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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H11NO2S.ClH
Molecular Weight 185.672
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL CYSTEINATE HYDROCHLORIDE

SMILES

Cl.CCOC(=O)[C@@H](N)CS

InChI

InChIKey=JFKJWWJOCJHMGV-WCCKRBBISA-N
InChI=1S/C5H11NO2S.ClH/c1-2-8-5(7)4(6)3-9;/h4,9H,2-3,6H2,1H3;1H/t4-;/m0./s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/international/ethyl-l-cysteine-hydrochloride.html | https://www.ncbi.nlm.nih.gov/pubmed/16309906 | https://www.ncbi.nlm.nih.gov/pubmed/15203134

Ethyl cysteinate is derivative of semi-essential proteinogenic amino acid Cysteine. Ethyl cysteinate is widely used in food additive, cosmetic, pharmaceutical area. Ethyl cysteinate is membrane-permeable, readily enters peripheral tissues and the brain, and increases intracellular pools of cysteine in these tissues via a membrane-associated carboxylesterase. The increased availability of cysteine directly alters the redox status of cells and enhances glutathione production. The enhanced biovailability of L-cysteine and L-glutathione would also promote the direct formation of the S-nitrosothiols, L-S-nitrosocysteine and L-S-nitrosoglutathione and the overall S-nitrosylation status of functional proteins in cells.

Originator

Sources: Experientia, Volume2, Pages 411-12, Journal, 1946

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: membrane-associated carboxylesterase
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
(99m)Tc-ethyl cysteinate dimer brain SPECT findings in early stage of dementia with Lewy bodies and Parkinson's disease patients: a correlation with neuropsychological tests.
2008 Jan
Patents

Patents

Sample Use Guides

The antiinflammatory activity of Ethyl cysteinate was assessed from it’s ability to inhibit the paw edema induced by carrageenan in Balb/C mice. The Ethyl cysteinate were administered ip at a dose of 150 lmol/kg and demonstrated a significant inhibition of the edema. The gastrointestinal toxicity profile of Ethyl cysteinate (84 mkM/kg) was evaluated in vivo following a 4-day oral dosage scheme in rats.
Route of Administration: Other
Ethyl cysteinate activity was evaluated in lipid peroxidation assay. The supernatant fraction hepatic microsomal membrane lipids. Lipid peroxidation was assessed by the formation of thiobarbituric acid (TBA)-reactive substances (e.g. malondialdehyde). Cysteine ethyl ester (1 uM) inhibited lipid peroxidation by 49%.
Name Type Language
ETHYL CYSTEINATE HYDROCHLORIDE
Systematic Name English
L-CYSTEINE, ETHYL ESTER, HYDROCHLORIDE
Common Name English
L-CYSTEINE ETHYL ESTER, HYDROCHLORIDE
WHO-DD  
Systematic Name English
ETHYL CYSTEINE HYDROCHLORIDE
Systematic Name English
L-CYSTEINE ETHYLESTER HYDROCHLORIDE
Systematic Name English
ETHYL L-CYSTEINE HYDROCHLORIDE [JAN]
Common Name English
CYSTEINE, ETHYL ESTER, HYDROCHLORIDE, L-
Common Name English
NSC-117387
Code English
L-cysteine ethyl ester, hydrochloride [WHO-DD]
Common Name English
ETHYL L-2-AMINO-3-MERCAPTOPROPIONATE HYDROCHLORIDE
Common Name English
ETHYL L-CYSTEINE HYDROCHLORIDE
JAN  
Systematic Name English
CYSTANIN
Brand Name English
L-CYSTEINE, ETHYL ESTER, HYDROCHLORIDE (1:1)
Common Name English
ETHYL L-CYSTEINATE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
EVMPD
SUB14334MIG
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
PRIMARY
ChEMBL
CHEMBL863
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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ECHA (EC/EINECS)
212-779-6
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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PUBCHEM
13358
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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SMS_ID
100000077082
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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EPA CompTox
DTXSID4046527
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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NSC
117387
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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FDA UNII
AM467TB2I1
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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RXCUI
236634
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
PRIMARY RxNorm
CAS
868-59-7
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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EVMPD
SUB21813
Created by admin on Fri Dec 15 19:50:14 GMT 2023 , Edited by admin on Fri Dec 15 19:50:14 GMT 2023
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