Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jaki R. Tamboli"'
Autor:
Chandrakant Bagul, Garikapati Koteswara Rao, Immadi Veena, Ravindra Kulkarni, Jaki R. Tamboli, Ravikumar Akunuri, Siddiq Pasha Shaik, Manika Pal-Bhadra, Ahmed Kamal
Publikováno v:
Molecular diversity.
A library of benzimidazole briged pyrazolo[1,5-a]pyrimidine (6a-q) was designed, synthesized and subjected for evaluation for cytotoxic potential. Antiproliferative activity, ranging from 3.1-51.5 μM, was observed against a panel of cancer cell line
Autor:
Manika Pal-Bhadra, Venkata Krishna Kanth Makani, Chandrakant Bagul, Jaki R. Tamboli, Garikapati Koteswara Rao, Ahmed Kamal
Publikováno v:
MedChemComm. 8:1810-1816
A series of pyrazolo[1,5-a]pyrimidines substituted at C5 with 1-phenylprop-2-en-1-one (6a-q) and 3-phenylprop-2-en-1-one (7a-k) was synthesized and evaluated for antiproliferative activity. Among them, 6h was found to be the most active compound agai
Autor:
Pranjal Sarma, Syed Farooq Adil, M. Janaki Ramaiah, Raksha Ganesh, Ahmed Kamal, S.N.C.V.L. Pushpavalli, Utpal Bhadra, Jaki R. Tamboli, Manika Pal-Bhadra
Publikováno v:
Bioorganic & Medicinal Chemistry. 21:6414-6426
A series of new conjugates of quinazolino linked 4β-amidopodophyllotoxins 10aa–af and 10ba–bf were synthesized and evaluated for their anticancer activity against human pancreatic carcinoma (Panc-1) as well as breast cancer cell lines such as MC
Autor:
Syed Farooq Adil, Ahmed Kamal, Jaki R. Tamboli, V. Lakshma Nayak, Sistla Ramakrishna, M.V.P.S. Vishnuvardhan
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 23:3208-3215
A series of pyrazolo[1,5-a]pyrimidine linked 2-aminobenzothizole conjugates (6a–t) were synthesized and evaluated for their anticancer activity against five human cancer cell lines. Among them two compounds 6p and 6m showed significant anticancer a
Autor:
Paidakula Suresh, Adla Mallareddy, Nishant Jain, Papagari Venkat Reddy, Thokhir Basha Shaik, Jaki R. Tamboli, Ahmed Kamal, Banala Ashwini Kumar, Shasi V. Kalivendi, P. Raju
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:2349-2358
A series of novel conjugates of 4-aza-2,3-didehydropodophyllotoxins ( 11a – w ) were synthesized by a straightforward one-step multicomponent synthesis that demonstrated cytotoxicity against five human cancer cell lines (breast, oral, colon, lung a
Publikováno v:
Letters in Drug Design & Discovery. 7:665-673
Publikováno v:
Letters in Drug Design & Discovery. 6:201-209
Publikováno v:
Letters in Drug Design & Discovery. 5:261-270
A series of phthalimido-dihydropyrimidones (19a-l) and naphthalimido-dihydropyrimidones (23a-l) have been synthesized and some representative compounds have been evaluated for their in vitro anticancer activity. Compounds 19d, 19f and 19j are selecti
Autor:
Jaki R. Tamboli, M. Janaki Ramaiah, A. Lavanya, Utpal Bhadra, Ahmed Kamal, Manika Pal-Bhadra, V. Haritha, Nibedita Patel, S.N.C.V.L. Pushpavalli, Kaustav Bhadra
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(20)
It has previously been shown that anthranilamide-pyrazolo[1,5-a]pyrimidine conjugates activate p53 and cause apoptosis in cervical cancer cells such as HeLa and SiHa. Here we establish the role of these conjugates in activating p53 pathway by phospho
Autor:
Ahmed Kamal, V. Lakshma Nayak, M.V.P.S. Vishnuvardhan, Jaki R. Tamboli, Sistla Ramakrishna, Syed Farooq Adil
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(1)
A series of different heteroaromatic linked 4β-amidopodophyllotoxin conjugates (16a-i, 17a-i and 18a-d) were synthesized and evaluated for anticancer activity against five human cancer cell lines. Among the series, one of the compound 17g showed sig