Molecule Details

O=C(CCl)N1CCN(Cc2ccco2)CC1
piperazine-chloroacetamide Enamine Mcule MolPort
Molecular Properties
SMILES:
O=C(CCl)N1CCN(Cc2ccco2)CC1
MW: 242.08
Fraction sp3: 0.55
HBA: 3
HBD: 0
Rotatable Bonds: 3
TPSA: 36.69
cLogP: 1.16
Covalent Warhead: ✔️
Covalent Fragment: ✔️
Source
Enamine SCR: Z2608820552
Enamine REAL: Z1562120730
Mcule: MCULE-3595033105
MolPort: MolPort-012-963-698
O=C(CCl)N1CCN(S(=O)(=O)c2cccs2)CC1

LON-WEI-8f408cad-3

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O=C(CCl)N1CCN(S(=O)(=O)c2cccc(F)c2)CC1

LON-WEI-8f408cad-4

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

AAR-POS-d2a4d1df-24

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

AAR-POS-d2a4d1df-27

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

AAR-POS-d2a4d1df-29

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

MAR-LAB-ca4662a6-2
0.582

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O=C(CCl)N1CCN(Cc2ccccc2)CC1

MAK-UNK-7c9d1431-24
0.558

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O=C(CCl)N1CCN(Cc2cccs2)CC1

AAR-POS-0daf6b7e-17
0.509

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O=C(CCl)N1CCN(Cc2cccs2)CC1

LON-WEI-8f408cad-5
0.509

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

AAR-POS-0daf6b7e-12
0.500

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

JOH-UNI-27ac80fd-23
0.500

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

MAK-UNK-7c9d1431-29
0.491

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

AAR-POS-0daf6b7e-2
0.483

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

MAR-TRE-6a44bbf2-61
0.482

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

AAR-POS-d2a4d1df-29
0.482

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

AAR-POS-d2a4d1df-35
0.475

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

MED-COV-4280ac29-15
0.475

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

AAR-POS-d2a4d1df-24
0.467

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Cc1ccccc1CN1CCN(C(=O)CCl)CC1

MAK-UNK-7c9d1431-20
0.467

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

AAR-POS-0daf6b7e-13
0.466

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

LON-WEI-8f408cad-7
0.466

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O=C(CCl)N1CCN(Cc2ccsc2)CC1

MAK-UNK-212f693e-8
0.466

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

JOK-SYG-18591e8f-1
0.460

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

MAK-UNK-6ca90168-14
0.458

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

PAU-UNI-8cdd41c7-1
0.456

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

MIH-UNI-e573136b-5
0.455

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

MED-COV-4280ac29-33
0.446

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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(Cc2ccc(CS(=O)(=O)F)cc2)CC1

JIA-UNI-93b03cae-1
0.443

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

MAK-UNK-af83ef51-1
0.439

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

NEH-REV-107bcf72-5
0.435

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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(Cc2cscc2Cl)CC1

SAD-SAT-bc31ec01-1
0.433

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

MAR-TRE-6a44bbf2-54
0.431

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

MAK-UNK-7c9d1431-16
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#Cc1cccc(CN2CCN(C(=O)CCl)CC2)c1

MAT-POS-ee51dedd-1
0.431

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CC(=O)Nc1ccc(S(=O)(=O)N2CCN(Cc3ccco3)CC2)cc1

MAR-TRE-fd17a9b8-74
0.429

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O=C(CCl)N1CCN(Cc2cccc3ccccc23)CC1

AAR-POS-d2a4d1df-40
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(Cc2ncc(Cc3ccccc3)s2)CC1

MED-COV-4280ac29-8
0.423

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

MED-COV-4280ac29-25
0.423

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

STE-KUL-2e0d2e88-7
0.420

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

SAD-SAT-581007d4-2
0.419

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

MAT-POS-2db6411e-2
0.419

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

SAD-SAT-581007d4-7
0.419

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

SAD-SAT-65574d3f-1
0.419

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

AHN-SAT-de2502ba-14
0.419

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

SAD-SAT-581007d4-1
0.419

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CCNc1ccccc1CN1CCN(C(=O)CCl)CC1

SEL-UNI-cd366922-6
0.418

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

SAD-SAT-5b1897b2-2
0.413

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O=C(CCl)N1CCN(CCCc2ccccc2)CC1

