Molecule Details

Cc1c(N)cncc1NC(=O)C(C)c1cccc(Cl)c1
3-aminopyridine-like Ordered
Molecular Properties
SMILES:
Cc1c(N)cncc1NC(=O)C(C)c1cccc(Cl)c1
MW: 289.766
Fraction sp3: 0.2
HBA: 3
HBD: 2
Rotatable Bonds: 3
TPSA: 68.01
cLogP: 3.36782
Covalent Warhead:
Covalent Fragment: ✔️
Order Status
Ordered: 2020-03-31
Synthesis Location: enamine
Shipped: synthesis in progress

aniline

CC(=O)Nc1cnccc1C

MAK-UNK-6435e6c2-8

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O=C(Nc1ccccc1)Nc1cccnc1

AAR-POS-d2a4d1df-11

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O=C(CC1CCCCC1)Nc1cccnc1

ALE-HEI-f28a35b5-9

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Nc1cncnc1

AAR-POS-d2a4d1df-18

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CC(NC(=O)CCl)c1cccc(Cl)c1

AAR-POS-0daf6b7e-10

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Cc1c(N)cncc1NC(=O)C(C)c1cccc(C#N)c1

TRY-UNI-714a760b-21
0.657

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Cc1c(N)cncc1NC(=O)C(C)c1ccccc1

TRY-UNI-714a760b-14
0.641

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

TRY-UNI-2eddb1ff-4
0.594

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

TRY-UNI-2eddb1ff-5
0.594

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

TRY-UNI-714a760b-18
0.594

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

JAN-GHE-83b26c96-4
0.594

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

JAN-GHE-83b26c96-5
0.594

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CC(C(=O)Nc1cnccc1Cl)c1cccc(Cl)c1

SAM-UNK-2684b532-7
0.580

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CC(=O)Nc1cnccc1-c1cncc(NC(=O)C(C)c2cccc(Cl)c2)c1C

MAK-UNK-f203cb68-13
0.575

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

MAK-UNK-f203cb68-22
0.568

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

TRY-UNI-714a760b-9
0.557

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CC(C)c1ncncc1NC(=O)C(C)c1cccc(Cl)c1

JAN-GHE-83b26c96-6
0.556

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CC(=O)Nc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

JAN-GHE-83b26c96-2
0.548

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

SAM-UNK-2684b532-6
0.541

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

SAM-UNK-2684b532-5
0.541

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Cc1c(N)cncc1NC(=O)Cc1cccc(Cl)c1

TRY-UNI-714a760b-3
0.535

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CC(=O)Nc1cnccc1Cc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

MAK-UNK-f203cb68-2
0.506

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CC(C(=O)Nc1cnccc1-n1cccn1)c1cccc(Cl)c1

JAN-GHE-83b26c96-3
0.500

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CC(=O)Nc1cnccc1-c1cc(C)c(NC(=O)C(C)c2cccc(Cl)c2)cn1

MAK-UNK-f203cb68-12
0.488

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

MAK-UNK-f203cb68-21
0.482

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

MAK-UNK-f203cb68-4
0.482

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Cc1c(N)cncc1NC(=O)CC1(c2cccc(Cl)c2)CCCCC1

WAR-XCH-72a8c209-2
0.482

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

MAK-UNK-f203cb68-19
0.440

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CC(=O)Nc1cnccc1-c1nccc(C)c1NC(=O)C(C)c1cccc(Cl)c1

MAK-UNK-f203cb68-11
0.440

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Cc1c(O)cncc1NC(=O)C(C)c1ccccc1

BEN-DND-93268d01-16
0.438

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Cc1c(N)cncc1NC(=O)Nc1ccccc1

TRY-UNI-714a760b-8
0.437

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

MAK-UNK-f203cb68-20
0.433

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Cc1c(N)cncc1NC(=O)C(C)C1CCCCC1

TRY-UNI-714a760b-13
0.427

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

MAT-POS-1e5f28a7-1
0.425

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CC(C(=O)Nc1nncn1C1CC1)c1cccc(Cl)c1

BRU-CON-67e07230-1
0.425

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Cc1ncncc1NC(=O)C(c1cccc(Cl)c1)C(C)C

