Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H16N2O3 |
Molecular Weight | 308.3312 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C(=O)C1=C(O)C2=CC=CC=C2N(C)C1=O)C3=CC=CC=C3
InChI
InChIKey=SGOOQMRIPALTEL-UHFFFAOYSA-N
InChI=1S/C18H16N2O3/c1-19(12-8-4-3-5-9-12)17(22)15-16(21)13-10-6-7-11-14(13)20(2)18(15)23/h3-11,21H,1-2H3
Roquinimex (Linomide, LS 2616) is a quinoline-3-carboxamide with pleiotropic immune modulating capacity and it has therapeutic effects in several experimental animal models of autoimmune diseases. Linomide has been evaluated in clinical trials for multiple sclerosis, and was indeed shown to have disease inhibitory effects. However, due to unexpected side effects recorded in patients treated with Linomide, premature termination of clinical trials was required. The basic mechanism(s) of action of Linomide in inducing beneficial effects in autoimmune diseases is still elusive. Some experimental evidence indicates that Linomide influences the regulation of the cytokine profile, resulting in the inhibition of autoimmune and inflammation pathologies. Roquinimex possesses potential antineoplastic activity. Roquinimex inhibits endothelial cell proliferation, migration, and basement membrane invasion; reduces the secretion of the angiogenic factor tumor necrosis factor alpha by tumor-associated macrophages (TAMs); and inhibits angiogenesis.
Roquinimex was in phase III clinical trials with Pharmacia Corporation in Europe and the US for the treatment of multiple sclerosis.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11407306
Curator's Comment: Linomide applied in models for autoimmune and
inflammation pathologies of the central nervous system.
Originator
Sources: http://adisinsight.springer.com/drugs/800001478
Curator's Comment: # Pfizer
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: GO:0002369 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10369127 |
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Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
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Immunomodulation by roquinimex decreases the expression of IL-23 (p19) mRNA in the brains of herpes simplex virus type 1 infected BALB/c mice. | 2004 Aug |
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H1521, a novel derivative of 4-hydroxyquinoline-3-carboxamide, suppresses the development of lupus in mice by inducing Th1 cytokine profile in T cells. | 2011 Apr |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10773855
Treatment of multiple sclerosis: 2.5 or 5 mg.
The target treatment consisted of Linomide 2 x 2.5 mg daily, administered orally as tablets for the planned treatment
period of 36 months. All patients started with
one tablet daily (i.e. 2.5 mg Linomide or placebo) and
if this dose was well tolerated, it was to be changed
into a 5 mg dose after 3 months of treatment.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9569049
Curator's Comment: Post-capillary endothelial cells (CVECs) were obtained by a
bead perfusion technique of the bovine coronary sinus.
Linomide (50-200 ug/ml) was not cytotoxic in vitro on resting capillary endothelial cells but blocked endothelial cell replication induced by VEGF.
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ACTIVE MOIETY