Molecule Details

Cc1ccncc1NC(=O)Cc1ccc2[nH]ccc2c1
3-aminopyridine-like Enamine Assayed
Molecular Properties
SMILES:
Cc1ccncc1NC(=O)Cc1ccc2[nH]ccc2c1
MW: 265.12
Fraction sp3: 0.12
HBA: 2
HBD: 2
Rotatable Bonds: 3
TPSA: 57.78
cLogP: 3.05
Covalent Warhead:
Covalent Fragment:
Source
Enamine REAL: s_22____3391102____16784198
Activity Data
Average Inhibition @ 20 µM - Fluorescence: 2.8551305
Average Inhibition @ 50 µM - Fluorescence: -2.3296125
Relative Solubility @ 20 µM: 1.0
Relative Solubility @ 100 µM: 1.0
Order Status
Ordered: 2020-06-20
Synthesis Location: enamine
Shipped: 2020-07-08

Cc1ccncc1NC(=O)Cc1ccc2[nH]ncc2c1

VLA-UCB-00f2c2b3-2
0.630

View
Cc1ccncc1NC(=O)Cc1ccc2nc[nH]c2c1

GAB-REV-70cc3ca5-18
0.532

View
Cc1ccc(CC(=O)Nc2cnccc2C)cc1

JAN-GHE-83b26c96-11
0.522

View
Cc1ccncc1NC(=O)Cc1cccc(I)c1

JAN-GHE-83b26c96-13
0.521

View
Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

TRY-UNI-714a760b-6
0.521

View
Cc1ccncc1NC(=O)Cc1cccc(CO)c1

EDJ-MED-e58735b6-2
0.521

View
Cc1ccncc1NC(=O)Cc1cccc(O)c1

ALP-POS-95b75b4d-2
0.521

View
Cc1ccncc1NC(=O)Cc1cccc(F)c1

ALP-POS-95b75b4d-1
0.514

View
Cc1ccncc1NC(=O)Cc1cccc(Br)c1

JAN-GHE-83b26c96-12
0.514

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

DAR-DIA-0cde14eb-1
0.513

View
Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

EDG-MED-0da5ad92-8
0.507

View
Cc1ccncc1NC(=O)Cc1cncc(Cl)c1

TRY-UNI-2eddb1ff-2
0.507

View
COc1cccc(CC(=O)Nc2cnccc2C)c1

EDJ-MED-e58735b6-1
0.500

View
Cc1ccncc1NC(=O)Cc1cccc(S(N)(=O)=O)c1

EDJ-MED-e58735b6-3
0.500

View
Cc1ccncc1NC(=O)Cc1ccccc1

TRY-UNI-714a760b-5
0.500

View
Cc1ccncc1NC(=O)Cc1cccc([S+](C)[O-])c1

DAR-DIA-0cde14eb-78
0.500

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

ALP-POS-95b75b4d-3
0.494

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

JAN-GHE-83b26c96-14
0.494

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

ANN-UNI-98d2bf15-2
0.494

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

DAR-DIA-0cde14eb-76
0.494

View
Cc1ccncc1NC(=O)Cc1cccc(-c2cn[nH]c2)c1

EDJ-MED-e58735b6-4
0.488

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

DAR-DIA-0cde14eb-2
0.487

View
Cc1ccncc1NC(=O)Cc1cccc(C#N)c1

TRY-UNI-714a760b-20
0.487

View
Cc1ccncc1NC(=O)Cc1ccc(Cl)c(OC2CC(=O)N2)c1

RAL-THA-901e9a10-8
0.483

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

DAR-DIA-0cde14eb-4
0.481

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

DAR-DIA-0cde14eb-3
0.481

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

DAR-DIA-0cde14eb-79
0.481

View
Cc1ccncc1NC(=O)Cc1ccc(S(N)(=O)=O)cc1

GAB-REV-70cc3ca5-20
0.480

View
Cc1ccncc1NC(=O)Cc1ccsc1

MIH-UNI-6b9ca91a-1
0.479

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

MAT-POS-e501d84c-1
0.476

View
Cc1ccncc1NC(=O)Cc1cccc(C2CC2)c1

ALP-POS-95b75b4d-4
0.475

View
Cc1ccncc1NC(=O)Cc1cccc(OC(F)(F)F)c1

ANN-UNI-98d2bf15-5
0.475

View
Cc1cc(CC(=O)Nc2cnccc2C)[nH]n1

EDJ-MED-c9f55a56-1
0.473

View
Cc1ccncc1NC(=O)Cc1cccc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-7
0.471

