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Compound InformationSONAR Target prediction
Name:

Alfaxalone

Unique Identifier:Prest1190
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C21H32O3
Molecular Weight:304.255 g/mol
X log p:-0.808  (online calculus)
Lipinksi Failures0
TPSA34.14
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:3
Rotatable Bond Count:1
Canonical Smiles:CC(=O)C1CCC2C3CCC4CC(O)CCC4(C)C3C(=O)CC21C

Found: 3 nonactive as graph: single | with analogs << Back 1 2 3
Species: 9606
Condition: TMPPre003
Replicates: 2
Raw OD Value: r im 12413.0000±0
Normalized OD Score: sc h 1.0635±0
Z-Score: 1.7655±0
p-Value: 0.0774842
Z-Factor: -8.44604
Fitness Defect: 2.5577
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Prestwick
Plate Number and Position:13|E3
Drug Concentration:50.00 nM
OD Absorbance:0 nm
Robot Temperature:23.50 Celcius
Date:2006-10-10 YYYY-MM-DD
Plate CH Control (+):22091.5±7532.35178
Plate DMSO Control (-):12139.5±7461.51552
Plate Z-Factor:-5.4357
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DBLink | Rows returned: 23<< Back 1 2 3 4 Next >> 
2754258 (3R,5R,10S,13R)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclop
enta[a]phenanthren-11-one
6540818 (3R,5S,8S,9R,10R,13S,14S,17R)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetrad
ecahydrocyclopenta[a]phenanthren-11-one
6572230 (3S,5R,8R,9S,10R,13S,14R,17S)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetrad
ecahydrocyclopenta[a]phenanthren-11-one
6603970 (3S,5S,8R,9R,10S,13S,14R,17R)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetrad
ecahydrocyclopenta[a]phenanthren-11-one
6604375 (3S,5S,8R,9R,10S,13S,14S,17R)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetrad
ecahydrocyclopenta[a]phenanthren-11-one
6918935 (3S,5S,8R,9S,10S,13R,14S,17R)-17-acetyl-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetrad
ecahydrocyclopenta[a]phenanthren-11-one

internal high similarity DBLink | Rows returned: 0

active | Cluster 7027 | Additional Members: 5 | Rows returned: 0

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