Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ibrahim Bin Sayeed"'
Autor:
Ahmed Kamal, K. Sirisha, Mohd Adil Shareef, Thipparapu Ganapathi, C. Ganesh Kumar, Ibrahim Bin Sayeed, Hemshikha Rajpurohit, Manasa Kadagathur, Bathini Nagendra Babu, Irfan Khan
Publikováno v:
ChemistrySelect. 4:2258-2266
Autor:
Bathini Nagendra Babu, C. Ganesh Kumar, Irfan Khan, Gopathi Ramu, Mohd Adil Shareef, Ahmed Kamal, Surender Singh Jadav, Ibrahim Bin Sayeed, K. Sirisha
Publikováno v:
MedChemComm. 10:806-813
A series of new 1,4-dihydroindeno[1,2-c]pyrazole tethered carbohydrazide hybrids (5a–u) were designed, synthesized and evaluated for their antimicrobial activity. Compounds 5d, 5g, 5j, 5k and 5q demonstrated significant activity against the entire
Autor:
Ahmed Kamal, Ibrahim Bin Sayeed, Apoorva Nagarajan, M.V.P.S. Vishnuvardhan, Srinivas Kantevari
Publikováno v:
Bioorganic Chemistry. 80:714-720
A library of new imidazopyridine linked triazole hybrid conjugates (8a-r) were designed, synthesized and evaluated for their cytotoxicity against four cancer cell lines namely, human lung (A549), human prostate (DU-145), human colon (HCT-116) and bre
Autor:
Ahmed Kamal, Praveen Reddy Adiyala, Kasinathuni Naga Visweswara Sastry, Ibrahim Bin Sayeed, Jeshma Kovvuri, Apoorva Nagarajan, Vedinthe Lakshma Nayak, Ram Awatar Maurya, Velma Ganga Reddy
Publikováno v:
ChemistrySelect. 2:8158-8161
α-Keto vinyl azides and 2-aminopyridines were coupled to yield 1-aryl-N-(2-arylimidazo[1, 2-a]pyridin-3-yl)methanimines in the presence of visible light using Ru(bpy)3Cl2.6H2O as a photocatalyst. This synthetic protocol allows the formation of 3 new
Autor:
Koteswara Rao Garikapati, Ibrahim Bin Sayeed, Apoorva Nagarajan, Venkata Krishna Kanth Makani, Ahmed Kamal, Abdullah Alarifi, Manika Pal-Bhadra, Mohd Adil Shareef
Publikováno v:
ChemistrySelect. 2:6480-6487
A new class of imidazothiazole-propenones was synthesized and investigated for their anti-proliferative activity against various human cancer cell lines. Promising activities were observed in five congeners 8 k, 8 l, 8 n, 8 o and 8 v with interesting
Autor:
Ahmed Kamal, V. Saidi Reddy, Abdullah Alarifi, V. Lakshma Nayak, Ibrahim Bin Sayeed, Kunta Chandrasekhar, M.V.P.S. Vishnuvardhan
Publikováno v:
MedChemComm. 8:1817-1823
A series of new triazolo linked 4β-amidopodophyllotoxin conjugates (9a-l) were synthesized using click chemistry and evaluated for their antitumor activity against four human cancer cell lines. Among them, two compounds (9c and 9j) showed significan
Publikováno v:
MedChemComm. 8:1000-1006
A library of imidazopyridine–propenone conjugates (8a–8u) were synthesized and evaluated for their antitumor activity against four human cancer cell lines, namely, prostate (DU-145), lung (A549), cervical (Hela) and breast (MCF-7) cancer cell lin
Autor:
Ibrahim Bin Sayeed, Kanugala Sirisha, Bathini Nagendra Babu, Irfan Khan, C. Ganesh Kumar, Syed Akbar, Ahmed Kamal, Thipparapu Ganapathi, Mohd Adil Shareef
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:126621
A series of new triazole fused imidazo[2,1-b]thiazole hybrids (9a-u) were designed, synthesized and evaluated as antimicrobial agents. Compounds 9c, 9d, 9e, 9j and 9l showed promising broad spectrum antimicrobial activity. Further, compound 9c exhibi
Synthesis of 2-anilinopyridine–arylpropenone conjugates as tubulin inhibitors and apoptotic inducers
Autor:
Ibrahim Bin Sayeed, M.V.P.S. Vishnuvardhan, Anver Basha Shaik, Praveen Reddy Adiyala, Vangala Santhosh Reddy, M. Kashi Reddy, Ahmed Kamal, Nishant Jain, Sumit S. Chourasiya, G. Bharath Kumar
Publikováno v:
RSC Advances. 5:97367-97380
A series of new (Z)-3-(arylamino)-1-(2-(arylamino)pyridin-3-yl)prop-2-en-1-one conjugates 9a–p were synthesized and evaluated for their cytotoxic activity against some human cancer cell lines. Some of the treated compounds like 9a, 9g and 9j showed
Autor:
Ibrahim Bin Sayeed, Venkatesh Tekumalla, Praveen Reddy Adiyala, Burri Nagaraju, Apoorva Nagarajan, Ahmed Kamal, Mohd Adil Shareef, V. Lakshma Nayak
Publikováno v:
Bioorganic chemistry. 76
Cancer chemotherapy has several limitations such as often insufficient differentiation between malign tissue and benign tissue. The clinical utility of the pyrrolo[2,1-c][1,4]benzodiazepines (PBDs) are inadequate because of the lack of selectivity fo