Molecule Details

Cc1ccncc1NC(=O)Nc1cccc(Cl)c1
Duplicate 3-aminopyridine-like MolPort Assayed
View on Fragalysis x2908
Molecular Properties
SMILES:
Cc1ccncc1NC(=O)Nc1cccc(Cl)c1
MW: 261.712
Fraction sp3: 0.08
HBA: 2
HBD: 2
Rotatable Bonds: 2
TPSA: 54.02
cLogP: 3.68742
Covalent Warhead:
Covalent Fragment: ✔️
Source
MolPort: MolPort-047-314-818
Activity Data
IC50 (µM) - Fluorescence: 64.4136105144302
IC50 (µM) - RapidFire: 45.6892627861479
Trypsin IC50 (µM): 99.0
pIC50 (µM) - Fluorescence 4.19102235706909
Average Inhibition @ 20 µM - Fluorescence: 32.14497
Average Inhibition @ 50 µM - Fluorescence: 58.708675
Average Inhibition @ 20 µM - RapidFire: 25.5825
Average Inhibition @ 50 µM - RapidFire: 64.135
Relative Solubility @ 20 µM: 0.99
Relative Solubility @ 100 µM: 0.96
Order Status
Ordered: 2020-03-31
Synthesis Location: enamine
Shipped: 2020-04-17
CS(=O)(=O)NCCc1ccccc1

AAR-POS-d2a4d1df-1

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Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

JAG-UCB-cedd89ab-8
1.000

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

TRY-UNI-714a760b-24
0.625

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Cc1ccncc1NC(=O)Nc1ccccc1

TRY-UNI-714a760b-4
0.621

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Cc1ccncc1NC(=O)Nc1ccccc1

ALE-HEI-f28a35b5-1
0.621

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

DAR-DIA-0cde14eb-6
0.612

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

DAR-DIA-0cde14eb-5
0.597

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

DAR-DIA-0cde14eb-7
0.588

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

DAR-DIA-0cde14eb-8
0.588

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Cc1c(N)cncc1NC(=O)Nc1cccc(Cl)c1

TRY-UNI-714a760b-9
0.585

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

DAR-DIA-0cde14eb-9
0.571

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

WAR-XCH-eb7b662f-7
0.567

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

DAR-DIA-23aa0b97-14
0.567

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

JOR-UNI-2fc98d0b-7
0.567

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

JAN-GHE-83b26c96-19
0.567

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

EDG-MED-0da5ad92-19
0.545

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

EDG-MED-0da5ad92-5
0.544

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Cc1ccncc1NC(=O)CCc1cccc(Cl)c1

ALP-POS-f13221e1-4
0.544

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

MAK-UNK-f203cb68-18
0.537

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

MAK-UNK-6ca90168-24
0.530

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Cc1ccncc1CC(=O)Nc1cccc(Cl)c1

EDJ-MED-49816e9b-1
0.530

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Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

TRY-UNI-714a760b-6
0.530

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

JAN-GHE-83b26c96-4
0.529

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

TRY-UNI-2eddb1ff-4
0.529

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

JAN-GHE-83b26c96-5
0.529

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

TRY-UNI-714a760b-18
0.529

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

TRY-UNI-2eddb1ff-5
0.529

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

JAN-GHE-83b26c96-10
0.529

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

EDG-MED-0da5ad92-3
0.522

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

JAN-GHE-83b26c96-9
0.522

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Cc1ccncc1NC(=O)Nc1cncc(C#N)c1

CHR-SOS-363cfb78-2
0.515

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

EDG-MED-0da5ad92-10
0.515

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

JAN-GHE-83b26c96-22
0.515

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

JAN-GHE-83b26c96-8
0.507

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

MAT-POS-1e5f28a7-1
0.500

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

JAN-GHE-83b26c96-23
0.500

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

SAM-UNK-2684b532-2
0.493

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

EDG-MED-0da5ad92-11
0.493

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

JAN-GHE-83b26c96-20
0.493

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Nc1cncc(NC(=O)Nc2cccc(Cl)c2)c1

