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1824609-67-7

1824609-67-7 Structure

1824609-67-7 Structure
IdentificationBack Directory
[Name]

2-Quinolinemethanol, 3-amino-α,α-dimethyl-
[CAS]

1824609-67-7
[Synonyms]

acloproxalap
Acloproxalap/ADX-629
2-(3-aminoquinolin-2-yl)propan-2-ol
2-Quinolinemethanol, 3-amino-α,α-dimethyl-
[Molecular Formula]

C12H14N2O
[MOL File]

1824609-67-7.mol
[Molecular Weight]

202.26
Chemical PropertiesBack Directory
[Boiling point ]

379.7±27.0 °C(Predicted)
[density ]

1.212±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

13.27±0.29(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Acloproxalap is a quinoline-based aldehyde scavenger that can be used in studies of diseases with toxic aldehyde accumulation, such as inflammatory diseases of the eye and skin, respiratory diseases such as pneumonia, organ diseases, and viral infection-related syndromes[1][2].
[in vivo]

Acloproxalap (compound I-6) (100 or 200 mg/kg, i.p. or p.o., everyday, 6 days) can effectively improve inflammation of the colon in acute ulcerative colitis (UC) female Swiss Webster mice[1].

Animal Model:Acute ulcerative colitis (UC) in female Swiss Webster mice[1]
Dosage:100 mg/kg, 200 mg/kg
Administration:Intraperitoneal injection for 100 mg/kg, oral gavage for 200 mg/kg; everyday; 6 days
Result:Inhibited weight loss in intraperitoneal injection mice significantly while there was no significant difference in the oral gavage group compared to the control group.
Both significantly reduced colonic histopathological parameters.
Animal Model:Male non-na?ve beagle dogs[2]
Dosage:3 mg/kg
Administration:Intravenous injection; once
Result:The pharmacokinetic parameters of Acloproxalap (compound I-1)
ParameterAcloproxalap (compound I-1)
t1/21.82 h
Tmax0.518 h
Clearance12.2 mL/kg/min
steady-state volume1385 mL/kg
AUC0-t4103 ng/mL*h
AUC0?inf_obs4137 ng/mL*h
Animal Model:Male non-na?ve beagle dogs[2]
Dosage:10 mg/kg
Administration:Oral gavage; once
Result:The pharmacokinetic parameters of Acloproxalap (compound I-1)
ParameterAcloproxalap (compound I-1)
t1/23.02 h
Tmax0.518 h
Cmax3558 ng/mL
AUC0-t9361 ng/mL*h
AUC0?inf_obs9546 ng/mL*h
BioA75%
[References]

[1] Susan Macdonald, et al. Treatment of inflammatory disorders. US20190105322
[2] Todd Brady, et al. Pharmaceutical formulations and uses thereof. WO2021231792
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