Linear 1 3-diarylpropanoids

Organic compounds contain a central propyl group (3 carbon chain) with one phenyl group bonded to the first and the third carbons in the propyl chain; the propyl chain may contain other functional groups, such as a carbon - carbon double bond.

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301 – 315 of 719 results

301

Medchemexpress LLC 4'-Methoxychalcone | 959-23-9 | 99.8% | 5 G

4'-Methoxychalcone regulates adipocyte differentiation through PPARγ activation. It also modulates the expression and secretion of various adipokines in adipose tissue that are involved in insulin sensitivity. This product is intended for research use only.

Regulates adipocyte differentiation via PPARγ activation
Modulates adipokine expression and secretion involved in insulin sensitivity
Increases mRNA expression of adipogenic genes during differentiation
Reduces upregulated mRNA expression of IL-6, PAI-1, and MCP-1
Causes an increase in PPARγ expression during differentiation
Exhibits antiproliferative activity and cytotoxicity against various human cell lines
Targets PPARγ
Derived from Piperaceae Piper nigrum Linn.
Classified as flavonoids, chalcones

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302

Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC

5000561452 AKT PAN C67E7 RABBIT MAB SIGNA

Pricing & Availability

303

Medchemexpress LLC 4'-Methoxychalcone | 959-23-9 | 99.8% | 50 G

4'-Methoxychalcone is a compound that regulates adipocyte differentiation through PPARγ activation. It modulates the expression and secretion of various adipokines in adipose tissue, which are involved in insulin sensitivity.

Regulates adipocyte differentiation via PPARγ activation.
Modulates adipokine expression and secretion.
Increases mRNA expression of adipogenic genes during differentiation.
Reduces upregulated mRNA expression of inflammatory markers in preadipocyte cells.
Exhibits antiproliferative and cytotoxic activity against various human and mouse cell lines.

Pricing & Availability

304

Apexbio Technology LLC 4-METHOXYCHALCONE 1-5000mg

4-Methoxychalcone-1 (CAS No 959-33-1) is a flavonoid derivative often studied in the field of biomedical research It originates from the chalcone family known for diverse biological activities Its mechanism of action involves the modulation of key signaling pathways potentially affecting inflammatory and oxidative stress responses In vitro it exhibits biological activity in the nanomolar to low micromolar range showcasing its potency Common applications include studies using various cancer cell lines where it is tested for antiproliferative effects It is also utilized in animal models to explore its therapeutic potential in disease contexts In drug screening it serves as a candidate for evaluating new therapeutic strategies due to its bioactive properties Experimental concentrations typically depend on the specific research design allowing for flexibility in application across different experimental setups ensuring adaptability to varied research objectives