Design,synthesis, and anticancer evaluation of acetamide and hydrazine analogues of pyrimidine

A library of acetamide and hydrazine analogues were generated on the pyrimidine ring through a multistep reaction starting from 5-nitro-pyrimidine-4,6-diol and pyrimidine-4,6-diol, respectively. The synthesized analogues were screened for in vitro cytotoxic activity against various human cancer cell lines like HCT-1 and HT-15 (colon), MCF-7(breast), PC-3 (prostrate), SF268 (CNS) using MTT method. From the bioassay results, it was observed that even though many of the synthesized derivatives exhibited a good potency against various screened cancer cell lines, compound 14a from the acetamide series was found to show potent anticancer activity on all the tested cancer cell lines with IC₅₀ value of 0.36μM on CNS cell line and 1.6μM on HT-21 cell line, and compound 19xxi from hydrazine series of pyrimidine showed potent activity against three tested cancer cell lines with IC₅₀ value of 0.76μM on HT-29 cell line, 2.6μM on HCT-15, and 3.2μM on MCF-7 cell line.     

New 1-alk(en)yl-1,3,5-trihydroxycyclohexanes from the Dufour gland of the African ant Crematogaster nigriceps

The Dufour gland of the African ant Crematogaster nigriceps contains a mixture of at least eight 1-heptadec(en)yl- and 1-nonadec(en)yl-1,3,5-trihydroxycyclohexane derivatives, the mono-unsaturated components being the major ones (about 65%). They are accompanied by small amounts of (Z,Z)-dienic derivatives (<10%). The structures, the relative and absolute configurations, and the preferred conformation of these new compounds have been established by spectroscopic and chemical methods, whereas the positions of the double bond in the alkenyl chains were determined by DMDS derivatisation followed by linked scan EIMS.     

Synthesis of the C1-C16 fragment of the ajudazols

The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.     

Explicitly realizing average Siegel theta series as linear combinations of Eisenstein series

We find nice representatives for the 0-dimensional cusps of the degree n Siegel upper half-space under the action of \(\Gamma _0(\mathcal N )\). To each of these, we attach a Siegel Eisenstein series, and then we make explicit a result of Siegel, realizing any integral weight average Siegel theta series of arbitrary level \(\mathcal N \) and Dirichlet character \(\chi _{_L}\) modulo \(\mathcal N \) as a linear combination of Siegel Eisenstein series.     

Effect of side groups on two-photon absorption of soluble polythiophenes

The effect of pendant side groups on two-photon absorption cross-section in a number of soluble fluorescent polythiophenes was investigated. Different side groups lead to different planarity and conformation of the polymer. As the side-group-induced planarity of the polymer chain increases, the two-photon absorption cross-section also increases. The increased delocalization of the π-electrons along the polymer backbone enhances the third-order optical nonlinearity. The aggregation of the polymer chain in solution lowers the quantum efficiency of fluorescence and decreases the two-photon absorption cross-section. This study demonstrates a novel method of enhancing the two-photon absorption cross-section by tuning the pendant side group.     

Development of visually evoked cortical activity in infant macaque monkeys studied longitudinally with fMRI

We studied the development of visual activation longitudinally in two infant monkeys aged 103-561 days using the BOLD fMRI technique under opiate anesthesia and compared the results with those obtained in three adult animals studied under identical conditions. Visual activation in primary visual cortex, V1, was strong and reliable in monkeys of the youngest and oldest ages, showing that functional imaging techniques give qualitatively similar results in infants and adults. Visual activation in extrastriate areas involved in processing motion (MT/V5) and form (V4) was not evident in the younger animals, but became more adult-like in the older animals. This delayed onset of measurable BOLD responses in extrastriate visual cortex may reflect delayed development of visual responses in these areas, although at this stage it is not possible to rule out either effects of anesthesia or of changes in cerebral vascular response mechanisms as the cause. The demonstration of visually evoked BOLD responses in young monkeys shows that the BOLD fMRI technique can usefully be employed to address functional questions of brain development.     

Effects of polymer adsorption on the effective viscosity in microchannel flows: phenomenological slip layer model from molecular simulations

Molecular simulations (Dissipative Particle Dynamics - DPD) were used to quantify the effect of polymer adsorption on the effective shear viscosity of a semi-dilute polymer solution in microchannel Poseuille flow. It is well known that polymer depletion layers develop adjacent to solid walls due to hydrodynamic forces, causing an apparent wall slip and reduced effective viscosity (increased total flow rate). We found that depletion layers also developed in the presence of hydrodynamically rough adsorbed layers on the wall. Polymer-polymer (steric) repulsion between flowing and adsorbed polymer expanded the depletion layer compared to no-adsorption cases, and the effective viscosity was reduced further. Desorption occurred for higher shear rates, reducing the repulsion effect and shrinking the depletion layers. A phenomenological algebraic model for the depletion layer thickness, including a shear modified adsorption isotherm, was developed based on the simulation data. The depletion layer model can be used together with the effective viscosity model we developed earlier.     

Preferential Siting of Aluminum Heteroatoms in the Zeolite Catalyst Al‐SSZ‐70

The adsorption and reaction properties of heterogeneous zeolite catalysts (e.g. for catalytic cracking of petroleum, partial oxidation of natural gas) depend strongly on the types and distributions of Al heteroatoms in the aluminosilicate frameworks. The origins of these properties have been challenging to discern, owing in part to the structural complexity of aluminosilicate zeolites. Herein, combined solid‐state NMR and synchrotron X‐ray powder diffraction analyses show the Al atoms locate preferentially in certain framework sites in the zeolite catalyst Al‐SSZ‐70. Through‐covalent‐bond 2D ²⁷Al{²⁹Si} J‐correlation NMR spectra allow distinct framework Al sites to be identified and their relative occupancies quantified. The analyses show that 94 % of the Al atoms are located at the surfaces of the large‐pore interlayer channels of Al‐SSZ‐70, while only 6 % are in the sub‐nm intralayer channels. The selective siting of Al atoms accounts for the reaction properties of catalysts derived from SSZ‐70.