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Details

Stereochemistry RACEMIC
Molecular Formula C10H10NO4S2.Na
Molecular Weight 295.31
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STEPRONIN SODIUM

SMILES

[Na+].CC(SC(=O)C1=CC=CS1)C(=O)NCC([O-])=O

InChI

InChIKey=LAKRODSFPQQVBB-UHFFFAOYSA-M
InChI=1S/C10H11NO4S2.Na/c1-6(9(14)11-5-8(12)13)17-10(15)7-3-2-4-16-7;/h2-4,6H,5H2,1H3,(H,11,14)(H,12,13);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C10H10NO4S2
Molecular Weight 272.321
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:32:06 GMT 2023
Edited
by admin
on Fri Dec 15 16:32:06 GMT 2023
Record UNII
FR96Q1BI9E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STEPRONIN SODIUM
WHO-DD  
Common Name English
TIOTEN
Common Name English
Stepronin sodium [WHO-DD]
Common Name English
STEPRONIN SODIUM SALT [MI]
Common Name English
SODIUM N-(2-MERCAPTOPROPIONYL)GLYCINE 2-THIOPHENECARBOXYLATE
Systematic Name English
GLYCINE, N-(1-OXO-2-((2-THIENYLCARBONYL)THIO)PROPYL)-, MONOSODIUM SALT
Systematic Name English
Code System Code Type Description
PUBCHEM
23691748
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID90999373
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
EVMPD
SUB04570MIG
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
SMS_ID
100000084978
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
CAS
78126-10-0
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
DRUG BANK
DBSALT002347
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
FDA UNII
FR96Q1BI9E
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY
MERCK INDEX
m10206
Created by admin on Fri Dec 15 16:32:06 GMT 2023 , Edited by admin on Fri Dec 15 16:32:06 GMT 2023
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY