Molecule Details

Nc1cncc(NC(=O)Nc2cccc(Cl)c2)c1
3-aminopyridine-like Enamine Assayed
View on Fragalysis x2964
Molecular Properties
SMILES:
Nc1cncc(NC(=O)Nc2cccc(Cl)c2)c1
MW: 262.7
Fraction sp3: 0.0
HBA: 3
HBD: 3
Rotatable Bonds: 2
TPSA: 80.04
cLogP: 2.9612
Covalent Warhead:
Covalent Fragment:
Source
Enamine SCR: Z4444622197
Activity Data
Average Inhibition @ 50 µM - Fluorescence: 14.95938
Average Inhibition @ 20 µM - RapidFire: 15.185
Average Inhibition @ 50 µM - RapidFire: 39.42
Relative Solubility @ 20 µM: 1.0
Relative Solubility @ 100 µM: 1.0
Order Status
Ordered: 2020-03-31
Synthesis Location: enamine
Shipped: 2020-04-27

aniline

N#Cc1cccc(NC(=O)Nc2cncc(N)c2)c1

DAR-DIA-23aa0b97-8
0.607

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Nc1cncc(NC(=O)Nc2ccccc2)c1

SID-ELM-2583a2cd-5
0.600

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

JOR-UNI-2fc98d0b-7
0.596

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

JAN-GHE-83b26c96-19
0.596

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

WAR-XCH-eb7b662f-7
0.596

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O=C(Nc1cccnc1)Nc1cccc(Cl)c1

DAR-DIA-23aa0b97-14
0.596

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

JAN-LUN-3e0f9c09-1
0.544

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

JAN-LUN-8953ce76-6
0.544

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

TRY-UNI-714a760b-9
0.538

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Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

TRY-UNI-714a760b-12
0.492

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Cc1ccncc1NC(=O)Nc1cccc(Cl)c1

JAG-UCB-cedd89ab-8
0.492

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N#Cc1cncc(NC(=O)Nc2cncc(N)c2)c1

DAR-DIA-23aa0b97-9
0.492

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CC(=O)Nc1cncc(N)c1

DAN-PUR-19f24f0c-1
0.481

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O=C(Nc1cccc(Cl)c1)Nc1ncnc2[nH]ncc12

JAG-UCB-cedd89ab-6
0.438

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O=C(Nc1cccnc1)Nc1cncc(Cl)c1

DAR-DIA-23aa0b97-15
0.429

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

JAG-UCB-cedd89ab-7
0.425

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O=C(Nc1cccc(Cl)c1)Nc1cncc(CC(=O)N2CCN(S(=O)(=O)c3cccc(F)c3)CC2)c1

ABB-MCD-f549d731-1
0.402

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Nc1cncc(NC(=O)N[C@@H]2CC[C@H]3O[C@@H]3C2)c1

FRA-FAC-9ed5a63a-5
0.394

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C=C(C(=O)Nc1cccc(Cl)c1)c1cccnc1

BEN-DND-61647d40-20
0.391

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Nc1cn(CC(=O)Nc2cccc(Cl)c2)nn1

JAG-UCB-252a2f58-1
0.380

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Cc1ccncc1CC(=O)Nc1cccc(Cl)c1

EDJ-MED-49816e9b-1
0.380

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

DAR-DIA-03336633-3
0.378

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O=C(Cc1cn[nH]c1)Nc1cccc(Cl)c1

MIC-UNK-66895286-2
0.377

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O=C(Nc1cccc(Cl)c1)[C@@]1(c2cccnc2)CO1

BEN-DND-61647d40-19
0.375

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O=C(CCl)CN(C(=O)Nc1cccc(Cl)c1)c1cncnc1

SEA-TRI-6388eba6-1
0.373

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

WAR-XCH-eb7b662f-3
0.369

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CNc1cncc(NC(=O)Nc2ccccc2)c1

SID-ELM-2583a2cd-6
0.369

View
O=C(Cc1cncc2cnccc12)Nc1cccc(Cl)c1

BEN-DND-61647d40-15
0.368

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Cc1[nH]ncc1CC(=O)Nc1cccc(Cl)c1

MIC-UNK-66895286-3
0.366

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C=CC(=O)CN(C(=O)Nc1cccc(Cl)c1)c1cncnc1

