ChemicalBook--->CAS DataBase List--->1018946-38-7

1018946-38-7

1018946-38-7 Structure

1018946-38-7 Structure
IdentificationBack Directory
[Name]

DWK-1339
[CAS]

1018946-38-7
[Synonyms]

DWK-1339
SNU-0039
DWK-1339;DWK 1339;DWK1339
2-(3,4-DiMethoxy-phenyl)-5-(3-Methoxy-propyl)-benzofuran
Benzofuran, 2-(3,4-diMethoxyphenyl)-5-(3-Methoxypropyl)-
2-(3,4-dimethoxyphenyl)-5-(3-methoxypropyl)-1-benzofuran
[Molecular Formula]

C20H22O4
[MDL Number]

MFCD22665705
[MOL File]

1018946-38-7.mol
[Molecular Weight]

326.39
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30mg/mL; DMSO: 30mg/mL; Ethanol: 2mg/mL
[form ]

A crystalline solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

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

DWK-1339 is an inhibitor of amyloid-β (Aβ) aggregation. It inhibits aggregation of monomeric Aβ (1-42) (Aβ42) and induces disaggregation of Aβ42 fibrils in vitro when used at concentrations ranging from 3.1 to 50 μM. DWK-1339 (10 μM) reduces Aβ42-induced toxicity in HT-22 cells. In vivo, DWK-1339 (10 mg/kg) increases step-through latency in a passive avoidance test and increases spontaneous alteration in the Y-maze compared with vehicle control mice in a mouse model of Aβ42-induced acute Alzheimer''s disease. It also decreases brain levels of Aβ42 and increases spontaneous alteration in the Y-maze in the APP/PS1 transgenic mouse model of Alzheimer''s disease.
[Uses]

DWK-1339, is an orally active and blood-brain-barrier-permeable Aβ-aggregation inhibitor, used in the research of Alzheimer''s disease.
[in vivo]

MDR-1339 (0.1-10 mg/kg, p.o.) dose-dependently restores the passive avoidance responses in mice models of Alzheimer's disease (AD), with an ED50 of 0.19 mg/kg. MDR-1339 (30 and 100 mg/kg, p.o. daily for 8 weeks) significantly improves spontaneous alternation, and reduces the Aβ1-40 and Aβ1-42 levels in APP/PS1 mice[1].

[storage]

Store at -20°C
[References]

[1] HEE-JIN HA. Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer’s Disease[J]. Journal of Medicinal Chemistry, 2017, 61 1: 396-402. DOI: 10.1021/acs.jmedchem.7b00844
Spectrum DetailBack Directory
[Spectrum Detail]

DWK-1339(1018946-38-7)1HNMR
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