Home | Screening data | Screen comparisons | Search for compounds | Structure search

Compound InformationSONAR Target prediction
Name:

LATHOSTEROL

Unique Identifier:SPE01500843
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:341.296 g/mol
X log p:3.679  (online calculus)
Lipinksi Failures0
TPSA0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:1
Rotatable Bond Count:5
Canonical Smiles:CC(C)CCCC(C)C1CCC2C3=CCC4CC(O)CCC4(C)C3CCC12C
Class:sterol
Source:Austeria rubens
Reference:J Biol Chem 248: 6697 (1973)
Generic_name:LANOSTEROL
Chemical_iupac_name:LANOSTEROL
Drug_type:Experimental
Kegg_compound_id:C01724
Drugbank_id:EXPT02002
Logp:7.63
Cas_registry_number:79-63-0
Drug_category:Lanosterol Synthase inhibitor
Organisms_affected:-1

Found: 2 active | as graph: single | with analogs << Back 1 2
Species: 4932
Condition: RGP1
Replicates: 2
Raw OD Value: r im 0.3965±0.00622254
Normalized OD Score: sc h 0.8229±0.0199773
Z-Score: -4.6220±0.459677
p-Value: 0.00000903334
Z-Factor: 0.0289704
Fitness Defect: 11.6146
Bioactivity Statement: Active
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:22|A3
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:26.50 Celcius
Date:2008-06-26 YYYY-MM-DD
Plate CH Control (+):0.040025±0.00027
Plate DMSO Control (-):0.4675±0.01743
Plate Z-Factor:0.8726
png
ps
pdf

DBLink | Rows returned: 277[1] << Back 21 22 23 24 25 26 27 28 29 30  Next >> [47]
5317337 n/a
5317423 (3S,10R,13S,17R)-17-(5,6-dimethylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1
H-cyclopenta[a]phenanthren-3-ol
5317775 2,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,10-diol
5317959 n/a
5318052 2-[(6S)-6,10-dimethyl-2-spiro[4.5]dec-9-enyl]propan-2-ol
5318507 n/a

internal high similarity DBLink | Rows returned: 112 Next >> 
SPE01504073 0.9167
SPE01504051 0.9189
SPE01500847 0.9189
SPE00107022 0.9189
SPE00300055 0.9444
NRB 03722 0.9706

active | Cluster 14237 | Additional Members: 2 | Rows returned: 0

Service provided by the Mike Tyers Laboratory