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Compound InformationSONAR Target prediction
Name:

2-(4,4-dimethylcyclohexyl)propan-2-ol

Unique Identifier:NRB 02318
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C11H22O
Molecular Weight:148.117 g/mol
X log p:-0.528  (online calculus)
Lipinksi Failures0
TPSA0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:1
Rotatable Bond Count:1
Canonical Smiles:CC(C)(O)C1CCC(C)(C)CC1
Generic_name:5-ALPHA-ANDROSTANE-3-BETA,17BETA-DIOL
Chemical_iupac_name:5-ALPHA-ANDROSTANE-3-BETA,17BETA-DIOL
Drug_type:Experimental
Drugbank_id:EXPT00530
Logp:3.73
Drug_category:Sex Hormone-Binding Globulin inhibitor
Organisms_affected:-1

Found: 1 active | as graph: single | with analogs
Species: 4932
Condition: SWE1
Replicates: 2
Raw OD Value: r im 0.6354±0.00643467
Normalized OD Score: sc h 0.8382±0.0241815
Z-Score: -9.8086±1.09272
p-Value: 8.13258e-20
Z-Factor: 0.230419
Fitness Defect: 43.9558
Bioactivity Statement: Active
Experimental Conditions
Library:Maybridge1000
Plate Number and Position:8|A8
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:21.40 Celcius
Date:2007-08-22 YYYY-MM-DD
Plate CH Control (+):0.03955±0.00272
Plate DMSO Control (-):0.74005±0.01428
Plate Z-Factor:0.9201
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DBLink | Rows returned: 2037[1] << Back 301 302 303 304 305 306 307 308 309 310  Next >> [340]
7098636 (3R,5R,8S,9S,10S,13S,14R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[
a]phenanthren-3-ol
7098637 (3R,5R,8S,9S,10S,13R,14R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[
a]phenanthren-3-ol
7098952 (1R,2R,12S)-bicyclo[10.1.0]tridecan-2-ol
7099854 n/a
7099855 n/a
7099924 (3S,4aR,6aR,6aR,6bR,8aR,12aR,14aR,14bS)-8a-(hydroxymethyl)-4,4,6a,6a,11,11,14b-heptamethyl-1,2,3,4a,5,6,
6b,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol

internal high similarity DBLink | Rows returned: 382 3 4 5 6 7 Next >> 
BTB 12413 0.9231
RJC 00940 0.9231
JFD 01247 0.9231
NRB 02212 0.9231
BTB 14986 0.9231
BTB 14459 0.9231

active | Cluster 1300 | Additional Members: 1 | Rows returned: 0

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