C3G (Cyanidin 3 Glucoside)

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Description

Overview of C3G

C3G (Cyanidin-3-Glucoside) is a naturally occurring anthocyanin pigment. It belongs to the flavonoid class. C3G is formed when cyanidin attaches to a glucose molecule at the 3-position. It is water-soluble and exhibits color changes in response to pH variations.

Chemical Properties

C3G
PubChem CID 197081
Molecular Formula C21H21ClO11
Molecular Weight 484.8 g/mol
Source Naturally occurring anthocyanin pigment in plants (e.g., berries, black rice, purple corn)
Major Constituents Cyanidin-3-O-glucoside, Chloride form
CAS 7084-24-4
Labeling For research use only; laboratory applications; not for human or veterinary use
Chemical Structure Depiction
Purity Typically ≥ 95% (verify with manufacturer certificate of analysis)
Classification Flavonoid, Anthocyanin, Glycoside
Storage Temperature  2–8 °C, protected from light and moisture
Solubility  Water–soluble; color changes with pH variations
Safety Handle using standard laboratory safety procedures; use personal protective equipment (PPE); avoid ingestion and contact with skin or eyes

Various Mechanisms of C3G

Free Radical Interaction

C3G has electron-donating properties. These properties allow it to interact with reactive oxygen species (ROS) in chemical and cellular model systems.

Signal Pathway Modulation

C3G can interact with NF-κB signaling components. It also influences associated molecular pathways under controlled experimental conditions.

Enzymatic and Kinase Interactions

C3G affects AMP-activated protein kinase (AMPK) phosphorylation. This modulation influences downstream molecular events related to cellular energy metabolism in vitro.

Research Applications

C3G is utilized in laboratory research to investigate its biochemical and molecular interactions. It is applied in studies of reactive oxygen species (ROS) modulation and redox chemistry. Researchers also examine signal transduction pathways, including NF-κB and kinase activity (e.g., AMPK). C3G is used in spectroscopic and analytical chemistry studies that leverage its water solubility and pH-dependent color changes. Additionally, it supports structure–function analyses of anthocyanins, glycoside linkages, and flavonoid stability, with all applications strictly limited to research use and not implying effects on living subjects.

Why Choose Purerawz for C3G?

Buy C3G for laboratory research use from our online shop. At Purerawz, we provide high-quality reference materials. Each research compound comes with a Certificate of Analysis for verification of purity and concentration.

Note:

C3G is an investigational compound currently undergoing clinical evaluation and has not been established as safe or effective for any therapeutic use

Disclaimer

This information is for educational purposes only and not medical advice. Products are for research use only. Research must follow IRB or IACUC guidelines. Verify information independently before purchasing. By ordering, you agree to our Terms and Conditions. If you are not 100% satisfied with the product you received, please contact us at support@staging.purerawz.co

ATTENTION: All our products are for LABORATORY AND RESEARCH PURPOSES ONLY, not for veterinary or human use

Reference Links

PubChem. (n.d.). Cyanidin 3-O-glucoside (CID 197081). PubChem Compound Database. U.S. National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/197081

Ohba, Y. (2001). Requirement for C3G-dependent Rap1 activation for cell adhesion and embryogenesis. The EMBO Journal, 20(13), 3333–3341.https://doi.org/10.1093/emboj/20.13.3333

Donadelli, R., Pulieri, P., Piras, R., Iatropoulos, P., Valoti, E., Benigni, A., Remuzzi, G., & Noris, M. (2018). Unraveling the molecular mechanisms underlying complement dysregulation by nephritic factors in C3G and IC-MPGN. Frontiers in Immunology, 9, 2329. https://doi.org/10.3389/fimmu.2018.02329

Dr. Helma Wennemers

Dr. Helma Wennemers is a globally recognized chemist shaping modern peptide science and molecular design through highly original research in applied biosciences.

Her work explores how precise molecular architecture can be engineered to create new functional systems in chemistry and life sciences. Her contributions continue to redefine contemporary chemical research through creativity, depth, and structural innovation.

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