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SML1628

Sigma-Aldrich

LMT-28

≥98% (HPLC)

Synonym(s):

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

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5 MG
$111.00
25 MG
$447.00

$111.00


Estimated to ship onApril 11, 2025


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5 MG
$111.00
25 MG
$447.00

About This Item

Empirical Formula (Hill Notation):
C17H29NO4
CAS Number:
Molecular Weight:
311.42
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

$111.00


Estimated to ship onApril 11, 2025


Request a Bulk Order

Quality Level

assay

≥98% (HPLC)

form

oil

color

colorless to light yellow, oil

shipped in

wet ice

storage temp.

−20°C

SMILES string

CC(C)[C@H](N1C([C@@H](C)[C@H](O)C(CCCCC)=C)=O)COC1=O

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

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.[1]
LMT-28 is an IL-6 antagonist that targets the IL-6 Receptor β subunit, Glycoprotein 130 (gp130).
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.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3


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