Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Munikumar Reddy Doddareddy"'
Autor:
Namfon Pantarat, Danuta S. Kalinowski, David E. Hibbs, Des R. Richardson, Munikumar Reddy Doddareddy, Jennifer Ong, Darius J.R. Lane, Vera Richardson, Michael L.-H. Huang, Angelica M. Merlot, Ashleigh M. Fordham, Sumit Sahni
Publikováno v:
Oncotarget
// Angelica M. Merlot 1 , Sumit Sahni 1 , Darius J.R. Lane 1 , Ashleigh M. Fordham 1 , Namfon Pantarat 1 , David E. Hibbs 2 , Vera Richardson 1 , Munikumar R. Doddareddy 2 , Jennifer A. Ong 2 , Michael L.H. Huang 1 , Des R. Richardson 1,* and Danuta
Autor:
Shalini Srivastava, Pratik M. Oza, Rajeshwar Narlawar, Ramesh R. Mamidi, Dulal Panda, David E. Hibbs, Anusri Bhattacharya, Emma C. L. Marrs, Kishore Kunal, Paul W. Groundwater, Vivian Wan Yu Liao, John D. Perry, Munikumar Reddy Doddareddy
Publikováno v:
IndraStra Global.
Inhibition of FtsZ assembly has been found to stall bacterial cell division. Here, we report the identification of a potent carbocyclic curcumin analogue (2d) that inhibits Bacillus subtilis 168 cell proliferation by targeting the assembly of FtsZ. 2
Autor:
David E. Hibbs, Munikumar Reddy Doddareddy, Paul W. Groundwater, Azadeh Matin, Rebecca H. Roubin, Navnath Gavande, Srinivas Nammi
Publikováno v:
Bioorganic & Medicinal Chemistry. 21:766-778
Twenty three dual PPARα and γ molecules of natural product origin, previously reported by our group, were further investigated for pan PPAR transactivation against PPARδ. The in vitro cell toxicity profile, as well as, in silico study of the most
Autor:
David E. Hibbs, Veronika Bender, Eve Diefenbach, Nicholas Manolios, Munikumar Reddy Doddareddy, Marina Ali, Laura Raguine
Publikováno v:
Chemical Biology & Drug Design. 81:167-174
Core peptide is a hydrophobic peptide, the sequence of which is derived from the T-cell antigen receptor alpha-chain transmembrane region. Previous studies have shown that core peptide can inhibit T-cell-mediated immune responses both in vitro and in
Autor:
Samuel D. Banister, Robert H. Mach, Jinquan Cui, Miral Manoli, Iman A. Moussa, Munikumar Reddy Doddareddy, Michael Kassiou
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:5493-5497
Imidazolidine and 1,4-diazepane analogs of N-(2-benzofuranyl)methyl-N′-(4-alkoxybenzyl)piperazines were prepared to explore the effect of ring contraction and expansion on σ receptor affinity and subtype selectivity within a series of cyclic diami
Publikováno v:
Bulletin of the Korean Chemical Society. 32:2008-2014
Serotonin or 5-hydroxytryptamine subtype 2C (5-HT2C) receptor belongs to class A amine subfamily of Gprotein-coupled receptor (GPCR) super family and its ligands has therapeutic promise as anti-depressant and -obesity agents. So far, bovine rhodopsin
Autor:
Dhanaji Achyutrao Thorat, Tae-Joon Hong, Ji-Sook Hahn, Yong Seo Cho, Munikumar Reddy Doddareddy, Ae Nim Pae, Seon Hee Seo
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:1714-1720
Structure based drug design (SBDD) was used to discover heat shock protein 90 (HSP90) inhibitors useful in the treatment of cancer. By using the crystal structure of HSP90-ligand complex (1uyi), a docking model was prepared and was validated by exter
Publikováno v:
ChemMedChem. 5:716-729
Ligand-based in silico hERG models were generated for 2 644 compounds using linear discriminant analysis (LDA) and support vector machines (SVM). As a result, the dataset used for the model generation is the largest publicly available (see Supporting
Autor:
Judy Lin, Rajeshwar Narlawar, Johannes Brussee, Munikumar Reddy Doddareddy, Adriaan P. IJzerman, J. Robert Lane
Publikováno v:
Journal of Medicinal Chemistry. 53:3028-3037
Many G protein-coupled receptors (GPCRs), including the adenosine A(1) receptor (A(1)AR), have been shown to be allosterically modulated by small molecule ligands. So far, in the absence of structural information, the exact location of the allosteric
Autor:
Yong Seo Cho, Ae Nim Pae, Byung Ho Lee, Munikumar Reddy Doddareddy, Kwang-Seok Oh, Shanthi Nagarajan, Hyunah Choo
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:2759-2766
Control of NF-kappaB release through the inhibition of IKKbeta has been identified as a potential target for the treatment of inflammatory and autoimmune diseases. We have employed structure based virtual screening scheme to identify lead like molecu