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. 2021 May 4;9:660424. doi: 10.3389/fchem.2021.660424

TABLE 2.

Anti-proliferative activity for compounds 3b, 3d, 4d, and 9b against human leukemia-lymphoma-derived cell lines and solid tumor-derived cell-lines.

Compounds CC50 (µM) a
CCRF-CEM b WIL-2NS c CCRF-SB d SK-MEL28 e SK-MES1 f DU145 g HeLa h CRL 7065 i
3b 0.5 ± 0.1 >100 0.35 ± 0.07 6.2 ± 1.3 6.8 ± 3.5 5.1 ± 0 7.1 ± 2.7 0.75 ± 0.05
3d 0.07 ±0.02 >100 7.9 ± 0.9 >100 >100 >100 >100 0.37 ± 0.04
4d 3.3 ±1.7 64 ± 10 0.51 ± 0.13 >100 >100 >100 >100 1.7 ± 0.1
9b 5.5 ±1.8 23 ± 7 8.5 ± 3.2 2.6±0.7 9.9±3.1 5.2 ± 0.4 5.4 ± 0.7 6.7 ± 2.4
Vincristine 0.003 ± 0.001 0.006 ± 0.002 0.003 ± 0.001 >4 0.01±0.02 0.02 ± 0.01 0.05 ± 0.02 >4
Doxorubicin 0.02±0.01 0.06±0.01 0.03±0.02 1.1±0.2 0.65±0.05 0.3 ± 0.1 1.8 ± 0.2 2.0 ± 0.2

Control is represented by CRL 7065 cell line. Vincristine and Doxorubicin were used as positive controls.

a

Compound concentration required to reduce cell proliferation by 50%, as determined by the MTT method, under conditions allowing untreated controls to undergo at least three consecutive rounds of multiplication. Data represent mean values (±SD) for three independent determinations.

b

CD4+ human acute T-lymphoblastic leukemia.

c

Human splenic B-lymphoblastoid cells.

d

Human acute B-lymphoblastic.

e

Human skin melanoma.

f

Human lung squamous carcinoma.

g

Human prostate carcinoma.

h

Human cervix carcinoma.

i

Human foreskin fibroblasts.