View
Cc1ccncc1NC(=O)Cc1cccc(OC2CC(=O)N2)c1

BRU-LEF-c49414a7-1
0.471

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(-c2ncc[nH]2)c1

RAL-THA-6b94ceba-9
0.464

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

DAR-DIA-0cde14eb-14
0.464

View
CCC(F)(F)c1cccc(CC(=O)Nc2cnccc2C)c1

DAR-DIA-0cde14eb-77
0.463

View
Cc1ccncc1NC(=O)CCc1ccc(F)cc1

BEN-DND-93268d01-5
0.461

View
Cc1ccncc1NC(=O)Cc1cncc(C#N)c1

TRY-UNI-2eddb1ff-1
0.456

View
Cc1ccncc1NC(=O)CCl

MAK-UNK-6ca90168-26
0.448

View
COc1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

MAT-POS-c9973a83-1
0.444

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

RAL-THA-6b94ceba-6
0.444

View
Cc1cc(CC(=O)Nc2cnccc2C)cc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-1
0.443

View
Cc1ccncc1NC(=O)Cc1cccc(CN2CCOCC2)c1

SAD-SAT-7d5528d9-1
0.442

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(-c2cnc[nH]2)c1

RAL-THA-6b94ceba-11
0.442

View
Cc1nnc(CC(=O)Nc2cnccc2C)s1

ALE-HEI-f28a35b5-3
0.440

View
Cc1ccncc1NC(=O)Cc1cnn(C2(C)CC2)c1

DAR-DIA-0cde14eb-61
0.439

View
Cc1ccncc1NC(=O)Cc1cnn(C2(I)CC2)c1

DAR-DIA-0cde14eb-64
0.439

View
Cc1ccncc1NC(=O)Cc1cc(N2CCCCC2)cc(C2(C)CC2)c1

DAR-DIA-0cde14eb-16
0.438

View
CCc1cc(CC(=O)Nc2cnccc2C)cc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-6
0.438

View
C#Cc1cc(CC(=O)Nc2cnccc2C)cc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-4
0.435

View
Cc1ccncc1NC(=O)Cc1cnn(C2(F)CC2)c1

DAR-DIA-0cde14eb-63
0.434

View
Cc1ccncc1NC(=O)Cc1cnn(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-62
0.434

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

RAL-THA-6b94ceba-13
0.434

View
Cc1ccncc1NC(=O)Cc1nc2ccccc2[nH]1

GAB-REV-70cc3ca5-9
0.434

View
CNC(=O)c1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

RAL-THA-6b94ceba-7
0.434

View
Cc1ccncc1NC(=O)CC1(CO)CC1

MAT-POS-590ac91e-6
0.432

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(-c2nnc[nH]2)c1

RAL-THA-6b94ceba-10
0.432

View
Cc1ccncc1NC(=O)CCCBr

ALE-HEI-f28a35b5-12
0.431

View
Cc1ccncc1NC(=O)Cc1ccccc1N

ANN-UNI-98d2bf15-1
0.429

View
CC(=O)NCc1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

RAL-THA-6b94ceba-5
0.429

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

RAL-THA-6b94ceba-15
0.429

View
Cc1ccncc1NC(=O)CC#N

ASH-SAT-43770c7d-9
0.429

View
Cc1ccncc1NC(=O)Cc1cc(Cl)c2c(c1)OCCO2

BAR-COM-0f94fc3d-28
0.425

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(NC2(C)CCC(F)(F)CC2)c1

MAT-POS-044491d2-6
0.424

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(OCc2ncc[nH]2)c1

RAL-THA-6b94ceba-1
0.424

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

WIL-MOD-03b86a88-5
0.424

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

WIL-MOD-03b86a88-3
0.424

View
CNS(=O)(=O)c1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

RAL-THA-6b94ceba-14
0.424

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

RAL-THA-6b94ceba-12
0.424

View
CNS(=O)(=O)Cc1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

RAL-THA-6b94ceba-16
0.424

View
COc1cc(CC(=O)Nc2cnccc2C)cc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-5
0.422

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

WIL-MOD-03b86a88-6
0.419

View
Cc1ccncc1NC(=O)Cc1cnn(C2(C#N)CC2)c1

DAR-DIA-0cde14eb-74
0.419

View
Cc1ccncc1NC(=O)CN(C)c1cc2ccccc2[nH]1

GAB-REV-70cc3ca5-7
0.419

View
COC(=O)NCc1cc(Cl)cc(CC(=O)Nc2cnccc2C)c1

RAL-THA-6b94ceba-8
0.419

View
Cc1ccncc1NC(=O)CCSCCS(C)(=O)=O

MAK-UNK-372b0df5-3
0.418

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(OC2CC(=O)N2)c1

TRY-UNI-2eddb1ff-7
0.418

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(OC2CC(=O)N2)c1

WIL-MOD-03b86a88-1
0.418

View
Cc1ccncc1NC(=O)Cc1cc(F)cc(OC2CC(=O)N2)c1

RAL-THA-901e9a10-2
0.418

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(NC23CC(N4CCCCC4)(C2)C3)c1

MAT-POS-044491d2-5
0.417

View
Cc1ccncc1NC(=O)CC1CC2(CC2)C1

MAT-POS-590ac91e-24
0.416

View
Cc1ccncc1NC(=O)CCOC1CC1

MAT-POS-590ac91e-10
0.416

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(C2COC2)c1

WIL-MOD-03b86a88-2
0.414

View
Cc1ccncc1NC(=O)CCCCC(=N)N

PET-SGC-6e7c5dc0-1
0.413

View
Cc1ccncc1NC(=O)Cc1ccccc1-c1ccccn1

THO-SYG-cc9e9a11-2
0.412

View
Cc1ccncc1NC(=O)Cc1nc2cccc(C)c2o1

GAB-REV-70cc3ca5-23
0.412

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

MAT-POS-044491d2-7
0.411

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(OC2COC2)c1

WIL-MOD-03b86a88-4
0.411

View
Cc1ccncc1NC(=O)CC(C)C(C)C

MAT-POS-590ac91e-11
0.411

View
Cc1ccncc1NC(=O)CCc1ccn[nH]1

MAT-POS-590ac91e-17
0.410

View
Cc1ccncc1NC(=O)CCNc1ccc2[nH]ncc2c1

GAB-REV-70cc3ca5-12
0.409

View
Cc1ccncc1NC(=O)Cc1cc(N2CCCCC2)cc(C2(Cl)CC2)c1

DAR-DIA-0cde14eb-17
0.409

View
Cc1ccncc1NC(=O)CC(C)(C)NC(=O)c1cccc2[nH]ccc12

GAB-REV-70cc3ca5-6
0.409

View
Cc1ccncc1NC(=O)Cc1cc(N2CCCCC2)cc(C2(F)CC2)c1

DAR-DIA-0cde14eb-18
0.409

View
Cc1ccncc1NC(=O)Cc1cc(N2CCCCC2)cc(C2(I)CC2)c1

DAR-DIA-0cde14eb-19
0.409

View
Cc1ccncc1NC(=O)Cc1cc(Cl)cc(OCc2cnc[nH]2)c1

RAL-THA-6b94ceba-3
0.409

View
COC1(CC(=O)Nc2cnccc2C)CC1

MAT-POS-590ac91e-9
0.408

View
Cc1ccncc1NC(=O)CC(O)C1CC1

MAT-POS-590ac91e-7
0.408

View
Cc1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.812

View
Cc1ccncc1NC(=O)Cc1ccc2[nH]ncc2c1

0.755

View
Cc1ccncc1NC(=O)NCCc1ccc2[nH]ccc2c1

0.698

View
Cc1ccncc1NC(=O)Cc1ccc2ccccc2c1

0.694

View
Cc1ccncc1NC(=O)C(=O)NCCc1ccc2[nH]ccc2c1

0.685

View
Cc1ccncc1NC(=O)Cc1ccc(CC(=O)Nc2cnccc2C)cc1

0.682

View
Cc1ccc(CC(=O)Nc2cnccc2C)cc1C

0.681

View
Cc1ccc(CC(=O)Nc2cnccc2C)cc1Br

0.673

View
Cc1cnccc1NC(=O)CCc1ccc2[nH]ccc2c1

0.673

View
Cc1ccncc1NC(=O)Cc1ccc2[nH]c(=O)[nH]c2c1

0.667

View
Cc1ccncc1NC(=O)c1ccc2[nH]ccc2c1

0.660

View
Cc1ccncc1NC(=O)Cc1ccc(O)cc1

0.660

View
Cc1ccncc1NC(=O)Cc1ccc2cn[nH]c2c1

0.654

View
Cc1ccncc1NCc1ccc2[nH]ccc2c1

0.653

View
Cc1ccncc1NC(=O)Cc1ccc(Br)cc1

0.646

View
Cc1ccncc1NC(=O)Cc1ccc(Cl)c(Cl)c1

0.640

View
Cc1ccncc1NC(=O)Cc1ccc(F)c(F)c1

0.640

View
Cc1ccncc1NC(=O)Cc1cccc(Br)c1

0.640

View
Cc1ccc(CC(=O)Nc2cnccc2C)cc1O

0.640

View
Cc1ccc(CC(=O)Nc2cnccc2C)cc1

0.638

View
Cc1ccncc1NC(=O)Cc1ccc(F)c(Br)c1

0.635

View
Cc1ccncc1NC(=O)Cc1ccc(Br)c(Cl)c1

0.635

View
Cc1ccncc1NC(=O)Cc1ccc(Br)c(F)c1

0.635

View
Cc1ccncc1NC(=O)Cc1ccncc1

0.630

View
Cc1cc2cc[nH]c2cc1NC(=O)Cc1ccc2[nH]ncc2c1

0.630

View
COc1cc(CC(=O)Nc2cnccc2C)ccc1C

0.627

View
Cc1cc2cc[nH]c2cc1NC(=O)Cc1ccncc1

0.627

View
Cc1cc(C)cc(CC(=O)Nc2cnccc2C)c1

0.625

View
CCc1ccc(CC(=O)Nc2cnccc2C)cc1

0.625

View
Cc1cnccc1NC(=O)Cc1ccc2[nH]ncc2c1

0.623

View
Cc1cccc(CC(=O)Nc2cnccc2C)c1

0.620

View
CC(=O)Nc1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.618

View
COc1ccc(CC(=O)Nc2cnccc2C)cc1OC

0.615

View
Cc1ccncc1NC(=O)Cc1ccc2c(c1)CCCC2

0.615

View
Cc1ccncc1NC(=O)Cc1ccc2c(c1)CCC2

0.615

View
Cc1ccncc1NC(=O)Cc1ccc(Cl)cc1

0.612

View
Cc1ccncc1NC(=O)Cc1ccc(F)cc1

0.612

View
Cc1ccncc1NC(=O)Cc1ccc(I)cc1

0.612

View
Cc1ccncc1NC(=O)Cc1ccc(CN)cc1

0.612

View
O=C(CCc1ccc2[nH]ccc2c1)Nc1cnccc1O

0.611

View
Cc1cc(C)n(-c2ccc(CC(=O)Nc3cnccc3C)cc2)n1

0.611

View
Cc1cc2cc[nH]c2cc1NC(=O)Cc1cccnc1

0.611

View
Cc1ccncc1NC(=O)Cc1cccc(Cl)c1

0.608

View
Cc1ccncc1NC(=O)Cc1cccc(I)c1

0.608

View
Cc1ccncc1NC(=O)Cc1ccc(-n2cccc2)cc1

0.608

View
COc1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.607

View
CSc1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.607

View
Cc1cc(C)c(CC(=O)Nc2cnccc2C)c(C)c1

0.604

View
Cc1ccncc1NC(=O)Cc1cncnc1

0.604

View
Cc1cnncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.604

View
Cc1ccncc1NC(=O)Cc1ccc2c(c1)OCCO2

0.604

View
Cc1ccncc1NC(=O)Cc1ccc(O)c(F)c1

0.604

View
Cc1ccncc1NC(=O)Cc1ccc2c(c1)COC2

0.604

View
Cc1ccncc1NC(=O)Cc1cnc2ccccc2c1

0.604

View
CC(=O)c1ccc(CC(=O)Nc2cnccc2C)cc1

0.600

View
Cc1ccc(CC(=O)Nc2cnccc2C)cn1

0.600

View
CCCc1ccc(CC(=O)Nc2cnccc2C)cc1

0.600

View
Cc1cncc(CC(=O)Nc2cnccc2C)c1

0.600

View
