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Compound InformationSONAR Target prediction
Name:

MENTHOL(-)

Unique Identifier:SPE01503134
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:136.106 g/mol
X log p:-0.347  (online calculus)
Lipinksi Failures0
TPSA0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:1
Rotatable Bond Count:1
Canonical Smiles:CC(C)C1CCC(C)CC1O
Class:terpene
Source:Mentha piperita and other Mentha spp
Therapeutics:analgesic (topical), antipruritic agent
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: 205 nonactive as graph: single | with analogs [1] << Back 1 2 3 4 5 6 7 8 9 10  Next >> [205]
Species: 4932
Condition: MKK1
Replicates: 2
Raw OD Value: r im 0.8650±0.104652
Normalized OD Score: sc h 0.9966±0.00560686
Z-Score: -0.0916±0.154841
p-Value: 0.913178
Z-Factor: -10.7851
Fitness Defect: 0.0908
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum_ED
Plate Number and Position:1|B3
Drug Concentration:50.00 nM
OD Absorbance:595 nm
Robot Temperature:30.00 Celcius
Date:2010-08-10 YYYY-MM-DD
Plate CH Control (+):0.09525±0.00506
Plate DMSO Control (-):0.9664999999999999±0.02195
Plate Z-Factor:0.8798
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DBLink | Rows returned: 2037[1] << Back 331 332 333 334 335 336 337 338 339 340 Next >> [340]
16057696 n/a
16057709 (5S,7S)-3-ethyladamantan-1-ol
16057773 (1S,4S,6R)-6,7,7-trimethylbicyclo[2.2.1]heptan-6-ol
16059117 cyclopentane; dicyclopentylmethanol; iron(+2) cation
16061344 (3S,5S,8S,9S,10S,13S,14S,17R)-17-[(2S,3S,5R)-3-hydroxy-5,6-dimethyl-heptan-2-yl]-10,13-dimethyl-2,3,4,5,
6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
16061351 n/a

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 4541 | Additional Members: 2 | Rows returned: 0

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