Molecule Details

Cc1cc(Cl)cc(CN2CCN(C(=O)CCl)CC2)c1
piperazine-chloroacetamide
Molecular Properties
SMILES:
Cc1cc(Cl)cc(CN2CCN(C(=O)CCl)CC2)c1
MW: 300.08
Fraction sp3: 0.5
HBA: 2
HBD: 0
Rotatable Bonds: 3
TPSA: 23.55
cLogP: 2.53
Covalent Warhead: ✔️
Covalent Fragment:
CS(=O)(=O)NCCc1ccccc1

AAR-POS-d2a4d1df-1

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O=C(CCl)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

PAU-UNI-8cdd41c7-1
0.735

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O=C(CCl)N1CCN(Cc2cc(F)cc(Cl)c2)CC1

SAD-SAT-581007d4-1
0.667

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O=C(CCl)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

MAT-POS-2db6411e-2
0.667

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O=C(CCl)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

SAD-SAT-581007d4-7
0.667

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COCc1cc(Cl)cc(CN2CCN(C(=O)CCl)CC2)c1

MED-COV-4280ac29-33
0.627

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(S(N)(=O)=O)c1

SAD-SAT-581007d4-4
0.600

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NS(=O)(=O)c1cc(Cl)cc(CN2CCN(C(=O)CCl)CC2)c1

SAD-SAT-581007d4-3
0.600

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O=C(CCl)N1CCN(Cc2cccc(Cl)c2)CC1

AAR-POS-d2a4d1df-35
0.561

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O=C(CCl)N1CCN(Cc2cccc(Cl)c2)CC1

MED-COV-4280ac29-15
0.561

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O=C(CCl)N1CCN(Cc2ccc(Cl)cc2)CC1

MAK-UNK-7c9d1431-29
0.556

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Cc1cccc(CN2CCN(C(=O)CCl)CC2)c1

AAR-POS-d2a4d1df-24
0.552

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Cc1cc(Cl)cc(CC2CCN(C(=O)CCl)CC2)c1

NIR-THE-0d6461ce-8
0.516

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O=C(CCl)N1CCN(Cc2ccccc2)CC1

MAK-UNK-7c9d1431-24
0.509

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Cc1ccc(CN2CCCN(C(=O)CCl)CC2)cc1

MAK-UNK-7c9d1431-21
0.500

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CC(=O)Nc1cc(C#N)cc(CN2CCN(C(=O)CCl)CC2)c1

TAM-UNI-d1c3dd9f-16
0.485

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CC(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

KIM-UNI-2ee5d8f9-1
0.483

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

AAR-POS-0daf6b7e-13
0.475

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

LON-WEI-8f408cad-7
0.475

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

MAK-UNK-212f693e-8
0.475

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CN(C)Cc1cccc(CN2CCN(C(=O)CCl)CC2)c1

JOK-SYG-18591e8f-1
0.469

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2ccnc(C#N)n2)c1

MAK-UNK-849bee6c-2
0.468

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N#Cc1ccc(CN2CCN(C(=O)CCl)CC2)cc1

MAK-UNK-6ca90168-14
0.467

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O=C(CCl)N1CCN(Cc2ccc3c(c2)OCO3)CC1

MAK-UNK-7c9d1431-14
0.462

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COc1ccc(CN2CCN(C(=O)CCl)CC2)cc1F

SAD-SAT-5b1897b2-5
0.462

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Cc1cc(Cl)cc(NC2CCN(C(=O)CCl)CC2)c1

NIR-THE-0d6461ce-9
0.462

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Cc1ccc(CN2CCN(C(=O)CCl)CC2)o1

MAR-LAB-ca4662a6-2
0.459

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CNc1ccc(Nc2cc(C)cc(CN3CCN(C(=O)CCl)CC3)c2)c(C#N)c1

MAK-UNK-849bee6c-18
0.456

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O=C(CCl)N1CCN(Cc2ccc(CS(=O)(=O)F)cc2)CC1

JIA-UNI-93b03cae-1
0.452

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Cc1ccccc1CN1CCN(C(=O)CCl)CC1

MAK-UNK-7c9d1431-20
0.452

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2ccc(N)cc2C#N)c1

MAK-UNK-849bee6c-19
0.450

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2ccc(NCC#N)cc2C#N)c1

MAK-UNK-10dfa458-43
0.444

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Cc1nc(CN2CCN(C(=O)CCl)CC2)cs1

SAD-SAT-5b1897b2-2
0.444

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2cccnc2C#N)c1

MAK-UNK-849bee6c-1
0.444

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(NCC(C)c2ccc(S(N)(=O)=O)cc2)c1