Cc1ccncc1NC(=O)C=Cc1ccc2[nH]ccc2c1

0.600

View
CC(C)(C)Oc1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.596

View
Cc1ccncc1NC(=O)Cc1cccc(F)c1

0.596

View
Cc1ccncc1NC(=O)Cc1ccc(-n2cnnc2)cc1

0.596

View
O=C(CCc1ccc2[nH]ccc2c1)Nc1ccncc1Br

0.593

View
Cc1cnccc1CC(=O)Nc1ccc2[nH]ccc2c1

0.593

View
Cc1ccncc1NC(=O)Cc1ccc2c(c1)OCO2

0.593

View
Cc1ccncc1NC(=O)Cc1ccc(C)c([N+](=O)[O-])c1

0.593

View
COc1cc(CC(=O)Nc2cnccc2C)ccc1Cl

0.593

View
CCCOc1ccc(CC(=O)Nc2cnccc2C)cc1OCCC

0.593

View
Cc1cnccc1CC(=O)Nc1cc2[nH]ccc2cc1C

0.593

View
Cc1ccncc1NC(=O)Cc1cccnc1

0.592

View
CCc1cnccc1NC(=O)CCc1ccc2[nH]ccc2c1

0.589

View
CC(=O)c1cnccc1NC(=O)CCc1ccc2[nH]ccc2c1

0.589

View
Cc1ccncc1NC(=O)Cc1ccc(-c2ccccc2)cc1

0.588

View
COc1ccc(CC(=O)Nc2cnccc2C)cc1

0.588

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

0.588

View
Cc1ccncc1NC(=O)Cc1ccc(CC(C)C)cc1

0.588

View
Cc1ccncc1NC(=O)Cc1ccc(C(C)(C)C)cc1

0.588

View
Cc1ccncc1NC(=O)Cc1ccc(C#N)cc1

0.588

View
Cc1ccncc1NC(=O)Cc1cncc(O)c1

0.588

View
Cc1ccncc1NC(=O)Cc1ccc(C(N)=O)cc1

0.588

View
Cc1ccncc1NC(=O)Cc1ccc([Si](C)(C)C)cc1

0.588

View
COc1cccc(CC(=O)Nc2cnccc2C)c1

0.585

View
Cc1cc2cc[nH]c2cc1NC(=O)Cc1cncnc1

0.585

View
Cc1cnn(-c2ccncc2NC(=O)CCc2ccc3[nH]ccc3c2)c1

0.583

View
Cc1nccn1-c1ccncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.583

View
O=C(CCc1ccc2[nH]ccc2c1)Nc1ccncc1F

0.582

View
COc1ccc(CC(=O)Nc2cnccc2C)cc1F

0.582

View
COc1cc(CC(=O)Nc2cnccc2C)ccc1O

0.582

View
Cc1ccncc1NC(=O)Cc1ccc2ncsc2c1

0.582

View
Cc1cc(Br)ncc1NC(=O)CCc1ccc2[nH]ccc2c1

0.582

View
Cc1ccncc1C(=O)NCCc1ccc2[nH]ccc2c1

0.582

View
O=C(CCc1ccc2[nH]ccc2c1)Nc1ccncc1I

0.582

View
O=C(CCc1ccc2[nH]ccc2c1)Nc1ccncc1O

0.582

View
Cc1ccncc1NC(=O)Cc1ncc[nH]1

0.580

View
Cc1cnccc1CC(=O)NCCc1ccc2[nH]ccc2c1

0.579

View
Cc1ccncc1CCNC(=O)CCc1ccc2[nH]ccc2c1

0.579

View
Cc1cnccc1NC(=O)NCCc1ccc2[nH]ccc2c1

0.579

View
CCCCc1ccc(CC(=O)Nc2cnccc2C)cc1

0.577

View
Cc1ccncc1NC(=O)Cc1ccc(C(F)(F)F)cc1

0.577

View
COc1cc(CC(=O)Nc2cnccc2C)cc(OC)c1

0.577

View

C(NC1=C(C)C=CN=C1)(=O)CC1C2=C(C=CC=C2)NC=1

0.852

View
C(NC1C=NC2=C(C=CC=C2)C=1)(CC1=CC=CC=C1)=O

0.822

View
C(NC1C=NC2=C(C=CC=C2)C=1)(=O)CC1=CC=C(C)C=C1

0.805

View
C(NC1C=NC2=C(C=CC=C2)C=1)(=O)CC1=CC=NC=C1

0.792

View
C(NC1C=NC2=C(C=CC=C2)C=1)(=O)CC1=CC=C(CC)C=C1

0.791

View


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