MAK-UNK-15efde89-1
0.413

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

DAV-CRI-d1e0885a-1
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(C(=O)CCl)CC1

SAD-SAT-1b030f84-9
0.409

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

SIM-SYN-f15aaa3a-1
0.407

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

JOH-UNI-27ac80fd-38
0.406

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O=C(CCl)N1CCN(Cc2scc3ccccc23)CC1

PAU-UNI-b2b6b158-1
0.406

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

MAK-UNK-7c9d1431-18
0.406

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Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

TAT-ENA-80bfd3e5-20
0.403

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Cc1ccccc1CN1CCCN(C(=O)CCl)CC1

AAR-POS-d2a4d1df-41
0.403

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

SAD-SAT-581007d4-4
0.403

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

NAU-LAT-64f4b287-3
0.403

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

TAM-UNI-d1c3dd9f-18
0.403

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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(Cc2cccc(CNC(=O)N3CCOCC3)c2)CC1

TAM-UNI-d1c3dd9f-12
0.400

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

SAD-SAT-bc31ec01-7
0.397

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

MAK-UNK-987948f6-2
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(CCl)N1CCN(Cc2cc(Cl)cc3ccccc23)CC1

PAU-UNI-19862c28-1
0.394

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

DAR-DIA-fb20be43-8
0.394

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

STE-KUL-2e0d2e88-1
0.394

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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

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

SAD-SAT-65574d3f-10
0.388

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

MAK-UNK-849bee6c-9
0.387

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

MAK-UNK-176ca439-3
0.387

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

MAK-UNK-cd94b63c-1
0.387

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

NEH-REV-107bcf72-3
0.386

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

MAK-UNK-c74072e5-1
0.386

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O=C(CCl)N1CCN(C(=O)c2ccoc2)CC1

SAD-SAT-3a925b8b-5
0.383

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

SAD-SAT-581007d4-3
0.382

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Nc1nc(CN2CCN(C(=O)CCl)CC2)ncc1Cc1ccccc1

MED-COV-4280ac29-19
0.382

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

MAK-UNK-704ed37c-11
0.380

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

MED-COV-4280ac29-24
0.378

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

DAR-DIA-fb20be43-3
0.378

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

DAR-DIA-fb20be43-7
0.378

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NS(=O)(=O)CCNc1ncccc1CN1CCN(C(=O)CCl)CC1

STU-CHA-464c0256-1
0.377

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NS(=O)(=O)c1ccc2cccc(CN3CCN(C(=O)CCl)CC3)c2c1

MIH-UNI-e573136b-4
0.373

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

DAR-DIA-fb20be43-6
0.373

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

MAK-UNK-e4a48a85-20
0.373

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

MAK-UNK-849bee6c-7
0.373

View
CCc1ccccc1NC(=O)CN1CCN(C(=O)CCl)CC1

MAR-TRE-6a44bbf2-27
0.371

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

SAD-SAT-65574d3f-9
0.371

View
O=C(CCl)N1CCN(C(=O)Nc2ccccc2)CC1

AHN-SAT-de2502ba-7
0.371

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

MAR-TRE-6a44bbf2-21
0.371

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

MAK-UNK-7c9d1431-9
0.371

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

SEL-UNI-cd366922-7
0.370

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

MAK-UNK-e4a48a85-21
0.368

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

TAM-UNI-d1c3dd9f-13
0.368

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O=C(CCl)N1CCN(C(=O)n2cccc2)CC1

MAK-UNK-52a1ef4b-1
0.368

View
Cc1cccc(C)c1NC(=O)CN1CCN(C(=O)CCl)CC1

TAT-ENA-80bfd3e5-30
0.368

View
NS(=O)(=O)Cc1nc2cccc(CN3CCN(C(=O)CCl)CC3)c2[nH]1

STU-CHA-0f79177c-1
0.367

View
O=C(CN1CCN(C(=O)CCl)CC1)Nc1cccc(F)c1

MAR-TRE-6a44bbf2-3
0.366

View
CCC(=O)N1CCN(Cc2ccco2)CC1

0.730

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

1.000

View
O=C(Cc1ccco1)N1CCN(Cc2ccco2)CC1

0.750

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCN(C(=O)CN2CCN(Cc3ccco3)CC2)CC1