MAK-UNK-af83ef51-17
0.444

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O=C(CCl)N1CCN(Cc2cscc2Cl)CC1

SAD-SAT-bc31ec01-1
0.443

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O=C(CCl)N1CCN(Cc2ccc(Cl)s2)CC1

AAR-POS-0daf6b7e-2
0.443

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N#Cc1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAT-POS-ee51dedd-1
0.439

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O=C(CCl)N1CCN(Cc2ccc3c(c2)OCCO3)CC1

MAR-TRE-6a44bbf2-54
0.439

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O=C(CCl)N1CCN(Cc2ccc3c(c2)OCCO3)CC1

MAK-UNK-7c9d1431-16
0.439

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COc1cc(C)c(CN2CCN(C(=O)CCl)CC2)cc1OC

SAD-SAT-65574d3f-10
0.439

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CCNc1ccc(Nc2cc(C)cc(CN3CCN(C(=O)CCl)CC3)c2)c(C#N)c1

MAK-UNK-af83ef51-22
0.439

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2ccc(NC(=O)CCl)cc2C#N)c1

MAK-UNK-849bee6c-24
0.439

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O=C(CCl)N1CCN(Cc2ccc3c(c2)CCO3)CC1

MAK-UNK-7c9d1431-18
0.435

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C=Cc1cc(NCC)ccc1Nc1cc(C)cc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-10dfa458-19
0.434

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CCNc1cc(Nc2cc(C)cc(CN3CCN(C(=O)CCl)CC3)c2)cc(C#N)n1

MAK-UNK-849bee6c-21
0.434

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CCNc1cnc(C#N)nc1Nc1cc(C)cc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-849bee6c-23
0.430

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CCNc1cc(Nc2cc(C)cc(CN3CCN(C(=O)CCl)CC3)c2)nc(C#N)n1

MAK-UNK-849bee6c-22
0.429

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2cc(NC(=O)CCl)nc(C#N)n2)c1

MAK-UNK-849bee6c-25
0.429

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O=C(CCl)N1CCN(Cc2cnc(-c3ccccc3)nc2)CC1

MAK-UNK-af83ef51-1
0.426

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Cc1cc(CN2CCN(C(=O)CCl)CC2)cc(Nc2nc(C#N)ncc2NC(=O)CCl)c1

MAK-UNK-849bee6c-26
0.425

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O=C(CCl)N1CCN(Cc2cc(Cl)cc3cnccc23)CC1

JOO-PER-58e158bd-1
0.425

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O=C(CCl)N1CCN(Cc2cc(Cl)cc3ccccc23)CC1

DAR-DIA-fb20be43-8
0.423

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COCCc1ccc(Cl)cc1CN1CCN(C(=O)CCl)CC1

MED-COV-4280ac29-37
0.423

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O=C(CCl)N1CCN(Cc2cc(Cl)cc3ccccc23)CC1

PAU-UNI-19862c28-1
0.423

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C=CC(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

SAD-SAT-581007d4-8
0.422

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O=C(CCl)N1CCN(Cc2cc(O)ccc2O)CC1

NEH-REV-107bcf72-5
0.422

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O=C(CCl)N1CCN(Cc2cccs2)CC1

AAR-POS-0daf6b7e-17
0.419

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O=C(CCl)N1CCN(Cc2ccco2)CC1

MAK-UNK-7c9d1431-28
0.419

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O=C(CCl)N1CCN(Cc2cccs2)CC1

LON-WEI-8f408cad-5
0.419

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CCNc1ccc(Nc2cc(C)cc(CN3CCN(C(=O)CCl)CC3)c2)c(C#N)n1

MAK-UNK-849bee6c-20
0.414

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O=C(CCl)N1CCN(Cc2ccc(Br)s2)CC1

AAR-POS-0daf6b7e-12
0.413

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O=C(CCl)N1CCN(Cc2ccc(Br)s2)CC1

JOH-UNI-27ac80fd-23
0.413

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Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

AAR-POS-d2a4d1df-41
0.412

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Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

TAT-ENA-80bfd3e5-20
0.412

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O=C(CCl)N1CCN(Cc2c(F)cccc2Cl)CC1

AHN-SAT-de2502ba-15
0.409

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Nc1csc(O)c1CN1CCN(C(=O)CCl)CC1

ASH-SAT-43770c7d-5
0.400

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N#Cc1nccc(Sc2cccc(CN3CCN(C(=O)CCl)CC3)c2)n1

