Molecule Details

Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC1
Duplicate 3-aminopyridine-like Enamine Assayed
View on Fragalysis x10392
Molecular Properties
SMILES:
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC1
MW: 286.762
Fraction sp3: 0.25
HBA: 2
HBD: 1
Rotatable Bonds: 3
TPSA: 41.99
cLogP: 3.71372
Covalent Warhead:
Covalent Fragment:
Source
Enamine Extended REAL: s_22____3391102____488342
Activity Data
IC50 (µM) - Fluorescence: 99.5
Trypsin IC50 (µM): 99.0
Average Inhibition @ 20 µM - Fluorescence: 38.411715
Average Inhibition @ 50 µM - Fluorescence: 61.618515
Average Inhibition @ 50 µM - RapidFire: 43.30332433
Relative Solubility @ 20 µM: 1.01
Relative Solubility @ 100 µM: 1.0
Order Status
Ordered: 2020-05-17
Synthesis Location: enamine
Shipped: 2020-06-10
O=C(Nc1ccccc1)Nc1cccnc1

AAR-POS-d2a4d1df-11

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Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC1

JAN-GHE-83b26c96-20
1.000

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Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC(=O)C1

BAR-COM-0f94fc3d-25
0.769

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Cc1ccncc1NC(=O)N(C)c1cccc(Cl)c1

EDG-MED-0da5ad92-3
0.521

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Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

TRY-UNI-714a760b-6
0.507

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Cc1ccncc1NC(=O)N(c1cccc(Cl)c1)c1cccc(Cl)c1

EDG-MED-0da5ad92-19
0.500

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Cc1ccncc1NC(=O)CCc1cccc(Cl)c1

ALP-POS-f13221e1-4
0.500

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Cc1ccncc1NC(=O)C1(Cc2cccc(Cl)c2)CCOCC1

SAD-SAT-7d5528d9-4
0.494

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Cc1ccncc1NC(=O)C(C)(C)c1cccc(Cl)c1

EDG-MED-0da5ad92-10
0.493

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Cc1ccncc1NC(=O)C(C)(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

MAK-UNK-f203cb68-18
0.493

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Cc1ccncc1NC(=O)C(C)(C)c1cccc(Cl)c1

JAN-GHE-83b26c96-22
0.493

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Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

JAG-UCB-cedd89ab-8
0.493

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Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

TRY-UNI-714a760b-12
0.493

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Cc1ccncc1NC(=O)C(=O)c1cccc(Cl)c1

MAK-UNK-6ca90168-24
0.486

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Cc1ccncc1NC(=O)C(CO)c1cccc(Cl)c1

EDG-MED-0da5ad92-5
0.480

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Cc1ccncc1NC(=O)C(F)(F)c1cccc(Cl)c1

JAN-GHE-83b26c96-23
0.480

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Cc1ccncc1NC(=O)[C@H](C)c1cccc(Cl)c1

TRY-UNI-2eddb1ff-5
0.467

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Cc1ccncc1NC(=O)[C@@H](C)c1cccc(Cl)c1

TRY-UNI-2eddb1ff-4
0.467

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Cc1ccncc1NC(=O)[C@H](C)c1cccc(Cl)c1

JAN-GHE-83b26c96-4
0.467

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Cc1ccncc1NC(=O)[C@@H](C)c1cccc(Cl)c1

JAN-GHE-83b26c96-5
0.467

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Cc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

TRY-UNI-714a760b-18
0.467

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Cc1ccncc1NC(=O)Nc1cccc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-6
0.462

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Cc1ccncc1NC(=O)C(c1cccc(Cl)c1)C(C)C

JAN-GHE-83b26c96-9
0.461

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Cc1ccncc1NC(=O)N(c1ccccc1)c1cccc(Cl)c1

SAM-UNK-2684b532-2
0.456

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Cc1ccncc1NC(=O)Cc1cccc(C2(F)CC2)c1

DAR-DIA-0cde14eb-2
0.456

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Cc1ccncc1NC(=O)Cc1cccc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-3
0.450

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Cc1ccncc1NC(=O)C(c1cccc(Cl)c1)N(C)C

JAN-GHE-83b26c96-10
0.449

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Cc1ccncc1NC(=O)Nc1cccc(C2(C)CC2)c1

DAR-DIA-0cde14eb-5
0.449

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Cc1ccncc1NC(=N)Cc1cccc(Cl)c1

EDG-MED-0da5ad92-6
0.446

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Cc1ccncc1NC(=O)Nc1cccc(C2(I)CC2)c1

