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Details

Stereochemistry EPIMERIC
Molecular Formula C10H11NO4S2.C6H14N2O2
Molecular Weight 419.516
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STEPRONIN LYSINE

SMILES

NCCCC[C@H](N)C(O)=O.CC(SC(=O)C1=CC=CS1)C(=O)NCC(O)=O

InChI

InChIKey=APCSLWMOGLTNCY-ZSCHJXSPSA-N
InChI=1S/C10H11NO4S2.C6H14N2O2/c1-6(9(14)11-5-8(12)13)17-10(15)7-3-2-4-16-7;7-4-2-1-3-5(8)6(9)10/h2-4,6H,5H2,1H3,(H,11,14)(H,12,13);5H,1-4,7-8H2,(H,9,10)/t;5-/m.0/s1

HIDE SMILES / InChI
Stepronin is clinically used as an expectorant. It inhibits airway secretion in vitro by both decreasing Cl- secretion from epithelial cells and mucus glycoprotein secretion from submucosal glands. The mucolytic activity of stepronine does not involve the gastric mucous coating and that the drug does not exert adverse effects on the gastric mucosa. It is a new chemical immunosuppressant drug, which has the effect of preventing graft-versus-host-disease (GVHD) in a mouse model. The mechanism by which this compound acts as an immunosuppressant appears to be similar to cyclosporine A (CyA), although, in contrast to CyA, it is not toxic for animals and humans. Stepronin has an antiviral effect as well and is able to block, indirectly, the human immunodeficiency virus–1 (HIV-1) replication in mononuclear cells in vitro.

Approval Year

Name Type Language
STEPRONIN LYSINATE
WHO-DD  
Preferred Name English
STEPRONIN LYSINE
Common Name English
MASOR
Brand Name English
STEPRONIN LYSINE SALT [MI]
Common Name English
STEPRONIN LYSINE SALT
MI  
Common Name English
Stepronin lysinate [WHO-DD]
Common Name English
MUCODIL
Brand Name English
L-LYSINE, COMPD. WITH N-(1-OXO-2-((2-THIENYLCARBONYL)THIO)PROPYL)GLYCINE (1:1)
Systematic Name English
Code System Code Type Description
SMS_ID
100000084959
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID20150551
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
EVMPD
SUB04569MIG
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
CAS
113790-28-6
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
FDA UNII
B0592FL1C4
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
PUBCHEM
44152559
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY
MERCK INDEX
m10206
Created by admin on Mon Mar 31 22:55:07 GMT 2025 , Edited by admin on Mon Mar 31 22:55:07 GMT 2025
PRIMARY Merck Index