MAK-UNK-849bee6c-17
0.398

View
NS(=O)(=O)c1ccc2cc(CN3CCN(C(=O)CCl)CC3)ccc2c1

SEL-UNI-cd366922-7
0.397

View
N#Cc1ccsc1CN1CCN(C(=O)CCl)CC1

DAV-CRI-d1e0885a-1
0.397

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CNCCSC(=O)c1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-176ca439-3
0.395

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CNCCSC(=O)c1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-cd94b63c-1
0.395

View
CNS(=O)(=O)c1ccc2ccc(CN3CCN(C(=O)CCl)CC3)cc2c1

TAM-UNI-d1c3dd9f-6
0.395

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CS(=O)(=O)N1CCc2ccc(CN3CCN(C(=O)CCl)CC3)cc2C1

TAM-UNI-d1c3dd9f-5
0.395

View
O=C(CCl)N1CCN(Cc2cc(O)cc3c2OCO3)CC1

NEH-REV-107bcf72-3
0.394

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COCc1cc(CN2CCN(C(=O)CCl)CC2)sc1Br

JOH-UNI-27ac80fd-38
0.394

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Cc1ccc(NC(=O)CN2CCN(C(=O)CCl)CC2)cc1

MAR-TRE-6a44bbf2-12
0.394

View
Cc1ccc(C(=O)N2CCN(C(=O)CCl)CC2)cc1

AAR-POS-d2a4d1df-25
0.393

View
Cc1ccc(C(=O)N2CCN(C(=O)CCl)CC2)cc1

AHN-SAT-de2502ba-8
0.393

View
CN(c1cccc(CN2CCN(C(=O)CCl)CC2)c1)c1ccnc(C#N)n1

MAK-UNK-849bee6c-15
0.393

View
O=C(CCl)N1CCN(Cc2ncc(Cc3ccccc3)s2)CC1

MED-COV-4280ac29-8
0.392

View
O=C(CCl)N1CCN(C(=O)CCl)CC1

SAD-SAT-1b030f84-9
0.391

View
O=C(CCl)N1CCN(C(=O)c2cc(O)cc(Cl)c2)CC1

SAD-SAT-581007d4-5
0.391

View
O=C(CCl)N1CCN(Cc2cn(Cc3ccccc3)nn2)CC1

STE-KUL-2e0d2e88-7
0.389

View
N#Cc1ncc(Sc2cccc(CN3CCN(C(=O)CCl)CC3)c2)cn1

MAK-UNK-849bee6c-16
0.388

View
CCNc1ccccc1CN1CCN(C(=O)CCl)CC1

SEL-UNI-cd366922-6
0.386

View
N#Cc1ncccc1-c1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-849bee6c-5
0.383

View
N#Cc1nccc(-c2cccc(CN3CCN(C(=O)CCl)CC3)c2)n1

MAK-UNK-849bee6c-6
0.383

View
N#Cc1ncc(-c2cccc(CN3CCN(C(=O)CCl)CC3)c2)cn1

MAK-UNK-849bee6c-7
0.382

View
O=C(CCl)N1CCN(Cc2ncc(Cc3ccsc3)s2)CC1

MAK-UNK-e4a48a85-20
0.382

View
Cc1cc(CN2CCN(C(=O)CCl)CC2)ccc1NCCNCN1CCC(O)CC1

MAK-UNK-e4a48a85-18
0.381

View
O=C(CCl)N1CCN(c2cccc(Cl)c2)CC1

SAD-SAT-65574d3f-9
0.381

View
CN(c1cnc(C#N)nc1)c1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAK-UNK-849bee6c-14
0.380

View
CCNc1ncc(C#N)cc1CN1CCN(C(=O)CCl)CC1

BRU-LEF-ae0885ba-1
0.378

View
CCNc1ncc(C#N)cc1CN1CCN(C(=O)CCl)CC1

DAR-DIA-fb20be43-4
0.378

View
CCNc1ncc(C#N)cc1CN1CCN(C(=O)CCl)CC1

PAU-UNI-52c0427f-1
0.378

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CNC(=O)Cc1c(C)cccc1CN1CCN(C(=O)CCl)CC1

STE-UNK-13e151dd-1
0.378

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CC(=O)NCCc1c[nH]c2c(CN3CCN(C(=O)CCl)CC3)cc(Cl)cc12

