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Table 1 EC50 of DT2216, Bcl-2 family protein inhibitors, or chemotherapy drugs against selective T cell lymphoma (TCL) cell lines

From: DT2216—a Bcl-xL-specific degrader is highly active against Bcl-xL-dependent T cell lymphomas

TCL cell lines

Chemotherapy drugs (nM)

Bcl-2 family inhibitors (μM)

DT2216 (μM)

Doxorubicin

Etoposide

Vincristine

ABT263

A-1155463

ABT199

S63845

(a selective Bcl-xL

(Bcl-2/xL)

(Bcl-xL)

(Bcl-2)

(Mcl-1)

degrader)

MyLa (CTCL)

124.60

199.50

8.60

0.04

0.0008

> 5

> 5

0.005

MJ (CTCL)

480

> 10,000

60

0.33

0.30

> 10

> 10

0.10

MAC2A (ALK-ALCL)

120

1260

< 1

0.06

0.009

1.80

> 10

0.28

L82 (ALK+ALCL)

30

110

< 1

0.07

0.03

2.38

1.55

0.02

DL40 (ALK-ALCL)

10

80

< 1

4.42

> 10

> 10

0.003

> 10

SMZ1 (PTCL-NOS)

10

100

1.50

9.71

> 10

> 10

0.05

> 10

FEPD (ALK-ALCL)

60

370

10

7.90

> 10

8.99

0.22

> 10

Human PLT

0.13

> 10

  1. The results were calculated from a representative experiment with 6 replicates per concentration for each compound. Similar results were also got in two or more assays
  2. EC50 the half maximal effective concentration, CTCL cutaneous TCL, ALK-ALCL anaplastic lymphoma kinase negative anaplastic large cell lymphoma, ALK+ALCL anaplastic lymphoma kinase positive anaplastic large cell lymphoma, PTCL-NOS peripheral TCL not otherwise specified, PLT platelets