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

/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 FMINZTNMQYSSFY-QOFLHBTFSA-N
Smiles C[C@]12CC[C@H]3[C@@H](CNC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)NC56CC7CC(CC(C7)C5)C6
InChI
InChI=1S/C29H42N2O2/c1-27-8-6-23-21(16-30-25-12-20(32)5-7-28(23,25)2)22(27)3-4-24(27)26(33)31-29-13-17-9-18(14-29)11-19(10-17)15-29/h12,17-19,21-24,30H,3-11,13-16H2,1-2H3,(H,31,33)/t17?,18?,19?,21-,22-,23-,24+,27-,28+,29?/m0/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C29H42N2O2
Molecular Weight 450.66
AlogP 3.84
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 0.0
Heavy Atoms 33.0

Pharmacology

Targets EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Enzyme Oxidoreductase
- 0.07-70000315.91 - - -
EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Homo sapiens
- 0.07-70000315.91 - - -

Cross References

Resources Reference
ChEMBL CHEMBL2282782
PubChem 9911625
SureChEMBL SCHEMBL8610451
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