Výsledky vyhledávání - "Veeresh Maddi"

Synthesis and antibacterial activity of a new series of 3-[3-(substituted phenyl)-1-phenyl-1H-pyrazol-5-yl]-2H-chromen-2-one derivatives

Autor: Mohan Agrawal, Pankaj Patil, Prashant Aragade, Prashant Shinde, Veeresh Maddi, R. Venkat Narayanan

Publikováno v: Journal of Enzyme Inhibition and Medicinal Chemistry. 27:849-853

A series of 3-[3-(substituted phenyl)-1-phenyl-1H-pyrazol-5-yl]-2H-chromen-2-one (4a-k) were synthesized by reaction of 3-[2,3-dibromo-3-(substituted phenyl)propanoyl]-2H-chromen-2-one (3 a-k) with phenyl hydrazine in presence of triethylamine in abs

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b02e0dba8b64fbba7f210d75b75c5e9
https://doi.org/10.3109/14756366.2011.622270

Zobrazit plný text záznamu

Synthesis, spectral studies and biological evaluation of a novel series of 2-substituted-5,6-diarylsubstituted imidazo(2,1-b)-1,3,4-thiadiazole derivatives as possible anti-tubercular agents

Autor: Mangala Ghatole, Veeresh Maddi, Malleshappa N. Noolvi, Mahesh B. Palkar, Laxmivenkat G. Nargund

Publikováno v: Medicinal Chemistry Research. 21:1313-1321

A novel series of 18 analogs of 2-substituted-5,6-diarylsubstituted imidazo(2,1-b)-1,3,4-thiadiazole 6a–r have been synthesized by the reaction of 2-amino-5-substituted-1,3,4-thiadiazoles 5a–d and an appropriately substituted α-bromo-1,2-(p-subs

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d418f458a7e078bcc0f1ea2ade55f74d
https://doi.org/10.1007/s00044-011-9646-9

Zobrazit plný text záznamu

Synthesis and evaluation of anti-inflammatory and analgesic activity of 3-[(5-substituted-1,3,4-oxadiazol-2-yl-thio)acetyl]-2H-chromen-2-ones

Autor: A. H. M. Vishwanathswamy, Pradeepkumar Ronad, Nista Ingale, Veeresh Maddi, Darbhamulla Satyanarayana, Shivalingrao Mamledesai, Mahesh B. Palkar

Publikováno v: Medicinal Chemistry Research. 21:16-26

A novel series of 3-[(5-substituted-1,3,4-oxadiazol-2-yl-thio)acetyl]-2H-chromen-2-one (7a–i) were synthesized by the condensation between the appropriately substituted 5-substituted-1,3,4-oxadiazolyl-2-thione (4a–i) derived from various existing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4af50f6366b0d0931c9ec83c1a30bbeb
https://doi.org/10.1007/s00044-010-9494-z

Zobrazit plný text záznamu

Synthesis and antimicrobial activity of 7-(2-substituted phenylthiazolidinyl)-benzopyran-2-one derivatives

Autor: Malleshappa N. Noolvi, Sheetal Sapkal, Veeresh Maddi, Satyanarayana Dharbhamulla, Pradeepkumar Ronad

Publikováno v: European Journal of Medicinal Chemistry. 45:85-89

A series of 7-(2-substituted phenylthiazolidinyl)-benzopyran-2-one derivatives have been synthesized by reaction of 7-amino-4-methyl-benzopyran-2-one (1) with an appropriate substituted aldehydes to obtain various Schiff bases (3a-k) which on treatme

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f9e5cab6850213f5d9c3aa98023106e
https://doi.org/10.1016/j.ejmech.2009.09.028

Zobrazit plný text záznamu

Synthesis and Antimycobacterial Activity of a Novel Series of Isonicotinylhydrazide Derivatives

Autor: Mahesh B. Palkar, Sandip Jaju, Shivalingarao Mamledesai, Darbhamulla Satyanarayana, Veeresh Maddi, Mangala Ghatole, Pradeepkumar Ronad

Publikováno v: Archiv der Pharmazie. 342:723-731

A novel series of 14 new isonicotinyl hydrazide derivatives 2a-g, 3a-g containing a 4-thiazolidinone / 2-azetidinone nucleus were synthesized by reacting N'-substituted arylidene / heteroarylidene isonicotinyl hydrazide 1a-g with thioglycollic acid i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::638b598c8647657bffae31a7ce789a7f
https://doi.org/10.1002/ardp.200900001

Zobrazit plný text záznamu

Synthesis and Antibacterial Activity of a New Series of 3‐[3‐(Substituted Phenyl)‐1‐Isonicotinoyl‐1H‐Pyrazol‐5‐yl]‐2H‐Chromen‐2‐one Derivatives

Autor: Shivalingarao Mamledesai, Mahesh B. Palkar, Darbhamulla Satyanarayana, Suresh Khode, Pradeepkumar Ronad, Prashant Aragade, Veeresh Maddi

Publikováno v: Archiv der Pharmazie. 342:361-366

A novel series of 3-[3-(substituted phenyl)-1-isonicotinoyl-1H-pyrazol-5-yl]-2H-chromen-2-one derivatives 4a-k have been synthesized by the reaction of 3-[2,3-dibromo-3-(substituted phenyl) propanoyl]-2H-chromen-2-one 3a-k and isonicotinic acid hydra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::45272dfbd15c18237a1a4ff8d8744a8a
https://doi.org/10.1002/ardp.200800156

Zobrazit plný text záznamu

Synthesis and pharmacological evaluation of a novel series of 5-(substituted)aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agents

Autor: Prashant Aragade, Veeresh Maddi, Suresh Khode, A. H. M. Thippeswamy, Mahesh B. Palkar, Darbhamulla Satyanarayana, Shivalingarao Mamledesai, Pradeep Kumar Ronad

Publikováno v: European Journal of Medicinal Chemistry. 44:1682-1688

A novel series of 5-(substituted)aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines (3a-l) were synthesized by reacting various substituted 3-aryl-1-(3-coumarinyl)propan-1-ones (2a-l) with phenylhydrazine in the presence of hot pyridine. Structures of all

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63149352ba2c77c9df2e0f83c3a24606
https://doi.org/10.1016/j.ejmech.2008.09.020

Zobrazit plný text záznamu

RATIONAL DESIGN OF ANTIBACTERIAL THIENOPYRIMIDINES BY 2D-QSAR STUDY

Autor: Imtiyaz Ahmed Khazi, Jameel Ahmed S. Mulla, Mahesh B. Palkar, Veeresh Maddi

Publikováno v: Journal of Drug Delivery and Therapeutics. 2

QSAR studies were performed on a set of 43 analogs of thienopyrimidine using V-Life Molecular Design Suite (MDS 3.5) QSAR plus module by using Multiple Linear Regression (MLR) and Partial Least Squares (PLS) Regression methods against a gram positive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2452bc064e5e93de59e8da844c5af501
https://doi.org/10.22270/jddt.v2i2.118

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání