Molecular Properties | |
SMILES: | O=C(Nc1c(Cl)ncn2c(O)nnc12)C1CCOc2ccc(Cl)cc21 |
MW: | 379.02 |
Fraction sp3: | 0.2 |
HBA: | 7 |
HBD: | 2 |
Rotatable Bonds: | 2 |
TPSA: | 101.64 |
cLogP: | 2.64 |
Covalent Warhead: | ✗ |
Covalent Fragment: | ✗ |
Order Status | |
Ordered: | 2020-09-29 |
Synthesis Location: | enamine |
Shipped: | synthesis in progress |
α-Halogen substituted N-heterocycles
4-halopyridine
2-halopyridine
halo-pyridine,_-diazoles_and_-triazoles
VLA-UCB-1dbca3b4-15
EDJ-MED-c8e7a002-17
EDJ-MED-c8e7a002-16
EDJ-MED-c8e7a002-14
EDJ-MED-c8e7a002-11
EDJ-MED-c8e7a002-6
EDJ-MED-c8e7a002-5
EDJ-MED-c8e7a002-4
EDJ-MED-c8e7a002-13
EDJ-MED-c8e7a002-12
EDJ-MED-c8e7a002-8
EDJ-MED-c8e7a002-3
EDJ-MED-c8e7a002-15
EDJ-MED-c8e7a002-10
EDJ-MED-c8e7a002-9
EDJ-MED-c8e7a002-7
EDJ-MED-c8e7a002-1
EDJ-MED-c8e7a002-2
EDJ-MED-97c1bf5c-5
0.739
JAG-UCB-52b62a6f-2
0.640
JAG-UCB-52b62a6f-3
0.640
JAG-UCB-52b62a6f-11
0.542
EDJ-MED-97c1bf5c-3
0.535
NAU-LAT-8502cac5-15
0.533
RAL-THA-b74298ba-1
0.528
EDJ-MED-97c1bf5c-4
0.520
JAG-UCB-a3ef7265-20
0.516
RAL-THA-b74298ba-3
0.516
EDG-MED-fe7487f8-9
0.516
JAG-UCB-c61058a9-41
0.516
JAG-UCB-119787ef-1
0.516
JAG-UCB-c61058a9-21
0.516
MAT-POS-968e8d9c-1
0.516
RAL-THA-b74298ba-2
0.516
JOH-UNI-1b27fa5e-6
0.516
RAL-THA-3d7a794f-4
0.511
JOH-UNI-1b27fa5e-7
0.511
MAT-UCB-70f7c0f7-6
0.510
JOH-UNI-16fcdf60-1
0.505
EDG-MED-fe7487f8-8
0.505
ERI-UCB-9c7ec71b-4
0.505
JOH-UNI-d0d90dc1-3
0.505
RAL-THA-b74298ba-4
0.505
JOH-SUS-a69c159d-6
0.505
NAU-LAT-8502cac5-11
0.500
JOH-UNI-f51e3bbc-3
0.500
JAG-UCB-c61058a9-2
0.500
NAU-LAT-8502cac5-16
0.500
JOH-UNI-1b27fa5e-4
0.500
NAU-LAT-8502cac5-14
0.495
RAL-THA-3d7a794f-1
0.495
PET-UNK-3e029fdc-1
0.495
NAU-LAT-8502cac5-10
0.495
LON-WEI-0a73fcb8-3
0.490
JAG-UCB-c61058a9-32
0.490
ERI-UCB-a38d41be-1
0.490
NAU-LAT-8502cac5-12
0.489
JAG-UCB-c61058a9-44
0.489
JAG-UCB-c61058a9-6
0.489
ADA-UCB-dc2b944c-9
0.485
JOH-SUS-a69c159d-7
0.485
ADA-UCB-dc2b944c-10
0.485
JOH-UNI-1b27fa5e-5
0.485
BEN-DND-c852c98b-8
0.485
BEN-DND-a7517465-10
0.485
RAL-THA-3d7a794f-3
0.484
ROB-UNI-569bc02e-3
0.484
RAL-THA-3d7a794f-2
0.484
VLA-UCB-53bdeed6-2
0.484
MIC-UNK-deda7a44-6
0.479
JAG-UCB-c61058a9-9
0.479
JAG-UCB-c61058a9-22
0.479
ROB-UNI-569bc02e-1
0.475
ADA-UCB-b1b30a00-7
0.475
JOH-SUS-a69c159d-3
0.475
ROB-UNI-569bc02e-6
0.474
JAN-GHE-f4ca5a00-22
0.474
LON-WEI-0a73fcb8-6
0.474
JOH-UNI-f51e3bbc-4
0.471
JAG-UCB-52b62a6f-12
0.470
JOH-SUS-a69c159d-5
0.470
NAU-LAT-8502cac5-13
0.469
BEN-DND-c852c98b-4
0.469
MIC-UNK-deda7a44-7
0.469
MAT-POS-b3e365b9-3
0.468
JAN-GHE-f4ca5a00-13
0.468
DAR-DIA-6a508060-6
0.468
NAU-LAT-b7d8c353-7
0.468
BRU-CON-c4e3408a-1
0.468
MAT-POS-b3e365b9-4
0.468
ADA-UCB-dc2b944c-11
0.465
JAG-UCB-c61058a9-7
0.463
NAU-LAT-b7d8c353-4
0.462
BEN-DND-b89db3f2-2
0.462
EDJ-MED-fb4b7746-1
0.461
JAG-UCB-52b62a6f-14
0.461
MAT-POS-2bb0cf2b-2
0.461
JOH-UNI-1b27fa5e-3
0.460
ROB-UNI-569bc02e-7
0.460
JOH-UNI-1b27fa5e-1
0.460
NAU-LAT-b7d8c353-1
0.458
MAK-UNK-919546f0-1
0.458
MAK-UNK-f481d203-1
0.458
MAK-UNK-f481d203-2
0.458
EDJ-MED-e9694d2b-1
0.458
DAR-DIA-6a508060-7
0.458
LON-WEI-0a73fcb8-7
0.458
ERI-UCB-9c7ec71b-2
0.458
VLA-UCB-53bdeed6-3
0.458
JAN-GHE-f4ca5a00-21
0.458
ALP-POS-8b8a49e1-3
0.456
JAG-UCB-52b62a6f-8
0.455
JAG-UCB-52b62a6f-9
0.455
BEN-DND-4f474d93-2
0.455
JAG-UCB-52b62a6f-17
0.455
ADA-UCB-dc2b944c-12
0.455
ALP-POS-ce760d3f-3
0.455
JOH-SUS-a69c159d-1
0.455