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Compound InformationSONAR Target prediction
Name:

3-alpha,21-Dihydroxy-5-alpha-pregnan-20-one

Unique Identifier:LOPAC 01126
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C21H34O3
Molecular Weight:301.231 g/mol
X log p:-0.154  (online calculus)
Lipinksi Failures0
TPSA17.07
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:3
Rotatable Bond Count:2
Canonical Smiles:CC12CCC(O)CC1CCC1C3CCC(C(=O)CO)C3(C)CCC12
Class:GABA
Action:Modulator
Selectivity:GABA-A

Found: 24 nonactive as graph: single | with analogs [1] << Back 1 2 3 4 5 6 7 8 9 10  Next >> [24]
Species: 4932
Condition: HOC1
Replicates: 2
Raw OD Value: r im 0.6251±0.0217789
Normalized OD Score: sc h 1.0597±0.00409604
Z-Score: 2.7429±0.0577525
p-Value: 0.00613308
Z-Factor: -0.105161
Fitness Defect: 5.0941
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Lopac
Plate Number and Position:12|B8
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:26.60 Celcius
Date:2005-11-24 YYYY-MM-DD
Plate CH Control (+):0.0411±0.00218
Plate DMSO Control (-):0.58045±0.01014
Plate Z-Factor:0.9244
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DBLink | Rows returned: 145[1] << Back 11 12 13 14 15 16 17 18 19 20  Next >> [25]
7056541 (3R,5S,8R,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-
cyclopenta[a]phenanthren-17-one
7056542 (3S,5S,8S,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-
cyclopenta[a]phenanthren-17-one
7056543 (3R,5S,8S,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-
cyclopenta[a]phenanthren-17-one
7064610 (2S)-1-(1-adamantyl)-2-hydroxy-propan-1-one
7064611 (2R)-1-(1-adamantyl)-2-hydroxy-propan-1-one
7092964 (2R,4aR,6aR,6aS,6bS,8aS,12aS,14aS,14bS)-2-hydroxy-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,6b,7,8,9,10
,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one

internal high similarity DBLink | Rows returned: 1
RJC 02364 1.0000

active | Cluster 17389 | Additional Members: 4 | Rows returned: 2
SPE00100652 0.4
SPE00100303 0

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