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Roquinimex

Roquinimex Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: TCI (Shanghai) Development Co., Ltd.  
Tel: 021-67121386
Email: Sales-CN@TCIchemicals.com
Company Name: VDM Biochemicals   
Tel: 0330-2528181
Email: sales@vdmbio.com
Company Name: TOKYO CHEMICAL INDUSTRY CO., LTD.  
Tel: 03-36680489
Email: Sales-JP@TCIchemicals.com
Company Name: TCI Europe  
Tel: 320-37350700
Email: sales@tcieurope.eu

Roquinimex manufacturers

  • Roquinimex
  • Roquinimex pictures
  • $30.00
  • 2026-07-27
  • CAS:84088-42-6
  • Purity: 99.65%
  • Supply Ability: 10g
Roquinimex Basic information
Product Name:Roquinimex
Synonyms:N-PHENYLMETHYL-1,2-DIHYDRO-4-HYDROXYL-N,1-DIMETHYL-2-OXO-QUINOLINE-3-CARBOXAMIDE;ROQUINIMEX;LINOMIDE;LS-2616;1,2-DIHYDRO-4-HYDROXY-N,1-DIMETHYL-2-OXO-N-PHENYL-3-QUINOLINECARBOXAMIDE;1,2-DIHYDRO-4-HYDROXY-N,N-DIMETHYL-2-OXO-N-PHENYL-3-QUINOLINECARBOXAMIDE;CS-1231;Roquinimex(Linomide)
CAS:84088-42-6
MF:C18H16N2O3
MW:308.33
EINECS:
Product Categories:Antitumour
Mol File:84088-42-6.mol
Roquinimex Structure
Roquinimex Chemical Properties
Melting point 200-204°
Boiling point 436.2±45.0 °C(Predicted)
density 1.357±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO: 11 mg/mL
form solid
pka4.50±1.00(Predicted)
color White to off-white
Merck 14,8259
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 36/37
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
HS Code 2933.49.2600
MSDS Information
ProviderLanguage
SigmaAldrich English
Roquinimex Usage And Synthesis
DescriptionRoquinimex is an immunomodulator with diverse biological activities. In vivo, roquinimex (80 mg/kg) increases the number of myocardial MHC class II-expressing cells, the ratio of cytotoxic to helper T cells, and survival and decreases necrotic lesion area in a mouse model of murine coxsackievirus B3-induced myocarditis. It induces IFN-γ production, reduces TNF-α and IL-1β production, prevents the development of proteinuria, and ameliorates nephritis in a mouse model of chronic graft versus host disease (GVHD). Roquinimex (300 mg/kg) decreases colonic myeloperoxidase (MPO) activity and mucosal damage in a mouse model of colitis induced by dextran sulfate (DSS; ). It also decreases tumor weight and tumor blood flow in a von Hippel-Lindau (VHL) type 2a paraganglioma mouse xenograft model.
UsesBiological response modifier; immunomodulator.
UsesAn immunomodulator with antitumour properties. Inhibits T-cell apoptosis in vivo; also inhibits angiogenesis in rats
DefinitionChEBI: 4-hydroxy-N,1-dimethyl-2-oxo-N-phenyl-3-quinolinecarboxamide is an aromatic amide.
Biological ActivityImmunomodulator with stimulatory and antitumor properties. Inhibits in vivo apoptosis of T-cells and inhibits angiogenesis in rats in vivo .
References[1] N. ILBCK. Effects of the immunomodulator LS 2616 on lymphocyte subpopulations in murine Coxsackievirus B3 myocarditis.[J]. Journal of immunology, 1989, 142 9 1: 3225-3228. DOI: 10.4049/jimmunol.142.9.3225
[2] ZHI-YONG XIAO. Roquinimex-mediated protection effect on the development of chronic graft-versus-host disease in mice is associated with induction of Th1 cytokine production and inhibition of proinflammatory cytokine production[J]. Life sciences, 2007, 81 19: Pages 1403-1410. DOI: 10.1016/j.lfs.2007.08.044
[3] Q LIU. Roquinimex inhibits dextran sodium sulfate-induced murine colitis.[J]. Inflammation Research, 2003, 52 2: 64-68. DOI: 10.1007/s000110300002
[4] D J GROSS. The antiangiogenic agent linomide inhibits the growth rate of von Hippel-Lindau paraganglioma xenografts to mice.[J]. Clinical Cancer Research, 1999, 5 11: 3669-3675.
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