Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Muraleedharan K. Manheri"'
Autor:
Jais Kurian, Muraleedharan K. Manheri, Ashan Manhas, Ramshad Kalluruttimmal, Mohammad Anas, Saheer V. Chaluvalappil, Varsha Kumari, Niti Kumar
Publikováno v:
ChemMedChem. 17(2)
Although many quinolones have shown promise as potent antimalarials, their clinical development has been slow due to poor performance in vivo. Insights into structural modifications that can improve their therapeutic potential will be very valuable i
Autor:
Archana Panthalattu Parambil, Muraleedharan K. Manheri, Lakshmi Chakkumkumarath, Divya Thekke Thattariyil, Ramshad Kalluruttimmal, Ashis Kumar Sen
Publikováno v:
The Analyst. 144:4210-4218
A sensor for the detection and quantification of H2S in biological samples should ideally meet a set of criteria such as fast detection, high sensitivity in the desired concentration range, high selectivity, non-interference from biomolecules like pr
Autor:
Karunagaran Devarajan, Nalini Venkatesan, Soumya Saroj, Muraleedharan K. Manheri, Sateeshkumar Kumbhakonam
Publikováno v:
Bioorganicmedicinal chemistry letters. 30(22)
New cisplatin analogs in which the diamminedichloro-Pt(II) unit is conjugated to dihydroquinoline- or tetrahydroquinoline frameworks were synthesized and subjected to biological evaluation in order to understand their effects on cellular redox homeos
Autor:
Muraleedharan K. Manheri, Devarajan Karunagaran, Nalini Venkatesan, Sateeshkumar Kumbhakonam, Soumya Saroj, Kasipandi Vellaisamy
Publikováno v:
New Journal of Chemistry. 42:2450-2458
A modular strategy that allows introduction of one or more reactive platinum units at chosen locations along a peptide sequence is presented. This makes use of diazides generated from serine and threonine as diamine equivalents which can be conjugate
Publikováno v:
Materials scienceengineering. C, Materials for biological applications. 112
A new group of non-ionic amphiphiles with short alkyl chains and functionalizable oxanorbornane-based head group for drug delivery application are presented. They can be prepared through a sequence that starts with cycloaddition of Boc-protected furf
Publikováno v:
RSC Advances. 6:29197-29201
Fine-tuning the gelation ability of aryl triazolyl peptide 1 by C-terminal modification led to the identification of 2 with the remarkable ability to form highly transparent gels in a wide range of solvents including oils. Good rheological properties
Publikováno v:
Chirality. 31(4)
Lipase-catalysed enantioselective acetylation and deacetylation routes were investigated to prepare 1,5,6-trisubstituted 7-oxabicyclo[2.2.1]hept-2-ene skeleton in enantio-pure form. The racemic alcohol (6) used in acetylation reaction was accessed th
Publikováno v:
Chemical communications (Cambridge, England). 53(32)
A simple replacement of a H atom by Br transformed non-gelating aryl triazolyl amino acid benzyl ester into a versatile gelator, which formed shape-persistent, self-healing and mouldable gels. The ‘bromo-aryl benzyl ester’ fragment was then trans
Autor:
Sridevi Duggirala, V. Senu Adeeba, Muraleedharan K. Manheri, Mukesh Doble, John Victor Napoleon, Rakesh P. Nankar
Publikováno v:
European journal of medicinal chemistry. 123
The dual effect of FtsZ inhibition and oxidative stress by a group of 1,2-dihydroquinolines that culminate in bactericidal effect on mycobacterium strains is demonstrated. They inhibited the non-pathogenic Mycobacterium smegmatis mc2 155 with MIC as
Publikováno v:
Synthesis. 2011:3379-3388
When subjected to tandem SN2-SNAr cyclization in the presence of alkyl or aralkyl amines, Baylis-Hillman acetates gave the corresponding 1,2-dihydroquinolines, which on simple exposure to light and oxygen afforded the corresponding 4- and 2-quinolone