Design, Synthesis and Biological Evaluation of Oxindole-Based Chalcones as Small-Molecule Inhibitors of Melanogenic Tyrosinase von Suthar, Sharad Kumar, Bansal, Sumit, Narkhede, Niteen, Guleria, Manju, Alex, Angel Treasa, Joseph, Alex

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Ingenuity pathway analysis of α -synuclein predicts potential signaling pathways, network molecules, biological functions, and its role in neurological diseases von Suthar, Sharad Kumar, Lee, Sang-Yoon

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The Role of Superoxide Dismutase 1 in Amyotrophic Lateral Sclerosis: Identification of Signaling Pathways, Regulators, Molecular Interaction Networks, and Biological Functions thro... von Suthar, Sharad Kumar, Lee, Sang-Yoon

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Design, synthesis, and biological evaluation of oxindole derivatives as antidepressive agents von Suthar, Sharad Kumar, Bansal, Sumit, Alam, Md. Maqusood, Jaiswal, Varun, Tiwari, Amit, Chaudhary, Anil, Alex, Angel Treasa, Joseph, Alex

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Bioinformatic Analyses of Canonical Pathways of TSPOAP1 and its Roles in Human Diseases von Suthar, Sharad Kumar, Alam, Mohammad Maqusood, Lee, Jihye, Monga, Jitender, Joseph, Alex, Lee, Sang-Yoon

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Molecular docking and biological evaluation of hydroxy-substituted (Z)-3-benzylideneindolin-2-one chalcones for the lead identification as tyrosinase inhibitors von Suthar, Sharad Kumar, Aggarwal, Vaibhav, Chauhan, Monika, Sharma, Ankesh, Bansal, Sumit, Sharma, Manu

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Recent Developments in Chimeric NSAIDs as Safer Anti-Inflammatory Agents von Suthar, Sharad Kumar, Sharma, Manu

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Truncation or proteolysis of α-synuclein in Parkinsonism von Suthar, Sharad Kumar, Lee, Sang-Yoon

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Tea: A native source of antimicrobial agents von Bansal, Sumit, Choudhary, Shivani, Sharma, Manu, Kumar, Suthar Sharad, Lohan, Sandeep, Bhardwaj, Varun, Syan, Navneet, Jyoti, Saras

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(+)-Cyanidan-3-ol inhibits epidermoid squamous cell carcinoma growth via inhibiting AKT/mTOR signaling through modulating CIP2A-PP2A axis von Monga, Jitender, Suthar, Sharad Kumar, Rohila, Deepak, Joseph, Alex, Chauhan, Chetan Singh, Sharma, Manu

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Design and synthesis of novel 2-phenyl-5-(1,3-diphenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazoles as selective COX-2 inhibitors with potent anti-inflammatory activity von Bansal, Sumit, Bala, Manju, Suthar, Sharad Kumar, Choudhary, Shivani, Bhattacharya, Shoumyo, Bhardwaj, Varun, Singla, Sumit, Joseph, Alex

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Novel quinolone substituted thiazolidin-4-ones as anti-inflammatory, anticancer agents: Design, synthesis and biological screening von Suthar, Sharad Kumar, Jaiswal, Varun, Lohan, Sandeep, Bansal, Sumit, Chaudhary, Anil, Tiwari, Amit, Alex, Angel Treasa, Joesph, Alex

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Chiral HPLC separation of enantiomeric blebbistatin derivatives and racemization analysis in vertebrate tissues von Suthar, Sharad Kumar, Rauscher, Anna Á., Winternitz, Máté, Gyimesi, Máté, Málnási-Csizmadia, András

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First-in-class drug candidate (MPH-220) efficiently improves spastic gait disorders by selective inhibition of fast skeletal muscle myosin-2 von Gyimesi, Mate, Horvath, Adam I., Turos, Demeter, Kumar Suthar, Sharad, Penzes, Mate, Canon, Louise, Kikuti, Carlos, Ruppel, Kathleen, Trivedi, Darshan V., Spudich, James A., Rauscher, Anna Á., Kovacs, Mihaly, Komoly, Samuel, Houdusse, Anne M., Malnasi-Csizmadia, Andras

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Single Residue Variation in Skeletal Muscle Myosin Enables Direct and Selective Drug Targeting for Spasticity and Muscle Stiffness von Gyimesi, Máté, Horváth, Ádám I., Túrós, Demeter, Suthar, Sharad Kumar, Pénzes, Máté, Kurdi, Csilla, Canon, Louise, Kikuti, Carlos, Ruppel, Kathleen M., Trivedi, Darshan V., Spudich, James A., Lőrincz, István, Rauscher, Anna Á., Kovács, Mihály, Pál, Endre, Komoly, Sámuel, Houdusse, Anne, Málnási-Csizmadia, András

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Quantitative structure–activity relationship (QSAR) studies as strategic approach in drug discovery von Patel, Harun M., Noolvi, Malleshappa N., Sharma, Poonam, Jaiswal, Varun, Bansal, Sumit, Lohan, Sandeep, Kumar, Suthar Sharad, Abbot, Vikrant, Dhiman, Saurabh, Bhardwaj, Varun

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Design and synthesis of novel 4-(4-oxo-2-arylthiazolidin-3-yl)benzenesulfonamides as selective inhibitors of carbonic anhydrase IX over I and II with potential anticancer activity von Suthar, Sharad Kumar, Bansal, Sumit, Lohan, Sandeep, Modak, Vikarm, Chaudhary, Anil, Tiwari, Amit

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Synthesis of lantadene analogs with marked in vitro inhibition of lung adenocarcinoma and TNF-α induced nuclear factor-kappa B (NF-κB) activation von Monika, Sharma, Ankesh, Suthar, Sharad Kumar, Aggarwal, Vaibhav, Lee, Hong Boon, Sharma, Manu

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The synthesis of non-steroidal anti-inflammatory drug (NSAID)–lantadene prodrugs as novel lung adenocarcinoma inhibitors via the inhibition of cyclooxygenase-2 (COX-2), cyclin D1 a... von Suthar, Sharad Kumar, Lee, Hong Boon, Sharma, Manu

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Improved Inhibitory and Absorption, Distribution, Metabolism, Excretion, and Toxicology (ADMET) Properties of Blebbistatin Derivatives Indicate That Blebbistatin Scaffold Is Ideal... von Gyimesi, Mate, Rauscher, Anna A., Suthar, Sharad Kumar, Hamow, Kamiran A., Oravecz, Kinga, Lorincz, Istvan, Borhegyi, Zsolt, Deri, Mate T., Kiss, Adam F., Monostory, Katalin, Szabo, Pal Tamas, Nag, Suman, Tomasic, Ivan, Krans, Jacob, Tierney, Patrick J., Kovacs, Mihaly, Kornya, Laszlo, Malnasi-Csizmadia, Andras

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