SEA-TRI-2dd971ce-1
0.364

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

JAN-LUN-3e0f9c09-2
0.364

View
O=C(Cc1cncc2ccncc12)Nc1cccc(Cl)c1

BEN-DND-61647d40-16
0.364

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

JAN-LUN-8953ce76-4
0.364

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Nc1cncc(NC(=O)CC2CCCCC2)c1

SID-ELM-2583a2cd-16
0.362

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Cc1cccc(NC(=O)Nc2cccnc2)c1

WAR-XCH-eb7b662f-6
0.358

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O=C1CC[C@@H](C(=O)Nc2cccc(Cl)c2)CN1

JAG-UCB-ef2c0e8e-10
0.352

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Cc1cc(O)ncc1CC(=O)Nc1cccc(Cl)c1

MIC-UNK-66895286-4
0.351

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

JAN-LUN-8953ce76-1
0.351

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

JAN-LUN-8953ce76-7
0.351

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C=CS(=O)(=O)CN(C(=O)Nc1cccc(Cl)c1)c1cncnc1

SEA-TRI-5a552082-1
0.351

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

JAN-LUN-3e0f9c09-4
0.351

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Cc1cncc(NC(=O)Cc2cccc(Cl)c2)c1

EDG-MED-0da5ad92-12
0.347

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

WAR-XCH-eb7b662f-4
0.343

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CC(C)(C)c1cccc(NC(=O)Nc2cccnc2)c1

WIL-UNI-5578df48-21
0.343

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Nc1cnc(Cl)c(NC(=O)Nc2ccccc2)c1

SID-ELM-8b394441-5
0.343

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CN(C)c1cncc(NC(=O)Nc2ccccc2)c1

SID-ELM-2583a2cd-7
0.338

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N#Cc1cccc(NC(=O)Nc2cccnc2)c1

JOR-UNI-61e7b1d5-2
0.338

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Cc1cc(Cl)cc(NC(=O)Nc2cccnc2)c1

WAR-XCH-eb7b662f-5
0.338

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N#Cc1cccc(NC(=O)Nc2cccnc2)c1

DAR-DIA-23aa0b97-5
0.338

View
N#Cc1cccc(NC(=O)Nc2cccnc2)c1

ANN-UNI-26382800-4
0.338

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N#Cc1cccc(NC(=O)Nc2cccnc2)c1

WAR-XCH-eb7b662f-1
0.338

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O=C(Cn1ncc2ccccc21)Nc1cccc(Cl)c1

BEN-DND-61647d40-11
0.338

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O=C(Nc1cccc(Cl)c1)C(c1cccnc1)N1C(=O)C=CC1=O

JAN-GHE-d851b096-2
0.338

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NC1=NC(Cc2cccc(NC(=O)Nc3cccnc3)c2)C(=O)N1

WIL-UNI-5578df48-27
0.337

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Cc1ncc(CCc2cccc(NC(=O)Nc3cccnc3)c2)[nH]1

BAR-COM-21d20d65-5
0.333

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O=C(Cc1cnc(O)c2ccccc12)Nc1cccc(Cl)c1

MIC-UNK-66895286-5
0.333

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O=C(Nc1cccnc1)c1cccc(Cl)c1

CHR-SOS-7098f804-12
0.333

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NC1=[SH]C(Cc2cccc(NC(=O)Nc3cccnc3)c2)C(=O)N1

WIL-UNI-5578df48-29
0.329

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CC(C)(C#N)c1cccc(NC(=O)Nc2cccnc2)c1

WIL-UNI-5578df48-19
0.329

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O=C(Nc1ccc(Cl)cc1)Nc1ccc(Cl)c(Cl)c1

MAK-UNK-0cb6a3ad-11
0.328

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N#Cc1cccc(NC(=O)Cc2cncc(N)c2)c1

DAR-DIA-23aa0b97-3
0.325

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N#Cc1cc(Cl)cc(NC(=O)Nc2cccnc2)c1

WAR-XCH-eb7b662f-2
0.324

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COC(C)(C)c1cccc(NC(=O)Nc2cccnc2)c1

WIL-UNI-5578df48-22
0.324

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CC(C)(C)c1cc(N)cc(NC(=O)Nc2cccnc2)c1

SAD-SAT-689b7d5a-3
0.324

View
N#Cc1cncc(NC(=O)Nc2cccnc2)c1

CHR-SOS-363cfb78-1
0.324

View
O=C(Cc1cccc(Cl)c1)Nc1cccnc1

EDG-MED-0da5ad92-2
0.324

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

MAK-UNK-129dcd6f-9
0.321

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CN(CCc1cccc(NC(=O)Nc2cccnc2)c1)C(N)=O

