| 
 | Compound Information | SONAR Target prediction |  | Name: | METHYLPREDNISOLONE |  | Unique Identifier: | SPE01500406 |  | MolClass: | Checkout models in ver1.5 and ver1.0 |  | Molecular Formula: |  |  | Molecular Weight: | 344.232 g/mol |  | X log p: | 3.897  (online calculus) |  | Lipinksi Failures | 0 |  | TPSA | 34.14 |  | Hydrogen Bond Donor Count: | 0 |  | Hydrogen Bond Acceptors Count: | 5 |  | Rotatable Bond Count: | 2 |  | Canonical Smiles: | CC1CC2C3CCC(O)(C(=O)CO)C3(C)CC(O)C2C2(C)C=CC(=O)C=C12 |  | Source: | semisynthetic |  | Therapeutics: | glucocorticoid |  | Generic_name: | Prednisolone |  | Chemical_iupac_name: | 11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17- dodecahydrocyclopenta[a]phenanthren-3-one
 |  | Drug_type: | Approved Drug |  | Pharmgkb_id: | PA451096 |  | Kegg_compound_id: | C07369 |  | Drugbank_id: | APRD00197 |  | Melting_point: | 235 oC |  | H2o_solubility: | 223 mg/L |  | Logp: | 1.705 |  | Cas_registry_number: | 50-24-8 |  | Drug_category: | Antineoplastic Agents; Glucocorticoids; Anti-inflammatory Agents; AdrenergicAgents; ATC:A07EA01; ATC:C05AA04; ATC:D07AA01; ATC:D07AA03; ATC:D07AC14;ATC:D07XA02;
 ATC:D10AA02; ATC:H02AB04; ATC:H02AB06; ATC:R01AD02; ATC:S01BA04;ATC:S01CB02;
 ATC:S02BA03; ATC:S03BA02
 |  | Indication: | For the treatment of primary or secondary adrenocortical insufficiency, such as congenital adrenal hyperplasia, thyroiditis. Also used to treat psoriatic arthritis,
 rheumatoid arthritis, ankylosing spondylitis, bursitis, acute gouty arthritis and
 epicondylitis. Also indicated for treatment of systemic lupus erythematosus,
 pemphigus and acute rhematic carditis. Can be used in the treatment of leukemias,
 lymphomas, thrombocytopenia purpura and autoimmune hemolytic anemia. Can be used to
 treat celiac disease, insulin resistance, ulcerative colitis and liver disorders.
 |  | Pharmacology: | Prednisolone is a synthetic glucocorticoid used as antiinflammatory or immunosuppressive agent. Prednisolone is indicated in the treatment of various
 conditions, including congenital adrenal hyperplasia, psoriatic arthritis, systemic
 lupus erythematosus, bullous dermatitis herpetiformis, seasonal or perennial
 allergic rhinitis, allergic corneal marginal ulcers, symptomatic sarcoidosis,
 idiopathic thrombocytopenic purpura in adults, leukemias and lymphomas in adults,
 and ulcerative colitis. Glucocorticoids are adrenocortical steroids and cause
 profound and varied metabolic effects. In addition, they modify the body-s immune
 responses to diverse stimuli.
 |  | Mechanism_of_action: | Glucocorticoids such as Prednisolone can inhibit leukocyte infiltration at the site of inflammation, interfere with mediators of inflammatory response, and suppress
 humoral immune responses. The antiinflammatory actions of glucocorticoids are
 thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control
 the biosynthesis of potent mediators of inflammation such as prostaglandins and
 leukotrienes. Prednisolone reduces inflammatory reaction by limiting the capillary
 dilatation and permeability of the vascular structures. These compounds restrict the
 accumulation of polymorphonuclear leukocytes and macrophages and reduce the release
 of vasoactive kinins. Recent research suggests that corticosteroids may inhibit the
 release of arachidonic acid from phospholipids, thereby reducing the formation of
 prostaglandins. Prednisolone is a glucocorticoid receptor agonist. On binding, the
 corticoreceptor-ligand complex translocates itself into the cell nucleus, where it
 binds to many glucocorticoid response elements (GRE) in the promoter region of the
 target genes. The DNA bound receptor then interacts with basic transcription
 factors, causing an increase or decrease in expression of specific target genes,
 including suppression of IL2 (interleukin 2) expression.
 |  | Organisms_affected: | Humans and other mammals | 
 
 
	
		| Species: | 4932 |  
		| Condition: | VPS1 |  
		| Replicates: | 2 |  
		| Raw OD Value: r im | 0.6334±0.00459619 |  
		| Normalized OD Score: sc h | 1.0169±0.0147493 |  
		| Z-Score: | 0.6804±0.606149 |  
		| p-Value: | 0.534286 |  
		| Z-Factor: | -9.52522 |  
		| Fitness Defect: | 0.6268 |  
		| Bioactivity Statement: | Nonactive |  | | Experimental Conditions |  |  | Library: | Spectrum |  | Plate Number and Position: | 17|B6 |  | Drug Concentration: | 50.00 nM |  | OD Absorbance: | 600 nm |  | Robot Temperature: | 26.60 Celcius |  | Date: | 2007-10-03 YYYY-MM-DD |  | Plate CH Control (+): | 0.0405±0.00098 |  | Plate DMSO Control (-): | 0.61695±0.11609 |  | Plate Z-Factor: | 0.3579 | 
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		| 4159 | 11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]ph enanthren-3-one
 |  
		| 4894 | 11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phena nthren-3-one
 |  
		| 5755 | (8S,9S,10S,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-oct ahydro-6H-cyclopenta[a]phenanthren-3-one
 |  
		| 6741 | (6S,8S,9S,10S,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15, 16-octahydro-6H-cyclopenta[a]phenanthren-3-one
 |  
		| 2733846 | (6R,8S,9R,10S,11S,13S,14R,17S)-11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15, 16-octahydro-6H-cyclopenta[a]phenanthren-3-one
 |  
		| 3011528 | (17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a ]phenanthren-3-one
 |  
 | internal high similarity DBLink  | Rows returned: 1 |  | 
 
 | active | Cluster 8234 | Additional Members: 4 | Rows returned: 0 |  | 
 
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