Structure-based design of nonpeptidic HIV protease inhibitors: the sulfonamide-substituted cyclooctylpyramones.
Skulnick, H.I., Johnson, P.D., Aristoff, P.A., Morris, J.K., Lovasz, K.D., Howe, W.J., Watenpaugh, K.D., Janakiraman, M.N., Anderson, D.J., Reischer, R.J., Schwartz, T.M., Banitt, L.S., Tomich, P.K., Lynn, J.C., Horng, M.-M., Chong, K.-T., Hinshaw, R.R., Dolak, L.A., Seest, E.P., Schwende, F.J., Rush, B.D., Howard, G.M., Toth, L.N., Wilkinson, K.F., Kakuk, T.J., Johnson, C.W., Cole, S.L., Zaya, R.M., Zipp, G.L., Possert, P.L., Dalga, R.J., Zhong, W.-Z., Williams, M.G., Romines, K.R.
J.Med.Chem.