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Chemical Structure| 289893-26-1 Chemical Structure| 289893-26-1

Structure of Arimoclomol maleate
CAS No.: 289893-26-1

Chemical Structure| 289893-26-1

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Arimoclomol maleate (BRX-220) is a co-inducer of heat shock proteins (HSPs). Arimoclomol protects motor neurons by enhancing Hsp expression, thereby directly affecting protein aggregation and the clearance of misfolded and assembled proteins through the ubiquitin-proteasome system.

Synonyms: BRX-220

4.5 *For Research Use Only !

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Product Details of Arimoclomol maleate

CAS No. :289893-26-1
Formula : C18H24ClN3O7
M.W : 429.85
SMILES Code : C(=C\C(O)=O)\C(O)=O.C(=NOC[C@@H](CN1CCCCC1)O)(Cl)C2=CN(=O)=CC=C2
Synonyms :
BRX-220
MDL No. :MFCD28143527

Safety of Arimoclomol maleate

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H314-H331
Precautionary Statements:P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P405-P501
Class:6.1(8)
UN#:2928
Packing Group:

Related Pathways of Arimoclomol maleate

DNA

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
primary rat motoneurons 0.1-100 μM 24 h Arimoclomol had no effect on neuronal survival under unstressed conditions but significantly increased motoneuron survival under stress conditions (e.g., staurosporin or H2O2-induced apoptosis and oxidative stress). Cell Mol Biol Lett. 2009;14(2):319-35
SK-N-SH cells 1 μM 24 h Arimoclomol reduced P23H-GFP aggregation and improved viability of mutant rhodopsin-expressing cells Cell Death Dis. 2014 May 22;5(5):e1236
NPC1I1061T human fibroblasts 0.5 mM 72 or 120 h To evaluate the effect of Arimoclomol on cholesterol storage in NPC1I1061T mutant cells, results showed no reduction in cholesterol storage. J Lipid Res. 2021;62:100114
rat myoblasts 10 μM 24 h reduced the formation of cytoplasmic inclusions, improved nuclear localization of TDP-43, and reduced cell death Sci Transl Med. 2016 Mar 23;8(331):331ra41
Neuronal-like cells 400 μM 9-11 days Arimoclomol increased the level and activity of GCase in neuronal cells derived from both neuronopathic and non-neuronopathic GD patients. EBioMedicine. 2018 Dec;38:142-153
Primary GD patient fibroblasts 100-400 μM 5 days Arimoclomol dose-dependently increased the amount of GCase in primary GD fibroblasts across all tested genotypes, including neuronopathic and non-neuronopathic associated mutations, and enhanced the folding, maturation, activity, and correct cellular localization of mutated GCase. EBioMedicine. 2018 Dec;38:142-153
iPSC-derived motor neurons 50μM 24 h reduced TDP-43 mislocalization and ubiquitin-positive aggregate formation Mol Neurobiol. 2023 Dec;60(12):6896-6915
fibroblasts 10–400μM 24 h ameliorated abnormal nuclear morphology and TDP-43 pathology in mutant VCP patient fibroblasts Mol Neurobiol. 2023 Dec;60(12):6896-6915

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Rats P23H rhodopsin transgenic rats Intraperitoneal injection 10 mg/kg Daily administration for 2 to 6 weeks Arimoclomol improved electroretinogram responses and prolonged photoreceptor survival, as assessed by measuring outer nuclear layer thickness in the retina Cell Death Dis. 2014 May 22;5(5):e1236
Mice FUSR521G mouse model Intraperitoneal injection 5, 10, 20 mg/kg Daily for 28 days Arimoclomol reversed cognitive deficits and improved cortical dendritic spine densities in FUSR521G mice without inducing heat shock protein expression. Neurotherapeutics. 2024 Sep;21(5):e00388
Mice Mutant VCP mouse model Oral (drinking water) 120 mg/kg Daily administration from 4 to 14 months of age Improved muscle strength and pathological features, reduced inflammatory cell infiltration and cytoplasmic mislocalization of TDP-43 Sci Transl Med. 2016 Mar 23;8(331):331ra41
Mice AR100 mouse model Oral (in drinking water) 120 mg/kg Daily administration from symptom onset until 18 months of age To evaluate the therapeutic potential of arimoclomol in a mouse model of spinal and bulbar muscular atrophy. Results showed that arimoclomol significantly improved hindlimb muscle force and contractile characteristics, rescued motor units, improved motor neuron survival, and upregulated the expression of vascular endothelial growth factor with neurotrophic activity. Brain. 2013 Mar;136(Pt 3):926-43

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2.33mL

0.47mL

0.23mL

11.63mL

2.33mL

1.16mL

23.26mL

4.65mL

2.33mL

 

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