0.750

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCN(Cc2ccco2)CC1

0.750

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

0.730

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

0.730

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

0.730

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

0.714

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

0.711

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

0.711

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

0.711

View
O=C(CCc1ccco1)N1CCN(Cc2ccco2)CC1

0.711

View
O=C(Cc1c(Cl)cccc1Cl)N1CCN(Cc2ccco2)CC1

0.707

View
O=C(CC(F)(F)F)N1CCN(Cc2ccco2)CC1

0.692

View
CN(C)CC(=O)N1CCN(Cc2ccco2)CC1

0.692

View
O=C(CC1CC1)N1CCN(Cc2ccco2)CC1

0.692

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

0.692

View
CCCC(=O)N1CCN(Cc2ccco2)CC1

0.692

View
O=C(CN1CCCC1)N1CCN(Cc2ccco2)CC1

0.692

View
O=C(CN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1)N1CCCC1

0.692

View
O=C(CN1CCCC1)N1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.692

View
O=C(Cc1c(F)cccc1F)N1CCN(Cc2ccco2)CC1

0.683

View
Cc1cccc(C)c1CC(=O)N1CCN(Cc2ccco2)CC1

0.683

View
C=C(Cl)CCC(=O)N1CCN(Cc2ccco2)CC1

0.683

View
CCC(CC)CC(=O)N1CCN(Cc2ccco2)CC1

0.683

View
O=C(CCC(=O)N1CCN(c2ccccc2)CC1)N1CCN(Cc2ccco2)CC1

0.683

View
O=C(N1CCC1)N1CCN(Cc2ccco2)CC1

0.676

View
O=C(N1CCCC1)N1CCN(Cc2ccco2)CC1

0.676

View
NC(=O)N1CCN(Cc2ccco2)CC1

0.676

View
CC(=O)N1CCN(Cc2ccco2)CC1

0.676

View
CSCC(=O)N1CCN(Cc2ccco2)CC1

0.675

View
N#CCC(=O)N1CCN(Cc2ccco2)CC1

0.675

View
CC(=O)CCC(=O)N1CCN(Cc2ccco2)CC1

0.675

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

0.675

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

0.675

View
O=C(CCC(=O)N1CCN(Cc2ccco2)CC1)N1CCOCC1

0.675

View
NC(=O)CCC(=O)N1CCN(Cc2ccco2)CC1

0.675

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

0.675

View
COCC(=O)N1CCN(Cc2ccco2)CC1

0.675

View
CC(CC(=O)N1CCN(Cc2ccco2)CC1)CC(=O)N1CCN(Cc2ccco2)CC1

0.675

View
O=C(CN1CCCCCCC1)N1CCN(Cc2ccco2)CC1

0.675

View
O=C(CN1CCCCCC1)N1CCN(Cc2ccco2)CC1

0.675

View
O=C(CN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1)N1CCCCCC1

0.675

View
O=C(CN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1)N1CCCCC1

0.675

View
O=C(Cc1ccccc1)N1CCN(Cc2ccco2)CC1

0.675

View
CCC(=O)N1CCN(C(=O)C(=O)N2CCN(Cc3ccco3)CC2)CC1

0.675

View
O=C(COc1ccccc1)N1CCN(Cc2ccco2)CC1

0.667

View
O=C(Cc1ccc(Cl)cc1)N1CCN(Cc2ccco2)CC1

0.667

View
Cc1cc(C)c(CC(=O)N2CCN(Cc3ccco3)CC2)c(C)c1

0.667

View
CC(C)(C)OCC(=O)N1CCN(Cc2ccco2)CC1

0.667

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCC1

0.667

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCCC1

0.667

View
O=C(COc1ccc(Cl)cc1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CSCc1ccco1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(c1c(Cl)cccc1Cl)N1CCN(Cc2ccco2)CC1

0.659

View
CC(C)CCC(=O)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CSC(F)F)N1CCN(Cc2ccco2)CC1

0.659

View
CS(=O)(=O)CC(=O)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CCC(F)F)N1CCN(Cc2ccco2)CC1

0.659

View
CC(F)(F)CC(=O)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CC(F)(F)C(F)(F)F)N1CCN(Cc2ccco2)CC1

0.659

View
O=C1CC(CC(=O)N2CCN(Cc3ccco3)CC2)C1

0.659

View
CCCCC(=O)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CC1CCCC1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(Cc1ccc(F)cc1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CCC(F)(F)F)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CC1CCC1)N1CCN(Cc2ccco2)CC1

0.659

View
CN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
O=C(CN1CCOCC1)N1CCN(Cc2ccco2)CC1

