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LMT-28

SIGMA/SML1628 - ≥98% (HPLC)

Synonym: (4S)-3-[(2S,3S)-3-Hydroxy-2-methyl-4-methylene-1-oxononyl]-4-(1-methylethyl)-2-oxazolidinone

CAS Number: 1239600-18-0
Empirical Formula (Hill Notation): C17H29NO4
Molecular Weight: 311.42
Linear Formula: C17H29NO4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML1628-5MG 5 mg
$108.00
1/EA
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45-SML1628-25MG 25 mg
$435.00
1/EA
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assay ≥98% (HPLC)
color colorless to light yellow, oil
form oil
InChI 1S/C17H29NO4/c1-6-7-8-9-12(4)15(19)13(5)16(20)18-14(11(2)3)10-22-17(18)21/h11,13-15,19H,4,6-10H2,1-3,5H3/t13-,14+,15+/m0/s1
InChI key UDXWSYOXIRPYFK-RRFJBIMHSA-N
Quality Level 100 
shipped in wet ice
SMILES string CC(C)[C@H](N1C([C@@H](C)[C@H](O)C(CCCCC)=C)=O)COC1=O
storage temp. −20°C
Biochem/physiol Actions: LMT-28 is a derivative of oxazolidinone. It has the ability to repress the activation of signal transducer and activator of transcription 3 (STAT3) stimulated by interleukin 6 (IL-6). Orally administered LMT-28 reduced arthritis and acute pancreatitis stimulated by collagen in mice pathologic models.
Biochem/physiol Actions: LMT-28 is an IL-6 antagonist that targets the IL-6 Receptor β subunit, Glycoprotein 130 (gp130). Its binding to gp130) results in inhibition of IL-6 activation, and downregulation of levels of p-STAT3. LMT-28 was shown to stimulate phosphorylation of STAT3 and JAK2 protein. IL-6 dysregulation is involved in inflammation and cancers. LMT-28 had inhbitory activity against IL-6–dependent TF-1 cell proliferation and also had therapeutic effect against pancreatitis.
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 12352200

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