Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mohana Rao Katiki"'
Publikováno v:
Letters in Drug Design & Discovery. 16:846-860
Background: In an effort to establish new drug candidates with improved antiproliferative activity, we report here a novel class of compounds designed rationally by the replacement of an ethyl group in tamoxifen with a methylene (1H-1,2,4-triazole) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b5ff8a077ea3f1a103b4e7efd8cac1c
https://doi.org/10.2174/1570180815666180621100314
https://doi.org/10.2174/1570180815666180621100314
Autor:
M. S. R. Murty, Mohana Rao Katiki, Kommula Dileep, G. Narender Reddy, B. Ramalingeswara Rao, C. Ganesh Kumar, Jagadeesh Babu Nanubolu
Publikováno v:
Letters in Organic Chemistry. 16:723-734
Two series of N-2-benzothiazolyl-4-(arylsulfonyl)-1-piperazineacetamides/propanamides were synthesized from substituted 2-aminobenzothiazoles and were assayed for their in vitro antimicrobial activities against a panel of different pathogenic bacteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1778c06f7f63ca442fd819bc20318eb6
https://doi.org/10.2174/1570178615666181113094539
https://doi.org/10.2174/1570178615666181113094539
Autor:
V. P. S. Vishnu Vardhan, Kommula Dileep, Busam Ramalingeswara Rao, Babu Nanubolu, Mohana Rao Katiki, M. S. R. Murty, Ramakrishna Sistla
Publikováno v:
Organic Communications, Vol 10, Iss 3, Pp 178-189 (2017)
A series of 1-(4-substituted)-4-(3-((1-(substituted)-1H-tetrazol-5-yl)thio)propyl)piperazine derivatives were ( 6a-t) synthesized by KF-Al2O3 mediated S-alkylation of 5-thio-substituted tetrazole with 1-(3-chloropropyl)-4-(4-substituted)piperazine. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84712bddcb90a8ff6d6007960a742354
Autor:
Dileep Kommula, M. S. R. Murty, Mohana Rao Katiki, Sai Shyam Narayanan, Ruby John Anto, B. Ramalingeswara Rao
Publikováno v:
Croatica Chemica Acta
Volume 92
Issue 3
Volume 92
Issue 3
The synthesis of a series of substituted hippuric acid (2-benzamidoacetic acid) derivatives containing arylsulfonylpiperazine nucleus (3a–j, 4a–j) is described. The compounds were synthesized by coupling hippuric/4-fluorohippuric acid with variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475aaa82dca53de03faab940efe6fd08
https://hrcak.srce.hr/226910
https://hrcak.srce.hr/226910
Autor:
Reddy Shetty Prakasham, Busam Ramalingeswara Rao, M. S. R. Murty, Ruby John Anto, Mohana Rao Katiki, Rachapudi B. N. Prasad, Bethala L. A. Prabhavathi Devi, Sudhreer K. Buddana, Sai S. Narayanan
Publikováno v:
Letters in Drug Design & Discovery. 13:968-981
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f886c865aabe9f2e656c3da1bd5f4f3
https://doi.org/10.2174/1570180813666160125222334
https://doi.org/10.2174/1570180813666160125222334
Autor:
Nishant Jain, Sowjanya Polepalli, Sudheer Kumar Buddana, Srujana Garimella, Jagadeesh Babu Nanubolu, M. S. R. Murty, Mohana Rao Katiki, Reddy Shetty Prakasham
Publikováno v:
Molecular Diversity. 20:687-703
A new class of compounds, structurally related to the breast cancer drug tamoxifen, was designed and synthesized. The McMurry coupling reaction was used as the key synthetic step in the preparation of these analogs, and the structural assignments wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37d96a0a7fc2c832ae19a8342f1e70a
https://doi.org/10.1007/s11030-016-9677-8
https://doi.org/10.1007/s11030-016-9677-8
Autor:
M. S. R. Murty, Rajesh Pamanji, Janapala Venkateswara Rao, Rayudu Venkateswara Rao, Kesur R. Ram, B. Ramalingeswara Rao, L. R. Velatooru, Mohana Rao Katiki
Publikováno v:
Medicinal Chemistry Research. 23:1661-1671
A series of 3-[3-[4-(substituted)-1-cyclicamine]propyl]thio-5-substituted[1,2,4]triazoles (8a–m) and 2-[3-[4-(substituted)-1-cyclicamine]propyl]-5-(substituted)-2,4-dihydro-3H[1,2,4]triazole-3-thiones (9a–h) were synthesized with good yields star
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02eae2c73d650728459d67f0f872adee
https://doi.org/10.1007/s00044-013-0757-3
https://doi.org/10.1007/s00044-013-0757-3
Publikováno v:
Medicinal Chemistry Research. 22:4980-4991
The synthesis of a series of substituted 2-(piperazin-1-yl)benzothiazole/benzoxazole coupled with 1,3,4-oxadiazole-2-thiol pharmacophore (8a–t) is described using a three carbon spacer (Jones and Helm, Drugs 69:1903–1910, 2009). The structures of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea2c3ce88594999c654f8670d8d1c0e8
https://doi.org/10.1007/s00044-013-0510-y
https://doi.org/10.1007/s00044-013-0510-y
Autor:
Lekshmi R Nath, Sophia Ran, Mohana Rao Katiki, Sridivya, Jayesh Antony, Shabna A, Rajan E, M. S. R. Murty, Paul A, Naresh Kumar, Minakshi Saikia, Ruby John Anto, Sankar S, Chandran H, Sriramya, Panakkal Ej, Vinod, Sophia Margaret Joseph
Publikováno v:
Scientific Reports. 5
Wrightia tinctoria is a constituent of several ayurvedic preparations against skin disorders including psoriasis and herpes, though not yet has been explored for anticancer potential. Herein, for the first time, we report the significant anticancer p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5599464d3bbda3f0bd63bf37071bcecd
https://doi.org/10.1038/srep12662
https://doi.org/10.1038/srep12662
Autor:
Lekshmi R Nath, Sankar S, Mohana Rao Katiki, Anju Paul, Sophia Margaret Joseph, Harsha Chandran, Jayesh Antony, Elizabeth Jayex Panakkal, Shabna A, Sophia Ran, Easwary Rajan, Ruby John Anto, Nishanth Kumar. S, M. S. R. Murty, I Sridivya, I Sriramya, Vinod, Minakshi Saikia
Publikováno v:
Scientific Reports
Wrightia tinctoria is a constituent of several ayurvedic preparations against skin disorders including psoriasis and herpes, though not yet has been explored for anticancer potential. Herein, for the first time, we report the significant anticancer p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26a4d7f11f0b98421a8e3683ff9619ff
https://doi.org/10.1038/srep11107
https://doi.org/10.1038/srep11107