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Compound InformationSONAR Target prediction
Name:

FLUMETHAZONE PIVALATE

Unique Identifier:SPE01500300
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:458.282 g/mol
X log p:3.904  (online calculus)
Lipinksi Failures0
TPSA60.44
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:6
Rotatable Bond Count:5
Canonical Smiles:CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)COC(=O)C(C)(C)C
Source:semisynthetic
Therapeutics:glucocorticoid, antiinflammatory
Generic_name:Flumethasone Pivalate
Chemical_iupac_name:[2-(6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octah
ydrocyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] 2,2-dimethylpropanoate
Drug_type:Approved Drug
Kegg_compound_id:D01464
Drugbank_id:APRD00975
Melting_point:219 oC (base only)
H2o_solubility:0.392 mg/L
Logp:4.212
Cas_registry_number:2002-29-1
Drug_category:Anti-inflammatory Agents; Glucocorticoids; Antipruritics; ATC:C05AA10; ATC:D07AC04
Indication:For the treatment of contact dermatitis, atopic dermatitis, exczema, psoriasis,
diaper rash and other skin conditions
Pharmacology:Flumethasone pivalate is a moderately potent difluorinated corticosteroid ester with
anti-inflammatory, antipruritic and vasoconstrictive properties. As it is a
privalate salt, its anti-inflammatory action is concentrated at the site of
application. This local effect on diseased areas results in a prompt decrease in
inflammation, exudation and itching.
Mechanism_of_action:Flumethasone is a glucocorticoid receptor agonist. The antiinflammatory actions of
corticosteroids are thought to involve lipocortins, phospholipase A2 inhibitory
proteins which, through inhibition arachidonic acid, control the biosynthesis of
prostaglandins and leukotrienes. The immune system is suppressed by corticosteroids
due to a decrease in the function of the lymphatic system, a reduction in
immunoglobulin and complement concentrations, the precipitation of lymphocytopenia,
and interference with antigen-antibody binding. Flumethasone binds to plasma
transcortin, and it becomes active when it is not bound to transcortin.
Organisms_affected:Humans and other mammals

Found: 205 nonactive as graph: single | with analogs [1] << Back 161 162 163 164 165 166 167 168 169 170  Next >> [205]
Species: 4932
Condition: MT2481-pdr1pdr3-2nd
Replicates: 2
Raw OD Value: r im 0.5746±0.00233345
Normalized OD Score: sc h 1.0045±0.00214536
Z-Score: 0.3890±0.0750646
p-Value: 0.697646
Z-Factor: -9.73096
Fitness Defect: 0.36
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:12|B5
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:25.80 Celcius
Date:2007-09-27 YYYY-MM-DD
Plate CH Control (+):0.040075±0.00114
Plate DMSO Control (-):0.5593±0.08074
Plate Z-Factor:0.4777
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DBLink | Rows returned: 5
3376 [2-(6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phe
nanthren-17-yl)-2-oxo-ethyl] 2,2-dimethylpropanoate
16158 [2-[(6S,9R,11S,14S,16R,17R)-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-o
ctahydrocyclopenta[a]phenanthren-17-yl]-2-oxo-ethyl] 2,2-dimethylpropanoate
171624 [2-[(6S,8S,10S,11S,13S,14S,16R,17R)-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14
,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxo-ethyl] 2,2-dimethylpropanoate
443980 [2-[(6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12
,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxo-ethyl] 2,2-dimethylpropanoate
5702055 [2-[(6S,9R,10S,11S,13S,16R,17R)-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,
16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxo-ethyl] 2,2-dimethylpropanoate

internal high similarity DBLink | Rows returned: 4
SPE01500231 0.9135
SPE01503210 0.9151
SPE01500145 0.9238
SPE01503299 0.9423

nonactive | Cluster 15366 | Additional Members: 3 | Rows returned: 2
Prest1095 0.267441860465116
SPE01503299 0

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