Molecule Details

O=C(CCl)N1CCN(Cc2ccc(Cl)s2)CC1
piperazine-chloroacetamide Enamine Mcule MolPort
View on Fragalysis x1334
Molecular Properties
SMILES:
O=C(CCl)N1CCN(Cc2ccc(Cl)s2)CC1
MW: 293.219
Fraction sp3: 0.55
HBA: 3
HBD: 0
Rotatable Bonds: 3
TPSA: 23.55
cLogP: 2.2845
Covalent Warhead: ✔️
Covalent Fragment:
Source
Enamine SCR: Z147647730
Enamine REAL: Z1562119728
Mcule: MCULE-8595318607
MolPort: MolPort-004-525-869
O=C(CCl)N1CCN(Cc2ccc(Br)s2)CC1

AAR-POS-0daf6b7e-12
0.673

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

JOH-UNI-27ac80fd-23
0.673

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

LON-WEI-8f408cad-5
0.564

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O=C(CCl)N1CCN(Cc2cccs2)CC1

AAR-POS-0daf6b7e-17
0.564

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

MAK-UNK-7c9d1431-29
0.519

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O=C(CCl)N1CCN(Cc2ccccc2)CC1

MAK-UNK-7c9d1431-24
0.500

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

JOH-UNI-27ac80fd-38
0.492

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

LON-WEI-8f408cad-7
0.491

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

MAK-UNK-212f693e-8
0.491

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

AAR-POS-0daf6b7e-13
0.491

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

MAK-UNK-7c9d1431-28
0.483

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O=C(CCl)N1CCN(Cc2cscc2Cl)CC1

SAD-SAT-bc31ec01-1
0.483

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

PAU-UNI-8cdd41c7-1
0.482

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

MAR-LAB-ca4662a6-2
0.475

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

MED-COV-4280ac29-15
0.475

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

JOH-UNI-27ac80fd-24
0.475

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

AAR-POS-d2a4d1df-35
0.475

View
O=C(CCl)N1CCN(Cc2ccc(Cl)s2)C[C@@H]1Cc1ccc(O)cc1

SEA-TRI-8252c13b-1
0.465

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O=C(CCl)N1CCN(Cc2cnc(Cc3ccccc3)s2)CC1

MED-COV-4280ac29-25
0.464

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O=C(CCl)N1CCN(Cc2ccc(-c3ccc4ccccc4c3CBr)s2)CC1

MAK-UNK-c74072e5-2
0.462

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

SAD-SAT-5b1897b2-2
0.459

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

MAK-UNK-6ca90168-14
0.458

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O=Cc1cc(-c2ccc(CN3CCN(C(=O)CCl)CC3)s2)ccc1[N+](=O)[O-]

MAK-UNK-c74072e5-10
0.455

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

MAK-UNK-7c9d1431-16
0.453

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

MAR-TRE-6a44bbf2-54
0.453

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O=C(CCl)N1CCN(S(=O)(=O)c2ccc(Cl)s2)CC1

AAR-POS-0daf6b7e-15
0.450

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O=C(CCl)N1CCN(Cc2scc3ccccc23)CC1

PAU-UNI-b2b6b158-1
0.448

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

AHN-SAT-de2502ba-15
0.444

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O=C(CCl)N1CCN(Cc2cnc(Cc3ccsc3)s2)CC1

MAK-UNK-e4a48a85-21
0.444

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Cc1ccccc1CN1CCN(C(=O)CCl)CC1

MAK-UNK-7c9d1431-20
0.443

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

SAD-SAT-581007d4-7
0.443

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

AAR-POS-d2a4d1df-24
0.443

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

SAD-SAT-581007d4-1
0.443

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

MAT-POS-2db6411e-2
0.443

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

JIA-UNI-93b03cae-1
0.443

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

SAD-SAT-581007d4-2
0.443

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O=C(CCl)N1CCN(Cc2ccc(-c3cccn3S(=O)(=O)c3ccccc3)s2)CC1