DAR-DIA-23aa0b97-13
0.492

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

MAK-UNK-f203cb68-3
0.487

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

SAM-UNK-2684b532-1
0.486

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Cc1ccncc1NC(=O)c1cccc(NC(=O)Nc2cccnc2)c1

MAK-UNK-129dcd6f-9
0.486

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Cc1ccncc1NC(=O)Nc1cnn(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-66
0.486

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Cc1ccncc1NC(=N)Cc1cccc(Cl)c1

EDG-MED-0da5ad92-6
0.485

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

BAR-COM-0f94fc3d-38
0.479

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

BAR-COM-0f94fc3d-25
0.473

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CC(=O)Nc1cnccc1C

MAK-UNK-6435e6c2-8
0.473

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CC(=O)Nc1cnccc1C

AAR-POS-d2a4d1df-3
0.473

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Cc1ccncc1NC(=O)Nc1cnn(C2(C)CC2)c1

DAR-DIA-0cde14eb-65
0.472

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Cc1ccncc1NC(=O)Nc1cnn(C2(I)CC2)c1

DAR-DIA-0cde14eb-68
0.472

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Cc1nnc(NC(=O)Nc2cnccc2C)s1

ALE-HEI-f28a35b5-2
0.470

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Cc1ccncc1NC(=O)Nc1cnn(C2(F)CC2)c1

DAR-DIA-0cde14eb-67
0.466

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O=C(Nc1cccc(Cl)c1)Nc1cnccc1CCNC(=O)NC1CCCCC1

DAR-DIA-03336633-3
0.460

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Cc1ccncc1NC(=O)c1ccncc1NC(=O)Nc1ccccc1

MAK-UNK-129dcd6f-15
0.459

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

JAN-GHE-83b26c96-21
0.456

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

MAK-UNK-f203cb68-19
0.456

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Cc1ccncc1NC(=O)Nc1cnn(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-69
0.453

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Cc1ccncc1NC(=O)NCCBr

ALE-HEI-f28a35b5-13
0.453

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

MAK-UNK-f203cb68-1
0.451

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

VLA-UCB-05e51b3f-2
0.450

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

MAK-UNK-f203cb68-9
0.450

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

SAM-UNK-2684b532-3
0.450

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

SAM-UNK-2684b532-4
0.450

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

TRY-UNI-9f475305-3
0.450

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Cc1ccncc1NC(=O)CCl

MAK-UNK-6ca90168-26
0.450

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Cc1ccncc1NC(=O)Cc1cccc(I)c1

JAN-GHE-83b26c96-13
0.443

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COc1ccccc1OC[C@H](C(=O)Nc1cnccc1C)c1cccc(Cl)c1

ADA-UCB-6c2cb422-9
0.442

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Cc1ccncc1NC(=O)c1ccc(Cl)cc1C(C)C(=O)Nc1cnccc1C

MAK-UNK-f203cb68-15
0.442

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Cc1ccncc1NC(=O)c1cncc(NC(=O)C(C)c2cccc(Cl)c2)c1C

MAK-UNK-f203cb68-22
0.440

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Cc1ccncc1NC(=O)Nc1cc(N2CCCCC2)cc(C2(C)CC2)c1

DAR-DIA-0cde14eb-20
0.439

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

TRY-UNI-2eddb1ff-3
0.437

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Cc1ccncc1NC(=O)c1ccccc1NC(=O)Nc1cccnc1

MAK-UNK-129dcd6f-4
0.436

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CCNc1ncc(C#N)cc1NC(=O)Nc1cnccc1C

TRY-UNI-1fd04853-2
0.434

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Cc1ccncc1NC(=O)c1ccc(NC(=O)Nc2ccccc2)cn1

MAK-UNK-129dcd6f-17
0.434

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C=CC(=O)Nc1cnccc1C

MAK-UNK-6ca90168-27
0.433

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

EDG-MED-0da5ad92-20
0.432

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Cc1ccncc1NC(=O)c1ncccc1NC(=O)Nc1ccccc1