BAR-COM-21d20d65-8
0.321

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NC(=O)[C@@H](F)CCc1cccc(NC(=O)Nc2cccnc2)c1

BAR-COM-21d20d65-9
0.321

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O=C(Cn1cnc2ccccc21)Nc1cccc(Cl)c1

BEN-DND-61647d40-13
0.321

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NC(=O)NC(=O)Cc1cccc(NC(=O)Nc2cccnc2)c1

WIL-UNI-5578df48-28
0.321

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N#CC(C(=O)Nc1cccc(Cl)c1)C(=O)c1cccs1

JOH-UNI-c7afdb96-5
0.320

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

TRY-UNI-714a760b-23
0.316

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O=C(Cn1nnc2ccccc21)Nc1cccc(Cl)c1

MAT-POS-3b92565d-14
0.316

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O=C(Cn1nnc2ccccc21)Nc1cccc(Cl)c1

BEN-DND-61647d40-12
0.316

View
O=C(Nc1cccnc1)Nc1cccc(Cc2ccccc2O)c1

WIL-UNI-5578df48-26
0.316

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O=C(Nc1cccnc1)Nc1csc(Cl)c1

MAK-UNK-d1e89583-7
0.314

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O=C(Nc1cccnc1)Nc1ccncc1Cl

MAK-UNK-d1e89583-4
0.314

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O=C(Cc1cccc(Cl)c1)Nc1cncnc1

JAN-GHE-5a013bed-9
0.314

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O=C(Cc1c[nH]c2ncccc12)Nc1cccc(Cl)c1

DAR-DIA-23aa0b97-12
0.312

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O=C(Nc1cncc(Cl)c1)c1cccc2[nH]ccc12

NAU-LAT-356bd3c2-2
0.312

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Cc1nc(NCCNC(=O)Nc2cccc(Cl)c2)cc(N2CCOCC2)n1

MAR-TRE-f5c2d31c-11
0.311

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Cc1cc2c(N)nc(=O)n(CC(=O)Nc3cccc(Cl)c3)c2s1

JAG-UCB-77729364-1
0.310

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O=S1(=O)CC(Nc2cccc(Cl)c2)C=N1

