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Arylphthalazines as potent, and orally bioavailable inhibitors of VEGFR-2 Journal article
Duncton M.A.J., Piatnitski Chekler E.L., Katoch-Rouse R., Sherman D., Wong W.C., Smith II L.M., Kawakami J.K., Kiselyov A.S., Milligan D.L., Balagtas C., Hadari Y.R., Wang Y., Patel S.N., Rolster R.L., Tonra J.R., Surguladze D., Mitelman S., Kussie P., Bohlen P., Doody J.F.. Arylphthalazines as potent, and orally bioavailable inhibitors of VEGFR-2[J]. Bioorganic and Medicinal Chemistry, 2009, 17(2), 731-740.
Authors:  Duncton M.A.J.;  Piatnitski Chekler E.L.;  Katoch-Rouse R.;  Sherman D.;  Wong W.C.; et al.
Favorite | TC[WOS]:38 TC[Scopus]:38 | Submit date：2019/01/16
Angiogenesis  Arylphthalazine  Inhibitor  Kdr  Kinase  Phthalazine  Vegfr-2  
Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines Journal article
Ouyang X., Piatnitski E.L., Pattaropong V., Chen X., He H.-Y., Kiselyov A.S., Velankar A., Kawakami J., Labelle M., Smith II L., Lohman J., Lee S.P., Malikzay A., Fleming J., Gerlak J., Wang Y., Rosler R.L., Zhou K., Mitelman S., Camara M., Surguladze D., Doody J.F., Tuma M.C.. Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines[J]. Bioorganic and Medicinal Chemistry Letters, 2006, 16(5), 1191-1196.
Authors:  Ouyang X.;  Piatnitski E.L.;  Pattaropong V.;  Chen X.;  He H.-Y.; et al.
Favorite | TC[WOS]:99 TC[Scopus]:104 | Submit date：2019/01/16
1,3,4-oxadiazole  Antimitotic Agent  Multiple-drug Resistance  Tubulin Polymerization Inhibitor