DAR-DIA-fb20be43-15
0.378

View
CCNc1cc(CN2CCN(C(=O)CCl)CC2)c(C#N)cn1

DAV-CRI-d1e0885a-2
0.377

View
N#Cc1ncc(CCc2cccc(CN3CCN(C(=O)CCl)CC3)c2)cn1

MAK-UNK-849bee6c-9
0.377

View
CC(=O)N1CCCc2cccc(CN3CCN(C(=O)CCl)CC3)c2C1

TAM-UNI-d1c3dd9f-13
0.377

View
CCC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.789

View
Cc1cc(Cl)cc(CN2CCN(C(=O)CO)CC2)c1

0.769

View
CC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.737

View
COCC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.732

View
Cc1cc(Cl)cc(CN2CCN(C(=O)CC(C)C)CC2)c1

0.732

View
Cc1cc(Cl)cc(CN2CCN(C(=O)CN3CCCC3)CC2)c1

0.732

View
CCC(=O)N1CCCN(Cc2cc(C)cc(Cl)c2)CC1

0.714

View
Cc1cc(Cl)cc(CN2CCN(CC(=O)N3CCCC3)CC2)c1

0.707

View
Cc1cc(Cl)cc(CN2CCN(C(=O)N3CCCC3)CC2)c1

0.700

View
Cc1cccc(CN2CCN(C(=O)CCl)CC2)c1

0.700

View
CCN(CC)CC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.698

View
Cc1cc(Cl)cc(CN2CCN(CC(=O)N3CCCCC3)CC2)c1

0.690

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C(C)(C)C)CC2)c1

0.683

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C(C)C)CC2)c1

0.683

View
COC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.683

View
Cc1cc(Cl)cc(CN2CCN(C(=O)N(C)C)CC2)c1

0.683

View
CNC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.683

View
Cc1cc(Cl)cc(CN2CCN(C(=O)CN3CCOCC3)CC2)c1

0.682

View
Cc1cc(Cl)cc(CN2CCN(C(=O)CN3C(=O)CCC3=O)CC2)c1

0.682

View
Cc1cc(Cl)cc(CN2CCCN(CC(=O)N3CCCC3)CC2)c1

0.674

View
CC(=O)N1CCCN(Cc2cc(C)cc(Cl)c2)CC1

0.667

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C3CC3)CC2)c1

0.667

View
Cc1ccc(CN2CCN(C(=O)CCl)CC2)cc1

0.667

View
CCOC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.651

View
Cc1cc(Cl)cc(CN2CCN(C(=O)N3CCOCC3)CC2)c1

0.651

View
CCNC(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.651

View
Cc1cc(Cl)cc(CN2CCCN(C(N)=O)CC2)c1

0.651

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C(C)O)CC2)c1

0.651

View
O=C(CCl)N1CCN(Cc2cccc(Cl)c2)CC1

0.650

View
CCC(=O)N1CCN(Cc2cc(C)cc(C)c2)CC1

0.641

View
CCC(=O)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.641

View
O=C(CCl)N1CCN(Cc2ccc(Cl)cc2)CC1

0.641

View
CCN1CCN(C(=O)CC2CCN(Cc3cc(C)cc(Cl)c3)CC2)CC1

0.638

View
Cc1cc(Cl)cc(CN2CCCN(C(=O)CC3CCCC3)CC2)c1

0.638

View
CC(=O)NCC(=O)N1CCCN(Cc2cc(C)cc(Cl)c2)CC1

0.638

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccccc3)CC2)c1

0.636

View
Cc1cc(Cl)cc(CN2CCN(C(=O)NC(C)(C)C)CC2)c1

0.636

View
COC(OC)C(=O)N1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.636

View
Cc1cc(Cl)cc(CN2CCN(CC(N)=O)CC2)c1

0.634

View
Cc1cc(C)cc(CN2CCN(C(=O)CO)CC2)c1

0.625

View
Cc1cc(Cl)cc(CN2CCN(C(=O)Cn3cnnn3)CC2)c1

0.625

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccc(F)cc3)CC2)c1

0.622

View
Cc1cc(Cl)cc(CN2CCCN(C(=O)C(C)C)CC2)c1

0.622

View
COC(=O)N1CCCN(Cc2cc(C)cc(Cl)c2)CC1

0.622

View
COc1cc(CN2CCN(C(=O)CCl)CC2)cc(OC)c1

0.619

View
Cc1cc(C)cc(CN2CCN(C(=O)CN(C)C)CC2)c1

0.610

View
CN(C)CC(=O)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.610

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C(=O)NC(C)C)CC2)c1

0.609

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3cccs3)CC2)c1

0.609

View
Cc1cc(Cl)cc(CN2CCCN(C(=O)C3CC3)CC2)c1

0.609

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccc(O)cc3)CC2)c1

