luteolin 7 sulfate

Luteolin 7-sulfate, derived from the marine plant Phyllospadix iwatensis Makino, suppresses TYR gene expression by intervening in a signaling pathway involving the cAMP-responsive element binding protein (CREB) and microphthalmia-associated transcription factor (MITF). This inhibition ultimately leads to a decrease in melanin synthesis.

Luteolin (monohydrate) is the hydrated form of Luteolin, a flavonoid that acts as a potent Nrf2 inhibitor. It possesses anti-inflammatory and anticancer properties, induces apoptosis and cell cycle arrest in multiple human cancer cell lines, including non-small lung cancer cells, and inhibits cell metastasis and angiogenesis [1].

Luteolin (Luteolol) belongs to the flavonoid group of natural products and is a Nrf2 inhibitor, PDE inhibitor. Luteolin has a wide range of biological activities including antitumor, antioxidant, anti-inflammatory, antimicrobial, antiviral, antiallergic, and procoagulant.

Luteolin (Standard) is a reference compound for analytical and biochemical research involving Luteolin. Luteolin (Standard) belongs to the flavonoid class and functions as a Nrf2 inhibitor and PDE inhibitor. Luteolin (Standard) is utilized in biomedical research focused on flavonoid signaling modulation, oxidative stress regulation, inflammatory pathway analysis, and enzyme inhibition profiling across tumor, infectious, and allergic disease models.