JAN-GHE-83b26c96-7
0.418

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Cc1c(N)cncc1NC(=O)Nc1cccc(C#N)c1

TRY-UNI-714a760b-23
0.412

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Cc1c(N)cncc1NC(=O)Cc1ccccc1

TRY-UNI-714a760b-2
0.411

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

JAN-GHE-83b26c96-9
0.405

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

JAN-GHE-83b26c96-10
0.395

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Cc1c(N)cncc1NC(=O)Cc1cccc(C#N)c1

TRY-UNI-714a760b-19
0.390

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CC(=O)Nc1cnccc1C(C(=O)C(C)c1cccc(Cl)c1)c1cnccc1C

MAK-UNK-f203cb68-10
0.389

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

EDG-MED-0da5ad92-5
0.388

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

TRY-UNI-2eddb1ff-3
0.385

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

JAN-GHE-83b26c96-8
0.381

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

TRY-UNI-714a760b-22
0.373

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

DAR-DIA-0cde14eb-11
0.372

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

DAR-DIA-0cde14eb-12
0.372

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Cc1cncc(NC(=O)Cc2cccc(Cl)c2)c1C

PET-UNK-8df914d1-3
0.372

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CCC(C(=O)Nc1cnncc1C)c1cccc(Cl)c1

JAN-GHE-83b26c96-1
0.370

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CC(C(=O)Nc1cncc2ccccc12)c1cccc(C2(F)CC2)c1

DAR-DIA-0cde14eb-57
0.367

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CC(C(=O)Nc1cncc2ccccc12)c1cccc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-56
0.367

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

SAM-UNK-2684b532-1
0.365

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Cc1c(N)cncc1NC(=O)NC1CCCCC1

TRY-UNI-714a760b-7
0.364

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

DAR-DIA-0cde14eb-10
0.360

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CC(C(=O)Nc1cncc2ccccc12)c1cccc(C2(C)CC2)c1

DAR-DIA-0cde14eb-55
0.360

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Cc1c(N)cncc1NC(=O)CC1CCCCC1

TRY-UNI-714a760b-1
0.359

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CC(=O)N1CCN(C(C(=O)Nc2cncc3ccccc23)c2cccc(Cl)c2)CC1

MIC-UNK-6ab519a7-1
0.359

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

DAR-DIA-0cde14eb-13
0.356

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

MAK-UNK-f203cb68-3
0.352

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CC(C(=O)Nc1cncc2ccccc12)c1cccc(C2(I)CC2)c1

DAR-DIA-0cde14eb-58
0.352

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CC(=O)Nc1ccc(C(C(=O)Nc2cncc3ccccc23)c2cccc(Cl)c2)cc1

MIC-UNK-d36ab305-1
0.351

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CN(C)c1ccc(C(C(=O)Nc2cncc3ccccc23)c2cccc(Cl)c2)cc1

MIC-UNK-d36ab305-4
0.347

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

DAR-DIA-0cde14eb-15
0.344

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

TRY-UNI-9f475305-3
0.341

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

SAM-UNK-2684b532-3
0.341

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

VLA-UCB-05e51b3f-2
0.341

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CC(C(=O)Nc1cncc2c1CCCC2)c1cccc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-41
0.340

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CC(C(=O)Nc1cncc2ccccc12)c1cccc(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-60
0.340

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CC(C(=O)Nc1cncc2c1CCCC2)c1cccc(C2(F)CC2)c1

DAR-DIA-0cde14eb-42
0.340

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O=C(Nc1cncc2ccccc12)C(CCc1ccc(F)cc1)c1cccc(Cl)c1

MIC-UNK-c66144cb-2
0.340

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Cc1cccc([C@H](C)C(=O)Nc2ccn[nH]2)c1

JAG-UCB-cedd89ab-5
0.338

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Cc1ccncc1NC(=O)C(C)c1ccccc1

AHN-SAT-202241f6-1
0.338

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Cc1ccncc1NC(=O)C(C)c1ccccc1

TRY-UNI-714a760b-17
0.338

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O=C(Nc1cncc2ccccc12)C(CCc1cccc(F)c1)c1cccc(Cl)c1

