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726419

2-(氯甲基)萘

Name: 2-(氯甲基)萘
Brand: ALDRICH

≥97.0%

别名:

β-Naphthylmethyl chloride, 2-Menaphthyl chloride, 2-Naphthylmethyl chloride

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关于此项目

经验公式（希尔记法）:

C₁₁H₉Cl

化学文摘社编号:

2506-41-4

分子量:

176.64

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

329764234

EC Number:

219-713-5

Beilstein/REAXYS Number:

742185

MDL number:

MFCD00046488

Assay:

≥97.0% (GC), ≥97.0%, 97.0-103.0% (T)

Form:

crystals

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属性

Quality Level

100

assay

≥97.0% (GC), ≥97.0%, 97.0-103.0% (T)

form

crystals

functional group

chloro

SMILES string

ClCc1ccc2ccccc2c1

InChI

1S/C11H9Cl/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2

InChI key

MPCHQYWZAVTABQ-UHFFFAOYSA-N

说明

Application

Improving insulin sensitivity: Research highlights dihydroberberine′s capacity to enhance insulin sensitivity through AMPK activation, offering a promising therapeutic strategy for managing insulin resistance and type 2 diabetes (Lewis and Falk, 2022).

Anti-inflammatory effects: A study conducted on the anti-inflammatory properties of dihydroberberine found significant reductions in inflammatory markers, suggesting its potential as an anti-inflammatory agent in metabolic syndrome (Dian et al., 2022).

Enhancing bioavailability: Investigations into the oral bioavailability of dihydroberberine demonstrate improvements over its precursor berberine, highlighting its superior pharmacokinetic profile which could lead to more effective clinical applications (Murakami, Bodor, and Bodor, 2023).

Glucose uptake mechanisms: Studies on dihydroberberine have shown its effectiveness in facilitating glucose uptake, an essential function for metabolic health, through its interaction with cellular transport mechanisms (Moon et al., 2021).