CIVENTICHEM CV-4057

Product NameCIVENTICHEM CV-4057
CAS248281-84-7
MFC19H17ClN2O3
MW356.8
EINECS692-155-1
MOL File248281-84-7.mol

Chemical Properties

Melting point	201 °C (decomp)
Boiling point	484.8±45.0 °C(Predicted)
Density	1.395±0.06 g/cm3(Predicted)
storage temp.	Sealed in dry,Room Temperature
solubility	Soluble in DMSO (>25 mg/ml)
form	solid
pka	4.50±1.00(Predicted)
color	Off-white
Stability	Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChI	1S/C19H17ClN2O3/c1-3-22(12-8-5-4-6-9-12)19(25)16-17(23)15-13(20)10-7-11-14(15)21(2)18(16)24/h4-11,23H,3H2,1-2H3
InChIKey	GKWPCEFFIHSJOE-UHFFFAOYSA-N
SMILES	OC(C1=C(C=CC=C1N(C2=O)C)Cl)=C2C(N(C3=CC=CC=C3)CC)=O

Safety Information

Hazard Codes	T
Risk Statements	25
Safety Statements	45
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 1
Storage Class	11 - Combustible Solids
Hazard Classifications	Carc. 2 Repr. 2 STOT RE 2

Usage And Synthesis

Description

Laquinimod (248281-84-7) is an immunomodulator1 that inhibits inflammation2 and autoimmunity3,4 via activation of the aryl hydrocarbon receptor (AhR)5. It has been investigated as a treatment for multiple sclerosis6 and has shown efficacy in Huntington’s disease models7,8.

Uses

Laquinimod (ABR-215062), an orally available carboxamide derivative, is a potent immunomodulator which prevents neurodegeneration and inflammation in the central nervous system. Laquinimod reduces astrocytic NF-κB activation to protect from Cuprizone-induced demyelination. Laquinimod hasthepotentialfor relapsing remitting (RR) and chronic progressive (CP) forms of multiple sclerosis (MS; RRMS or CPMS) as well as neurodegenerative diseasesresearch[1][2][3][4].

Definition

ChEBI: Laquinimod is an aromatic amide.

Synthesis

Benzoic acid, 2-chloro-6-[[3-(ethylphenylamino)-1,3-dioxopropyl]methylamino]-, methyl ester

1379595-99-9

248281-84-7

b) To a stirred solution of anhydrous tetrahydrofuran (50 mL) of the compound (CAS:1379595-99-9) (10 mmol) was added sodium methanolate (3.6 mmol, 0.5 M, dissolved in methanol) in batches under nitrogen protection. The reaction mixture was heated to reflux for 2 hours. Upon completion of the reaction, the mixture was cooled and the solvent was partially evaporated to give a concentrated solution containing the insoluble salt. The concentrated solution was dissolved in a solvent mixture of methanol (30 mL), 10 M aqueous sodium hydroxide (1.07 mL, 10.7 mmol) and water (15.0 mL). Subsequently, 5 M aqueous hydrochloric acid (2.4 mL, 12.0 mmol) was slowly added to neutralize the reaction mixture. The precipitated crystalline precipitate was collected by filtration, washed with cold methanol and dried to afford the target product 5-chloro-N-ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide in 87% yield and 98.9% purity.

in vitro

abr-215062 was shown to completely inhibit the development of murine acute experimental autoimmune encephalomyelitis (eae) [1].

in vivo

abr-215062 dose-dependently inhibited disease and showed better disease inhibitory effects as compared to roquinimex (linomide). furthermore, abr-215062 inhibited the inflammation of both cd4+ t cells and macrophages into central nervous tissues [2].

IC 50

NF-κB

References

[1] STIG JÖNSSON. Synthesis and Biological Evaluation of New 1,2-Dihydro-4-hydroxy-2-oxo-3-quinolinecarboxamides for Treatment of Autoimmune Disorders: Structure−Activity Relationship[J]. Journal of Medicinal Chemistry, 2004, 47 8: 2075-2088. DOI:10.1021/jm031044w
[2] VEIT ROTHHAMMER. Aryl Hydrocarbon Receptor Activation in Astrocytes by Laquinimod Ameliorates Autoimmune Inflammation in the CNS.[J]. Neurology(R) neuroimmunology & neuroinflammation, 2021. DOI:10.1212/nxi.0000000000000946
[3] KALLIOPI PITAROKOILI . Laquinimod exerts strong clinical and immunomodulatory effects in Lewis rat experimental autoimmune neuritis[J]. Journal of neuroimmunology, 2014, 274 1: Pages 38-45. DOI:10.1016/j.jneuroim.2014.06.012
[4] MARTINA OTT. Laquinimod, a prototypic quinoline-3-carboxamide and aryl hydrocarbon receptor agonist, utilizes a CD155-mediated natural killer/dendritic cell interaction to suppress CNS autoimmunity.[J]. Journal of Neuroinflammation, 2019: 49. DOI:10.1186/s12974-019-1437-0
[5] J. KAYE. Laquinimod arrests experimental autoimmune encephalomyelitis by activating the aryl hydrocarbon receptor[J]. Proceedings of the National Academy of Sciences, 2016, 27 1: E6145-E6152. DOI:10.1073/pnas.1607843113
[6] J. THÖNE R L. Laquinimod in the treatment of multiple sclerosis: a review of the data so far[J]. Drug Design, Development and Therapy, 2016, 10 1: 1111-1118. DOI:10.2147/dddt.s55308
[7] LUCIANNE DOBSON. Laquinimod dampens hyperactive cytokine production in Huntington’s disease patient myeloid cells[J]. Journal of Neurochemistry, 2016, 137 5: 782-794. DOI:10.1111/jnc.13553
[8] MARTA GARCIA-MIRALLES. Laquinimod rescues striatal, cortical and white matter pathology and results in modest behavioural improvements in the YAC128 model of Huntington disease.[J]. Scientific Reports, 2016: 31652. DOI:10.1038/srep31652

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