Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Niranjana Kumar Arigari"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::717c5b83a8025433c2ae0a65b5d6e099
https://doi.org/10.1002/jhet.4332
https://doi.org/10.1002/jhet.4332
Autor:
Komuraiah Buduma, Niranjana Kumar Arigari, K.V.N.S. Srinivas, Srinivas Chinde, Paramjit Grover, J. Kotesh Kumar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:2159-2163
A simple and efficient method for the selective synthesis of 2-pyrdones from 4H-pyrans using iodine as catalyst and ethanol as solvent was developed. The present method is equally effective for both aromatic and hetero aromatic ring containing 4H-pyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b59035b94b143b07348ddf1472c7c8
https://doi.org/10.1016/j.bmcl.2016.03.071
https://doi.org/10.1016/j.bmcl.2016.03.071
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::745c07bfa5413718e59e9f8b74a7f7f6
https://doi.org/10.1002/jhet.2505
https://doi.org/10.1002/jhet.2505
Autor:
Paramjit Grover, Komuraiah Buduma, Niranjana Kumar Arigari, K.V.N.S. Srinivas, J. Kotesh Kumar, Srinivas Chinde
Publikováno v:
ChemInform. 47
A simple and efficient method for the selective synthesis of 2-pyrdones from 4H-pyrans using iodine as catalyst and ethanol as solvent was developed. The present method is equally effective for both aromatic and hetero aromatic ring containing 4H-pyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a73b1f3250790cc24a3a02d2771d49b
https://doi.org/10.1002/chin.201633145
https://doi.org/10.1002/chin.201633145
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c2adb04995b76300aaedbe6069ac97a
https://pubmed.ncbi.nlm.nih.gov/26873414
https://pubmed.ncbi.nlm.nih.gov/26873414
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d203ba79e43c952fa9ad86b63a722a
https://pubmed.ncbi.nlm.nih.gov/25743216
https://pubmed.ncbi.nlm.nih.gov/25743216