DR. GAUTAM PANDA
 
...

 

Scientist E- II
Medicinal and Process Chemistry Division
Central Drug Research Institute
Chattar Manzil Palace
Lucknow 226001, UP, India


 
 
Phone No. +91-0522-2612411-18 (7 lines), 4603 (off), 4385 (lab), 9450657049 (Cell)
Fax No. +91-0522-2623405, 2623938
E- Mail gautam.panda@gmail.com,gautam_panda@cdri.res.in
Educational Qualifications M.Sc. (IIT Kharagpur, 1993), Ph.D. (University of Hyderabad, 2000)
Research Experience (Area)

2002 (February)-todate, Scientist, CDRI, Lucknow;

 
POST -DOCTORAL RESEARCH
 

Visiting Fellow, National Tsing Hua University, Taiwan; NSERC

Visiting Postdoctoral Fellow, Department of Chemistry, University of Ottawa with Prof. Howard Alper (http://www.science.ca/scientists/scientistprofile.php?pID=248) and National Research Council, Ottawa, Canada with Dr. Prabhat Arya (http://steacie.nrc-cnrc.gc.ca/personal/arya/arya_index_e.html)
 
CURRENT AREAS OF INTEREST

Synthetic Organic Chemistry; Bioorganic and Medicinal Chemistry; Chemical Biology
Sub Area of Research:
i) Design, synthesis and development of target based new chemical entities for Breast Cancer, Tuberculosis and Malaria;
ii) [6-5-6] and [6-5-5]tricyclic core embedded new heterocycles (Taiwaniaquinoid like structures) as anticancer agents;
iii) Organic synthesis of target and diversity oriented natural products (alkaloids) and amino acid based natural product like designed chiral molecules through identification of new synthetic methodologies;
iv) Design, synthesis and bioevaluation of benzofused oxaheterocycles using b-Hydroxy-a-tosyloxy Esters obtained from Sharpless epoxidation and dihydroxylation reaction
Ongoing/Completed Project Title:
a)“Design and Development of Tissue Selective Antiestrogens” of Rs. 11,59,000/- from DST, New Delhi has been completed as Principal Investigator (PI). b) “Design and Synthesis of Novel SERMs for the management of Osteoporosis and other estrogen related disorders” of Rs. 17,00,000/- from ICMR, New Delhi is ongoing as PI. c)“Diversity Oriented Organic Synthesis of Small But Smart Molecules In Drug Discovery Research” of Rs. 20,00,000/- from DST, New Delhi is ongoing as PI. d)Member of Task force project on “Reproductive Health Research” funded by Ministry of Health. e)Member of CSIR Task force project on “Microbial Infections” and “Synthetic Biology and Metabolic Engineering of Azadirachtin biosynthetic pathway”. f)“Amino Acids as chiral Synthons: Development of new synthetic protocols for creating Natural Products and related diversity in quest for anticancer agent” of Rs. 35 lakhsfrom DST,New Delhi is ongoing as PI. g)“Design, synthesis and evaluation of new chemical entities against atypical mycobacterium, Mycobacterium fortuitum” of Rs. 40 lakhs from ICMR, New Delhi and is ongoing as PI.

Awards/Fellowships
CDRI Incentive Award on original research paper of Impact Factor >4.00 and >5.00 in 2007 and 2008 respectively
Visited Heinerich Heine University, Duesseldorf, Germany for three months under Indian National Science Academy, India - DFG, Germany Exchange Fellowship Programme
 
GROUP MEMBERS
Present Group Members: Krishna, Subal, Ritesh, Sanjit, Priyanka, Saurav, Amit, Sudipta, Sankalan and Priyanka Misra.
Past Group Members: Shagufta (PDF with A. IJzerman, Leiden/Amsterdam Centre for Drug Research, University of Leiden, Netherland; Jitendra (PDF with Peter Wipf, University of Pittsburgh and Subhas Sinha, The Scripps Research Institute, USA; Ajay (PDF with S.B. Park, Seol); Sajal (PDF with Alfred Hassner, Israel); Maloy (PDF in USA).
SELECTED PUBLICATIONS
 
