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L-Cycloserine - 10mM in DMSO, high purity , CAS No.339-72-0

  • Moligand™
  • 10mM in DMSO
Item Number
L423473
Grouped product items
SKUSizeAvailabilityPrice Qty
L423473-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90

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™, 10mM in DMSO
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 -80°C
Shipped InIce chest + Ice pads
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

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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Chemical and Physical Properties

Refractive Index1.48
Melt Point(°C)146°C

Related Documents

Solution Calculators