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

Compound InformationSONAR Target prediction
Name:

TETRAHYDROCORTISONE

Unique Identifier:SPE01701047
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C21H32O5
Molecular Weight:333.23 g/mol
X log p:-2.158  (online calculus)
Lipinksi Failures0
TPSA34.14
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:5
Rotatable Bond Count:2
Canonical Smiles:CC12CCC(O)CC1CCC1C3CCC(O)(C(=O)CO)C3(C)CC(=O)C12
Source:exmicrobial degradation of cortisone
Reference:J Biol Chem 111: 599 (1935); 114: 613 (1936);124: 459 (1938); Z Naturforsch B 18:
284 (1963)

Found: 101 nonactive as graph: single | with analogs [1] << Back 91 92 93 94 95 96 97 98 99 100  Next >> [101]
Species: 4932
Condition: TOP1
Replicates: 2
Raw OD Value: r im 0.5964±0.00318198
Normalized OD Score: sc h 0.9919±0.00376703
Z-Score: -0.1300±0.0542886
p-Value: 0.896658
Z-Factor: -10.8462
Fitness Defect: 0.1091
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:7|G10
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:25.50 Celcius
Date:2006-04-26 YYYY-MM-DD
Plate CH Control (+):0.038775000000000004±0.00125
Plate DMSO Control (-):0.5789249999999999±0.01705
Plate Z-Factor:0.9060
png
ps
pdf

DBLink | Rows returned: 10<< Back 1 2
621102 17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,4,5,6,7,8,9,12,14,15,16-dodecahydrocyclopenta[a]phena
nthrene-3,11-dione
6429565 (3R,5S,17R)-3,17-dihydroxy-17-(2-hydroxyacetyl)-2,3,4,5,6,7,8,9,10,12,13,14,15,16-tetradecahydro-1H-cycl
openta[a]phenanthren-11-one
6429566 (3R,5R,17R)-3,17-dihydroxy-17-(2-hydroxyacetyl)-2,3,4,5,6,7,8,9,10,12,13,14,15,16-tetradecahydro-1H-cycl
openta[a]phenanthren-11-one
6710632 (3R,5R,10S,13S,17R)-3,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,12,14,15,16-dodec
ahydro-1H-cyclopenta[a]phenanthren-11-one

internal high similarity DBLink | Rows returned: 1
NRB 03728 0.9583

active | Cluster 7027 | Additional Members: 5 | Rows returned: 0

Service provided by the Mike Tyers Laboratory