Samanta, K.; and Panda, G. (2010): BF3.OEt2 Mediated Regioselective Ring Opening of Amino Acids Derived Chiral Aziridines: An Easy Route Towards 2,5-Substituted Chiral Piperazines, and Piperazine Core of the Natural Product Piperazinomycin; Chemistry an Asian Journal, accepted.
Das, S. K.; Das, S. K.; and Panda, G. (2010): Formal total synthesis of Rhaphidecursinol A. Eur. J. Org. Chem. 2010, 5100–5107.
Samanta, K.; and Panda, G. (2010): A New Synthesis of Amino Acids Based Enantiomerically Pure N- Di-Tosyl Protected Substituted 2,3,4,4a,5,6-Hexahydro-1H-pyrazino[1,2-a]quinoxalines, Organic and Biomolecular Chemistry, 2010, 8, 2823.
Das, S. K.; Srivastava, A. K.; and Panda, G. (2010): A new route to protected 1,4-oxazepanes and 1,4-diazepanes from Garner aldehyde. Tetrahedron Letters, 51, 1483-1485.
Singh, R.; and Panda, G. (2010): Sc(OTf)3 catalyzed one pot Domino approach for general and efficient synthesis of unsymmetrical and symmetrical 9-arylxanthenes. Organic and Biomolecular Chemistry, 8, 1097–1105.
Samanta, K., Chatterjee, B., Mishra, J. K., Dwivedi, S. D., Naik, L.V., Choudhry, P., Bid, H. K., Konwar, R., Chattopadhyay, N., and Panda, G. (2010): Anti-tumor Activity of a new series of Benzoxazepine Derivatives in Breast Cancer. Bioorganic & Medicinal Chemistry Letters 20, 283–287.
Das, S. K., Singh, R., and Panda, G. (2009): A new synthetic route to unsymmetrical 9-arylxanthenes. European Journal of Organic Chemistry, Issue 28, 4757-4761.
Parai, M. K., and Panda, G. (2009): A convenient synthesis of chiral amino acid derived 3,4-dihydro-2H-benzo[b][1,4]thiazines and antibiotic levofloxacin. Tetrahedron Letters, 50, 4703-4705.
Singh, R., Parai, M. K., and Panda, G. (2009): Application of Nazarov cyclization to access [6-5-6] and [6-5-5]tricyclic core embedded New Heterocycles : An easy entry to structures related to Taiwaniaquinoids. Organic and Biomolecular Chemistry, 7, 1858-1867.
Das, S. K., Dinda, S. K., and Panda, G. (2009): Enantioselective synthesis of a functionalized 1-benzoxepine derivative. European Journal of Organic Chemistry, Issue 2, 204–207.
Kumar, S., Das, S. K., Dey, S., Maity, P., Guha, M., Choubey, V., Panda, G., and Bandyopadhyay, U. (2008): Antiplasmodial Activity of [(Aryl)arylsulfanylmethyl]pyridines. Antimicrobial Agents and Chemotherapy, 52, 705–715.
Das, S. K., and Panda, G. (2008): b-Hydroxy-a-tosyloxy Esters as Chiral Building Blocks for the Enantioselective Synthesis of Benzo-annulated Oxa-heterocycles: Scope and Limitations. Tetrahedron, 64, 4162-4173.
Srivastava, A. K., and Panda, G. (2008): Total Synthesis of (-)-Balanol, its all Stereoisomers, their N-tosyl analogues and fully protected Ophiocordin: An easy access to hexahydroazepine cores from Garner aldehydes. Chemistry A European Journal, 14, 4675-4688.
Mishra J.K., Garg, P., Dohare, P., Kumar, A., Siddiqi, M.I., Ray, M., and Panda, G. (2007): Amino acid-based enantiomerically pure 3-substituted 1,4-benzodiazepin-2-ones: a new class of anti-ischemic agents. Bioorganic Medicinal Chemistry Letters; 17, 1326-13231.
Mishra, J. K., and Panda, G. (2007): Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions. Journal of Combinatorial Chemistry; 9, 321-338.
Shagufta and Panda, G. (2007): A new example of a steroid-amino acid hybrid: construction of constrained nine membered D-ring steroids; Organic Biomolecular Chemistry; 5, 360-366.
Mishra, J. K.; Rao, J. S., Sastry, G. N., and Panda, G. (2006): Regioselective aminoethylation in 1,4-Benzodiazepin-2-one Under Conventional Heating And Microwave Irradiation. Tetrahedron Letters, 47, 3357-3360.
Mishra, J. K., and Panda, G. (2005): A convenient two step syntheses of amino acids derived chiral-3-substituted-1,4-benzodiazepin-2-ones. Synthesis, 1881-1887.
Das, S. K., Shagufta, and Panda, G. (2005): An Easy Access to Unsymmetric Trisubstituted Methane Derivatives (TRSMs). Tetrahedron Letters, 46, 3097-3102.
Panda, G., Shagufta, Mishra, J.K., Chaturvedi, V,, Srivastava, A,K,, Srivastava, R., and Srivastava, B,S. (2004): Diaryloxy methano phenanthrenes: a new class of antituberculosis agents. Bioorganic Medicinal Chemistry, 12, 5269-5276.
Panda, G. and Rao, N. V. (2004): A Short Synthetic Approach to Chiral Serine Azido Derivatives. Synlett, 4, 714-716.
Arya, P., Panda, G., Rao, N.V., Alper, H., Bourque, S.C., and Manzer, L.E. (2001): Solid-Phase Catalysis: A Biomimetic Approach toward Ligands on Dendritic Arms to Explore Recyclable Hydroformylation Reactions. Journal of American Chemical Society, 123, 2889-2890.
Mehta, G., Panda, G., and Sarma, P.V.V.S. (1998): A Short Synthesis of Bucky-Bowl C3 hemifullerene (triindenotrifullrene). Tetrahedron Letters, 5835-5836.
Mehta, G., and Panda, G. (1997): A New Synthesis of Corannulene. Tetrahedron Letters, 38, 2145-2148.
Mehta, G., and Panda, G. (1997): Bucky-bowls: A Simple, Conceptually New Synthesis of C2v-semibuckminsterfullerene (C30H12, [5,5]-fulvalene circulene). Journal of Chemical Society Chemical Communication, 2081-2082.
 
PATENT FILED
 

Diaryloxy Methano Phenanthrenes: A New Class of Antituberculosis Agents, G. Panda, Shagufta, Jitendra Kumar Mishra, Vinita Chaturvedi, Anil K. Srivastava, Manju, Ranjana Srivastava and Brahm S. Srivastava, 1178DEL2004 Filing date 24/06/04