MAK-UNK-c74072e5-1
0.438

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

ASH-SAT-43770c7d-5
0.435

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

NEH-REV-107bcf72-5
0.435

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

MAT-POS-ee51dedd-1
0.431

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

MAK-UNK-7c9d1431-14
0.431

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

DAV-CRI-d1e0885a-1
0.431

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

MED-COV-4280ac29-33
0.424

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O=C(CCl)N1CCN(Cc2cccc3ccccc23)CC1

MED-COV-4280ac29-31
0.424

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O=C(CCl)N1CCN(Cc2cccc3ccccc23)CC1

AAR-POS-d2a4d1df-40
0.424

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

MED-COV-4280ac29-8
0.423

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

JOK-SYG-18591e8f-1
0.415

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

DAR-DIA-fb20be43-8
0.414

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

PAU-UNI-19862c28-1
0.414

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

MAK-UNK-e4a48a85-20
0.411

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O=C(CCl)N1CC2CC1CN2Cc1ccc(Cl)s1

MAK-UNK-3f402c2b-16
0.409

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

SAD-SAT-1b030f84-9
0.409

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

SAD-SAT-5b1897b2-5
0.409

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

MAK-UNK-7c9d1431-18
0.406

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O=C(CCl)N1CCN(Oc2ccsc2)CC1

MAK-UNK-212f693e-9
0.403

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

SAD-SAT-581007d4-3
0.403

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CNC(=O)c1ccc(C#N)cc1CN1CCN(C(=O)CCl)CC1

TAM-UNI-d1c3dd9f-17
0.403

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O=C(CCl)N1CCN(Cc2nc(-c3cccs3)no2)CC1

NAU-LAT-64f4b287-3
0.403

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O=C1Cc2c(cccc2CN2CCN(C(=O)CCl)CC2)CCN1

TAM-UNI-d1c3dd9f-14
0.400

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O=C(CCl)N1CCC(C(=O)N2CCN(Cc3ccc(-c4ccccc4[N+](=O)[O-])s3)CC2)CC1

SAD-SAT-9a6c5cf3-3
0.400

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

STE-KUL-2e0d2e88-7
0.400

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

DAR-DIA-fb20be43-2
0.400

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

MAK-UNK-7c9d1431-21
0.400

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

JOO-PER-58e158bd-1
0.397

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

SAD-SAT-bc31ec01-7
0.397

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CCNc1ccccc1CN1CCN(C(=O)CCl)CC1

SEL-UNI-cd366922-6
0.397

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

MAK-UNK-af83ef51-1
0.397

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C=CC(=O)N1CCN(Cc2ccc(CC)s2)CC1

SAD-SAT-b55127ae-10
0.397

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

MED-COV-4280ac29-37
0.394

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O=C(CN1CCN(C(=O)CCl)CC1)Nc1ccc(F)cc1

MAR-TRE-6a44bbf2-47
0.394

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

MIH-UNI-e573136b-5
0.391

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O=C(CCl)N1CCN(CCCc2ccccc2)CC1

MAK-UNK-15efde89-1
0.391

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

STE-UNK-13e151dd-1
0.389

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

TOB-UNK-c2aba166-1
0.389

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

SAD-SAT-65574d3f-10
0.388

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

NEH-REV-107bcf72-3
0.386

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

MAR-TRE-6a44bbf2-12
0.385

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COCCc1cc(Br)sc1CN1CCN(C(=O)CCl)CC1

JOH-UNI-27ac80fd-39
0.384

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CC(=O)Nc1ccc(C#N)cc1CN1CCN(C(=O)CCl)CC1

TAM-UNI-d1c3dd9f-18
0.384

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O=C(CCl)N1CCN(C(=O)c2ccco2)CC1

AAR-POS-d2a4d1df-29
0.383

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O=C(CCl)N1CCN(C(=O)c2ccco2)CC1

MAR-TRE-6a44bbf2-61
0.383

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

SAD-SAT-581007d4-4
0.382

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Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

