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916056-79-6

916056-79-6 Structure

916056-79-6 Structure
IdentificationBack Directory
[Name]

ADX-102 (NS-2)
[CAS]

916056-79-6
[Synonyms]

Reproxalap
ADX-102 (NS-2)
ADX-102 (Reproxalap
2-Quinolinemethanol, 3-amino-6-chloro-α,α-dimethyl-
[Molecular Formula]

C12H13ClN2O
[MDL Number]

MFCD28502442
[MOL File]

916056-79-6.mol
[Molecular Weight]

236.7
Chemical PropertiesBack Directory
[Boiling point ]

410.5±40.0 °C(Predicted)
[density ]

1.324±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 100 mg/mL (422.48 mM; Need ultrasonic)
[form ]

Solid
[pka]

13.07±0.29(Predicted)
[color ]

Light yellow to yellow
[InChI]

InChI=1S/C12H13ClN2O/c1-12(2,16)11-9(14)6-7-5-8(13)3-4-10(7)15-11/h3-6,16H,14H2,1-2H3
[InChIKey]

GUHFUVLKYSQIOQ-UHFFFAOYSA-N
[SMILES]

CC(C1=C(N)C=C2C(=N1)C=CC(Cl)=C2)(O)C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Reproxalap (ADX-102) is an active aldehyde sequestering agent. Reproxalap reduces the PKCα activity. Reproxalap blocks caspase 3/7 activation. Reproxalap protects cells from the cytotoxicity of C18:0-al. Reproxalap has anti-inflammatory and pain-relieving effects. Reproxalap is used in studies of dry eye, allergic conjunctivitis, and non-infectious anterior uveitis[1][2][3][4][5].
[in vivo]

Reproxalap (30-100 mg/kg, once or twice a day) shows a dose-dependent reduction in pain-related behaviors in acute pain models[3].
Reproxalap (10 mg/kg, intraperitoneal injection, single dose) significantly reduces the formation of N-retinyl-phosphatidylethanolamine (A2E) in the retinas of mice with macular degeneration[5].
Reproxalap (25-50 μg, IVT, injected in five doses after LPS (HY-D1056) induction) can improve eye scores in uveitis rats[5].

Animal Model:Carrageenaninduced and Complete Freund’s Adjuvant (CFA)-induced models in mice[3]
Dosage:30, 100 mg/kg; once a day or twice a day
Administration:
Result:Was effective in thermal hyperalgesia in the CFA-induced model at both 100 mg/kg QD and BID doses; in the carrageenan-induced model, and was effective at 30 mg/kg BID and 100 mg/kg BID doses.
Was effective in mechanical allodynia only in the CFA-induced model at a 100 mg/kg BID dose; in the carrageenan-induced model, was not effective.
Had a mild effect on swelling in the CFA-induced model at 30 mg/kg BID and 100 mg/kg BID doses; in the carrageenan-induced model, had a mild effect at a 100 mg/kg QD dose.
Animal Model:A mouse knockout model (abcr-/-) of macular degeneration (MD) [5]
Dosage:10 mg/kg; single dose
Administration:Intraperitoneal injection (i.p.)
Result:Reduced the formation of N-retinylidene-N-retinylethanolamine (A2E) in the retina by 71% without affecting dark adaptation or body weight.
Animal Model:A rat model of lipopolysaccharide (LPS)-induced uveitis[5]
Dosage:10 mg/kg 50 μg at hours 1, 3, 7, 10 and 17, after LPS induction, or injection 25 μg at 1 hour after LPS induction
Administration:Intravitreal (IVT)
Result:Improved the eye examination scores, enhancing the retinal-choroidal ratings.
[IC 50]

PKCα; Caspase 3; Caspase-7
[References]

[1] Ochoa CA, et al. Aldehyde Trapping by ADX-102 Is Protective against Cigarette Smoke and Alcohol Mediated Lung Cell Injury. Biomolecules. 2022 Mar 2;12(3):393. DOI:10.3390/biom12030393
[2] Rizzo WB, et al. Sj?gren-Larsson syndrome: A biochemical rationale for using aldehyde-reactive therapeutic agents. Mol Genet Metab Rep. 2021 Dec 23;30:100839. DOI:10.1016/j.ymgmr.2021.100839
[3] Susan Macdonald, et al. ADX-102, a novel aldehyde trap, reduces nociceptive behavior in mouse models of carrageenan and CFA induced pain.
[4] Reproxalap Phase 2b Dry Eye Disease Results.
[5] Susan G. Macdonald, Ph.D., et al. Novel Small Molecule Aldehyde Sequestering Agents Demonstrate Broad Therapeutic Potential for Ocular Inflammation.
Spectrum DetailBack Directory
[Spectrum Detail]

ADX-102 (NS-2)(916056-79-6)1HNMR
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