DAR-DIA-0cde14eb-8
0.443

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CCC(O)(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

BAR-COM-0f94fc3d-38
0.443

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Cc1ccncc1NC(=O)Cc1cccc(C2(C)CC2)c1

DAR-DIA-0cde14eb-1
0.443

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Cc1ccncc1NC(=O)Nc1cccc(C2(F)CC2)c1

DAR-DIA-0cde14eb-7
0.443

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COC(=O)C(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

MAT-POS-1e5f28a7-1
0.443

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Cc1ccncc1NC(=O)C1(C#N)CCOC1

MAT-POS-590ac91e-27
0.440

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Cc1ccncc1NS(=O)(=O)c1cccc(Cl)c1

JAN-GHE-83b26c96-21
0.438

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Cc1ccncc1NC(=O)CC(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

MAK-UNK-f203cb68-3
0.434

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Cc1ccncc1NC(=O)C(c1ccccc1)c1cccc(Cl)c1

SAM-UNK-2684b532-1
0.432

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Cc1ccncc1NC(=O)Nc1cccc(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-9
0.432

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Cc1ccncc1NC(=O)Cc1cccc(C2(I)CC2)c1

DAR-DIA-0cde14eb-4
0.432

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CCCC(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

JAN-GHE-83b26c96-8
0.432

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Cc1ccncc1NC(=O)CCl

MAK-UNK-6ca90168-26
0.431

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Nc1ccc(NC(=O)C2(c3cccc(Cl)c3)CCOCC2)cn1

MAR-TRE-04c86cea-78
0.427

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CC(=O)Nc1cnccc1C

AAR-POS-d2a4d1df-3
0.426

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CC(=O)Nc1cnccc1C

MAK-UNK-6435e6c2-8
0.426

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Cc1ccncc1NC(=O)C(C)c1cccc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-11
0.422

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Cc1ccncc1NC(=O)C12CC(CO1)C2

MAT-POS-590ac91e-4
0.419

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Cc1nnc(N(C(=O)Nc2cnccc2C)c2cccc(Cl)c2)s1

SAM-UNK-2684b532-4
0.419

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Cc1ccncc1NC(=O)N(Cc1ccccc1)c1cccc(Cl)c1

EDG-MED-0da5ad92-20
0.419

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CC(=O)N1CCN(C(C(=O)Nc2cnccc2C)c2cccc(Cl)c2)CC1

VLA-UCB-05e51b3f-2
0.419

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Cc1ccncc1NC(=O)Cc1cccc(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-14
0.417

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Cc1ccncc1NC(=O)CC1(CO)CC1

MAT-POS-590ac91e-6
0.417

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Cc1ccncc1NC(=O)N(CCC1CCCCC1)c1cccc(Cl)c1

MAT-POS-136e7878-1
0.416

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Cc1ccncc1NC(=O)C12CCC(CO1)C2

MAT-POS-590ac91e-29
0.416

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Cc1ccncc1NC(=O)CCCBr

ALE-HEI-f28a35b5-12
0.414

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Cc1ccncc1NC(=O)C1CCC2(Cc3cccc2c3)C1

SAD-SAT-7d5528d9-26
0.414

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Cc1ccncc1NC(=O)C1CCN(Cc2cccc(Cl)c2)CC1

SAD-SAT-7d5528d9-7
0.414

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Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

EDG-MED-0da5ad92-8
0.413

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Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

TRY-UNI-2eddb1ff-2
0.413

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Cc1ccncc1NC(=O)[C@@]12COC[C@@H]1C2

MAT-POS-590ac91e-3
0.413

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Cc1ccncc1NC(=O)C1(n2cccn2)CCNCC1

MAR-TRE-67513f76-79
0.412

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COC1(CC(=O)Nc2cnccc2C)CC1

MAT-POS-590ac91e-9
0.411

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Cc1ccncc1NC(=O)C(C)c1cccc(C2(C)CC2)c1

DAR-DIA-0cde14eb-10
0.410

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Cc1ccncc1NC(=O)NC1(c2cccnc2)CCCCC1

WAR-XCH-e55cba98-9
0.407

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Cc1ccncc1NC(=O)C(C(=O)C(C)c1cccc(Cl)c1)c1cnccc1C

MAK-UNK-f203cb68-19
0.407

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Cc1ccncc1NC(=O)C(C)c1cccc(C2(F)CC2)c1

DAR-DIA-0cde14eb-12
0.405

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Cc1ccncc1NC(=O)C(C)c1cccc(C2(I)CC2)c1

DAR-DIA-0cde14eb-13
0.405

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Cc1ccncc1NC(=O)[C@@H]1CC(=O)N(C)[C@@H]1c1cccc(Cl)c1

MAR-TRE-4b834d9a-26
0.404

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Cc1ccc(CC(=O)Nc2cnccc2C)cc1

JAN-GHE-83b26c96-11
0.403

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Cc1ccncc1NC(=O)C1(CCNS(C)(=O)=O)CCCCC1

ASH-UNK-40b46b30-11
0.402

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CC(=O)Nc1cnccc1C(C)(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

MAK-UNK-f203cb68-9
0.402

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Cc1nnc(C(C(=O)Nc2cnccc2C)c2cccc(Cl)c2)s1

TRY-UNI-9f475305-3
0.402

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Cc1nnc(C(C(=O)Nc2cnccc2C)c2cccc(Cl)c2)s1

SAM-UNK-2684b532-3
0.402

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Cc1ccncc1NC(=O)c1nccc(C)c1NC(=O)C(C)c1cccc(Cl)c1

MAK-UNK-f203cb68-20
0.402

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Cc1ccncc1NC(=O)Cc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

MAK-UNK-f203cb68-4
0.400

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Cc1ccncc1NC(=O)c1cc(C)c(NC(=O)C(C)c2cccc(Cl)c2)cn1

MAK-UNK-f203cb68-21
0.400

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Cc1ccncc1NC(=O)CC1CC2(CC2)C1

MAT-POS-590ac91e-24
0.400

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Cc1ccncc1NC(=O)CCc1nc2cc(Cl)ccc2o1

GAB-REV-70cc3ca5-22
0.398

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Cc1ccncc1NC(=O)CC1(c2cccc(S(N)(=O)=O)c2)CCC1

CHR-SOS-e960e883-6
0.398

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Cc1ccncc1NC(=O)CC1(C#N)CCC1

MAT-POS-590ac91e-15
0.395

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C=CC(=O)Nc1cnccc1C

MAK-UNK-6ca90168-27
0.394

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Cc1ccncc1NC(=O)CNC1(c2ccccc2)CCCCC1

WAR-XCH-e55cba98-11
0.393

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O=C(Nc1nncn1C1CC1)C1(c2cccc(Cl)c2)CCCCC1

NAU-LAT-e1818702-6
0.393

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Cc1ccncc1NC(=O)CC#N

ASH-SAT-43770c7d-9
0.391

View
Cc1ccncc1NC(=O)C(C)c1cccc(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-15
0.391

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Cc1ccncc1NC(=O)Cc1cccc(C2CC2)c1

ALP-POS-95b75b4d-4
0.390

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Cc1ccncc1NC(=O)Cc1cccc(O)c1

ALP-POS-95b75b4d-2
0.390

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Cc1ccncc1CC(=O)Nc1cccc(Cl)c1

EDJ-MED-49816e9b-1
0.390

View
Cc1ccncc1NC(=O)Cc1cccc(CO)c1

EDJ-MED-e58735b6-2
0.390

View
Cc1ccncc1NC(=O)Cc1cccc(I)c1

JAN-GHE-83b26c96-13
0.390

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CC(=O)Nc1cnccc1CC(C(=O)Nc1cnccc1C)c1cccc(Cl)c1

MAK-UNK-f203cb68-1
0.389

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Cc1ccncc1NC(=O)CC1(c2cccc(S(N)(=O)=O)c2)CCCC1

CHR-SOS-e960e883-5
0.389

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CC(=O)Nc1ccc(NCC(=O)Nc2cnccc2C)cc1

GAB-REV-70cc3ca5-21
0.387

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Cc1ccncc1NC(=O)CC1CCCCC1

ALE-HEI-f28a35b5-6
0.387

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Cc1ccncc1NC(=O)CC1CCCCC1

EDG-MED-0da5ad92-4
0.387

View
Cc1ccncc1NC(=O)CC1CCCCC1

TRY-UNI-714a760b-10
0.387

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Cc1ccncc1NC(=O)C1CCC12CCC2

MAT-POS-590ac91e-22
0.387

View
Cc1ccncc1NC(=O)Cc1cccc(F)c1

ALP-POS-95b75b4d-1
0.385

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Cc1ccncc1NC(=O)CCc1ccccn1

BEN-DND-93268d01-4
0.385

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Cc1ccncc1NC(=O)Cc1cccc(Br)c1

JAN-GHE-83b26c96-12
0.385

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Cc1ccncc1NC(=O)C(C)c1cncc(Cl)c1

