Molecule Details

O=C(CCl)N1CCN(Cc2cc(O)cc(Cl)c2)CC1
Duplicate piperazine-chloroacetamide Enamine Assayed
Molecular Properties
SMILES:
O=C(CCl)N1CCN(Cc2cc(O)cc(Cl)c2)CC1
MW: 302.06
Fraction sp3: 0.46
HBA: 3
HBD: 1
Rotatable Bonds: 3
TPSA: 43.78
cLogP: 1.93
Covalent Warhead: ✔️
Covalent Fragment:
Source
Enamine SCR: Z4450620215
Activity Data
IC50 (µM) - Fluorescence: 12.91844908314
IC50 (µM) - RapidFire: 1.56892614752099
Trypsin IC50 (µM): 99.0
pIC50 (µM) - Fluorescence 4.88878962218181
Average Inhibition @ 20 µM - Fluorescence: 74.96829
Average Inhibition @ 50 µM - Fluorescence: 89.51881
Average Inhibition @ 20 µM - RapidFire: 92.7299912844281
Average Inhibition @ 50 µM - RapidFire: 98.8615965175399
Order Status
Shipped: 2020-05-13
CS(=O)(=O)NCCc1ccccc1

AAR-POS-d2a4d1df-1

View

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

SAD-SAT-581007d4-7
1.000

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

PAU-UNI-8cdd41c7-1
0.735

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

KIM-UNI-2ee5d8f9-1
0.720

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

SAD-SAT-581007d4-1
0.667

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

SAD-SAT-581007d4-2
0.667

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

SAD-SAT-581007d4-8
0.655

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

MED-COV-4280ac29-33
0.627

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

SAD-SAT-581007d4-3
0.600

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

MED-COV-4280ac29-15
0.561

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

AAR-POS-d2a4d1df-35
0.561

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

MAK-UNK-7c9d1431-29
0.556

View
O=C(CCl)N1CCN(Cc2ccccc2)CC1

MAK-UNK-7c9d1431-24
0.509

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

SAD-SAT-581007d4-5
0.508

View
O=C(CCl)N1CCN(Cc2ccsc2)CC1

AAR-POS-0daf6b7e-13
0.500

View
O=C(CCl)N1CCN(Cc2ccsc2)CC1

MAK-UNK-212f693e-8
0.500

View
O=C(CCl)N1CCN(Cc2ccsc2)CC1

LON-WEI-8f408cad-7
0.500

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

SAD-SAT-581007d4-4
0.477

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

AAR-POS-d2a4d1df-24
0.475

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

NEH-REV-107bcf72-5
0.468

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

MAK-UNK-6ca90168-14
0.467

View
O=C(CCl)N1CCN(Cc2cscc2Cl)CC1

SAD-SAT-bc31ec01-1
0.467

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

MAK-UNK-7c9d1431-14
0.462

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

NEH-REV-107bcf72-3
0.456

View
O=C(CCl)N1CC2CC1CN2Cc1cc(O)cc(Cl)c1

MAK-UNK-df1a028e-6
0.455

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

JIA-UNI-93b03cae-1
0.452

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

MAK-UNK-af83ef51-1
0.448

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

JOK-SYG-18591e8f-1
0.446

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

TAM-UNI-d1c3dd9f-16
0.443

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

AAR-POS-0daf6b7e-2
0.443

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

MAR-TRE-6a44bbf2-54
0.439

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

MAK-UNK-7c9d1431-16
0.439

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

MAT-POS-ee51dedd-1
0.439

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

SAD-SAT-5b1897b2-5
0.439

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

JOH-UNI-27ac80fd-23
0.435

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

AAR-POS-0daf6b7e-12
0.435

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

AHN-SAT-de2502ba-15
0.431

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

JOO-PER-58e158bd-1
0.425

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

MED-COV-4280ac29-37
0.423

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

DAR-DIA-fb20be43-8
0.423

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

PAU-UNI-19862c28-1
0.423

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

ASH-SAT-43770c7d-5
0.422

View
O=C(CCl)N1CCN(Cc2ccco2)CC1

MAK-UNK-7c9d1431-28
0.419

View
O=C(CCl)N1CCN(Cc2cccs2)CC1

LON-WEI-8f408cad-5
0.419

View
O=C(CCl)N1CCN(Cc2cccs2)CC1

AAR-POS-0daf6b7e-17
0.419

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

MAK-UNK-7c9d1431-18
0.414

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

MAR-LAB-ca4662a6-2
0.413

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

MAK-UNK-7c9d1431-21
0.409

View
Cc1ccccc1CN1CCN(C(=O)CCl)CC1

MAK-UNK-7c9d1431-20
0.406

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

SAD-SAT-5b1897b2-2
0.400

View
C#CCN1CCN(C(=O)CCl)CC1

TOB-UNK-c2aba166-1
0.400

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

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

SAD-SAT-65574d3f-10
0.397

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

JOH-UNI-27ac80fd-38
0.394

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

SAD-SAT-1b030f84-9
0.391

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

STE-KUL-2e0d2e88-7
0.389

View
O=C(CCl)N1CCN(C(=O)c2cscc2Cl)CC1

SAD-SAT-1b030f84-5
0.387

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