MIC-UNK-c66144cb-1
0.337

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Cc1ccncc1NC(=O)c1ccc(C(C)C(=O)Nc2cnccc2C)cc1Cl

MAK-UNK-f203cb68-17
0.333

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Cc1ccncc1NC(=O)c1cc(Cl)cc(C(C)C(=O)Nc2cnccc2C)c1

MAK-UNK-f203cb68-16
0.333

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O=C(Nc1cncc2ccccc12)C(CCC1CCCCC1)c1cccc(Cl)c1

ALP-POS-3b848b35-4
0.330

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O=C(Nc1cncc2ccccc12)C(CCC1CCCCC1)c1cccc(Cl)c1

MIC-UNK-c66144cb-3
0.330

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

MAK-UNK-f203cb68-1
0.330

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CC(C(=O)Nc1cncc2c1CCCC2)c1cccc(C2(C)CC2)c1

DAR-DIA-0cde14eb-40
0.330

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

JAN-GHE-83b26c96-22
0.329

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

EDG-MED-0da5ad92-10
0.329

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O=C(NC(C(=O)O)c1cccc(Cl)c1)c1cncnc1

MAR-TRE-8190bb11-59
0.329

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

ADA-UCB-6c2cb422-9
0.327

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CC(C(=O)Nc1cncc2c1CCCC2)c1cccc(C2(I)CC2)c1

DAR-DIA-0cde14eb-44
0.326

View
Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

JAG-UCB-cedd89ab-8
0.325

View
Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

TRY-UNI-714a760b-12
0.325

View
CC(C)c1ccncc1NC(=O)Cc1cccc(Cl)c1

MAT-POS-bb423b95-5
0.321

View
CC(C(=O)Nc1cnccc1O)c1ccccc1

BEN-DND-93268d01-15
0.321

View
Cc1ncncc1NC(=O)Cc1cccc(Cl)c1

ABI-SAT-4d06482b-2
0.317

View
CC(C(=O)Nc1cncc2c1CCCC2)c1cccc(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-43
0.316

View
Cc1ccncc1NC(=O)C(C)c1cc(Cl)cc(OC2CC(=O)N2)c1

TRY-UNI-2eddb1ff-8
0.316

View
CC(NC(=O)CCl)c1cccc(Cl)c1

AAR-POS-0daf6b7e-10
0.315

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(C(C)C(N)=O)c1

WIL-MOD-03b86a88-3
0.315

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CC(=O)Nc1cnccc1-c1ccc(C(C)C(=O)Nc2cnccc2C)cc1Cl

MAK-UNK-f203cb68-8
0.312

View
Cc1cc(CN(C(=O)NC2CC2)C(=O)C(C)c2cccc(Cl)c2)no1

TRY-UNI-9f475305-8
0.312

View
CNCCOC(C(=O)Nc1cccnc1)c1cccc(Cl)c1

ADA-UNI-f8e79267-10
0.311

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CC(=O)NC(c1cccc(Cl)c1)c1nnc(C)s1

WIL-LEE-1f71e281-3
0.309

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COc1ccc2cncc(NC(=O)Cc3cccc(Cl)c3)c2c1

