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Compound InformationSONAR Target prediction
Name:

MEDRYSONE

Unique Identifier:SPE01500380
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:312.234 g/mol
X log p:1.024  (online calculus)
Lipinksi Failures0
TPSA34.14
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:3
Rotatable Bond Count:1
Canonical Smiles:CC1CC2C3CCC(C(C)=O)C3(C)CC(O)C2C2(C)CCC(=O)C=C12
Source:semisynthetic
Therapeutics:glucocorticoid
Generic_name:Medrysone
Chemical_iupac_name:17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocycl
openta[a]phenanthren-3-one
Drug_type:Approved Drug
Pharmgkb_id:PA450346
Kegg_compound_id:C14643
Drugbank_id:APRD01091
Melting_point:156.5 oC
Logp:3.291
Cas_registry_number:2668-66-8
Drug_category:Topical anti-inflammatory Agent; ATC:S01BA08
Indication:For the treatment of allergic conjunctivitis, vernal conjunctivitis, episcleritis,
and epinephrine sensitivity.
Pharmacology:Medrysone is a topical anti-inflammatory corticoidsteroids for ophthalmic use. In
patients with increased intraocular pressure and in those susceptible to a rise in
intraocular pressure, there is less effect on pressure with medrysone than with
dexamethasone or betamethasone. Corticoidsteroids inhibit the edema, fibrin
deposition, capillary dilation, and phagocytic migration of the acute inflammatory
response, as well as capillary proliferation, deposition of collagen, and scar
formation.
Mechanism_of_action:There is no generally accepted explanation for the mechanism of action of ocular
corticosteroids. However, corticosteroids are thought to act by the induction of
phospholipase A2 inhibitory proteins, collectively called lipocortins. It is
postulated that these proteins control the biosynthesis of potent mediators of
inflammation such as prostaglandins and leukotrienes by inhibiting the release of
their common precursor, arachidonic acid. Arachidonic acid is released from membrane
phospholipids by phospholipase A2.
Organisms_affected:Humans and other mammals

Found: 205 nonactive as graph: single | with analogs [1] << Back 51 52 53 54 55 56 57 58 59 60  Next >> [205]
Species: 4932
Condition: MDH1
Replicates: 2
Raw OD Value: r im 0.7537±0.00523259
Normalized OD Score: sc h 0.9603±0.0186144
Z-Score: -2.2189±0.806532
p-Value: 0.052254
Z-Factor: -2.41936
Fitness Defect: 2.9516
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Spectrum
Plate Number and Position:12|H4
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:26.00 Celcius
Date:2007-08-07 YYYY-MM-DD
Plate CH Control (+):0.0407±0.00130
Plate DMSO Control (-):0.7637499999999999±0.02024
Plate Z-Factor:0.9275
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DBLink | Rows returned: 42<< Back 1 2 3 4 5 6 7 Next >> 
242492 (6S,8S,9S,10R,11S,13R,14S,17S)-17-acetyl-11-hydroxy-6,10,11,13-tetramethyl-2,6,7,8,9,12,14,15,16,17-deca
hydro-1H-cyclopenta[a]phenanthren-3-one
247839 (6S,8S,9S,10R,11S,13R,14S,17S)-17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dode
cahydrocyclopenta[a]phenanthren-3-one
248319 17-acetyl-11-hydroxy-10,12,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthre
n-3-one
440105 (8S,9S,10R,11R,13R,14S)-17-acetyl-11-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyc
lopenta[a]phenanthren-3-one
2825556 (11R)-17-acetyl-11-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanth
ren-3-one
4161786 17-acetyl-8-hydroxy-13-methyl-1,2,6,7,9,10,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

internal high similarity DBLink | Rows returned: 132 3 Next >> 
SPE00307023 0.9167
SB 01709 0.9167
NRB 04205 0.9167
NRB 03896 0.9167
NRB 03850 0.9167
NRB 03833 0.9167

active | Cluster 7623 | Additional Members: 3 | Rows returned: 0

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