MAK-UNK-849bee6c-6
0.383

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

MAK-UNK-849bee6c-5
0.383

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

MAK-UNK-849bee6c-7
0.382

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

MAK-UNK-849bee6c-17
0.381

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

MAK-UNK-849bee6c-2
0.381

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

TAM-UNI-d1c3dd9f-6
0.377

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

MAK-UNK-176ca439-3
0.377

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

MAK-UNK-cd94b63c-1
0.377

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

MAK-UNK-849bee6c-9
0.377

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

TAM-UNI-d1c3dd9f-5
0.377

View
N#Cc1ccc(-c2cc(CN3CCN(C(=O)CCl)CC3)cc3cnccc23)cc1

FAB-UNK-7ad5ab26-2
0.376

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

MAK-UNK-6ca90168-15
0.375

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

SAD-SAT-bc31ec01-5
0.375

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

AAR-POS-0daf6b7e-21
0.373

View
O=C(CCl)N1CCN(Cc2cccc(CNC(=O)N3CCOCC3)c2)CC1

TAM-UNI-d1c3dd9f-12
0.372

View
O=C(CCl)N1CCN(Cc2cccc3ccccc23)CC1

AAR-POS-d2a4d1df-40
0.371

View
O=C(CCl)N1CCN(Cc2cccc3ccccc23)CC1

MED-COV-4280ac29-31
0.371

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

MAK-UNK-849bee6c-16
0.370

View
O=C(CCl)N1CCN(Cc2cc(F)cc3ccccc23)CC1

DAR-DIA-fb20be43-2
0.370

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

MAK-UNK-849bee6c-18
0.369

View
N#Cc1nccc(CCc2cccc(CN3CCN(C(=O)CCl)CC3)c2)n1

MAK-UNK-849bee6c-8
0.369

View
CCNc1ncc(OC)cc1CN1CCN(C(=O)CCl)CC1

DAR-DIA-fb20be43-5
0.368

View
Cc1nc(CN2CCN(C(=O)CCl)CC2)c(NCc2cccc(O)c2)c(=O)[nH]1

MAK-UNK-e4a48a85-27
0.368

View
CCNc1ccccc1CN1CCN(C(=O)CCl)CC1

SEL-UNI-cd366922-6
0.366

View
O=C(CCl)N1CCN(CC2=CC3OCOC3C=C2)CC1

SAD-SAT-bc31ec01-7
0.366

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

MAK-UNK-704ed37c-11
0.365

View
N#Cc1nccc(Oc2cccc(CN3CCN(C(=O)CCl)CC3)c2)n1

MAK-UNK-849bee6c-13
0.365

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

MAK-UNK-849bee6c-19
0.365

View
N#Cc1nccc(Nc2cccc(CN3CCN(C(=O)CCl)CC3)c2)n1

MAK-UNK-849bee6c-3
0.365

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

MED-COV-4280ac29-6
0.364

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

MAK-UNK-849bee6c-25
0.364

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

MAK-UNK-e4a48a85-20
0.364

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

MAK-UNK-849bee6c-22
0.364

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

MAK-UNK-849bee6c-14
0.362

View
NS(=O)(=O)c1cc(Cl)cc(C(=O)N2CCN(C(=O)CCl)CC2)c1

SAD-SAT-581007d4-6
0.362

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

NIR-THE-0d6461ce-8
0.362

View
O=C(CCl)N1CCN(Cc2cc(Cl)ccc2CNS(=O)(=O)N2CCOCC2)CC1

STU-CHA-6d5cfe2b-1
0.361

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

DAR-DIA-fb20be43-15
0.361

View
CC(=O)NCCc1cn(C)c2cc(CN3CCN(C(=O)CCl)CC3)ccc12

TAM-UNI-d1c3dd9f-19
0.361

View
O=C(CSCc1cccc(CN2CCN(C(=O)CCl)CC2)c1)CN1CCC(O)CC1

MAK-UNK-e4a48a85-7
0.361

View
NS(=O)(=O)CCc1ccccc1CN1CCN(C(=O)CCl)CC1

MIH-UNI-e573136b-5
0.361

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

MAK-UNK-849bee6c-1
0.360

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

MAK-UNK-849bee6c-15
0.360

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

0.789

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

0.769

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

0.732

View
O=C(CN1CCCC1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.732

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

0.718

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

0.714

View
O=C(CN1CCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCCC1

0.707

View
O=C(N1CCCC1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.700

View
O=C(C(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCCC1

0.700

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

0.700

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

0.698

View
O=C(CN1CCOCC1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.682

View
O=C(CN1C(=O)CCC1=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.682

View
O=C(CN1CCCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCCC1

0.674

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

0.667

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

0.667

View
O=C(C1CC1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.667

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

0.667

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

0.667

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

0.667

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

0.667

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

0.652

View
O=C(N1CCOCC1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.651

View
O=C(c1ccc(O)cc1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.651

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

0.651

View
O=C(C(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCOCC1

0.651