TRY-UNI-2eddb1ff-3
0.385

View
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC1

1.000

View
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.913

View
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCCC1

0.913

View
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCCCC1

0.894

View
Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCOCC1

0.857

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Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.830

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Cc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC(=O)C1

0.816

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Cc1cccc(C2(C(=O)Nc3cnccc3C)CC2)c1

0.787

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Cc1ccncc1NC(=O)C1(c2cccc(Br)c2)CC1

0.771

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Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.760

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Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCCC1

0.760

View
O=C(Nc1cnccc1O)C1(c2cccc(Cl)c2)CC1

0.755

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Cc1ccncc1NC(=O)C1(c2cccc(F)c2)CC1

0.755

View
Cc1cnncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.750

View
COc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.745

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Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCCCC1

0.745

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Cc1ccncc1NC(=O)C1(c2ccc(Cl)cc2)CC1

0.745

View
COc1cccc(C2(C(=O)Nc3cnccc3C)CC2)c1

0.740

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Cc1ccncc1NC(=O)C1(c2ccccc2)CC1

0.739

View
CC(=O)c1cnccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.725

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Cc1ccc(Cl)cc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.723

View
Cc1ccccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.723

View
Cc1ccncc1NC(=O)C1(c2cccnc2)CC1

0.723

View
O=C(Nc1ccncc1Br)C1(c2cccc(Cl)c2)CC1

0.720

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O=C(Nc1ccncc1F)C1(c2cccc(Cl)c2)CC1

0.720

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Cc1c(Cl)cncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.720

View
O=C(Nc1ccncc1I)C1(c2cccc(Cl)c2)CC1

0.720

View
Cc1cccc(C2(C(=O)Nc3cnccc3C)CCC2)c1

0.720

View
Cc1cccc(C2(C(=O)Nc3cnccc3C)CCCC2)c1

0.720

View
Cc1cc(Cl)ncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.720

View
Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCOCC1

0.717

View
CCc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.712

View
Cc1ccncc1NC(=O)C1(c2cccc(C(F)(F)F)c2)CC1

0.712

View
Cc1ccncc1NC(=O)C1(c2cccc(C#N)c2)CC1

0.712

View
Cc1ncncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.706

View
Cc1ccncc1NC(=O)C1(c2cccc(Br)c2)CCCC1

0.706

View
Cc1cccc(C2(C(=O)Nc3cnccc3C)CCCCC2)c1

0.706

View
Cc1ccncc1NC(=O)C1(c2cccc(Br)c2)CCC1

0.706

View
Cc1cc(C(F)(F)F)ncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.698

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Cc1ccncc1NC(=O)C1(c2ccncc2)CC1

0.696

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Cc1ccc(C)c(NC(=O)C2(c3cccc(Cl)c3)CC2)c1

