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Compound InformationSONAR Target prediction
Name:

CAMPHOR (1R)

Unique Identifier:SPE01500156
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:136.106 g/mol
X log p:-0.875  (online calculus)
Lipinksi Failures0
TPSA17.07
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:1
Rotatable Bond Count:0
Canonical Smiles:CC1(C)C2CCC1(C)C(=O)C2
Class:terpene
Source:Cinnamomum camphora
Therapeutics:analgesic, antiinfective, antipruritic
Generic_name:5ALPHA-ANDROSTAN-3,17-DIONE
Chemical_iupac_name:5ALPHA-ANDROSTAN-3,17-DIONE
Drug_type:Experimental
Drugbank_id:EXPT00262
Drug_category:Estradiol 17 Beta-Dehydrogenase 1 inhibitor
Organisms_affected:-1

Found: 205 nonactive as graph: single | with analogs [1] << Back 11 12 13 14 15 16 17 18 19 20  Next >> [205]
Species: 4932
Condition: ARX1
Replicates: 2
Raw OD Value: r im 0.6896±0.017112
Normalized OD Score: sc h 0.9950±0.00846079
Z-Score: -0.2648±0.438175
p-Value: 0.76481
Z-Factor: -34.4834
Fitness Defect: 0.2681
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:9|E9
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:25.30 Celcius
Date:2007-10-11 YYYY-MM-DD
Plate CH Control (+):0.040075±0.00066
Plate DMSO Control (-):0.67765±0.02321
Plate Z-Factor:0.8676
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DBLink | Rows returned: 1448[1] << Back 231 232 233 234 235 236 237 238 239 240  Next >> [242]
7140382 (5R,8S,9R,10R,13R,14S)-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthr
ene-3,17-dione
7140383 (5R,8S,9R,10S,13R,14S)-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthr
ene-3,17-dione
7160826 (3R)-3-methylcyclopentadecan-1-one
7160827 (3S)-3-methylcyclopentadecan-1-one
7163286 n/a
7164431 (1R,4R,6R)-5,5,6-trimethylnorbornan-2-one

internal high similarity DBLink | Rows returned: 172 3 Next >> 
RJC 02257 0.9231
RJC 02979 0.9231
JFD 02406 0.9231
BTBG 00073 0.9231
BTB 14425 0.9231
BTB 13696 0.9231

active | Cluster 10613 | Additional Members: 2 | Rows returned: 0

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