Yuguang Wang
Schering-Plough Research Institute
Kenilworth
NJ 07033
USA
Name/email consistency: high
- Sulfide analogues as potent and selective M(2) muscarinic receptor antagonists. Wang, Y., Chackalamannil, S., Hu, Z., McKittrick, B.A., Greenlee, W., Ruperto, V., Duffy, R.A., Lachowicz, J.E. Bioorg. Med. Chem. Lett. (2002)
- Design and synthesis of xanthine analogues as potent and selective PDE5 inhibitors. Wang, Y., Chackalamannil, S., Hu, Z., Boyle, C.D., Lankin, C.M., Xia, Y., Xu, R., Asberom, T., Pissarnitski, D., Stamford, A.W., Greenlee, W.J., Skell, J., Kurowski, S., Vemulapalli, S., Palamanda, J., Chintala, M., Wu, P., Myers, J., Wang, P. Bioorg. Med. Chem. Lett. (2002)
- Improving the oral efficacy of CNS drug candidates: discovery of highly orally efficacious piperidinyl piperidine M2 muscarinic receptor antagonists. Wang, Y., Chackalamannil, S., Hu, Z., Greenlee, W.J., Clader, J., Boyle, C.D., Kaminski, J.J., Billard, W., Binch, H., Crosby, G., Ruperto, V., Duffy, R.A., Cohen-Williams, M., Coffin, V.L., Cox, K.A., Grotz, D.E., Lachowicz, J.E. J. Med. Chem. (2002)
- Design and synthesis of ether analogues as potent and selective M2 muscarinic receptor antagonists. Wang, Y., Chackalamannil, S., Chang, W., Greenlee, W., Ruperto, V., Duffy, R.A., McQuade, R., Lachowicz, J.E. Bioorg. Med. Chem. Lett. (2001)
- Design and synthesis of piperidinyl piperidine analogues as potent and selective M2 muscarinic receptor antagonists. Wang, Y., Chackalamannil, S., Hu, Z., Clader, J.W., Greenlee, W., Billard, W., Binch, H., Crosby, G., Ruperto, V., Duffy, R.A., McQuade, R., Lachowicz, J.E. Bioorg. Med. Chem. Lett. (2000)
