 10.1016/j.bmcl.2012.07.077. Epub 2012 Aug 8. Bioorg Med Chem Lett. 2012. PMID: 22944118

2

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

Banerjee A, Narayana L, Raje FA, Pisal DV, Kadam PA, Gullapalli S, Kumar H, More SV, Bajpai M, Sangana RR, Jadhav S, Gudi GS, Khairatkar-Joshi N, Merugu RR, Voleti SR, Gharat LA. Banerjee A, et al. Among authors: gullapalli s. Bioorg Med Chem Lett. 2013 Dec 15;23(24):6747-54. doi: 10.1016/j.bmcl.2013.10.027. Epub 2013 Oct 26. Bioorg Med Chem Lett. 2013. PMID: 24231362

3

Design, synthesis and pharmacological evaluation of novel polycyclic heteroarene ethers as PDE10A inhibitors: part II.

Das S, Shelke DE, Harde RL, Avhad VB, Khairatkar-Joshi N, Gullapalli S, Gupta PK, Gandhi MN, Bhateja DK, Bajpai M, Joshi AA, Marathe MY, Gudi GS, Jadhav SB, Mahat MY, Thomas A. Das S, et al. Among authors: gullapalli s. Bioorg Med Chem Lett. 2014 Aug 1;24(15):3238-42. doi: 10.1016/j.bmcl.2014.06.028. Epub 2014 Jun 19. Bioorg Med Chem Lett. 2014. PMID: 24980052

4

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

Lingam VS, Dahale DH, Rathi VE, Shingote YB, Thakur RR, Mindhe AS, Kummari S, Khairatkar-Joshi N, Bajpai M, Shah DM, Sapalya RS, Gullapalli S, Gupta PK, Gudi GS, Jadhav SB, Pattem R, Thomas A. Lingam VS, et al. Among authors: gullapalli s. J Med Chem. 2015 Oct 22;58(20):8292-308. doi: 10.1021/acs.jmedchem.5b01240. Epub 2015 Oct 7. J Med Chem. 2015. PMID: 26421921

5

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

Banerjee A, Yadav PS, Bajpai M, Sangana RR, Gullapalli S, Gudi GS, Gharat LA. Banerjee A, et al. Among authors: gullapalli s. Bioorg Med Chem Lett. 2012 May 1;22(9):3223-8. doi: 10.1016/j.bmcl.2012.03.025. Epub 2012 Mar 23. Bioorg Med Chem Lett. 2012. PMID: 22487174

6

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

Gullapalli S, Amrutkar D, Gupta S, Kandadi MR, Kumar H, Gandhi M, Karande V, Narayanan S. Gullapalli S, et al. Neuropharmacology. 2010 Jun;58(8):1215-9. doi: 10.1016/j.neuropharm.2010.03.001. Epub 2010 Mar 7. Neuropharmacology. 2010. PMID: 20214912

7

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

Charrua A, Cruz CD, Narayanan S, Gharat L, Gullapalli S, Cruz F, Avelino A. Charrua A, et al. Among authors: gullapalli s. J Urol. 2009 Jan;181(1):379-86. doi: 10.1016/j.juro.2008.08.121. Epub 2008 Nov 17. J Urol. 2009. PMID: 19010489

8

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

Gullapalli S, Ramarao P. Gullapalli S, et al. Neuropharmacology. 2002 Mar;42(4):467-75. doi: 10.1016/s0028-3908(01)00200-3. Neuropharmacology. 2002. PMID: 11955518

9

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

Gullapalli S, Gurumoorthy K, Kaul CL, Ramarao P. Gullapalli S, et al. Eur J Pharmacol. 2002 Jan 25;435(2-3):187-94. doi: 10.1016/s0014-2999(01)01593-x. Eur J Pharmacol. 2002. PMID: 11821025

10

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

Gullapalli S, Nemmani KV, Ramarao P. Gullapalli S, et al. Pharmacol Biochem Behav. 2002 May;72(1-2):93-9. doi: 10.1016/s0091-3057(01)00726-2. Pharmacol Biochem Behav. 2002. PMID: 11900774

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