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Dive into the research topics where R. Sateesh Chandra Kumar is active.

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Featured researches published by R. Sateesh Chandra Kumar.


Bioorganic & Medicinal Chemistry Letters | 2011

Synthesis and antiglycation potentials of bergenin derivatives

T. Vijaya Kumar; Ashok K. Tiwari; A. Robinson; K. Suresh Babu; R. Sateesh Chandra Kumar; D. Anand Kumar; Amtul Zehra; J. Madhusudna Rao

Bergenin (1), major bioactive compound isolated from methanolic extract of Mallotus philippinensis, displayed moderate AGE inhibition activity (IC(50)=186.73 μM). A series of derivatives of bergenin (3a-k) containing variety of aromatic acids were synthesized under mild conditions by modification of sugar part. Selective esterification of hydroxyl groups on the sugar part enhanced antiglycation potential of bergenin. Compounds 3j and 3k exhibited potent antiglycation activity with the IC(50) values of 60.75 and 12.28 μM, respectively.


Journal of Asian Natural Products Research | 2013

Synthesis, anticancer, and antibacterial activities of piplartine derivatives on cell cycle regulation and growth inhibition

J. Ujwal Kumar; G. Shankaraiah; R. Sateesh Chandra Kumar; V. V. Pitke; G. Tirupathi Rao; B. Poornima; K. Suresh Babu; Amere Subbarao Sreedhar

A series of piplartine derivatives were synthesized via Baylis–Hillman reaction and evaluated for anticancer and antibacterial activities. The cytotoxicity of these compounds was examined in two different human tumor cell lines, IMR-32 and HeLa. The antibacterial activity was examined in Staphylococcus aureus and Pseudomonas aeruginosa. The results showed that compounds 2b, 2e, and 2j were found to be the most active compounds, which displayed line no cytotoxicity, but G2–M cell cycle arrest in tumor cells, and showed cytostatic effects in bacteria.


Tetrahedron Letters | 2010

Stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer

R. Sateesh Chandra Kumar; G. Venkateswar Reddy; G. Shankaraiah; K. Suresh Babu; J. Madhusudana Rao


Tetrahedron Letters | 2009

Stereoselective syntheses of 11-α-methoxycurvularin and 11-β-methoxycurvularin

G. Venkateswar Reddy; R. Sateesh Chandra Kumar; K. Suresh Babu; J. Madhusudana Rao


Tetrahedron Letters | 2010

Stereoselective synthesis (+)-cephalosporolide D

G. Venkateswar Reddy; R. Sateesh Chandra Kumar; Eppakayala Sreedhar; K. Suresh Babu; J. Madhusudana Rao


Tetrahedron-asymmetry | 2009

A simple and efficient enantioselective route to 2,6-disubstituted piperidines: synthesis of (2R,6S)-isosolenopsin A and (2S,6R)-isosolenopsin

R. Sateesh Chandra Kumar; Eppakayala Sreedhar; G. Venkateswar Reddy; K. Suresh Babu; J. Madhusudana Rao


Tetrahedron Letters | 2011

Stereoselective synthesis of (+)-radicamine B

G. Shankaraiah; R. Sateesh Chandra Kumar; B. Poornima; K. Suresh Babu


Tetrahedron-asymmetry | 2009

The first total synthesis of neohelmanticins A–D, amino derivatives of the 1,2-dihydroxypropane core and biological evaluation

Eppakayala Sreedhar; R. Sateesh Chandra Kumar; G. Venkateswar Reddy; A. Robinson; K. Suresh Babu; J. Madhusudana Rao; P.V. Srinivas


Chemistry Letters | 2009

Gallium(III) Chloride-catalyzed Sakurai Reaction of α-Amido Sulfones with Allyltrimethylsilane: Access to Synthesis of 2,6-Disubstituted Piperidine Alkaloid Derivatives

R. Sateesh Chandra Kumar; G. Venkateswar Reddy; K. Suresh Babu; J. Madhusudana Rao


Synlett | 2012

Formal Total Synthesis of (–)-5,6-Dihydrocineromycine B

G. Venkateswar Reddy; R. Sateesh Chandra Kumar; Bandi Siva; K. Suresh Babu; J. Madhusudana Rao

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K. Suresh Babu

Indian Institute of Chemical Technology

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G. Venkateswar Reddy

Indian Institute of Chemical Technology

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J. Madhusudana Rao

Indian Institute of Chemical Technology

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Eppakayala Sreedhar

Indian Institute of Chemical Technology

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G. Shankaraiah

Indian Institute of Chemical Technology

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A. Robinson

Indian Institute of Chemical Technology

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B. Poornima

Indian Institute of Chemical Technology

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Amere Subbarao Sreedhar

Centre for Cellular and Molecular Biology

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Amtul Zehra

Indian Institute of Chemical Technology

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Ashok K. Tiwari

Indian Institute of Chemical Technology

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