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. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: Bioorg Med Chem. 2018 Feb 10;26(8):1547–1559. doi: 10.1016/j.bmc.2018.01.032

Table 3.

Anti-angiogenesis properties of substituted phthalimidines.

compound structure % nitritea vessel lengthb # of vesselsc
11 graphic file with name nihms944639t8.jpg 101 105.1±4.9 19.5±0.5
21 graphic file with name nihms944639t9.jpg 72 42.1±3.3 14.0±1.4
9 graphic file with name nihms944639t10.jpg 50 83.1±2.4 18.2±0.4
22 graphic file with name nihms944639t11.jpg 49 42.8±9.2 8.6±2.7
24 graphic file with name nihms944639t12.jpg 11.5 86.4±2.8 22.0±0.5
20 graphic file with name nihms944639t13.jpg 9.2 48.2±1.9d 14.6±0.6d
a

nitrite data extrapolated from Table 1; presented as mean % of control

b

vessel length in µm, obtained at 10µg/mL; presented as mean ± S.E.M

c

vessel number obtained at 10µg/mL; values presented as mean ± S.E.M

d

compound 20 screened at 5µg/mL; values presented as mean ± S.E.M