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11.
Ahmad VU Khan A Farooq U Kousar F Khan SS Nawaz SA Abbasi MA Choudhary MI 《Chemical & pharmaceutical bulletin》2005,53(4):378-381
Three new tricyclic cis-clerodane type diterpenoids trivially named as limbatolide A (1), limbatolide B (2) and limbatolide C (3) have been isolated from the roots of Otostegia limbata along with two known compounds; oleanic acid and beta-sitosterol. The structure elucidation of the new compounds was based primarily on two-dimensional (2D) NMR techniques. Compounds 1-3 displayed inhibitory potential in a concentration-dependent manner against acetylcholinesterase (AChE; EC 3.1.1.7) and butyrylcholinesterase (BChE; EC 3.1.1.8) enzymes, respectively. 相似文献
12.
Choudhary MI Siddiqui ZA Musharraf SG Nawaz SA Atta-Ur-Rahman 《Natural product research》2005,19(4):311-317
The microbial transformation of prednisone (17alpha,21-dihydroxy-pregna-1,4-diene-3,11,20-trione) (1) by Cunninghamella elegans afforded two metabolites, 17alpha,21-dihydroxy-5alpha-pregn-1-ene-3,11,20-trione (2) and 17alpha,20S,21-trihydroxy-5alpha-pregn-1-ene-3,11-dione (3), while the fermentation of 1 with Fusarium lini, Rhizopus stolonifer and Curvularia lunata afforded a metabolite 1,4-pregnadiene-17alpha,20S,21-triol-3,11-dione (4). Compound 3 was found to be a new metabolite. Their structures were elucidated on the basis of spectroscopic techniques. Compound 3 showed inhibitory activity against lipoxygenase enzyme. 相似文献
13.
Begum N Hyder MI Kabir SE Hossain GM Nordlander E Rokhsana D Rosenberg E 《Inorganic chemistry》2005,44(26):9887-9894
Treatment of Mn(2)(CO)(10) with 3,4-toluenedithiol and 1,2-ethanedithiol in the presence of Me(3)NO.2H(2)O in CH(2)Cl(2) at room temperature afforded the dinuclear complexes Mn(2)(CO)(6)(mu-eta(4)-SC(6)H(3)(CH(3))S-SC(6)H(3)(CH(3))S) (1), and Mn(2)(CO)(6)(mu-eta(4)-SCH(2)CH(2)S-SCH(2)CH(2)S) (2), respectively. Similar reactions of Re(2)(CO)(10) with 3,4-toluenedithiol, 1,2-benzenedithiol, and 1,2-ethanedithiol yielded the dirhenium complexes Re(2)(CO)(6)(mu-eta(4)-SC(6)H(3)(CH(3))S-SC(6)H(3)(CH(3))S) (3), Re(2)(CO)(6)(mu-eta(4)-SC(6)H(4)S-SC(6)H(4)S) (4), and Re(2)(CO)(6)(SCH(2)CH(2)S-SCH(2)CH(2)S) (5), respectively. In contrast, treatment of Mn(2)(CO)(10) with 1,3-propanedithiol afforded the trimanganese compound Mn(3)(CO)(6)(mu-eta(2)-SCH(2)CH(2)CH(2)S)(3) (6), whereas Re(2)(CO)(10) gave only intractable materials. The molecular structures of 1, 3, and 6 have been determined by single-crystal X-ray diffraction studies. The dimanganese and dirhenium carbonyl compounds 1-5contain a binucleating disulfide ligand, formed by interligand disulfide bond formation between two dithiolate ligands identical in structure to that of the previously reported dimanganese complex Mn(2)(CO)(6)(mu-eta(4)-SC(6)H(4)S-SC(6)H(4)S). Complex 6, on the other hand, forms a unique example of a mixed-valence trimangenese carbonyl compound containing three bridging 1,3-propanedithiolate ligands. The solution properties of 6 have been investigated by UV-vis and EPR spectroscopies as well as electrochemical techniques. 相似文献
14.
The dependence of the diffusion parameters including slowing down area, neutron diffusion length and migration length on the voided volume fraction in water has been studied experimentally. For this purpose, the PIEAS Neutron Transport Facility (PNTF) comprised of a 10 Ci Am–Be neutron source and a water filled aluminum tank with Perspex voided tubes has been designed and fabricated. A BF3 detector was used for the neutron counting. The slowing down area was determined at the cadmium cutoff level. The diffusion parameters were determined first in the absence of voids. The experimentally measured values of the slowing down area, the diffusion length and the migration length have been found in good agreement with the corresponding values determined by other workers. By varying void volume fraction from 0% to 7.5%, the experimental measurements show a monotonic increase in the slowing down area from 58.71±2.6 to 71.28±3.2 cm2, in the diffusion length from 2.95±0.13 to 3.11±0.13 cm and in the migration length from 8.21±0.165 to 8.99±0.169 cm. Our measurements show that the diffusion parameters exhibit a quadratic dependence on the void volume fraction. 相似文献
15.