MAK-UNK-129dcd6f-18
0.430

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CO[C@H](C)C(=O)Nc1cnccc1C

MAT-POS-590ac91e-1
0.429

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CO[C@@H](C)C(=O)Nc1cnccc1C

MAT-POS-590ac91e-2
0.429

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Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

EDG-MED-0da5ad92-8
0.429

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Cc1ccncc1NC(=O)CC#N

ASH-SAT-43770c7d-9
0.429

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Cc1ccncc1NC(=O)Nc1cc(N2CCCCC2)cc(C2(F)CC2)c1

DAR-DIA-0cde14eb-22
0.429

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Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

TRY-UNI-2eddb1ff-2
0.429

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

MAK-UNK-f203cb68-21
0.429

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

MAK-UNK-f203cb68-4
0.429

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CO[C@H](C)C(=O)Nc1cnccc1C

ERI-UCB-5b47150d-1
0.429

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

SAD-SAT-7d5528d9-7
0.427

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O=C(Nc1cccc(Cl)c1)Nc1nccc2[nH]ncc12

JAG-UCB-cedd89ab-7
0.427

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Cc1ccncc1NC(=O)NC1CCCCC1

TRY-UNI-714a760b-11
0.426

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Cc1ccncc1NC(=O)NC1CCCCC1

ALE-HEI-f28a35b5-7
0.426

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Cc1ccncc1NC(=O)C(C)c1ccccc1

TRY-UNI-714a760b-17
0.426

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Cc1ccncc1NC(=O)C(C)c1ccccc1

AHN-SAT-202241f6-1
0.426

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Cc1ccncc1NC(=O)Cc1cc(Cl)cc(NC23CC(C2)C3)c1

MAT-POS-e501d84c-1
0.425

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Cc1ccncc1NC(=O)Nc1cc(N2CCCCC2)cc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-21
0.424

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Cc1ccncc1NC(=O)Cc1cc(Cl)cc(NS(C)(=O)=O)c1

WIL-MOD-03b86a88-5
0.423

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Cc1ccncc1NC(=O)c1cncc(NC(=O)Nc2ccccc2)c1

MAK-UNK-129dcd6f-16
0.423

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

SAD-SAT-7d5528d9-4
0.422

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O=C(O)CCCc1cncc(NC(=O)Nc2cccc(Cl)c2)c1

JAN-LUN-8953ce76-6
0.421

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Cc1ccncc1NC(=O)Nc1ccccc1CCNS(C)(=O)=O

SIM-DEM-f31d0e65-1
0.421

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O=C(O)CCCc1cncc(NC(=O)Nc2cccc(Cl)c2)c1

JAN-LUN-3e0f9c09-1
0.421

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Cc1ccncc1NC(=O)NNc1cccc(Cl)c1

0.795

View
Cc1ccncc1NC(=O)CNC(=O)Nc1cccc(Cl)c1

0.766

View
CC(=O)Nc1cccc(NC(=O)Nc2cnccc2C)c1

0.744

View
Cc1ccncc1NC(=S)Nc1cccc(Cl)c1

0.727

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COc1ccncc1NC(=O)Nc1cccc(Cl)c1

0.717

View
Cc1ccncc1NC(=O)NCc1cccc(Cl)c1

0.717

View
COc1cccc(NC(=O)Nc2cnccc2C)c1

0.711

View
COC(=O)Nc1cccc(NC(=O)Nc2cnccc2C)c1

0.711

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Cc1ccncc1NC(=O)CNc1cccc(Cl)c1

0.702

View
Cc1ccncc1NC(=O)C(=O)NNc1cccc(Cl)c1

0.702

View
CSc1cccc(NC(=O)Nc2cnccc2C)c1

0.696

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CCc1cccc(NC(=O)Nc2cnccc2C)c1

0.696

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Cc1ccccc1NC(=O)Nc1cccc(Cl)c1

0.690

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Cc1ccncc1C(=O)Nc1cccc(Cl)c1

0.667

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Cc1ccncc1NC(=O)c1cccc(Cl)c1

0.667

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

0.667

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

0.667

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

0.667

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CCOc1cccc(NC(=O)Nc2cnccc2C)c1

0.667

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Cc1ccncc1NC(=O)N(C)CC(=O)Nc1cccc(Cl)c1

