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Exploration of Drug Science
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T3
From:
Rational design of novel phenol ether derivatives as non-covalent proteasome inhibitors through 3D-QSAR, molecular docking and ADMET prediction
Table 3
The structures and activities of newly designed non-covalent proteasome inhibitors
ID
Substituent
Predicted pIC
50
Synthetic accessibility
Drug-likeness Lipinski
R
1
R
2
R
3
CoMFA
CoMSIA
C20
H
H
H
7.303
7.164
3.02
Yes
D1
Me
H
H
7.311
7.306
3.14
Yes
D2
H
CHO
H
7.369
7.233
3.56
Yes
D3
H
COOH
H
7.322
7.233
3.63
Yes
D4
H
NH
2
H
7.317
7.207
3.56
Yes
D5
H
H
F
7.394
7.190
3.20
Yes
D6
H
H
CHO
7.436
7.613
3.18
Yes
D7
H
H
COOH
7.435
7.652
3.29
Yes
D8
7.323
7.287
2.61
Yes
D9
Me
H
F
7.416
7.331
3.32
Yes
D10
Me
H
CHO
7.498
7.756
3.30
Yes
D11
Me
H
COOH
7.432
7.792
3.41
Yes
D12
H
COOH
F
7.425
7.258
3.79
Yes
D13
H
COOH
CHO
7.466
7.680
3.79
Yes
D14
H
COOH
COOH
7.458
7.718
3.89
Yes
D15
H
NH
2
F
7.388
7.232
3.73
Yes
D16
H
NH
2
CHO
7.437
7.649
3.72
Yes
D17
H
NH
2
COOH
7.431
7.688
3.82
Yes
D18
Me
CHO
COOH
7.349
7.792
3.94
Yes
D19
Me
COOH
F
7.346
7.364
3.91
Yes
D20
Me
COOH
CHO
7.450
7.788
3.90
Yes
D21
Me
COOH
COOH
7.362
7.823
4.01
Yes
D22
Me
NH
2
F
7.442
7.373
3.85
Yes
D23
Me
NH
2
CHO
7.522
7.794
3.83
Yes
D24
Me
NH
2
COOH
7.468
7.828
3.94
Yes
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