0.659

View
CC(=O)N1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
CCN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
O=C(CN(Cc1ccco1)Cc1ccco1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CN1CCN(C(=O)N2CCCC2)CC1)N1CCN(Cc2ccco2)CC1

0.659

View
O=C(CN1CCOCC1)N1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
O=C(CN1CCCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1)N1CCCC1

0.659

View
CC(=O)N1CCN(C(=O)CN2CCN(Cc3ccco3)CC2)CC1

0.659

View
CN1CCN(C(=O)CN2CCN(Cc3ccco3)CC2)CC1

0.659

View
O=C(CO)N1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
CCC(=O)N1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

View
O=C(CN1CCSSCC1)N1CCN(Cc2ccco2)CC1

0.659

View
NC(=O)CN1CCN(CC(=O)N2CCN(Cc3ccco3)CC2)CC1

0.659

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

0.659

View
CCC(=O)N1CCCN(Cc2ccco2)CC1

0.659

View
O=C(N1CCCCCC1)N1CCN(Cc2ccco2)CC1

0.658

View
O=C(c1ccc(C(=O)N2CCN(Cc3ccco3)CC2)cc1)N1CCN(Cc2ccco2)CC1

0.658

View
O=C(N1CCCCC1)N1CCN(Cc2ccco2)CC1

0.658

View
O=C(C(=O)N1CCN(Cc2ccco2)CC1)N1CCCC1

0.658

View
O=C(C(=O)N1CCN(Cc2ccco2)CC1)N1CCC1

0.658

View
O=C(CC(O)C(Cl)(Cl)Cl)N1CCN(Cc2ccco2)CC1

0.651

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

0.651

View
O=C(Cc1ccccc1Cl)N1CCN(Cc2ccco2)CC1

0.651

View
CCCC(CCC)CC(=O)N1CCN(Cc2ccco2)CC1

0.651

View
O=C(CC1CC1(Cl)Cl)N1CCN(Cc2ccco2)CC1

0.651

View
O=C(N1CCN(Cc2ccco2)CC1)C12CC(F)(C1)C2

0.650

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCCCC1

0.650

View
O=C(CN1CCN(Cc2ccco2)CC1)N1CCCCCC1

0.650

View
O=C(Cc1c(F)cccc1Cl)N1CCN(Cc2ccco2)CC1

0.644

View
Cc1cccc(Cl)c1CC(=O)N1CCN(Cc2ccco2)CC1

0.644

View
O=C(CN1CCN(c2ccccc2F)CC1)N1CCN(Cc2ccco2)CC1

0.644

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

0.192

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

0.192

View
O=C(c1ccco1)N1CCNCC1

0.190

View
CC(Cl)C(=O)N1CCN(C(=O)c2ccco2)CC1

0.189

View
O=C(c1ccco1)N1CCN(C(=O)c2ccco2)CC1

0.189

View
CC(=O)N1CCN(C(=O)c2ccco2)CC1

0.189

View
O=CN1CCN(C(=O)c2ccco2)CC1

0.189

View
CCN1CCN(C(=O)c2ccco2)CC1

0.182

View
CN1CCN(C(=O)c2ccco2)CC1

0.182

View
O=C(c1ccco1)N1CCN(Cc2ccco2)CC1

0.182

View
O=C(NCCN1CCN(C(=O)c2ccco2)CC1)c1ccco1

0.182

View
Cl.O=C(c1ccco1)N1CCNCC1

0.182

View
CN(C)CCN1CCN(C(=O)c2ccco2)CC1

0.182

View
CN(CC(=O)NCc1ccco1)C(=O)CCl

0.180

View
CC(=O)N1CCN(Cc2ccc(C)o2)CC1

0.178

View
CN1CCN(C(=O)c2ccco2)CC1.Cl

0.174

View
CCN1CCN(C(=O)c2ccco2)CC1.Cl

0.174

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

0.123

View
N1(CC2OC=CC=2)CCN(C(C)=O)CC1

0.918

View
N1(CC2OC=CC=2)CCN(C=O)CC1

0.851

View
N1(CC(Cl)Cl)CCN(C(=O)C2OC=CC=2)CC1

0.813

View
C(N1CCN(CC)CC1)(=O)C1OC=CC=1

0.810

View
N1(CC2OC(Br)=CC=2)CCN(C(C)=O)CC1

0.810

View

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