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L-Cystine - 99%, high purity , CAS No.56-89-3

  • Moligand™
  • ≥99%
Item Number
C108225
Grouped product items
SKUSizeAvailabilityPrice Qty
C108225-25g
25g
In stock
$20.90
C108225-100g
100g
In stock
$35.90
C108225-500g
500g
In stock
$134.90

Basic Description

SynonymsL-cystine|56-89-3|cystine|L-Cystin|L-Dicysteine|beta,beta'-Dithiodialanine|L-Cysteine disulfide|1-Cystine|3,3'-Dithiodialanine|Cystine, L-|Dicysteine|Cystine (L)-|Cystine acid|(H-Cys-OH)2|Cysteine disulfide|Cystin|Alanine, 3,3'-dithiodi-|Alanine, 3,3'-dit
Specifications & PurityMoligand™, ≥99%
Biochemical and Physiological MechanismsCystinuria is characterized with renal transport and excretion of L-Cystine. Cysteine is one of the functional amino acids that are associated with growth, reproduction, maintenance and immunity. Cysteine is a source of disulfide linkage in protein and is
Storage TempProtected from light,Desiccated
Shipped InNormal
GradeMoligand™
Product Description

A non-essential amino acid vital for human development

Associated Targets

DRD1 Tclin D(1A) dopamine receptor 0 Activities

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

ESR1 Tclin Estrogen receptor 0 Activities

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

GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities

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

HRH3 Tclin Histamine H3 receptor 0 Activities

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

KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities

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

HDAC6 Tclin Histone deacetylase 6 0 Activities

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

SLC6A2 Tclin Sodium-dependent noradrenaline transporter 0 Activities

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

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

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

SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

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

POLK Tbio DNA polymerase kappa 0 Activities

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

PGR Tclin Progesterone receptor 0 Activities

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

PDE3A Tclin cGMP-inhibited 3',5'-cyclic phosphodiesterase A 0 Activities

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

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

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

PDE4A Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4A 0 Activities

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

DRD3 Tclin D(3) dopamine receptor 0 Activities

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

CHRM2 Tclin Muscarinic acetylcholine receptor M2 0 Activities

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

ACHE Tclin Acetylcholinesterase 0 Activities

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

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

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

ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

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

ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

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

AR Tclin Androgen receptor 0 Activities

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

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

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

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

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

ADORA3 Tchem Adenosine receptor A3 0 Activities

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

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

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

TBXA2R Tclin Thromboxane A2 receptor 0 Activities

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

F2 Tclin Prothrombin 0 Activities

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

OPRM1 Tclin Mu-type opioid receptor 0 Activities

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

Names and Identifiers

Pubchem Sid488183988
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183988
IUPAC Name (2R)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]disulfanyl]propanoic acid
INCHI InChI=1S/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m0/s1
InChi Key LEVWYRKDKASIDU-IMJSIDKUSA-N
Canonical SMILES C([C@@H](C(=O)O)N)SSC[C@@H](C(=O)O)N
Isomeric SMILES C([C@@H](C(=O)O)N)SSC[C@@H](C(=O)O)N
WGK Germany 3
PubChem CID 67678
Molecular Weight 240.3
Beilstein 1728094

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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22 results found

Lot NumberCertificate TypeDateItem
E2428196Certificate of AnalysisApr 26, 2024 C108225
E2428183Certificate of AnalysisApr 26, 2024 C108225
E2428182Certificate of AnalysisApr 26, 2024 C108225
E2428197Certificate of AnalysisApr 26, 2024 C108225
C2405291Certificate of AnalysisFeb 22, 2024 C108225
C2405305Certificate of AnalysisFeb 22, 2024 C108225
C2405295Certificate of AnalysisFeb 22, 2024 C108225
C2405294Certificate of AnalysisFeb 22, 2024 C108225
C2405293Certificate of AnalysisFeb 22, 2024 C108225
C2405292Certificate of AnalysisFeb 22, 2024 C108225
C2405290Certificate of AnalysisFeb 22, 2024 C108225
C2321981Certificate of AnalysisJul 03, 2022 C108225
C2321980Certificate of AnalysisJul 03, 2022 C108225
G2230057Certificate of AnalysisJul 03, 2022 C108225
G2230059Certificate of AnalysisJul 03, 2022 C108225
G2230060Certificate of AnalysisJul 03, 2022 C108225
J2326104Certificate of AnalysisFeb 28, 2022 C108225
C2222461Certificate of AnalysisFeb 28, 2022 C108225
C2222427Certificate of AnalysisFeb 28, 2022 C108225
C2222426Certificate of AnalysisFeb 28, 2022 C108225
C2222417Certificate of AnalysisFeb 28, 2022 C108225
A2219154Certificate of AnalysisFeb 11, 2022 C108225

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Chemical and Physical Properties

SolubilitySoluble in dilute acid and alkali solutions, extremely insoluble in water, insoluble in ethanol.
SensitivityLight sensitive.
Specific Rotation[α]-222.5 ° (C=1, 1mol/L HCl)
Melt Point(°C)260-261°C

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 2782

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References

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