Venkata Madhavi Yaddanapudi

Employment

• NIPER,Hyderabad Assistant Professor
  2013 - Present
• Dr. Reddys Laboratories, IPDO Scientist
  2008 - 2013

Education

• Indian Institute of Chemical Technology PhD
  2001 - 2007

Projects & Funding

Projects & funding information is unavailable.

Publications (17)

• Cinnamamide: An insight into the pharmacological advances and structure activity relationships
  European Journal of medicinal chemistry 2019 DOI: 10.1016/j.ejmech.2019.07.064
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• Facile synthesis of 1,2,3-triazole-fused indolo- and pyrrolo[1,4]diazepines, DNA-binding and evaluation of their anticancer activity
  Bio-Organic Chemistry 2019 DOI: 10.1016/j.bioorg.2019.103306
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• Natural product derived promising anti-MRSA drug leads: A review
  Bioorganic & Medicinal Chemistry 2019 DOI: 10.1016/j.bmc.2019.07.023
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• Promising antibacterial agents against multidrug resistant Staphylococcus aureus
  2019 DOI: 10.1016/j.bioorg.2019.103252
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• Catalyst‐Free Facile Synthesis of Polycyclic Indole/Pyrrole Substituted-1,2,3-triazoles
  Organic & Biomolecular Chemistry 2019 DOI: 10.1039/C9OB01560D
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• Synthesis of Indolo[1,2-b ]isoquinoline Derivatives by Lewis Acid-Catalyzed Intramolecular Friedel-Crafts Alkylation Reaction
  European Journal Of Organic Chemistry 2018 DOI: 10.1002/ejoc.201800162
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• "Targeting AMPK in Diabetes and Diabetic Complications: Energy homeostasis, Autophagy and Mitochondrial health"
  Current Medicinal Chemistry 2018
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• Synthesis of new 3-phenylquinazolin-4(3H)-one derivatives as potent antibacterial agents effective against methicillin- and vancomycin-resistant Staphylococcus aureus (MRSA and VRSA)
  BioOrganic Chemistry 2018 DOI: 10.1016/j.bioorg.2018.08.012
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• Synthesis of 1,2,3-triazole linked 4(3H)-Quinazolinones as potent antibacterial agents against multidrug-resistant Staphylococcus aureus
  European Journal Of Medicinal Chemistry 2018 DOI: 10.1016/j.ejmech.2018.08.070
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• Synthesis and evaluation of new 4-oxoquinazolin-3(4H)-yl)benzoic acid and benzamide derivatives as potent antibacterial agents effective against multidrug resistant Staphylococcus aureus
  Bioorganic chemistry 2018 DOI: 10.1016/j.bioorg.2018.11.007
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