CAS 36413-91-9

Geiparvarin

Description:

Geiparvarin, with the CAS number 36413-91-9, is a chemical compound that belongs to the class of flavonoids, specifically a type of flavonol. It is derived from natural sources, particularly from certain plants, and is known for its potential biological activities. Geiparvarin exhibits antioxidant properties, which may contribute to its role in protecting cells from oxidative stress. Additionally, it has been studied for its anti-inflammatory and antimicrobial effects, making it of interest in pharmacological research. The compound's structure features a flavonoid backbone, which is characterized by a chromone ring fused to a phenolic ring, contributing to its reactivity and interaction with biological systems. While research is ongoing, Geiparvarin's potential applications in medicine and health supplements are being explored, particularly in the context of its therapeutic benefits. However, further studies are necessary to fully understand its mechanisms of action and efficacy in various biological contexts.

Formula: C₁₉H₁₈O₅

InChI: InChI=1S/C19H18O5/c1-12(15-11-17(20)19(2,3)24-15)8-9-22-14-6-4-13-5-7-18(21)23-16(13)10-14/h4-8,10-11H,9H2,1-3H3/b12-8+

InChI key: InChIKey=OUTLLBZGJYDUQE-XYOKQWHBSA-N

SMILES: O(C/C=C(\C)/C=1OC(C)(C)C(=O)C1)C=2C=C3C(=CC2)C=CC(=O)O3

Synonyms:

• 2H-1-Benzopyran-2-one, 7-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-, (E)-
• 2H-1-Benzopyran-2-one, 7-[[(2E)-3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-buten-1-yl]oxy]-
• 2H-1-Benzopyran-2-one, 7-[[(2E)-3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl]oxy]-
• 7-[[(2E)-3-(4,5-Dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-buten-1-yl]oxy]-2H-1-benzopyran-2-one
• Geiparvarin
• NSC 142227

Geiparvarin

CAS: 36413-91-9

Geiparvarin is a cytotoxic compound, which is a plant-derived chemical with notable bioactivity. It is sourced from the roots of the Daflon plant, known for various natural compounds with potential therapeutic effects. Geiparvarin acts by interfering with cellular processes, leading to apoptosis in malignant cells. This mode of action is particularly significant in the study and development of anticancer therapies.

Purity: Min. 95%

Ref: 3D-FG137872