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S-Benzyl-L-cysteine - 98%, high purity , CAS No.3054-01-1, Inhibitor of Alanine/serine/cysteine transporter 2

  • Moligand™
  • ≥98%
Item Number
B109016
Grouped product items
SKUSizeAvailabilityPrice Qty
B109016-5g
5g
In stock
$15.90
B109016-25g
25g
In stock
$41.90
B109016-100g
100g
In stock
$150.90

Basic Description

SynonymsS-Benzyl-L-cysteine|3054-01-1|H-Cys(Bzl)-OH|Benzylcysteine|S-Benzylcysteine|(R)-S-Benzylcysteine|L-S-Benzylcysteine|3-Benzylthioalanine|L-Cysteine, S-(phenylmethyl)-|(R)-2-amino-3-(benzylthio)propanoic acid|Alanine, 3-(benzylthio)-, L-|(2R)-2-amino-3-benz
Specifications & PurityMoligand™, ≥98%
Shipped InNormal
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of Alanine/serine/cysteine transporter 2

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KYAT1 Tbio Kynurenine--oxoglutarate transaminase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TLR2 Tchem Toll-like receptor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KIF11 Tchem Kinesin-like protein KIF11 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC1A5 Tchem Neutral amino acid transporter B(0) 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC7A10 Tbio Asc-type amino acid transporter 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GRIN3A Tclin Glutamate receptor ionotropic, NMDA 3A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488188566
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488188566
IUPAC Name (2R)-2-amino-3-benzylsulfanylpropanoic acid
INCHI InChI=1S/C10H13NO2S/c11-9(10(12)13)7-14-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1
InChi Key GHBAYRBVXCRIHT-VIFPVBQESA-N
Canonical SMILES C1=CC=C(C=C1)CSCC(C(=O)O)N
Isomeric SMILES C1=CC=C(C=C1)CSC[C@@H](C(=O)O)N
WGK Germany 3
Alternate CAS 3054-01-1,25988-62-9,25988-62-9
PubChem CID 193613
MeSH Entry Terms S-benzyl-L-cysteine;S-benzylcysteine;S-benzylcysteine, 2-13C-labeled
Molecular Weight 211.28
Beilstein 1879358
Reaxy-Rn 1879358

Certificates

Certificate of Analysis(COA)

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5 results found

Lot NumberCertificate TypeDateItem
C2310706Certificate of AnalysisMar 16, 2023 B109016
A1519095Certificate of AnalysisOct 24, 2022 B109016
A2218106Certificate of AnalysisDec 10, 2021 B109016
A2218151Certificate of AnalysisDec 10, 2021 B109016
E2325170Certificate of AnalysisDec 10, 2021 B109016

Chemical and Physical Properties

Specific Rotation[α]29 ° (C=1, 1mol/L NaOH)
Melt Point(°C)209-214°C

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 1879358

Related Documents

References

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11. Atefeh Rafiei,Lekha Sleno.  (2014-12-03)  Comparison of peak-picking workflows for untargeted liquid chromatography/high-resolution mass spectrometry metabolomics data analysis..  Rapid communications in mass spectrometry : RCM,  29  ((1)): (119-127).  [PMID:25462372]
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