摘要:
Novel 3-N-cycloalkyl-5-substituted-2-thioxothiazolidin-4-one derivatives that are effective for use in treating viral infections are described. Also described are pharmaceutical compositions comprising the 3-N-cycloalkyl-5-substituted-2-thioxothiazolidin-4-one derivatives and methods for using the compounds or compositions.
摘要:
Novel 3-N-cycloalkyl-5-substituted-2-thioxothiazolidin-4-one derivatives that are effective for use in treating viral infections are described. Also described are pharmaceutical compositions comprising the 3-N-cycloalkyl-5-substituted-2-thioxothiazolidin-4-one derivatives and methods for using the compounds or compositions.
摘要:
Compounds that are useful in treating or preventing viral infections, such as influenza, are described herein. Further described are compositions made from these compounds and methods for using the compounds and their compositions in treating or preventing viral infections.
摘要:
Compounds that are useful in treating or preventing viral infections, such as influenza, are described herein. Further described are compositions made from these compounds and methods for using the compounds and their compositions in treating or preventing viral infections.
摘要:
In the method for operating an interference multiple access communications system, wherein the improvement comprises the steps of employing a distributed scheduler within a Media Access Controller (MAC) for Multiuser Detection (MUD) enabled Mobile Ad-hoc Networks (MANETS) to increase spectral efficiency by increasing spectral use and providing a way to dynamically allocate virtual channels to achieve maximum channel reuse in different network topologies and different link patterns and to ameliorate any hidden or exposed node problems.
摘要:
A method of expressing auxin synthetase gene specifically in cotton seed coat and fiber, which comprises constructing plant expression vector capable of expressing auxin synthetase gene specifically by fusing a tissue-specific promoter with an auxin synthetase gene, and then integrating the construct into a cotton genome. The method can significantly improve the yield and the quality of cotton fiber, thereby providing fiber with high quality for textile industry.
摘要:
An electric reciprocating motion device includes a motor having a rotary shaft for outputting a reciprocating rotational power and a motion head coupling with the rotary shaft and being driven to move in a reciprocating motion along an axis of the rotary shaft and in a predetermined swing angle range. The motor is a spring motor including a motor unit and a torsion spring having two ends affixing at a motor housing and to the rotary shaft respectively. After the rotary shaft outputs a mechanical torque at one rotational direction, the torsion spring applies a spring force against the rotary shaft to drive the rotary shaft to rotate backward for generating the reciprocating rotational power. Using the spring motor in the electric reciprocating motion device, the device achieves the goals of simple mechanical structure, small volume, easy to install, and low in cost.
摘要:
The subject invention discloses materials and methods for the design, synthesis, and biochemical evaluation of chromogenic substrate compounds for sialidases of bacterial, viral, protozoa, and vertebrate (including humans) origin. These compounds are based upon N-acetylneuraminic acid glycosides. In particular, this invention provides a novel class of these compounds as chromogenic substrates of these sialidases which yield chromogenic products after reactions catalyzed by sialidase take place. Also provided are methods of making these substrate compounds, methods of diagnosis and prognosis of sialidase related diseases using these substrate compounds.
摘要:
A method of inhibiting bacterial sialidase comprising administering to a subject an inhibiting effective amount of a compound of formula I: ##STR1## wherein A is CO.sub.2 H, PO.sub.2 H, or SO.sub.2 H; B is N; R.sub.1 and R.sub.2 are H; R.sub.3 and R.sub.4 are, independently, H, OH, NO.sub.2, guanidino, or alkyl or alkenyl of from 1 to 3 carbons where the alkyl or alkenyl is unsubstituted or is substituted, independently, with one or more of OH, NH2, or halide; R.sub.5 is H; and R.sub.6 is COCH.sub.3, or COCI.sub.3 ; or an analog, pharmaceutically acceptable salt, derivative, or mixture thereof. A method of preventing a bacterial or trypanosomal infection using the compounds of formula I. A method of treating a bacterial or trypanosomal infection using the compounds of formula I. A pharmaceutical composition comprising a pharmaceutically acceptable carrier admixed with an inhibiting effective amount of a compound of formula I. A method of making a pharmaceutical composition, comprising admixing a pharmaceutically acceptable carrier with an inhibiting effective amount of a compound of formula I.
摘要:
A sialidase inhibitor of the shown formula I: ##STR1## where dashed lines d.sub.1 and d.sub.2, X.sub.1, R.sub.1, R.sub.2, R.sub.6, R.sub.3, R.sub.4 and R.sub.5 are as described in the specification; or an analog, pharmaceutically acceptable salt, or derivative of the inhibitor, with the proviso that the inhibitor is not HNBA GBA or Neu5Ac2en. The inhibitor in a composition with a pharmaceutically acceptable carrier. Methods of making a pharmaceutical composition of an acceptable carrier and the inhibitor. Methods of inhibiting sialidase and methods of treating and preventing bacterial or trypanosomal infection using the inhibitor.