Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kotesh Kumar, Jonnala"'
Autor:
Shilpi Singh, Satya Srinivas Kalvagunta Venkata Naga, Devendar Ponnam, Niranjana Kumar Arigari, Pallavi Misra, Abha Meena, Kotesh Kumar Jonnala, Suaib Luqman
Publikováno v:
Journal of Heterocyclic Chemistry. 58:2090-2101
Autor:
Chinthala, Yakaiah, Kumar Domatti, Anand, Sarfaraz, Alam, Singh, Shailendra Pratap, Kumar Arigari, Niranjan, Gupta, Namita, Satya, Srinivas K.V.N., Kotesh Kumar, Jonnala, Khan, Feroz, Tiwari, Ashok K., Paramjit, Grover
Publikováno v:
In European Journal of Medicinal Chemistry December 2013 70:308-314
Autor:
Kotesh Kumar Jonnala, Pooja Sharma, Setty Oh, Niranjana Kumar Arigari, Manjulatha K, Feroz Khan, Satya Srinivas Kvn, Yakaiah Chinthala
Publikováno v:
Journal of Heterocyclic Chemistry. 53:1902-1910
A series of new andrographolide-1,2,3-triazole derivatives, , were synthesized from a natural bioactive labdane type diterpenoid, andrographolide. All the derivatives were screened against human cancer cell lines MCF7, MDA-MB-231, COLO205, HepG2, K56
Autor:
K.V.N. Satya Srinivas, Komuraiah Buduma, Kotesh Kumar Jonnala, Pooja Sharma, Paramjit Grover, Niranjana Kumar Arigari, Aparna Shukla, Ashok Kumar Tiwari, Srinivas Chinde, Feroz Khan, Anand Kumar Dommati
Publikováno v:
Bioorganicmedicinal chemistry letters. 26(6)
A series of eleven novel bisindole derivatives were synthesized and screened for anticancer and antiobesity potentials in in vitro mode. The reaction of 1-ethoxy carbonyl 4-pyperidone 1a with indole-3-carboxaldehyde 1b in presence of catalytic amount
Autor:
Kotesh Kumar Jonnala, et al. et al.
Publikováno v:
ChemInform. 46
Among the synthesized compounds, derivatives (IIIg)—(IIIi) show potential cytotoxic activities towards several human cancer cell lines.
Autor:
Sarfaraz Alam, Ashok Kumar Tiwari, Sneha Thakur, Shalini Tirunagari, Srinivas K.V.N.S., Niranjana Kumar Arigari, Yakaiah Chinthala, Kotesh Kumar Jonnala, Feroz Khan, Srinivas Chinde, Paramjit Grover, Anand Kumar Domatti
Publikováno v:
European journal of medicinal chemistry. 93
A series of novel chalcone-triazole derivatives were synthesized and screened for in vitro anticancer activity on the human cancer cell lines IMR32 (neuroblastoma), HepG2 (hepatoma) and MCF-7 (breast adenocarcinoma), DU-145 (prostate carcinoma), and
Autor:
Singh Shilpi, Vijaya Dubey, Zehra Amtul, Niranjan Kumar Arigari, Ashok Kumar Tiwari, K.V.N.S. Srinivas, Devendar Ponnam, Luqman Suiab, Sarfaraz Alam, Kotesh Kumar Jonnala, Lubna Siddiqui, Sridhar Balasubramanian, Feroz Khan
Publikováno v:
European journal of medicinal chemistry. 87
A new series of 1,9-acetals of forskolin were synthesized by treating with aromatic and aliphatic aldehydes using Ceric ammonium nitrate as catalyst and evaluated for anticancer and α-glucosidase inhibition activities. Among the synthesized compound