EDJ-MED-00c1612e-1
0.308

View
COc1ccc2cncc(NC(=O)Cc3cccc(Cl)c3)c2c1

PET-UNK-8df914d1-1
0.308

View
Cc1ccncc1NC(=O)CCc1cccc(Cl)c1

ALP-POS-f13221e1-4
0.306

View
CC(=O)Nc1cnccc1-c1cc(Cl)cc(C(C)C(=O)Nc2cnccc2C)c1

MAK-UNK-f203cb68-7
0.305

View
Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

TRY-UNI-714a760b-6
0.305

View
CNCCC(C(=O)Nc1cccnc1)c1cccc(Cl)c1

ADA-UNI-f8e79267-11
0.303

View
CC(C(=O)Nc1cncc(Cl)c1Cl)c1cccc(Cl)c1

0.688

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

0.673

View
Cc1cccc(C(C)C(=O)Nc2cncc(Cl)c2C)c1

0.660

View
CC(C(=O)Nc1cncc2ccccc12)c1cccc(Cl)c1

0.660

View
CC(C(=O)Nc1cncc(Cl)c1Br)c1cccc(Cl)c1

0.660

View
Cc1cnncc1NC(=O)C(C)c1cccc(Cl)c1

0.653

View
Cc1cncc(NC(=O)C(C)c2cccc(Cl)c2)c1

0.653

View
CC(C(=O)Nc1ccc(Cl)nc1C(N)=O)c1cccc(Cl)c1

0.647

View
Cc1cncc(C)c1NC(=O)C(C)c1cccc(Cl)c1

0.646

View
Cc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.646

View
CC(C(=O)Nc1cncc(F)c1)c1cccc(Cl)c1

0.640

View
Cc1cnccc1NC(=O)C(C)c1cccc(Cl)c1

0.640

View
COc1cccc(C(C)C(=O)Nc2cncc(Cl)c2C)c1

0.635

View
CC(=O)Nc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.633

View
Cc1c(NC(=O)C(C)c2cccc(Cl)c2)cccc1C(N)=O

0.627

View
Cc1cnc(Cl)c(NC(=O)C(C)c2cccc(Cl)c2)c1

0.627

View
Cc1cc(Cl)ncc1NC(=O)C(C)c1cccc(Cl)c1

0.627

View
Cc1cc(NC(=O)C(C)c2cccc(Cl)c2)c(C)cn1

0.627

View
CC(C(=O)Nc1cnccc1O)c1cccc(Cl)c1

0.627

View
Cc1cc(NC(=O)C(C)c2cccc(Cl)c2)c(C)c(C)c1O

0.627

View
Cc1c(NC(=O)C(C)c2cccc(Cl)c2)cnn1C

0.627

View
Cc1ccccc1NC(=O)C(C)c1cccc(Cl)c1

0.625

View
CC(C(=O)Nc1cncnc1)c1cccc(Cl)c1

0.625

View
COC(=O)c1[nH]c(C)cc1NC(=O)C(C)c1cccc(Cl)c1

0.623

View
CC(C(=O)Nc1cnccc1OC(C)(C)C)c1cccc(Cl)c1

0.623

View
CC(C(=O)Nc1cc(F)ccc1F)c1cccc(Cl)c1

0.620

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(Cl)n1

0.620

View
Cc1c(F)cccc1NC(=O)C(C)c1cccc(Cl)c1

0.620

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(C)n1

0.620

View
Cc1nc(Cl)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.620

View
Cc1cc(F)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.620

View
Cc1cc(O)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.620

View
COC(=O)c1cncc(NC(=O)C(C)c2cccc(Cl)c2)c1

0.615

View
CC(=O)Nc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

0.615

View
Cc1ncc(NC(=O)C(C)c2cccc(Cl)c2)c(C)n1

0.615

View
CC(C)c1ncncc1NC(=O)C(C)c1cccc(Cl)c1

0.615

View
CC(C(=O)Nc1cc(Cl)ccc1F)c1cccc(Cl)c1

0.612

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(C)c1

0.612

View
CC(C(=O)Nc1ccccc1F)c1cccc(Cl)c1

0.612

View
Cc1cc(S(N)(=O)=O)cc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.611