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

0.651

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

0.651

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

0.650

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

0.650

View
O=C(CCl)N1CCN(Cc2ccc(O)c(Cl)c2)CC1

0.643

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

0.641

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

0.641

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

0.636

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

0.636

View
O=C(c1ccccc1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.636

View
O=C(Cn1cnnn1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.625

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

0.625

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

0.622

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

0.622

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

0.619

View
O=C(C1CC1)N1CCCN(Cc2cc(O)cc(Cl)c2)CC1

0.609

View
O=C(c1ccccc1O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.609

View
O=C(NC1CC1)C(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.609

View
O=C(c1cccs1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.609

View
O=C(CC1CCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCCC1

0.609

View
O=C(c1cccc(O)c1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.609

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

0.609

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

0.609

View
O=C(O)C1CCN(C(=O)N2CCN(Cc3cc(O)cc(Cl)c3)CC2)CC1

0.609

View
O=C(O)CN1CCCN(Cc2cc(O)cc(Cl)c2)CC1

0.605

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

0.600

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

0.596

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

0.595

View
Oc1cc(Cl)cc(CN2CCCC2)c1

0.595

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

0.591

View
CN1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.590

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

0.590

View
O=C(c1ccco1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

View
O=C(c1ccccn1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

View
O=C(c1ccsc1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

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

0.583

View
O=C(c1ccoc1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

View
O=C(C1CCCO1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

View
O=C(c1ccccc1)N1CCCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

View
CN1CCCC1C(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.583

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

0.581

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

0.581

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

0.581

View
O=C(O)C1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.581

View
OCCN1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.575

View
Oc1cc(Cl)cc(CN2CCN(CCN3CCCC3)CC2)c1

0.575

View
Oc1cc(Cl)cc(CN2CCC(F)CC2)c1

0.575

View
NC(=O)c1ccc(N2CCN(Cc3cc(O)cc(Cl)c3)CC2)cc1

0.574

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

0.571

View
O=C(CN1CCCC1)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.571

View
O=C(CC1CCN(Cc2cc(O)cc(Cl)c2)CC1)N1CCOCC1

0.571

View
Cn1cccc1C(=O)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.571

View
O=C(c1ccc(O)cc1)N1CCN(Cc2cc(Cl)cc(Cl)c2)CC1

0.568

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

0.568

View
NC(=O)C1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.568

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

0.568

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

0.568

View
O=C(Cc1cccc(Cl)c1)N1CCN(Cc2cccc(O)c2)CC1

0.565

View
O=C(CN1CCN(Cc2cc(O)cc(Cl)c2)CC1)NC1CC1

0.565

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

0.565

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

0.565

View
O=C(C1CCN(Cc2cc(O)cc(Cl)c2)CC1)C(F)(F)F

0.565

View
O=C(O)C(O)C1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.565

View
CN1CCN(C(=O)C2CCN(Cc3cc(O)cc(Cl)c3)CC2)CC1

0.562

View
Oc1cc(Cl)cc(CN2CCC(F)(F)CC2)c1

0.561

View
N#CCN1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.561

View
O=S1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.561

View
O=S1(=O)CCN(Cc2cc(O)cc(Cl)c2)CC1

0.561

View
Oc1cc(Cl)cc(CN2CCN(CC(F)(F)F)CC2)c1

0.561

View
Oc1cc(Cl)cc(CN2CCN(CC(F)F)CC2)c1

0.561

View
O=C(c1cccnc1)N1CCN(Cc2cc(O)cc(Cl)c2)CC1

0.560

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

0.558

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

0.558

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

0.556

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

0.181

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

0.055

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

0.829

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

0.789

View
C(N1CCN(CC2=CC=C(Cl)C=C2)CC1)(=O)C(Cl)Cl

0.786

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

0.785

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

0.778

View


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