MAK-UNK-942dcb71-5
0.309

View
CC(=O)NC(Cc1ccc(O)cc1)C(=O)Nc1cccc(Cl)c1

TRY-UNI-9f475305-11
0.308

View
O=C(NCCNc1cc(N2CCOCC2)ncn1)Nc1cccc(Cl)c1

MAR-TRE-f5c2d31c-36
0.308

View
NC1([C@H](O)CCc2cccc(NC(=O)Nc3cccnc3)c2)CC1

BAR-COM-21d20d65-1
0.306

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

CHR-SOS-7098f804-21
0.306

View
O=C(Nc1cccnc1)Nc1cccc(CCC2(CO)CC2)c1

BAR-COM-21d20d65-4
0.305

View
O=C(Nc1cccnc1)Nc1cccc(CCC(O)CCO)c1

WIL-UNI-5578df48-24
0.305

View
O=C(Nc1cc[nH]c1)Nc1cccc(F)c1

CAS-DEP-751a2458-3
0.304

View
C=CC(=O)N(c1cccc(Cl)c1)C(C(=O)Nc1cccc(Cl)c1)c1cccnc1

JAN-GHE-d851b096-9
0.303

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

MAK-UNK-129dcd6f-16
0.301

View
C=CC(=O)N(c1ccc(NC(C)=O)cc1)N(C(=O)Nc1cccc(Cl)c1)c1cccnc1

JAN-GHE-d851b096-3
0.300

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

TRY-UNI-714a760b-3
0.299

View
O=C(Nc1cn[nH]c1)Nc1cccc(-c2cccnc2)c1

CAS-DEP-167c18e3-4
0.299

View
N#Cc1ccncc1NC(=O)c1cccc(NC(=O)Nc2cccnc2)c1

MAK-UNK-10dfa458-24
0.298

View
NC1NCC(c2cccc(NC(=O)Nc3cccnc3)c2)O1

WIL-UNI-5578df48-23
0.298

View
O=C(Nc1cccnc1)Nc1cccc(CCCc2ccc[nH]2)c1

BAR-COM-21d20d65-3
0.298

View
CCC[C@](C)(O)CCc1cccc(NC(=O)Nc2cccnc2)c1

BAR-COM-21d20d65-6
0.298

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

0.649

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

0.649

View
CC1=CN=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.649

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

0.596

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

0.554

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

0.545

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

0.536

View
CC(=O)NC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.536

View
O=C(NC1=C[NH]N=C1)NC1=CC(Cl)=CC=C1

0.533

View
NNC(=O)NC1=CC=CC(Cl)=C1

0.528

View
CC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.526

View
CC(=O)NC1=CC=C(NC(=O)NC2=CC=CC(Cl)=C2)C=C1

0.526

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

0.526

View
CN1C=C(NC(=O)NC2=CC=CC(Cl)=C2)C=N1

0.525

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

0.517

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

0.517

View
NCC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.517

View
CC1=CC=C(NC(=O)NC2=CC=CC(Cl)=C2)C=N1

0.516

View
O=C(NC1=CC(Cl)=CC=C1)NC1=CN=C2C=CC=CC2=C1

0.515

View
CC1=CC=C(NC(=O)NC2=CC=CC(Cl)=C2)C=C1

0.508

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

0.508

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

0.508

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

0.508

View
CC1=CC=C(NC(=O)NC2=CC=CC(Cl)=C2)C=C1C

0.500

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

0.500

View
O=C(NC1=CC(Cl)=CC=C1)NC1=N[NH]C=C1

0.500

View
O=C(NNC1=CC=NC=C1)NC1=CC(Cl)=CC=C1

0.500

View
CNC1=CC=C(NC(=O)NC2=CC=CC(Cl)=C2)C=N1

0.500

View
COC(=O)NC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.500

View
CC(C)C(=O)NC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.500

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

0.500

View
O=C(NNC1=CN=CC(Br)=C1)NC1=CC(Cl)=CC=C1

0.493

View
C#CC1=CC(NC(=O)NC2=CC(Cl)=CC=C2)=CC=C1

0.492

View
COC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.492

View
CSC1=CC=CC(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.492

View
O=C(NC1=CC(Cl)=CC=C1)NC1=CN=C2CCCC2=C1

0.486

View
CCN1C=C(NC(=O)NC2=CC=CC(Cl)=C2)C=N1

0.485

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

0.482

View
NC(=O)CN1C=C(NC(=O)NC2=CC=CC(Cl)=C2)C=N1

0.478

View
O=C(NNC1=CN=CC(Cl)=N1)NC1=CC(Cl)=CC=C1