0.667

View
CCSc1cccc(NC(=O)Nc2cnccc2C)c1

0.667

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

0.667

View
Cc1ccncc1NC(=O)Nc1cccc(C(C)(C)O)c1

0.667

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Cc1ccncc1NC(=O)Nc1ccc(O)c(Cl)c1

0.660

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Cc1ccc(C)c(NC(=O)Nc2cccc(Cl)c2)c1

0.659

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Cc1ccc(NC(=O)Nc2cccc(Cl)c2)cc1NC(=O)c1ccncc1

0.653

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Cc1ccncc1C(C)NC(=O)Nc1cccc(Cl)c1

0.653

View
Cc1ccncc1NC(=O)NCCc1cccc(Cl)c1

0.653

View
Cc1ccncc1NC(=O)Nc1cccc(OC(C)C)c1

0.653

View
Cc1ccncc1NC(=O)Nc1cccc(OC(F)F)c1

0.653

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COCc1cccc(NC(=O)Nc2cnccc2C)c1

0.653

View
Cc1ccncc1NC(=O)Nc1cccc(CC(F)(F)F)c1

0.653

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Cc1ccc(Cl)cc1NC(=O)Nc1cccnc1

0.652

View
Cc1ccncc1NC(=O)NNc1cc(Cl)cc(Cl)c1

0.652

View
Cc1ccncc1NC(=O)Nc1csc(Cl)c1

0.652

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Cc1cc(C)cc(NC(=O)Nc2cnccc2C)c1

0.651

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CN1CCN(c2ccncc2NC(=O)Nc2cccc(Cl)c2)CC1

0.647

View
Cc1cccc(NC(=O)Nc2cccc(CNC(=O)Nc3cnccc3C)c2)c1

0.647

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

0.646

View
Cc1cnccc1NC(=O)NNc1cccc(Cl)c1

0.646

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Cc1ccncc1NC(=O)C(=O)N(C)CC(=O)Nc1cccc(Cl)c1

