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5-carboxypyranopetunidin 3-O-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 403982-49-0 Structure
  • Basic information

    1. Product Name: 5-carboxypyranopetunidin 3-O-β-D-glucopyranoside
    2. Synonyms:
    3. CAS NO:403982-49-0
    4. Molecular Formula:
    5. Molecular Weight: 547.449
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 403982-49-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-carboxypyranopetunidin 3-O-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-carboxypyranopetunidin 3-O-β-D-glucopyranoside(403982-49-0)
    11. EPA Substance Registry System: 5-carboxypyranopetunidin 3-O-β-D-glucopyranoside(403982-49-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 403982-49-0(Hazardous Substances Data)

403982-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403982-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,9,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 403982-49:
(8*4)+(7*0)+(6*3)+(5*9)+(4*8)+(3*2)+(2*4)+(1*9)=150
150 % 10 = 0
So 403982-49-0 is a valid CAS Registry Number.

403982-49-0Downstream Products

403982-49-0Relevant articles and documents

Antioxidant and cellular activities of anthocyanins and their corresponding vitisins A - Studies in platelets, monocytes, and human endothelial cells

Garcia-Alonso, Maria,Rimbach, Gerald,Rivas-Gonzalo, Julian C.,De Pascual-Teresa, Sonia

, p. 3378 - 3384 (2004)

During red wine aging, there is a loss of anthocyanins and the formation of various other pigments, so-called vitisins A, which are formed through the chemical interaction of the original anthocyanins with pyruvic acid. The objective of this study was to investigate the antioxidant activities of the most abundant anthocyanins present in red wine (glycosides of delphinidin, petunidin, and malvidin) and their corresponding vitisins A. Anthocyanins exhibited a higher iron reducing as well as 2,2′-azinobis (3-ethyl-benzothiazoline-6-sulfonate) and peroxyl radical scavenging activity than their corresponding vitisins A. Delphinidin showed the highest antioxidant effect of the tested compounds in all of the assays used, Furthermore, we studied the effect of anthocyanins and vitisins A on platelet aggregation and monocyte and endothelial function. Anthocyanins and vitisins did not affect nitric oxide production and tumor necrosis factor-α (TNF-α) secretion in lipopolysaccharide plus interferon-γ-activated macrophages. Furthermore, anthocyanins and vitisins did not change collagen-induced platelet aggregation in vitro. However, anthocyanins and to a lesser extent vitisins exhibited protective effects against TNF-α-induced monocyte chemoattractant protein production in primary human endothelial cells.

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