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c2[nH]ncc12

0.611

View
CC(C(=O)Nc1cncc(Br)c1)c1cccc(Cl)c1

0.608

View
Cc1c(NC(=O)C(C)c2cccc(Cl)c2)cccc1NC(=O)N(C)C

0.608

View
Cc1ccc(F)cc1NC(=O)C(C)c1cccc(Cl)c1

0.608

View
Cc1ccc(F)c(NC(=O)C(C)c2cccc(Cl)c2)c1

0.608

View
Cc1ncccc1NC(=O)C(C)c1cccc(Cl)c1

0.608

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(C)c1O

0.608

View
Cc1cnc(NC(=O)C(C)c2cccc(Cl)c2)[nH]1

0.608

View
Cc1nccn1-c1ccncc1NC(=O)C(C)c1cccc(Cl)c1

0.607

View
CC(C(=O)Nc1ccccc1Cl)c1cccc(Cl)c1

0.604

View
COc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

0.604

View
Cc1cc(Br)ncc1NC(=O)C(C)c1cccc(Cl)c1

0.604

View
CSc1ccncc1NC(=O)C(C)c1cccc(Cl)c1

0.604

View
CC(C(=O)Nc1cccc2cn[nH]c12)c1cccc(Cl)c1

0.604

View
CC(C(=O)Nc1ccc(F)cc1Cl)c1cccc(Cl)c1

0.600

View
Cc1ccc(C)c(NC(=O)C(C)c2cccc(Cl)c2)c1

0.600

View
CC(C(=O)Nc1cccnc1Cl)c1cccc(Cl)c1

0.600

View
CC(C(=O)Nc1ccc(F)cc1F)c1cccc(Cl)c1

0.600

View
Cc1cscc1NC(=O)C(C)c1cccc(Cl)c1

0.600

View
Cc1cnc(NC(=O)C(C)c2cccc(Cl)c2)nc1

0.600

View
CC(C(=O)Nc1cccnc1)c1cccc(Cl)c1

0.600

View
CC(C(=O)Nc1ccc(Cl)cc1C(N)=O)c1cccc(Cl)c1

0.600

View
Cc1ncc(NC(=O)C(C)c2cccc(Cl)c2)cn1

0.600

View
Cc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1C(N)=O

0.596

View
CC(C(=O)Nc1ccncc1Br)c1cccc(Cl)c1

0.596

View
CC(C(=O)Nc1ccncc1F)c1cccc(Cl)c1

0.596

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(Br)n1

0.596

View
Cc1nc(Br)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.596

View
Cc1nccc(NC(=O)C(C)c2cccc(Cl)c2)c1Cl

0.596

View
Cc1c(C#N)cccc1NC(=O)C(C)c1cccc(Cl)c1

0.596

View
Cc1cccc(C(C)C(=O)Nc2cncc(Cl)c2Cl)c1

0.596

View
Cc1nnccc1NC(=O)C(C)c1cccc(Cl)c1

0.596

View
CC(C(=O)Nc1ccncc1I)c1cccc(Cl)c1

0.596

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(O)n1

0.596

View
Cc1cc(C(N)=O)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.596

View
Cc1nn(C)c(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.596

View
CC(C(=O)Nc1ccncc1O)c1cccc(Cl)c1

0.596

View
Cc1nn(C)cc1NC(=O)C(C)c1cccc(Cl)c1

0.596

View
COC(=O)Nc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.596

View
CC(C(=O)Nc1cncnc1N(C)C)c1cccc(Cl)c1

0.593

View
CC(C(=O)Nc1ccc(Cl)cc1F)c1cccc(Cl)c1

0.592

View
CC(C(=O)Nc1ccc(Cl)cc1O)c1cccc(Cl)c1

0.592

View
CC(C(=O)Nc1cnccc1-n1cccn1)c1cccc(Cl)c1

0.589

View
CCn1cc(NC(=O)C(C)c2cccc(Cl)c2)c(C(N)=O)n1

0.589

View
Cc1cc(I)ccc1NC(=O)C(C)c1cccc(Cl)c1

0.588

View
CC(C(=O)Nc1cc(F)ccc1Cl)c1cccc(Cl)c1

0.588

View
Cc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1F

0.588

View
CC(C(=O)Nc1ccccc1C(N)=O)c1cccc(Cl)c1

0.588

View
COc1ccc(Cl)c(NC(=O)C(C)c2cccc(Cl)c2)c1

0.588

View
Cc1n[nH]c(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.588

View
Cc1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1O

0.588

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(O)c1

0.588

View
Cc1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(F)c1

0.588

View
CNC(=O)c1cccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.585

View
CC(C(=O)Nc1cc(Br)cnc1Cl)c1cccc(Cl)c1

0.585

View
COc1c(C)ccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.585

View
CC(=O)Nc1c(C)ccc(NC(=O)C(C)c2cccc(Cl)c2)c1C

0.585

View
CC(C(=O)Nc1cncc(Cl)c1Cl)c1cccc(F)c1

0.585

View
Cc1ccc(C(N)=O)cc1NC(=O)C(C)c1cccc(Cl)c1

0.585

View
COC(=O)c1ccc(NC(=O)C(C)c2cccc(Cl)c2)c(C)c1

0.585

View

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

0.851

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

0.810

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

0.798

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

0.786

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

0.786

View


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