AAR-POS-d2a4d1df-41
0.382

View
Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

TAT-ENA-80bfd3e5-20
0.382

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

MAK-UNK-704ed37c-11
0.380

View
O=C(CCl)N1CCC(C(=O)N2CCN(S(=O)(=O)c3ccc(Cl)s3)CC2)CC1

SAD-SAT-f2e2579e-3
0.378

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CCNc1cccc(C#N)c1CN1CCN(C(=O)CCl)CC1

MED-COV-4280ac29-24
0.378

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COc1cc(CN2CCN(C(=O)CCl)CC2)c2ccccc2c1

DAR-DIA-fb20be43-7
0.378

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CCNc1ccc(C#N)cc1CN1CCN(C(=O)CCl)CC1

DAR-DIA-fb20be43-3
0.378

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

MAK-UNK-704ed37c-12
0.377

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O=C(CCl)N1CCN(C(=O)c2ccc(Br)s2)CC1

JOH-UNI-27ac80fd-25
0.377

View
O=C1NCCCc2cccc(CN3CCN(C(=O)CCl)CC3)c21

TAM-UNI-d1c3dd9f-15
0.377

View
O=C(CCl)N1CCN(C/C=C/c2ccccc2)CC1

SAD-SAT-65574d3f-1
0.375

View
O=C(CCl)N1CCN(C/C=C/c2ccccc2)CC1

AHN-SAT-de2502ba-14
0.375

View
N#Cc1csc(NCO)c1CN1CCN(C(=O)CCl)CC1

DAV-CRI-d1e0885a-5
0.375

View
CC(=O)Nc1scc(C#N)c1CN1CCN(C(=O)CCl)CC1

DAV-CRI-d1e0885a-6
0.375

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N#Cc1cc(CN2CCN(C(=O)CCl)CC2)c2ccccc2c1

DAR-DIA-fb20be43-6
0.373

View
O=C(NCCN1CCN(C(=O)CCl)CC1)c1ccccc1

STE-KUL-2e0d2e88-1
0.373

View
O=C(CCl)N1CCN(C(=O)C2CC2)CC1

SAD-SAT-5b1897b2-9
0.370

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

SEL-UNI-cd366922-7
0.370

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CCC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.771

View
O=C(CO)N1CCN(CC2=CC=C(Cl)S2)CC1

0.755

View
CC(C)CC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.698

View
CC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.694

View
CN(C)CC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.685

View
COCC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.685

View
O=C(CCl)N1CCN(CC2=CC=C(Br)S2)CC1

0.673

View
O=C(O)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.667

View
O=C(CN1CCCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.661

View
O=C(CN1C(=O)CCC1=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.655

View
CNC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.654

View
CCN(CC)CC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.649

View
CC(O)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.648

View
CCC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.643

View
O=C(C1CC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.642

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CN(C)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.642

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ClC1=CC=C(CN2CCN(CC3=CC=C(Cl)S3)CC2)S1

0.636

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CC(C)(C)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.630

View
CC(C)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.630

View
COC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.630

View
O=C(CC1=CC=C(Cl)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.627

View
O=C(CC1=CC=CC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.627

View
O=C(CN1CCOCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.627

View
O=C(CC1=CC=CC=C1F)N1CCN(CC2=CC=C(Cl)S2)CC1

0.623

View
O=C(N1CCCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.618

View
O=C(C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1)N1CCCC1

0.618

View
CCOC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.618

View
O=C(CC1=CC=CS1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.617

View
O=C(CC1CCCCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.617

View
O=C(N1CCNCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.614

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CC(C)(C)OC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.614

View
O=C(N1CCOCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.607

View
CCNC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.607

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CCN(CC)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.607

View
CC1=CC=C(CC(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)C=C1

0.607

View
O=C(CCC1CCCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.597

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O=C(CN1CCN(CC2=CC=C(Cl)S2)CC1)N1CCCC1

0.596

View
O=C(N1CCCCC1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.596

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NC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.596

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CCC(CC)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.596

