Molecule Category Free-form
Source Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Structure

InChI Key LFCPEBOSWGHACP-UHFFFAOYSA-N
Smiles CCCCC(=O)Nc1ccc(Cl)c(c1)N2N=C(CCC)N(Cc3ccc(cc3F)c4ccccc4S(=O)(=O)NC(=O)c5cc(Cl)ccc5Cl)C2=O
InChI
InChI=1S/C36H33Cl3FN5O5S/c1-3-5-11-34(46)41-25-15-17-29(39)31(20-25)45-36(48)44(33(42-45)8-4-2)21-23-13-12-22(18-30(23)40)26-9-6-7-10-32(26)51(49,50)43-35(47)27-19-24(37)14-16-28(27)38/h6-7,9-10,12-20H,3-5,8,11,21H2,1-2H3,(H,41,46)(H,43,47)

Physicochemical Descriptors

Property Name Value
Molecular Formula C36H33Cl3FN5O5S
Molecular Weight 773.1
AlogP 8.68
Hydrogen Bond Acceptor 6.0
Hydrogen Bond Donor 2.0
Number of Rotational Bond 13.0
Polar Surface Area 136.63
Molecular species ACID
Aromatic Rings 4.0
Heavy Atoms 51.0

Pharmacology

EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Oryctolagus cuniculus
- 0.19-0.19 - - -

Cross References

Resources Reference
ChEMBL CHEMBL2236976
PubChem 76333473