Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Radhakrishnan Sureshbabu"'
Autor:
Romina Croci, Margherita Pezzullo, Delia Tarantino, Mario Milani, Shwu-Chen Tsay, Radhakrishnan Sureshbabu, Yi-Jin Tsai, Eloise Mastrangelo, Jacques Rohayem, Martino Bolognesi, Jih Ru Hwu
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91765 (2014)
Noroviruses (NV) are +ssRNA viruses responsible for severe gastroenteritis; no effective vaccines/antivirals are currently available. We previously identified Suramin (9) as a potent inhibitor of NV-RNA dependent RNA polymerase (NV-RdRp). Despite sig
Externí odkaz:
https://doaj.org/article/3bb15fd0144147289af16ceed90b73e6
Autor:
B. Gunasekaran, Radhakrishnan Sureshbabu, A. K. Mohanakrishnan, G. Chakkaravarthi, V. Manivannan
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 9, Pp o2069-o2069 (2009)
In the title compound, C20H19NO6S, the phenyl ring of the phenylsulfonyl group makes a dihedral angle of 83.35 (5)° with the indole ring system. The molecular structure exhibits a number of short intramolecular C—H...O contacts.
Externí odkaz:
https://doaj.org/article/333ae40767f34a7a83cb18fe140279d0
Autor:
B. Gunasekaran, Radhakrishnan Sureshbabu, A. K. Mohanakrishnan, G. Chakkaravarthi, V. Manivannan
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 8, Pp o1856-o1856 (2009)
In the title compound, C26H25NO6S, the phenyl ring forms a dihedral angle of 82.5 (1)° with the indole ring system. The molecular structure is stabilized by weak intramolecular C—H...O interactions and the crystal structure is stabilized by weak i
Externí odkaz:
https://doaj.org/article/c8abf10c0b82438ab40f986ef06afe04
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o264-o264 (2009)
In the title compound, C24H25NO8S, the indole unit is planar and makes a dihedral angle of 79.73 (11)° with the phenyl ring of the sulfonyl substituent. The molecules in the unit cell are stabilized by C—H...O and C—H...π intermolecular interac
Externí odkaz:
https://doaj.org/article/0150f690ba0d45998d651b9c0cf8ddb9
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 4, Pp o732-o732 (2008)
In the title compound, C19H18BrNO5S, the plane of the phenyl ring forms a dihedral angle of 76.99 (6)° with the indole ring system. The Br atom is disordered over two positions, with site-occupancy factors of 0.833 (14) and 0.167 (14). The molecular
Externí odkaz:
https://doaj.org/article/8c2a694d2b044bceb4ce0483518e5c31
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 4, Pp o751-o751 (2008)
In the title molecule, C15H12BrNO2S, the indole mean plane and phenyl ring are nearly orthogonal to each other, forming a dihedral angle of 88.19 (13)°. The Br atom is disordered over two close positions with occupancies of 0.56 (4) and 0.44 (4). Th
Externí odkaz:
https://doaj.org/article/c16fbaf7c7a648b78da803c58ebdf6b2
Autor:
Hsu-Chan Hsiao, Chih-Man Yang, Radhakrishnan Sureshbabu, Hsing-Wen Sung, Wei-Lun Chiang, Tzu-Tsen Lin, Wei-Tso Chia, Hung-Yi Liu
Publikováno v:
Journal of Controlled Release. 199:53-62
Eradicating subcutaneous bacterial infections remains a significant challenge. This work reports an injectable system of hollow microspheres (HMs) that can rapidly produce localized heat activated by near-infrared (NIR) light and control the release
Autor:
Ming Hua Hsu, Kou Hung Wu, Cheng Ying Hsieh, Fa Kuen Shieh, Pi Wen Ko, Kuan Chuan Pao, Lin Chiang Sherlock Huang, Radhakrishnan Sureshbabu, Shih Ching Chou
Publikováno v:
Applied Radiation and Isotopes. 89:53-57
This work presents a novel approach for labeling hippuric acid with I-131 using microwaves. It utilizes copper(II) acetate as a catalyst of the labeling. The process involves the use of this catalytic copper(II) acetate at low dilutions that were nev
Publikováno v:
Journal of Heterocyclic Chemistry. 49:913-918
An efficient synthesis of carbazole analogs has been achieved via interaction of N-protected-2-methylindoles with N,N-dimethylformamide dimethylacetal as well as N,N-dimethylacetamide dimethylacetal in the presence of pyrrolidine or 1,4-diazabicyclo(
Publikováno v:
Synthetic Communications. 42:526-533
An efficient synthesis of 2-(3′-bromo-3′-phenylallyl)indoles has been developed via direct carbon–carbon bond formation between bromomethylindoles/indolylmethylacetates and phenylacetylene.