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DR. GAUTAM PANDA |
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Scientist E- II
Medicinal and Process Chemistry Division
Central Drug Research Institute
Chattar Manzil Palace
Lucknow 226001, UP, India
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| 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;
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| POST
-DOCTORAL RESEARCH |
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| CURRENT
AREAS OF INTEREST |
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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.
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| Awards/Fellowships
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CDRI Incentive
Award on original research paper of Impact Factor >4.00
and >5.00 in 2007 and 2008 respectively |
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Visited Heinerich Heine
University, Duesseldorf, Germany for three months under
Indian National Science Academy, India - DFG, Germany
Exchange Fellowship Programme |
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| GROUP
MEMBERS |
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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).
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| SELECTED
PUBLICATIONS |
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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. |
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Das, S. K.; Das, S. K.;
and Panda, G. (2010):
Formal total synthesis of Rhaphidecursinol A. Eur. J.
Org. Chem. 2010, 5100–5107. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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Das, S. K., Shagufta,
and Panda, G. (2005):
An Easy Access to Unsymmetric Trisubstituted Methane Derivatives
(TRSMs). Tetrahedron Letters, 46, 3097-3102. |
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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. |
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Panda, G.
and Rao, N. V. (2004): A Short Synthetic
Approach to Chiral Serine Azido Derivatives. Synlett,
4, 714-716. |
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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. |
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Mehta, G., Panda,
G., and Sarma, P.V.V.S. (1998):
A Short Synthesis of Bucky-Bowl C3 hemifullerene (triindenotrifullrene).
Tetrahedron Letters, 5835-5836. |
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Mehta, G., and Panda,
G. (1997): A New Synthesis of
Corannulene. Tetrahedron Letters, 38, 2145-2148. |
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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. |
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| PATENT
FILED |
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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 |
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