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ChemicalBook--->CAS DataBase List--->1239600-18-0

1239600-18-0

1239600-18-0 Structure

1239600-18-0 Structure
IdentificationBack Directory
[Name]

LMT-28
[CAS]

1239600-18-0
[Synonyms]

LMT-28
LMT-28 >=98% (HPLC)
2-Oxazolidinone, 3-[(2S,3S)-3-hydroxy-2-methyl-4-methylene-1-oxononyl]-4-(1-methylethyl)-, (4S)-
[Molecular Formula]

C17H29NO4
[MDL Number]

MFCD30187587
[MOL File]

1239600-18-0.mol
[Molecular Weight]

311.42
Chemical PropertiesBack Directory
[Boiling point ]

452.9±38.0 °C(Predicted)
[density ]

1.065±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

100 mg/mL in DMSO (321.11 mM),
[form ]

oil
[pka]

13.97±0.20(Predicted)
[color ]

colorless to light yellow, oil
[Water Solubility ]

< 0.1 mg/mL Water (insoluble)
Hazard InformationBack Directory
[Uses]

LMT-28 is an orally active and the first synthetic IL-6 inhibitor that functions through direct binding to gp130. LMT-28 shows low toxicity and selectively inhibits IL-6-induced phosphorylation of STAT3, JAK2, and gp130[1].
[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.
[in vivo]

LMT-28 (0-0.5 mg/kg; p.o.; once daily for 15 days) alleviates CIA in mice[1].
LMT-28 (0.25 or 1 mg/kg; p.o.) ameliorates the progression of pancreatitis in mice. LMT-28 binds directly and specifically to gp130, and thereby inhibits the interaction of gp130 with the IL-6/IL-6Rα complex[1].

Animal Model:Six-week-old male DBA/1J mice (collagen-induced arthritis mice, CIA)[1]
Dosage:0-0.5 mg/kg
Administration:Oral; once daily for 15 days
Result:Markedly reduced the serum levels of cartilage oligomeric matrix protein (COMP) by 50%, serum amyloid P (SAP) by 55%, and anti-CII IgG by 62%.
[IC 50]

IL-6
[References]

[1] Hong SS, et al. A Novel Small-Molecule Inhibitor Targeting the IL-6 Receptor β Subunit, Glycoprotein 130. J Immunol. 2015 Jul 1;195(1):237-45. DOI:10.4049/jimmunol.1402908
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