Welcome to LookChem.com Sign In|Join Free
  • or
α-D-Fructofuranose 6-phosphate, also known as D-fructose 6-phosphate or F6P, is an important intermediate in the metabolism of glucose. It is formed during the first step of glycolysis, where the enzyme hexokinase or glucokinase phosphorylates glucose at the sixth carbon atom, converting it into glucose 6-phosphate. This molecule then undergoes an isomerization reaction catalyzed by phosphohexose isomerase, resulting in the formation of fructose 6-phosphate. In its α-D-fructofuranose form, the molecule has a furanose ring structure, which is a key component in various metabolic pathways, including glycolysis, gluconeogenesis, and the pentose phosphate pathway. α-D-fructofuranose 6-phosphate plays a crucial role in energy production and the synthesis of essential biomolecules within cells.

41452-28-2

Post Buying Request

41452-28-2 Suppliers

Recommended suppliers

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

41452-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41452-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41452-28:
(7*4)+(6*1)+(5*4)+(4*5)+(3*2)+(2*2)+(1*8)=92
92 % 10 = 2
So 41452-28-2 is a valid CAS Registry Number.

41452-28-2Downstream Products

41452-28-2Relevant academic research and scientific papers

Competitive inhibitors of type B ribose 5-phosphate isomerases: design, synthesis and kinetic evaluation of new d-allose and d-allulose 6-phosphate derivatives

Mariano, Sandrine,Roos, Annette K.,Mowbray, Sherry L.,Salmon, Laurent

experimental part, p. 869 - 880 (2009/08/07)

This study reports syntheses of d-allose 6-phosphate (All6P), d-allulose (or d-psicose) 6-phosphate (Allu6P), and seven d-ribose 5-phosphate isomerase (Rpi) inhibitors. The inhibitors were designed as analogues of the 6-carbon high-energy intermediate pos

Anomerization of Furanose Sugars and Sugar Phosphates

Pierce, John,Serianni, Anthony S.,Barker, Robert

, p. 2448 - 2456 (2007/10/02)

Thermodynamic and kinetic parameters for the ring-opening and -closing reactions of several aldo- and ketofuanoses and their phosphate esters have been determined by NMR line-width and saturation-transfer methods.Cyclic forms interconvert via a single, acyclic carbonyl form under either acid or base catalysis.Ring-opening rates do not correlate with thermodynamic stability of the rings.For aldofuranose phosphates, α anomers open faster than β anomers; for ketofuranose phosphates the converse is observed.Intramolecular catalysis of anomerization by the phosphate group of sugar phosphates is documented.Biological and mechanistic implications of the observed kinetics are discussed.

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 41452-28-2