Methylprednisolone

Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunomodulating properties. Methylprednisolone binds to and activates specific nuclear receptors, resulting in altered gene expression and inhibition of proinflammatory cytokine production. This agent also decreases the number of circulating lymphocytes, induces cell differentiation, and stimulates apoptosis in sensitive tumor cell populations.

General

Type : Drug,Steroid,Phenanthrene,Not A\/B H target

Chemical_Nomenclature : (6S,8S,9S,10R,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

Canonical SMILES : CC1CC2C3CCC(C3(CC(C2C4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O

InChI : InChI=1S\/C22H30O5\/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20\/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3\/t12-,14-,15-,17-,19+,20-,21-,22-\/m0\/s1

InChIKey : VHRSUDSXCMQTMA-PJHHCJLFSA-N

Other name(s) : Medrol,Medrone,Urbason,Medrate,Metastab,Metrisone,Promacortine,Suprametil,Solumedrol,Depo-Medrol,Methylone,Solu-Medrol


MW : 374.48

Formula : C22H30O5

CAS_number : 83-43-2

PubChem : 6741

UniChem : VHRSUDSXCMQTMA-PJHHCJLFSA-N

IUPHAR :

Wikipedia : Methylprednisolone

Target

Families : Methylprednisolone ligand of proteins in family: BCHE

Stucture :

Protein :

References (2)

Title : Amplification of neuromuscular transmission by methylprednisolone involves activation of presynaptic facilitatory adenosine A receptors and redistribution of synaptic vesicles - Oliveira_2014_Neuropharmacol_89C_64
Author(s) : Oliveira L , Costa AC , Noronha-Matos JB , Silva I , Cavalcante WL , Timoteo MA , Corrado AP , Dal Belo CA , Ambiel CR , Alves-do-Prado W , Correia-de-Sa P
Ref : Neuropharmacology , 89C :64 , 2014
Abstract : Oliveira_2014_Neuropharmacol_89C_64
ESTHER : Oliveira_2014_Neuropharmacol_89C_64
PubMedSearch : Oliveira_2014_Neuropharmacol_89C_64
PubMedID: 25220030

Title : Hydrolysis of methylprednisolone acetate by human serum cholinesterase -
Author(s) : Myers C , Lockridge O , La Du BN
Ref : Drug Metabolism & Disposition: The Biological Fate of Chemicals , 10 :279 , 1982
PubMedID: 6125364