Zobrazeno 1 - 10
of 12
pro vyhledávání: '"M. P. Narasimha Rao"'
Autor:
J Haritha, M Reddi Narasimha Rao, B Indira Padmaja, N Raja Reddy, N Suresh Babu, K V Guru Charan Karthik
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 3, Pp 1640-1646 (2020)
Purpose: The aim of the present study was to compare and evaluate the retention of dislodged crowns by addition of one horizontal circumferential groove (HCG) to preparation and/or casting and with two luting cements. Materials and Methods: A total o
Externí odkaz:
https://doaj.org/article/2446d76e282f4cf7abf7acfdadd2647d
Autor:
Burri Nagaraju, V. Lakshma Nayak, Jeshma Kovvuri, Ravikumar Akunuri, M. P. Narasimha Rao, Ahmed Kamal, A. Ajitha, Narayan Nagesh
Publikováno v:
European Journal of Medicinal Chemistry. 143:1563-1577
A series of new β-carboline-bisindole compounds were designed, synthesized and evaluated for their antiproliferative activity against human cancer cell lines, such as A549 (lung cancer), DU-145 (prostate cancer), HeLa (cervical cancer) and MCF-7 (br
Autor:
M. P. Narasimha Rao, Nishant Jain, P. Swapna, Ahmed Kamal, Kishore Mullagiri, Jeshma Kovvuri, Sowjanya Polepalli, Vijaykumar D. Nimbarte, Pompi Das
Publikováno v:
ChemMedChem. 9:1463-1475
A series of imidazo[2,1-b][1,3,4]thiadiazole-linked oxindoles composed of an A, B, C and D ring system were synthesized and investigated for anti-proliferative activity in various human cancer cell lines; test compounds were variously substituted at
Autor:
Ahmed Kamal, V. Lakshma Nayak, M.V.P.S. Vishnuvardhan, M. P. Narasimha Rao, Swapna Ponnampalli, Bagul Chandrakant, Kishore Mullagiri
Publikováno v:
Med. Chem. Commun.. 5:1644-1650
A series of imidazothiadiazole–benzimidazole conjugates (3a–z) were synthesized and evaluated for their cytotoxic activity against a set of four selected human cancer cell lines. Amongst them, compounds 3b and 3y exhibited significant antiprolife
Autor:
Nagula Shankaraiah, M. P. Narasimha Rao, Vunnam Srinivasulu, V. Lakshma Nayak, Ahmed Kamal, Yellaiah Tangella, Manda Sathish, Narayana Nagesh
Publikováno v:
Asian Journal of Organic Chemistry. 3:68-76
An efficient regio-selective aryl CH activation and tandem o-hydroxylation method for 2-arylbenzimidazoles has been developed by using a Pd(OAc)2/oxone/Cs2CO3 catalytic system. This reaction was successfully optimized by using various catalysts, oxid
Autor:
Rajesh V.C.R.N.C. Shetti, Ahmed Kamal, P. Swapna, Anver Basha Shaik, M. P. Narasimha Rao, Soma Gupta
Publikováno v:
European Journal of Medicinal Chemistry. 62:661-669
A number of linezolid-like oxazolidino-sulfonamides (7a–y and 8a–b) were designed and synthesized with a view to develop antimicrobial agents with improved properties. Most of the synthesized compounds showed good to moderate activity against a p
Autor:
V. Lakshma Nayak, M. P. Narasimha Rao, Nagula Shankaraiah, Ahmed Kamal, Vunnam Srinivasulu, Manda Sathish, Narayana Nagesh, Yellaiah Tangella
Publikováno v:
ChemInform. 45
The cytotoxicity of the products was investigated with some of the compounds being effective in selected human cancer cell lines.
Autor:
M. P. Narasimha Rao, Narayana Nagesh, Kishore Mullagiri, K. Vidyasagar, Jeshma Kovvuri, Vunnam Srinivasulu, Vangala Santhosh Reddy, Chandrakant Bagul, Ahmed Kamal, P. Swapna, Anver Basha Shaik
Publikováno v:
Organicbiomolecular chemistry. 12(15)
A series of β-carboline–benzimidazole conjugates bearing a substituted benzimidazole and an aryl ring at C3 and C1 respectively were designed and synthesized. The key step of their preparation was determined to involve condensation of substituted
Autor:
Vangala Santhosh Reddy, Anver Basha Shaik, Santosh Karnewar, M. Kashi Reddy, Srigiridhar Kotamraju, Ahmed Kamal, Chandan Kishor, M. P. Narasimha Rao, Ananthamurthy Nagabhushana, Anthony Addlagatta, Kallaganti V. S. Ramakrishna, Sumit S. Chourasiya, G. Bharath Kumar
Publikováno v:
ChemMedChem. 8(12)
A library of imidazopyridine-oxindole conjugates was synthesised and investigated for anticancer activity against various human cancer cell lines. Some of the tested compounds, such as 10 a, 10 e, 10 f, and 10 k, exhibited promising antiproliferative
Autor:
Rajesh V.C.R.N.C. Shetti, Inshad Ali Khan, Sunil Kumar, M. P. Narasimha Rao, Nitin Pal Kalia, Sandeep Sharma, Bagul Chandrakant, P. Swapna, Anver Basha Shaik, Farheen Sultana, Ahmed Kamal
Publikováno v:
European journal of medicinal chemistry. 64
In an effort to discover new anti-tubercular agents, a series of new diarylpyrrole–oxazolidinone conjugates have been designed and synthesized. The anti-tubercular activity of these new conjugates ( 4a – n and 5a – d ) against Mycobacterium tub