0.609

View
Cc1cc(Cl)cc(CN2CCC(CC(=O)N3CCCC3)CC2)c1

0.609

View
Cc1cc(Cl)cc(CN2CCN(C)CC2)c1

0.605

View
CCN1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.605

View
Cc1cc(Cl)cc(CN2CCN(CC(=O)N(C)C)CC2)c1

0.605

View
Cc1ccc(CN2CCCN(C(=O)CCl)CC2)cc1

0.605

View
Cc1cc(Cl)cc(CN2CCN(CCC(=O)O)CC2)c1

0.605

View
O=C(CO)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.600

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C(=O)NC3CC3)CC2)c1

0.596

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3cc(C)oc3C)CC2)c1

0.596

View
CCOC(=O)N1CCCN(Cc2cc(C)cc(Cl)c2)CC1

0.596

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccoc3)CC2)c1

0.596

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccccc3F)CC2)c1

0.596

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C3CCCN3C)CC2)c1

0.596

View
Cc1cc(Cl)cc(CN2CCN(C(=O)N3CCC(C(=O)O)CC3)CC2)c1

0.596

View
COCC(=O)N1CCN(Cc2cc(C)cc(C)c2)CC1

0.595

View
Cc1cc(C)cc(CN2CCN(C(=O)CC(C)C)CC2)c1

0.595

View
Cc1cc(C)cc(CN2CCN(C(=O)CN3CCCC3)CC2)c1

0.595

View
COCC(=O)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.595

View
CC(C)CC(=O)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.595

View
Cc1cc(Cl)cc(CN2CCCC2)c1

0.595

View
Cc1cc(C)cc(CN2CCN(C(=O)c3ccc(Cl)cc3)CC2)c1

0.591

View
COc1cc(CN2CCN(C(=O)CCl)CC2)cc(OC)c1OC

0.591

View
Cc1cc(Cl)cc(CN2CCCN(CC(=O)O)CC2)c1

0.591

View
CC(=O)N1CCN(Cc2cc(C)cc(C)c2)CC1

0.590

View
CC(=O)N1CCN(Cc2cc(Cl)cc(CN3CCN(C(C)=O)CC3)c2)CC1

0.590

View
CC(=O)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.590

View
CCc1ccc(CN2CCN(C(=O)CCl)CC2)cc1

0.585

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccco3)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)C3CCCO3)CC2)c1

0.583

View
COc1ccc(C(=O)N2CCN(Cc3cc(C)cc(Cl)c3)CC2)cc1

0.583

View
Cc1cc(Cl)cc(CN2CCCN(C(=O)c3ccccc3)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccccn3)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccccc3O)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3ccsc3)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3cccc(F)c3)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(C(=O)c3cccn3C)CC2)c1

0.583

View
Cc1cc(Cl)cc(CN2CCN(c3nc(C)cc(C)n3)CC2)c1

0.581

View
CCC(=O)N1CCCN(Cc2cc(C)cc(C)c2)CC1

0.581

View
CCC(=O)N1CCCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.581

View
CCC(=O)N1CCN(Cc2cc(F)cc(Cl)c2)CC1

0.581

View
O=C(CCl)N1CCCN(Cc2ccc(Cl)cc2)CC1

0.581

View
CCN(CC)C(=O)CN1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.578

View
CCNC(=O)CN1CCN(Cc2cc(C)cc(Cl)c2)CC1

0.578

View
Cc1cc(Cl)cc(CN2CCN(C(C)(C)C(N)=O)CC2)c1

0.578

View
Cc1cc(Cl)cc(CN2CCN(CCN3CCCC3)CC2)c1

0.575

View
Cc1cc(Cl)cc(CN2CCC(C(=O)N3CCN(C)CC3)CC2)c1

0.574

View
Cc1cc(Cl)cc(CN2CCN(c3ccc(C(N)=O)cc3)CC2)c1

0.574

View
Cc1cc(Cl)cc(CN2CCN(C(C)C(=O)N3CCCC3)CC2)c1

0.574

View
Cc1cc(C)cc(CN2CCN(CC(=O)N3CCCC3)CC2)c1

0.571

View

N1(CC2C=CC=C(Cl)C=2)CCN(C(C)=O)CC1

0.839

View
N1(CC2C=CC=C(C)C=2)CCN(C(C)=O)CC1

0.830

View
C(N1CCN(CC2C=CC=C(C)C=2)CC1)(=O)C(Cl)Cl

0.827

View
C(N1CCN(CC2C=CC=C(C)C=2)CC1)(=O)C1=CC=CC(Cl)=C1

0.801

View
N1(CC2=CC(Cl)=CC(Cl)=C2)CCN(C(C)=O)CC1

0.799

View


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