Sonali Rudra

Employment

• Adamas University Professor of Practice
  2024 - Present
• TCG Lifesciences (India) Associate Director
  2008 - 2023
• Ranbaxy Research Labs Group Leader
  1999 - 2008

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (11)

• Synthesis of stereo-enriched bis glyco-cyclohexylamines by a one pot dual Petasis reaction
  Tetrahedron Letters 2024 DOI: 10.1016/j.tetlet.2024.155025
  +Save
• Discovery of KB-0742, a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of CDK9 for MYC-Dependent Cancers
  Journal of Medicinal Chemistry 2023 DOI: 10.1021/acs.jmedchem.3c01233
  +Save
• Diastereo- and regioselective petasis aryl and allyl boration of ninhydrins towards synthesis of functionalized indene-diones and dihydrobenzoindeno-oxazin-ones
  Molecular Diversity 2023 DOI: 10.1007/s11030-022-10496-4
  +Save
• Synthesis, anti-cancer activity and molecular docking studies of new nicotinamide containing EP4 antagonists
  Journal of Molecular Structure 2022 DOI: 10.1016/j.molstruc.2022.132730
  +Save
• Synthesis of δ,δ‐Diaryl‐α‐cyanoacrylamides and δ,δ‐Diarylallylidiene Malononitriles by Pd(OAc)2 Catalyzed Mizoroki‐Heck Reaction
  ChemistrySelect 2021 DOI: 10.1002/slct.202103376
  +Save
• Synthesis and biological activity of novel oxazolidinones
  Bioorganic & Medicinal Chemistry Letters 2009 DOI: 10.1016/j.bmcl.2009.09.054
  +Save
• Synthesis and antibacterial activity of potent heterocyclic oxazolidinones and the identification of RBx 8700
  Bioorganic & Medicinal Chemistry Letters 2007 DOI: 10.1016/j.bmcl.2007.10.061
  +Save
• Small-molecule inhibitors of PDE-IV and -VII in the treatment of respiratory diseases and chronic inflammation
  Expert Opinion on Investigational Drugs 2007 DOI: 10.1517/13543784.16.10.1585
  +Save
• Synthesis and SAR of novel oxazolidinones: Discovery of ranbezolid
  Bioorganic & Medicinal Chemistry Letters 2005 DOI: 10.1016/j.bmcl.2005.06.063
  +Save
• Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes
  Bioorganic & Medicinal Chemistry 2003 DOI: 10.1016/s0968-0896(02)00606-5
  +Save