0.478

View
CC1=C(NC(=O)NC2=CC=CC(Cl)=C2)C=NO1

0.477

View
CC1=N[NH]C(NC(=O)NC2=CC=CC(Cl)=C2)=C1C

0.476

View
O=C(NNC(=O)NC1=CC(Cl)=CC=C1)NC1=CC=NC=C1

0.475

View
O=C(NNC1=CC(Cl)=CC=C1)NC1=CC=CC(Cl)=C1

0.475

View
O=C(NC1=CC=C(CC2=CC=NC=C2)C=C1)NC1=CC(Cl)=CC=C1

0.471

View
CC1=N[NH]C(NC(=O)NC2=CC=CC(Cl)=C2)=C1

0.469

View
NC1=CC=C(CNC(=O)NC2=CC=CC(Cl)=C2)C=C1

0.462

View
CC1=N[NH]C(C)=C1NC(=O)NC1=CC=CC(Cl)=C1

0.462

View
NC1=CC=C(C(=O)NC2=CC=CC(Cl)=C2)N=C1

0.460

View
O=C(NC1=CC(Cl)=CC=C1)C1=CN=CC(C(=O)NC2=CC=CC(Cl)=C2)=C1

0.459

View
O=C(NNC1=CC=NC=C1Cl)NC1=CC(Cl)=CC=C1

0.456

View
O=C(NC1=CC(Cl)=CC=C1)C1=C(Cl)C=NC=C1Cl

0.452

View
O=C(NC1=CC(Cl)=CC=C1)NN1C=NN=C1

0.452

View
C[C@H](NC(=O)NC1=CC=CC(Cl)=C1)C1=CN=CC(F)=C1

0.451

View
CC(NC(=O)NC1=CC(Cl)=CC=C1)C1=CN=CC(F)=C1

0.451

View
O=C(NC1=CC(Cl)=CC=C1)NC1=CN(C2=CC=CC=C2)N=C1

0.451

View
O=C(NC1=CC(Cl)=CC=C1)NC1=CC=C2OCCOC2=C1

0.448

View
FC1=CN=CC(NC(=S)NC2=CC=CC(Cl)=C2)=C1

0.446

View
S=C(NC1=CC(Cl)=CC=C1)NC1=CN=CC(Br)=C1

0.446

View
CC1=CN=CC(NC(=S)NC2=CC=CC(Cl)=C2)=C1

0.446

View
NC1=NC=NC=C1CNC(=O)NC1=CC=CC(Cl)=C1

0.444

View
O=C(NC1=CC(Cl)=CC=C1)NC1=CC=C2SC=NC2=C1

0.443

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

0.443

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

0.443

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

0.443

View
O=C(NC1=CC=C(N2CCCCC2)N=C1)NC1=CC(Cl)=CC=C1

0.438

View
O=C(NNC(=O)NC1=CC=CC(Cl)=C1)NC1=CC(F)=CC(F)=C1

0.438

View
O=C(NC1=CC(Cl)=CC=C1)C1=CN=CC(Cl)=N1

0.438

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

0.437

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

0.435

View
NC1=CC=C(C(=O)NC2=CC=CC(Cl)=C2)C=C1

0.435

View
O=C(NNC1=CC=CC(Cl)=C1)NC1=CC(F)=CN=C1

0.435

View
O=C(NNC1=CC(Cl)=CC=C1)NC1=CN=CC(Br)=C1

0.435

View
CC1=CN=CC(NC(=O)NNC2=CC=CC(Cl)=C2)=C1

0.435

View
CC1=CC=CC(NC(=O)NC2=CN=CC(C)=C2)=C1

0.429

View
CN1CCN(C2=CC=C(NC(=O)NC3=CC=CC(Cl)=C3)C=N2)CC1

0.427

View
NC1=CC=CC(C(=O)NC2=CC=CC(Cl)=C2)=C1

0.422

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

0.418

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

0.418

View
NC1=CC=CC(NC(=O)NC2=CC=CC=C2)=C1

0.417

View
O=C(NNC1=CC(Cl)=CC=C1)NC1=CC=CN=C1

0.412

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

0.409

View
CC1=CN=CC(NC(=O)NC2=CC=CC(F)=C2)=C1

0.409

View
CC(=O)NC1=CC=CC(NC(=O)NC2=CN=CC(F)=C2)=C1

0.409

View
COC(=O)C1=CN=CC(NC(=O)NNC2=CC=CC(Cl)=C2)=C1

0.405

View
CC1=CC=CC(NC(=O)NC2=CN=CC(F)=C2)=C1

0.403

View
C#CC1=CC(C(=O)NC2=CC(Cl)=CC=C2)=CN=C1

0.400

View
O=C(NCC1=CC=CC(Cl)=C1)NC1=CC(F)=CN=C1

0.397

View
O=C(NNC1=CC=CC(Cl)=C1)C(=O)NC1=CC(F)=CN=C1

0.397

View
O=C(NCC1=CC(Cl)=CC=C1)NC1=CN=CC(Br)=C1

0.397

View
CC1=CN=CC(NC(=O)NCC2=CC=CC(Cl)=C2)=C1

0.397

View
O=C(NNC1=CC(Cl)=CC=C1)C(=O)NC1=CN=CC(Br)=C1

0.397

View
CC1=CN=CC(NC(=O)C(=O)NNC2=CC=CC(Cl)=C2)=C1

0.397

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

0.397

View
COC(=O)C1=CN=CC(C(=O)NC2=CC=CC(Cl)=C2)=C1

0.394

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

0.391

View
O=C(CNC1=CC=CC(Cl)=C1)NC1=CC(F)=CN=C1

0.389

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

0.382

View
NC1=CC=CC(NC(=O)C2=CC=CC(Cl)=C2)=C1

0.379

View
O=C(NCC1=CC(Cl)=CC=C1)NC1=CC=CN=C1

0.375

View
Clc1cccc(NC(=O)Nc2cccnc2)c1

0.596

View
Clc1cc(Cl)cc(NC(=O)Nc2cccnc2)c1

0.369

View
Clc1ccc(NC(=O)Nc2cccnc2)cc1Cl

0.358

View
Clc1ccc(NC(=O)Nc2cccnc2)cc1

0.338

View
Cc1ccc(NC(=O)Nc2cccnc2)cc1Cl

0.338

View


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