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Compound InformationSONAR Target prediction
Name:

ESTRONE HEMISUCCINATE

Unique Identifier:SPE01503676
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C22H26O5
Molecular Weight:344.232 g/mol
X log p:5.334  (online calculus)
Lipinksi Failures1
TPSA60.44
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:5
Rotatable Bond Count:5
Canonical Smiles:CC12CCC3C(CCc4cc(OC(=O)CCC(O)=O)ccc34)C1CCC2=O
Therapeutics:estrogen

Found: 88 nonactive | as graph: single | with analogs [1] << Back 21 22 23 24 25 26 27 28 29 30  Next >> [88]
Species: 4932
Condition: ELG1
Replicates: 2
Raw OD Value: r im 0.7031±0.00190919
Normalized OD Score: sc h 0.9856±0.0028319
Z-Score: -0.9033±0.16761
p-Value: 0.369698
Z-Factor: -10.0646
Fitness Defect: 0.9951
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:22|H9
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:27.40 Celcius
Date:2007-10-10 YYYY-MM-DD
Plate CH Control (+):0.03985±0.00073
Plate DMSO Control (-):0.7005250000000001±0.18279
Plate Z-Factor:0.0434
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DBLink | Rows returned: 72 Next >> 
3274 4-[(13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl)oxy]-4-oxo-butanoic
acid
5702254 4-[[(13S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl]oxy]-4-oxo-bu
tanoic acid
6553596 4-[[(8R,9R,13S,14R)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl]oxy
]-4-oxo-butanoic acid
6978338 4-[[(8R,9R,13R,14R)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl]oxy
]-4-oxo-butanoate
6978339 4-[[(8R,9R,13R,14R)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl]oxy
]-4-oxo-butanoic acid
7067988 4-[[(8R,9S,13S,14R)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl]oxy
]-4-oxo-butanoate

internal high similarity DBLink | Rows returned: 0

active | Cluster 13348 | Additional Members: 15 | Rows returned: 2
SPE01500286 0.306451612903226
SPE01501181 0.25

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