Basic information Safety Supplier Related

CIVENTICHEM CV-4057

Basic information Safety Supplier Related

CIVENTICHEM CV-4057 Basic information

Product Name:
CIVENTICHEM CV-4057
Synonyms:
  • CIVENTICHEM CV-4057
  • LAQUINIMOD,5-CHLORO-4-HYDROXY-1-METHYL-2-OXO-1,2-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL-PHENYL-AMIDE
  • ABR-215062 (Laquinimod)
  • CIVENTICHEM
  • CS-82
  • ABR215062; ABR 215062 (LAQUINIMOD)
  • 5-Chloro-4-hydroxy-1-Methyl-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid ethyl-phenyl-aMide
  • LaquiniMod, SAIK-MS coMpound, ABR-215062
CAS:
248281-84-7
MF:
C19H17ClN2O3
MW:
356.8
EINECS:
692-155-1
Product Categories:
  • Inhibitors
  • api
  • Heterocycles
Mol File:
248281-84-7.mol
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CIVENTICHEM CV-4057 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.
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
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CIVENTICHEM CV-4057 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.

Definition

ChEBI: Laquinimod is an aromatic amide.

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].

References

J?nsson et al. (2004), Synthesis and Biological Evaluation of New 1,2-Dihydro-4-hydroxy-2-oxo-3-quinolinecarboxamides for Treatment of Autoimmune Disorders: Structure-Activity Relationship; Med. Chem. 47 2075 Rothhammer et al. (2021); Aryl Hydrocarbon Receptor Activation in Astrocytes by Laquinimod Ameliorates Autoimmune Inflammation in the CNS, Neurol. Neuroimmunol. Neuroinflamm., 8 e946 Pitarokoili et al. (2014), Laquinimod exerts strong clinical and immunomodulatory effects in Lewis rat experimental autoimmune neuritis; Neuroimmunol., 274 38 Ott et al. (2019), Laquinimod, a prototypic quinoline-3-carboxamide and aryl hydrocarbon receptor agonist, utilizes CD155-mediated natural killer/dendritic cell interaction to suppress CNS autoimmunity; Neuroinflammation, 16 49 Kaye et al. (2016), Laquinimod arrests experimental autoimmune encephalitis by activating the aryl hydrocarbon receptor; Natl. Acad. Sci. USA., 113 E6145 Th?ne and Linker (2016), Laquinimod in the treatment of multiple sclerosis: a review of the data so far; Drug Des. Devel. Ther., 10 1111 Dobson et al. (2016), Laquinimod dampens hyperactive cytokine production in Huntington’s disease patient myeloid cells; Neurochem., 137 782 Garcia-Miralles et al. (2016), Laquinimod rescues striatal, cortical and white matter pathology and results in modest behavioural improvements in the YAC128 model of Huntington disease; Rep., 6 31652

CIVENTICHEM CV-4057Supplier

Shanghai Boyle Chemical Co., Ltd.
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Email
sales@boylechem.com
JinYan Chemicals(ShangHai) Co.,Ltd.
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13817811078
Email
sales@jingyan-chemical.com
Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
shanghai Rainbow MediTech.Co.Ltd.
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21-021-64968085,64968086-5815,5812 13918693646
Email
bd@rainbowpharma.cn
Hangzhou Yuhao Chemical Technology Co., Ltd
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0571-82693216
Email
info@yuhaochemical.com