(1S,3AS,3BS,9AR,9BS,11AS)-9A,11A-DIMETHYL-7-OXO-N-PHENYL-2,3,3A,3B,4,5,7,8,9,9A,9B,10,11,11A-TETRADECAHYDRO-1H-CYCLOPENTA[I]PHENANTHRIDINE-1-CARBOXAMIDE

/static/temp/default.svg Search structure
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 NEXQLYFTKBAWDD-HQKDKDJQSA-N
Smiles C[C@]12CC[C@H]3[C@@H](CNC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)Nc5ccccc5
InChI
InChI=1S/C25H32N2O2/c1-24-13-11-20-18(15-26-22-14-17(28)10-12-25(20,22)2)19(24)8-9-21(24)23(29)27-16-6-4-3-5-7-16/h3-7,14,18-21,26H,8-13,15H2,1-2H3,(H,27,29)/t18-,19-,20-,21+,24-,25+/m0/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C25H32N2O2
Molecular Weight 392.53
AlogP 3.27
Hydrogen Bond Acceptor 3.0
Hydrogen Bond Donor 2.0
Number of Rotational Bond 2.0
Polar Surface Area 58.2
Molecular species NEUTRAL
Aromatic Rings 1.0
Heavy Atoms 29.0

Pharmacology

Targets EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Enzyme Oxidoreductase
- 1.4-714331826.16 - - -
EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Homo sapiens
- 1.4-714331826.16 - - -

Cross References

Resources Reference
ChEMBL CHEMBL2282767
PubChem 15250735
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