Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C4H9NO2S |
Molecular Weight | 135.185 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H](N)CS
InChI
InChIKey=MCYHPZGUONZRGO-VKHMYHEASA-N
InChI=1S/C4H9NO2S/c1-7-4(6)3(5)2-8/h3,8H,2,5H2,1H3/t3-/m0/s1
Mecysteine is used as a mucolytic in respiratory disorders associated with productive cough. Mecysteine is known as a mucolytic
agent, it breaks down mucus. It works by breaking some
of the chemical bonds between the molecules in mucus. It is given orally in a usual dose of 200 mg three times daily before meals reduced to 200 mg twice daily after 6 weeks. A rapid clinical effect can be achieved by giving 200 mg four times daily for the first 2 days. Mecysteine has also been given by inhalation.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Mucus glycoproteins Sources: https://www.ncbi.nlm.nih.gov/pubmed/6185664 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | VISCLAIR Approved UseVisclair is used together with other medicines to help in the treatment of conditions in which thick mucus is a problem. e.g. chronic obstructive pulmonary disease, sinusitis (inflamed nasal tubes), secretory otitis and in the symptomatic relief of cough with sputum or phlegm. |
|||
Primary | VISCLAIR Approved UseVisclair is used together with other medicines to help in the treatment of conditions in which thick mucus is a problem. e.g. chronic obstructive pulmonary disease, sinusitis (inflamed nasal tubes), secretory otitis and in the symptomatic relief of cough with sputum or phlegm. |
|||
Primary | VISCLAIR Approved UseVisclair is used together with other medicines to help in the treatment of conditions in which thick mucus is a problem. e.g. chronic obstructive pulmonary disease, sinusitis (inflamed nasal tubes), secretory otitis and in the symptomatic relief of cough with sputum or phlegm. |
PubMed
Title | Date | PubMed |
---|---|---|
Cysteine methyl ester modified glassy carbon spheres for removal of toxic heavy metals from aqueous media. | 2005 Aug 7 |
|
Maillard reaction products derived from thiol compounds as inhibitors of enzymatic browning of fruits and vegetables: the structure-activity relationship. | 2005 Jun |
|
Kinetics and mechanistic studies of the hydrolysis of diisocyanate-derived bis-thiocarbamates of cysteine methyl ester. | 2006 Mar |
|
Mathematical modelling and simulation of adsorption processes at spherical microparticles. | 2006 Mar 13 |
|
Kinetics of Cisplatin and its monohydrated complex with sulfur-containing compounds designed for local otoprotective administration. | 2006 Nov |
|
Observation of cysteine thiolate and -S...H-O intermolecular hydrogen bond. | 2006 Nov 23 |
|
Electrospray ionization and triple quadrupole tandem mass spectrometry study of some biologically relevant homo- and heterodimeric cadmium thiolate conjugates. | 2006 Oct |
|
One-electron reduction of S-nitrosothiols in aqueous medium. | 2006 Oct 15 |
|
Antidiabetic zinc(II)-N-acetyl-L-cysteine complex: evaluations of in vitro insulinomimetic and in vivo blood glucose-lowering activities. | 2007 |
|
Antiinflammatory and antifibrogenic effects of s-ethyl cysteine and s-methyl cysteine in the kidney of diabetic mice. | 2007 May |
|
Protective and alleviative effects from 4 cysteine-containing compounds on ethanol-induced acute liver injury through suppression of oxidation and inflammation. | 2007 Sep |
|
Aurintricarboxylic acid inhibits influenza virus neuraminidase. | 2009 Feb |
|
Synthesis, structural characterisation and anti-proliferative activity of NHC gold amino acid and peptide conjugates. | 2009 Sep 21 |
|
Redetermination of di-μ-sulfido-bis-{[(2R)-2-acet-oxy-2-amino-ethane-1-thiol-ato-κN,S]oxidomolybdenum(V)}. | 2010 Apr 24 |
|
hi2-1, a QTL which improves harvest index, earliness and alters metabolite accumulation of processing tomatoes. | 2010 Nov |
|
Gold nanoparticles conjugated to benzoylmercaptoacetyltriglycine and L-cysteine methylester. | 2010 Oct 1 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://en.pharmacodia.com/web/drug/1_12336.html
Curator's Comment: Mecysteine has also been given by inhalation.
It is given orally in a usual dose of 200 mg three times daily before meals reduced to 200 mg twice daily after 6 weeks. A rapid clinical effect can be achieved by giving 200 mg four times daily for the first 2 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6185664
The effects of L-cysteine methyl ester (Mecysteine) on behavior of mucus glycoproteins in canine tracheal secretory cells were investigated histologically and histochemically. Low concentrations (10(-7) and 10(-6)M) of L-cysteine methyl ester produced, as histological changes, decreases in the total goblet cell number and the thickness of the acini of submucosal glands, and an increase in the acinar inner diameter. On the other hand, L-cysteine methyl ester at 10(-5) and 10(-4)M produced an increase in the thickness of the acini and a slight decrease in the acinar inner diameter.
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C74536
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
41531
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
CHEMBL1622757
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
2485-62-3
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
SUB08688MIG
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
1375
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
29145
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
29426
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | RxNorm | ||
|
219-625-7
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
1653
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
C66067
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
DTXSID8048365
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
C017507
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
100000081968
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
RQ6L463N3B
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
Mecysteine
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | |||
|
m7126
Created by
admin on Fri Dec 15 16:23:30 GMT 2023 , Edited by admin on Fri Dec 15 16:23:30 GMT 2023
|
PRIMARY | Merck Index |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)