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NC(=O)CN1CCN(CC2=CC=C(Cl)S2)CC1

0.596

View
O=C(O)CN1CCN(CC2=CC=C(Cl)S2)CC1

0.596

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O=C(O)C1=CC=C(CN2CCN(CC3=CC=C(Cl)S3)CC2)S1

0.596

View
O=C(O)CCN1CCN(CC2=CC=C(Cl)S2)CC1

0.593

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CC(C)CC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.590

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O=C(CN1C=NN=N1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.587

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O=C(C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1)N1CCOCC1

0.586

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CC(C)(C)NC(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.586

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COC(OC)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.586

View
O=C(CC1=CC=C(Cl)S1)N1CCN(CC2=CC=C(Br)S2)CC1

0.583

View
CC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.579

View
O=C(COC1=CC=C(F)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.578

View
O=C(CCCC1=CC=CC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.578

View
O=C(CN1CCN(CC2=CC=C(Cl)S2)CC1)N1CCCCCC1

0.576

View
O=C(CN1CCN(CC2=CC=C(Cl)S2)CC1)N1CCCCC1

0.576

View
O=C(C1=CC=CC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.576

View
O=C(C1=CC=C(Cl)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.576

View
O=C(C1=CC=C(O)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.576

View
CC1=CC=C(OCC(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)C=C1

0.569

View
O=C(C1=C(Cl)C=CC=C1Cl)N1CCN(CC2=CC=C(Cl)S2)CC1

0.567

View
O=C(C1=CC=C(F)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.567

View
O=C(C1=CSC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.567

View
O=C(CCl)N1CCN(CC2=CC=CS2)CC1

0.564

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O=C(CC1=CC(F)=CC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.561

View
COC1=CC=C(CCC(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)C=C1

0.561

View
O=C(C1=CC=CS1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.557

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CC1=CC=C(C(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)C=C1

