17087-37-5 Usage
Uses
Used in Pharmaceutical Industry:
(1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is used as a potential therapeutic agent for the treatment of diabetes and metabolic disorders. Its ability to inhibit certain enzymes and modulate cellular processes makes it a candidate for further research and development in this field.
Used in Enzyme Inhibition Research:
In the field of biochemistry, (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is utilized for studying enzyme inhibition. Its structure allows it to interact with specific enzymes, providing insights into enzyme function and potential therapeutic targets.
Used in Cellular Process Modulation:
(1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is also used in cellular biology to investigate its effects on cellular processes. Understanding how (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol influences cellular mechanisms could lead to the development of new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 17087-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17087-37:
(7*1)+(6*7)+(5*0)+(4*8)+(3*7)+(2*3)+(1*7)=115
115 % 10 = 5
So 17087-37-5 is a valid CAS Registry Number.
17087-37-5Relevant academic research and scientific papers
Proton and Zinc(II) Complexes of 2-(Polyhydroxyalkyl)thiazolidine-4-carboxylic acid Derivatives
Gajda, Tamas,Nagy, Laszlo,Burger, Kalman
, p. 3155 - 3160 (2007/10/02)
The protonation and zinc-ion co-ordination equilibria of 2-(polyhydroxyalkyl)thiazolidine-4-carboxylic acid derivatives have been studied by potentiometric titration in the range pH 1.5-8.In most cases the formation of complexes with a metal-to-ligand ratio of 1:2 was demonstrated, but at above pH 6 mixed-ligand complexes involving hydroxide-ion co-ordination were also observed.The protonation and complex-formation constants were shown to depend on the structure of the polyhydroxy chains.In the case of the protonation constants this is due to the rearrangement of the intramolecular hydrogen-bonding network, while the complex-formation constants depend on the conformation of the OH groups on the first carbon atoms of the polyol chains.
