摘要:
A compound of the formula or the pharmaceutically acceptable salt thereof; wherein a, b, c, d, e, j, R1, R2, R3, and R4 are as defined herein and are useful to treat inflammation and other immune disorders.
摘要:
The present invention relates to compounds of the formula I and the pharmaceutically acceptable forms thereof; wherein X, Y, a, b, c, d, R1, R2, R3, R4 and R5 are as defined herein. Moreover, the present invention is also directed at pharmaceutical compositions comprising a compound of the formula I and a pharmaceutically acceptable carrier. Furthermore, the present invention is directed at methods of using the herein described compounds and compositions for treating or preventing a disorder or condition that can be treated or prevented by antagonizing the CCR1 receptor in a mammal.
摘要:
A compound of the formula XXXI or the pharmaceutically acceptable salt thereof; wherein R1, R2, and R3 are as defined herein and the compound is useful in the preparation or use of compounds that treat inflammation and other immune disorders.
摘要:
A compound of the formula or the pharmaceutically acceptable salt thereof; wherein R1, R2, R3 and R4 are as defined above useful to treat inflammation and other immune disorders.
摘要:
A phosphor composition consisting essentially of particles of zinc sulfide electroluminescent phosphor activated with from about 0.7% by weight of about 1.3% by weight of manganese, based upon the total weight of the phosphor composition, wherein the electroluminescent emission of the phosphor has an x color coordinate value of from about 0.522 to about 0.532 and a y color coordinate value of from about 0.460 to about 0.470 and an efficiency of greater than about 5.6 lumens per watt at 115V/400 Hz. A solid state process for producing the foregoing phosphor comprises a multiple firing in order to incorporate manganese, chloride and copper ions into the zinc sulfide lattice. Controlled levels of manganese yield highly efficient electroluminescent phosphors.
摘要:
Novel compounds related structurally to Brefeldin A useful as antiviral, antifungal, antiproliferative, immunosuppresive and detoxifying agents as well as pharmaceutical compositions and methods based thereon are disclosed.