0.694

View
Cc1ccncc1NC(=O)C1(c2c(Cl)cccc2Cl)CC1

0.694

View
O=C(Nc1cccc2ccncc12)C1(c2cccc(Cl)c2)CC1

0.692

View
O=C(Nc1cccc2cnccc12)C1(c2cccc(Cl)c2)CC1

0.692

View
O=C(Nc1cnccc1O)C1(c2cccc(Cl)c2)CCC1

0.692

View
O=C(Nc1cnccc1O)C1(c2cccc(Cl)c2)CCCC1

0.692

View
Cc1ccncc1NC(=O)C1(c2cccc(F)c2)CCCC1

0.692

View
Cc1ccncc1NC(=O)C1(c2cccc(F)c2)CCC1

0.692

View
Cc1ccncc1NC(=O)C1(c2cccc(Br)c2)CCCCC1

0.692

View
Cc1cc(Br)ncc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.692

View
Cc1ccncc1NC(=O)NC1(c2cccc(Cl)c2)CC1

0.692

View
Cc1cc(Cl)ccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.688

View
Cc1cc(C)cc(C2(C(=O)Nc3cnccc3C)CC2)c1

0.688

View
Cc1cc(NC(=O)C2(c3cccc(Cl)c3)CC2)c(C)cn1

0.686

View
Cc1cnncc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.686

View
Cc1cnncc1NC(=O)C1(c2cccc(Cl)c2)CCCC1

0.686

View
Cc1ccc(Cl)cc1NC(=O)C1(c2cccnc2)CC1

0.686

View
COc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.685

View
COc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCCC1

0.685

View
O=C(Nc1cncc(Cl)c1Cl)C1(c2cccc(Cl)c2)CC1

0.680

View
Cc1ccncc1NC(=O)C1(c2ccc(Cl)cc2)CCCC1

0.680

View
Cc1ccncc1NC(=O)C1(c2cccc(F)c2)CCCCC1

0.679

View
COc1cccc(C2(C(=O)Nc3cnccc3C)CCCC2)c1

0.679

View
O=C(Nc1ccnc2ccncc12)C1(c2cccc(Cl)c2)CC1

0.679

View
Cc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CC(=O)C1

0.679

View
Cc1ccncc1CNC(=O)C1(c2cccc(Cl)c2)CC1

0.679

View
Cc1ccncc1NC(=O)C(=O)NC1(c2cccc(Cl)c2)CC1

0.679

View
Cc1cccc(NC(=O)C2(c3cccc(Cl)c3)CC2)c1Cl

0.673

View
Cc1cccc(NC(=O)C2(c3cccc(Cl)c3)CC2)c1C

0.673

View
Cc1ccncc1NC(=O)C1(c2ccccc2)CCCC1

0.673

View
Cc1ccncc1NC(=O)C1(c2ccccc2)CCC1

0.673

View
Cc1cnncc1NC(=O)C1(c2cccc(Cl)c2)CCCCC1

0.673

View
Cc1ccncc1NC(=O)C1(c2ccc(Cl)c(Cl)c2)CCC1

0.673

View
COc1ccncc1NC(=O)C1(c2cccc(Cl)c2)CCCCC1

0.673

View
Cc1ccc(F)cc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.667

View
Cc1cc(O)ccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.667

View
Cc1ncccc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.667

View
Cc1ccncc1NC(=O)C1(c2ccc(Cl)cc2)CCCCC1

0.667

View
Cc1ccncc1C(C)NC(=O)C1(c2cccc(Cl)c2)CC1

0.667

View
O=C(Nc1ccncc1)C1(c2cccc(Cl)c2)CC1

0.667

View
Cc1ccncc1NC(=O)NC1(c2cccc(Cl)c2)CCCC1

0.667

View
Cc1ccncc1NC(=O)N1CCC(C)(c2cccc(Cl)c2)CC1

0.667

View
Cc1ccncc1S(=O)(=O)NC(=O)C1(c2cccc(Cl)c2)CC1

0.667

View
O=C(Nc1ccncc1Br)C1(c2cccc(Cl)c2)CCC1

0.660

View
O=C(Nc1ccncc1Br)C1(c2cccc(Cl)c2)CCCC1

0.660

View
O=C(Nc1ccncc1F)C1(c2cccc(Cl)c2)CCC1

0.660

View
O=C(Nc1ccncc1F)C1(c2cccc(Cl)c2)CCCC1

0.660

View
Cc1cc(Cl)ncc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.660

View
O=C(Nc1ccncc1I)C1(c2cccc(Cl)c2)CCC1

0.660

View
O=C(Nc1ccncc1I)C1(c2cccc(Cl)c2)CCCC1

0.660

View
Cc1ccncc1NC(=O)C1(c2ccc3c(c2)OCO3)CC1

0.660

View
Cc1ccncc1NC(=O)C1(Cc2cccc(Cl)c2)CC1

0.660

View
Cc1ccccc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.660

View
O=C(Nc1cccnc1)C1(c2cccc(Cl)c2)CC1

0.660

View
Cc1ccc(NC(=O)C2(c3cccc(Cl)c3)CC2)c(C)c1

0.660

View
Cc1ccncc1NC(=O)C1(c2cccnc2)CCCC1

0.660

View
Cc1cscc1NC(=O)C1(c2cccc(Cl)c2)CC1

0.660

View
CCc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCC1

0.655

View
CCc1cnccc1NC(=O)C1(c2cccc(Cl)c2)CCCC1

0.655

View
O=C(Nc1cnccc1O)C1(c2cccc(Cl)c2)CCOCC1

0.655

View
CCC(C(=O)Nc1cccnc1)c1ccccc1

0.200

View
O=C(Nc1cccnc1)C1(c2ccccc2)CC1

0.194

View
C(NC1=C(C)C=CN=C1)(=O)C(CC)C1=CC=CC=C1

0.790

View
C(NC1=C(C)C=CN=C1)(=O)C(C)C1=CC=C(Cl)C=C1

0.766

View
C(NC1=CN=CC(Cl)=C1C)(=O)C(CC)C1=CC=CC=C1

0.765

View
C(NC1=C(C)C=CN=C1)(=O)C(CC)C1=CC=C(Br)C=C1

0.744

View
C(NC1=C(C)C=CN=C1)(=O)C(C1=CC=C(CC(C)C)C=C1)C

0.741

View


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