Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jagadeesh Mavinahalli"'
Autor:
Salunkhe Videsh, Madhu bala, Avinash Dhanave, Tanaji Mengawade, Vamsi Madgula, Mahesh Thakkar, Keshav Naik, Bheemashankar Kulkarni, Rahul D. Kaduskar, Dhananjay N. Umrani, Santosh Kurhade, Sachin Joshi, Amit Bhalerao, Sreekanth R. Rouduri, Vishal V Pathade, Rajkanth Petla, Swagatam Ray, Narayanan Hariharan, Kasim A. Mookhtiar, Satheesh Veerappa Avaragolla, Debnath Bhuniya, Jagadeesh Mavinahalli, Ashwini Tambe, Vaibhav Jain, Siddhartha De, Amol A. Raje, Ahmed Nadeem
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:1867-1873
In a pursuit to identify reversible and selective BTK inhibitors, two series based on 7H-pyrrolo[2,3-d]pyrimidine and 1H-pyrrolo[2,3-b]pyridine as the hinge binding core, have been identified. Structure activity relationship (SAR) exploration led to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59344b4bbaa9f604c182b2a0a030bcea
https://doi.org/10.1016/j.bmcl.2017.02.026
https://doi.org/10.1016/j.bmcl.2017.02.026
Autor:
Jagadeesh, Mavinahalli N a, Chandrasekhar, Jayaraman a, b, *
Publikováno v:
In Chemical Physics Letters 1999 305(3):298-302
Autor:
Lei Zhou, Jagadeesh Mavinahalli, Thorsten Wohland, Rajamani Lakshminarayanan, Roger W. Beuerman, Lin Guo, Charles Tang, L. Y. Chen, Chandra S. Verma, Jing Li, Shouping Liu, L. B. Ong
Publikováno v:
Amino Acids. 40:123-133
Understanding the molecular mechanisms of antimicrobial peptide-membrane interactions is crucial in predicting the design of useful synthetic antimicrobial peptide analogues. Defensins are small (3-5 kDa) cysteine-rich cationic proteins which constit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefdc00aeb879194d95ef7a3fb3d2ab9
https://doi.org/10.1007/s00726-010-0565-8
https://doi.org/10.1007/s00726-010-0565-8
Autor:
Arumugam Madhumalar, Roger W. Beuerman, Chandra S. Verma, David P. Lane, Jagadeesh Mavinahalli
Publikováno v:
BMC Genomics, Vol 11, Iss Suppl 1, p S5 (2010)
BMC Genomics
BMC Genomics
The N terminal transactivation domain of p53 is regulated by ligases and coactivator proteins. The functional conformation of this region appears to be an alpha helix which is necessary for its appropriate interactions with several proteins including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::022cb60245d2343d7ae29b2c171486d0
https://doaj.org/article/df4126c675c344b499b0b8e99b19828b
https://doaj.org/article/df4126c675c344b499b0b8e99b19828b
Publikováno v:
Journal of Molecular Modeling; Feb2000, Vol. 6 Issue 2, p226-233, 8p
Publikováno v:
Journal of Molecular Modeling; February 2000, Vol. 6 Issue: 2 p226-233, 8p