Welcome to LookChem.com Sign In|Join Free
  • or
3-(benzo[d][1,3]dioxol-5-yl)-4-oxo-4H-chromen-7-yl acetate is a complex organic compound with the molecular formula C17H10O7. It is a derivative of the flavone class of compounds, characterized by the presence of a benzo[d][1,3]dioxole ring and a chromene core. This specific compound features an acetate group attached to the 7-yl position of the chromene ring. It is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, which are being studied for their potential applications in pharmaceuticals and cosmetology. The compound's structure and properties make it a subject of interest in the field of natural product chemistry and drug development.

5574-40-3

Post Buying Request

5574-40-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5574-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5574-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5574-40:
(6*5)+(5*5)+(4*7)+(3*4)+(2*4)+(1*0)=103
103 % 10 = 3
So 5574-40-3 is a valid CAS Registry Number.

5574-40-3Downstream Products

5574-40-3Relevant academic research and scientific papers

The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone

Mays, Jared R.,Hill, Stephanie A.,Moyers, Justin T.,Blagg, Brian S.J.

experimental part, p. 249 - 266 (2010/04/05)

The natural products novobiocin and derrubone have both demonstrated Hsp90 inhibition and structure-activity relationships have been established for each scaffold. Given these compounds share several key structural features, we hypothesized that incorporation of elements from each could provide insight to structural features important for Hsp90 inhibition. Thus, chimeric analogues of novobiocin and derrubone were constructed and evaluated. These studies confirmed that the functionality present at the 3-position of the isoflavone plays a critical role in determining Hsp90 inhibition and suggests that the bicyclic ring system present in both novobiocin and derrubone do not share similar modes of binding.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5574-40-3