Tawarah Khalid M. Jibril Ibrahim Bani-Fwaz Mutasem Z. 《Transition Metal Chemistry》2000,25(6):659-663
The kinetics of the photolytic CO-substitution of CpFe(CO)2SCOR [Cp = C5H5, Bu
t
C5H4, 1,3-Bu2
t
C5H3; R = Me, Bu
t
, Ph, 2-(O2N)C6H4, 3-(O2N)C6H4, 4-(O2N)C6H4, 3,5-(O2N)2C6H3] with PPh3 were studied in CH2Cl2 at 0 °C by i.r. spectroscopy. The reactions yielded exclusively the mono-CO-substituted derivatives, CpFe-(CO)(PPh3) SCOR, and were found to follow second order kinetics with first order dependence on the concentration of each reactant. The differences in rates are discussed in terms of current knowledge pertaining to such reactions. An associative mechanism is proposed to account for the kinetic data of the reactions described. 相似文献
16.
Reactions of various η6-arene-η5-cyclopentadienyliron or substituted cyclopentadienyliron cations with trimethyl, triethyl or triphenyl phosphite under either thermal or photochemical conditions all resulted in the replacement of the arene ligand with three phosphite ligands to give η5-tris(trimethyl, triethyl or triphenyl phosphite)-η5-cyclopentadienyliron or substituted cyclopentadienyliron cations. The yields of the phosphite complexes were higher from photolysis than from the analogous thermolysis. Photolysis of the η6-chlorobenzene-η5-cyclopentadienyliron cation (IX) carried out in the presence of a more basic or more electron-rich aromatic ligand resulted in the exchange of the chlorobenzene of IX with the more basic arene, thus providing synthetic routes to cyclopentadienyliron complexes that may be difficult to prepare by other means. New complexes synthesized in this way are the η6-2-phenylethyl tosylate-η5-cyclopentadienyliron cation and the CpFe+ complexes of thiophene, 2-methylthiophene, 3-methylthiophene and 2,5-dimethylthiophene. 相似文献
17.
In order to determine the effect of airborne emission of trace elements, e.g. Br, Rb Cs, Sc and Na on roadside ecosystem, concentrations were determined in different species of plants from an urban park at Lahore. For monitoring purpose attention was paid to the leaves ofSapindus mukorossis, Alstonia scholaris andDiospyros embryopteris. Different varieties of tissues were found to have different concentration of trace elements when compared among themselves. The concentration of trace element deposition was compared with the values reported in literature. Significant pollution was observed. 相似文献
18.
I. Ihsanullah Y. Iqbal T. N. Khattak 《Journal of Radioanalytical and Nuclear Chemistry》2005,266(2):361-366
Summary Date samples were irradiated with different doses using a gamma-irradiator. Levels of moisture, protein, fibre and fats were
determined on monthly basis for 5 months. Generally, the moisture contents of control date samples packed in white polythene
decreased from 14.1±1.1 to 9.7±0.8% over a 5-month period while the irradiated samples were in the range of 10.4-11.2%, however,
no proper pattern of change was observed. After 5-month storage, the protein level of irradiated samples was reduced to 1.00-1.30%,
while the percent fibre levels were found to be in the range of 2.40-2.48. Similarly, the fat level decreases from 1.06±0.12
to 0.68±0.06 for control date sample while after 5-month the decrease in fat content was 0.45±0.04%, 0.44±0.04%, 0.44±0.05%,
0.42±0.05% and 0.40±0.04% for samples irradiated with 20, 50, 100, 200 and 300 krads, respectively. 相似文献
19.
John R. Beswick W. David Cotterill Muhammad Iqbal Robert Livingstone 《Journal of heterocyclic chemistry》1993,30(3):623-626
Reaction between some naphtho[2,1-b]pyrans and 1,1-diphenylethene affords 9,9-diphenyl-1,9,10,10a-tetrahydro-2H-phenaleno[1,9-bc]pyrans. 相似文献
20.
Zhang Y Salaita K Lim JH Lee KB Mirkin CA 《Langmuir : the ACS journal of surfaces and colloids》2004,20(3):962-968
This paper describes a simple and convenient strategy for reducing the dimensions of organic micro-and nanostructures on metal surfaces. By varying electrochemical desorption conditions, features patterned by dip-pen nanolithography or micro contact printing and made of linear alkanethiols or selenols can be gradually desorbed in a controlled fashion. The process is referred to as electrochemical whittling because the adsorbate desorption is initiated at the exterior of the feature and moves inward as a function of time. The whittling process and adsorbate desorption were studied as a function of substrate morphology, adsorbate head and tail groups, and electrolyte solvent and salt. Importantly, one can independently address different nanostructures made of different adsorbates and effect their miniaturization based upon ajudicious selection of adsorbate, applied potential, and supporting electrolyte. Some of the physical and chemical origins of these observations have been elucidated. 相似文献