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Methylprednisolone-acetate

Inhibitor and substrate

General

Type : Steroid,Drug,Acetate,Phenanthrene

Chemical_Nomenclature : [2-[(6S,10R,11S,13S,17R)-11,17-dihydroxy-6,10,13-trimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

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

InChI : InChI=1S\/C24H32O6\/c1-13-9-16-17-6-8-24(29,20(28)12-30-14(2)25)23(17,4)11-19(27)21(16)22(3)7-5-15(26)10-18(13)22\/h5,7,10,13,16-17,19,21,27,29H,6,8-9,11-12H2,1-4H3\/t13-,16?,17?,19-,21?,22-,23-,24-\/m0\/s1

InChIKey : PLBHSZGDDKCEHR-UFBGDBPHSA-N

Other name(s) : 11beta,17alpha,21-Trihydroxy-6alpha-methyl-1,4-pregnadiene-3,20-dione,Methylprednisolone acetate,SCHEMBL3437554

MW : 416.51

Formula : C24H32O6

CAS_number : 53-36-1

PubChem : 45357932

UniChem : PLBHSZGDDKCEHR-UFBGDBPHSA-N

IUPHAR :

Wikipedia :

Target

Families : Methylprednisolone-acetate ligand of proteins in family: BCHE

Stucture :

Protein :

References (1)

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