0.557

View
O=C(C1=CC=C(Br)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.557

View
CC1=CC=C(C(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)S1

0.557

View
O=C(CCl)N1CCN(CC2=CC=C(C3=CC=C(Br)C=C3)S2)CC1

0.556

View
O=C(CCl)N1CCN(CC2=CC=C(C3=CC=CC=C3Cl)S2)CC1

0.554

View
O=C(CC1CCCC1)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.554

View
CC(=O)NCC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.554

View
O=C(C1=C(F)C=CC=C1F)N1CCN(CC2=CC=C(Cl)S2)CC1

0.548

View
O=C(NC1CC1)C(=O)N1CCN(CC2=CC=C(Cl)S2)CC1

0.548

View
O=C(CCC1=CC=C(Cl)S1)N1CCN(CC2=CC=C(Br)S2)CC1

0.547

View
O=C(C1CC1)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.541

View
ClC1=CC=C(CN2CCCN(CC3=CC=C(Cl)S3)CC2)S1

0.540

View
O=C(OC1=CC=CC=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.540

View
CCC1=CC=C(C(=O)N2CCN(CC3=CC=C(Cl)S3)CC2)C=C1

0.540

View
O=C(CCl)N1CCN(CC2=CC=C(C3=CC=CC(Cl)=C3)S2)CC1

0.537

View
CC(C)C(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.532

View
COC(=O)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.532

View
O=C(C1=CC=C(Cl)C=C1Cl)N1CCN(CC2=CC=C(Cl)S2)CC1

0.531

View
O=C(C1=CC=C(C(F)(F)F)C=C1)N1CCN(CC2=CC=C(Cl)S2)CC1

0.531

View
O=C(C1=CC=CC=C1F)N1CCN(CC2=CC=C(Cl)S2)CC1

0.531

View
CCN1CCN(C(=O)CC2CCN(CC3=CC=C(Cl)S3)CC2)CC1

0.530

View
O=C(CN1CCCN(CC2=CC=C(Cl)S2)CC1)N1CCCC1

0.524

View
O=C(CC1=CC=C(Cl)S1)N1CCN(CC2=CC=CS2)CC1

0.524

View
O=C(CCl)N1CCN(CC2=CC=C(C3=CC=CC=C3F)S2)CC1

0.522

View
O=C(CCC1=CC=CC=C1)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.522

View
ClC1=CC=C(CN2CCSSCC2)S1

0.510

View
O=C(CC1=CC=C(Cl)S1)N1CCN(CC2=CN=CS2)CC1

0.508

View
O=C(CCl)N1CCN(CC2=CC=C(C3=CC(F)=CC=C3)S2)CC1

0.507

View
O=C(CC1CCN(CC2=CC=C(Cl)S2)CC1)N1CCCC1

0.500

View
O=C(CCC1=CC=C(Cl)S1)N1CCN(CC2=CC=CS2)CC1

0.493

View
O=C(C1=CC=CC=C1)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.493

View
O=C(C1=CC=C(Cl)C=C1)N1CCCN(CC2=CC=C(Cl)S2)CC1

0.493

View
CCN1CCN(C(=O)CC2=CC=C(Cl)S2)CC1

0.483

View
O=C(CCC1=CC=C(Cl)S1)N1CCN(CC2=CC=C(Cl)C=C2)CC1

0.470

View
Cl.ClCC(=O)N1CCN(Cc2ccc(Cl)s2)CC1

0.977

View
CCC(=O)N1CCN(Cc2ccc(Cl)s2)CC1

0.771

View
COCC(=O)N1CCN(Cc2ccc(Cl)s2)CC1

0.685

View
Clc1ccc(CN2CCN(CC2)C(=O)CC#N)s1

0.685

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

0.685

View
Clc1ccc(CN2CCN(CC2)C(=O)C2CC2)s1

0.642

View
Clc1ccc(CN2CCN(CC2)C(=O)CN2CCOCC2)s1

0.627

View
NC(=O)CN1CCN(Cc2ccc(Cl)s2)CC1

0.596

View
OCCN1CCN(Cc2ccc(Cl)s2)CC1

0.577

View
CC(C)(C#N)C(=O)N1CCN(Cc2ccc(Cl)s2)CC1

0.567

View
CC(=O)NCCNC(=O)N1CCN(Cc2ccc(Cl)s2)CC1

0.565

View
Cl.ClCC(=O)N1CCN(Cc2cccs2)CC1

0.554

View
CN1CCN(Cc2ccc(Cl)s2)CC1

0.549

View
Clc1ccc(CN2CCNCC2)s1

0.529

View
CC(C)NC(=O)CN1CCN(Cc2ccc(Cl)s2)CC1

0.508

View
CC(C)(C)NC(=O)CN1CCN(Cc2ccc(Cl)s2)CC1

0.508

View
Clc1ccc(CN2CCNC(=O)C2)s1

0.441

View
CN(CC(=O)NC1CC1)C(=O)CN1CCN(Cc2ccc(Cl)s2)CC1

0.425

View
CCN1CCN(CC1)C(=O)c1ccc(Cl)s1

0.333

View
CCN(CC(=O)N1CCNC(=O)C1)Cc1ccc(Cl)s1

0.329

View
Clc1ccc(s1)C(=O)N1CCN(CC=C)CC1

0.318

View
CN(CC(=O)N1CCNC(=O)C1)Cc1ccc(Cl)s1

0.316

View
CN1CCN(CC1)C(=O)c1ccc(Cl)s1

0.286

View
CC(C)C(=O)NCCN(Cc1ccc(Cl)s1)C=O

0.264

View
N1(CC2SC(Cl)=CC=2)CCN(C(C)=O)CC1

0.930

View
N1(CC2SC(Cl)=CC=2)CCN(C=O)CC1

0.871

View
N1(CC2SC=CC=2)CCN(C(C)=O)CC1

0.836

View
N1(CC2SC(Cl)=CC=2)CCN(C)C(=O)C1

0.822

View
C(N1CCN(CC)CC1)(C1SC(Cl)=CC=1)=O

0.821

View


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