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L-Cycloserine - 97%, high purity , CAS No.339-72-0

  • Moligand™
  • ≥97%
Item Number
S136251
Grouped product items
SKUSizeAvailabilityPrice Qty
S136251-1g
1g
In stock
$10.90
S136251-5g
5g
In stock
$32.90
S136251-25g
25g
In stock
$145.90

Basic Description

SynonymsL-Cycloserine|339-72-0|Levcycloserine|(S)-4-Aminoisoxazolidin-3-one|Levcicloserina|Levcycloserinum|(4S)-4-amino-1,2-oxazolidin-3-one|Cyclo-L-serine|(S)-4-Amino-3-isoxazolidone|(S)-4-Amino-3-isoxazolidinone|(S)-(-)-Cycloserine|Cycloserine, l-|(-)-cycloseri
Specifications & PurityMoligand™, ≥97%
Biochemical and Physiological MechanismsBlocks sphingosine biosynthesis by inhibition of ketosphinganine synthetase. Cytotoxicity toward neuroblastoma and medulloblastoma cells mediated by suppression of ganglioside synthesis.
Storage TempStore at 2-8°C
Shipped InWet ice
GradeMoligand™
Product Description

L-Cycloserine is an irreversible inhibitor of 3-ketodihydrosphingosine synthetase, which is the first enzyme of the sphingolipid pathway, and causes the synthesis of sphingolipids to decrease. In vitro studies demonstrated that L-cyloserine inhibits 3-ketodihydrosphingosine synthetase 100 times more than D-Cycloserine .Research regarding L-Cycloserine and its effect on the immune response suggest that L-Cycloserine increases the level of IL-4 producing helper T cells and suppress the adhesion molecules CD29 and CD98. L-Cycloserine also inhibits SPTLC (serine palmitoyltransferase (SPT)), and HIV-1 investigations in the CD4+ lymphoid cell line (CEM) have shown that L-Cycloserine can inhibit HIV-1 replication.
An irreversible inhibitor of 3-ketodihydrosphingosine synthetase

Associated Targets

DRD1 Tclin D(1A) dopamine receptor 0 Activities

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

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

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

CBX1 Tbio Chromobox protein homolog 1 0 Activities

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

SLC36A1 Tchem Proton-coupled amino acid transporter 1 0 Activities

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

TXNRD1 Tclin Thioredoxin reductase 1, cytoplasmic 0 Activities

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

BLM Tchem Bloom syndrome protein 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)

BCHE Tclin Cholinesterase 0 Activities

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

Names and Identifiers

Pubchem Sid488189861
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189861
IUPAC Name (4S)-4-amino-1,2-oxazolidin-3-one
INCHI InChI=1S/C3H6N2O2/c4-2-1-7-5-3(2)6/h2H,1,4H2,(H,5,6)/t2-/m0/s1
InChi Key DYDCUQKUCUHJBH-REOHCLBHSA-N
Canonical SMILES C1C(C(=O)NO1)N
Isomeric SMILES C1[C@@H](C(=O)NO1)N
Alternate CAS 339-72-0
PubChem CID 449215
Molecular Weight 102.09
Beilstein 80799

Certificates

Certificate of Analysis(COA)

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9 results found

Lot NumberCertificate TypeDateItem
G2426302Certificate of AnalysisJul 04, 2024 S136251
G2426303Certificate of AnalysisJul 04, 2024 S136251
G2426304Certificate of AnalysisJul 04, 2024 S136251
D2318859Certificate of AnalysisMar 16, 2023 S136251
D2318860Certificate of AnalysisMar 16, 2023 S136251
D2318867Certificate of AnalysisMar 16, 2023 S136251
D2318869Certificate of AnalysisMar 16, 2023 S136251
D2318878Certificate of AnalysisMar 16, 2023 S136251
D2318918Certificate of AnalysisMar 16, 2023 S136251

Chemical and Physical Properties

Solubilityinsoluble in EtOH; ≥42.9 mg/mL in H2O; ≥8.78 mg/mL in DMSO
Refractive Index1.48
Melt Point(°C)146°C

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