0.642

View
Cc1ccncc1NC(=O)NC(c1ccccc1)c1cccc(Cl)c1

0.640

View
COC(C)C(=O)Nc1cccc(NC(=O)Nc2cnccc2C)c1

0.640

View
Cc1ccncc1NC(=O)NCc1cccc(NC(=O)NCc2ccncc2)c1

0.640

View
Cc1ccncc1NC(=O)Nc1cccc(NC2CCCC2)c1

0.640

View
Cc1ccncc1NC(=O)Nc1cccc(-n2ccnn2)c1

0.640

View
Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

0.638

View
Cc1cscc1NC(=O)Nc1cccc(Cl)c1

0.636

View
Cc1cccc(NC(=O)Nc2cccc(Cl)c2)c1C

0.636

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

0.633

View
Cc1ccncc1NC(=O)C(C)(C)Cc1cccc(Cl)c1

0.633

View
Cc1cnccc1CNC(=O)Nc1cccc(Cl)c1

0.633

View
Cc1ccncc1NC(=O)C(=O)NCc1cccc(Cl)c1

0.633

View
Cc1cnccc1C(=O)Nc1cccc(Cl)c1

0.630

View
Cc1cc(O)ccc1NC(=O)Nc1cccc(Cl)c1

0.630

View
Cc1cc(NC(=O)Nc2cnccc2C)ccc1O

0.630

View
CC(=O)Nc1cc(NC(=O)Nc2cnccc2C)ccc1C

0.630

View
Cc1ccc(NC(=O)Nc2cnccc2C)cc1

0.628

View
Cc1ccncc1CNC(=O)CNC(=O)Nc1cccc(Cl)c1

0.627

View
CCC(NC(=O)Nc1cnccc1C)c1cccc(Cl)c1

0.627

View
Cc1ccncc1NC(=O)NCCCc1cccc(Cl)c1

0.627

View
Cc1ccncc1NC(=O)NCC(O)c1cccc(Cl)c1

0.627

View
COC(=O)Cc1cccc(NC(=O)Nc2cnccc2C)c1

0.627

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

0.627

View
Cc1ccncc1NC(=O)Nc1cccc(-c2nnc(C)n2C)c1

0.627

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

0.625

View
Cc1ccc(NC(=O)Nc2cccc(Cl)c2)c(C)c1

0.622

View
Cc1ccccc1NC(=O)NNC(=O)Nc1cccc(Cl)c1

0.622

View
Cc1cncc(NC(=O)Nc2cccc(Cl)c2)c1

0.622

View
Cc1ccncc1NC(=O)Nc1cc(C)c(O)c(C)c1

0.622

View
Cc1ccncc1NC(=O)C(C)(C)Oc1cccc(Cl)c1

0.620

View
Cc1ccccc1NC(=O)Nc1cnccc1C

0.619

View
Cc1ccncc1NC(=O)C(=O)N1CCCN(C(=O)Nc2cccc(Cl)c2)CC1

0.618

View
Cc1c(NC(=O)Nc2cccc(Cl)c2)cnn1C

0.617

View
Cc1oncc1NC(=O)Nc1cccc(Cl)c1

0.617

View
CC(=O)Nc1ccc(NC(=O)Nc2cnccc2C)cc1C

0.617

View
Cc1ccc(-c2ccnn2C)cc1NC(=O)Nc1cccc(Cl)c1

0.615

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COCCOc1cccc(NC(=O)Nc2cnccc2C)c1

0.615

View
Cc1ccncc1NC(=O)NCCOc1cccc(Cl)c1

0.615

View
Cc1ccncc1NC(=O)Nc1cccc(COC(C)C)c1

0.615

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

0.615

View
Cc1ccncc1NC(=O)NC(CO)c1cccc(Cl)c1

0.615

View
Cc1ccncc1NC(=O)NC1(Cc2cccc(Cl)c2)CC1

0.615

View
CCC(C)Oc1cccc(NC(=O)Nc2cnccc2C)c1

0.615

View
CC(=O)Nc1ccc(NC(=O)Nc2cnccc2C)cc1

0.614

View
Cc1ccncc1NC(=O)Nc1cccc(C)c1C

0.614

View
Cc1ccncc1NC(=O)Nc1ccc(O)cc1

0.614

View
Cc1ccncc1NC(=O)CCc1cccc(Cl)c1

0.612

View
CCOc1cc(NC(=O)Nc2cnccc2C)ccc1C

0.612

View
Cc1ccncc1NC(=O)c1ccc(Cl)cc1Cl

0.609

View
Cc1ccc(Cl)cc1NC(=O)Nc1cccc(O)c1

0.609

View
CC(=O)Nc1cc(NC(=O)Nc2cccc(Cl)c2)ccc1C

0.609

View
Cc1cccc(NC(=O)C(=O)Nc2cnccc2C)c1

0.609

View
Cc1ccncc1C(=O)Nc1ccccc1C(=O)Nc1cccc(Cl)c1

0.608

View
Cc1cnccc1CCNC(=O)Nc1cccc(Cl)c1

0.608

View
CC(=O)Nc1cccc(CNC(=O)Nc2cnccc2C)c1

0.608

View
Cc1ccc(NC(=O)Nc2cccc(Cl)c2)cc1C

0.605

View
O=C(NNc1ccncc1Cl)Nc1cccc(Cl)c1

0.604

View
CNC(=O)COc1cccc(NC(=O)Nc2cnccc2C)c1

0.604

View
CCOC(=O)Cc1cccc(NC(=O)Nc2cnccc2C)c1

0.604

View
O=C(Nc1cccnc1)Nc1ccc(Cl)c(Cl)c1

0.192

View
O=C(Nc1cc(Cl)cc(Cl)c1)Nc1cnccc1C(F)(F)F

0.181

View
O=C(Nc1cccnc1)Nc1cc(Cl)cc(Cl)c1

0.160

View
O=C(Nc1cccnc1)Nc1cccc(Cl)c1

0.139

View
Cc1c(Cl)cccc1NC(=O)Nc1cccnc1

0.100

View
Cc1ccc(Cl)cc1NC(=O)Nc1cccnc1

0.086

View


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