85504-89-8 Usage
Description
(1R)-1-C-(4-Carboxythiazolidin-2-yl)-L-arabinitol is a chemical compound that belongs to the class of thiazolidine carboxylic acids. It is an enantiomer of a naturally occurring compound known as D-pinitol, which has been found to have potential therapeutic effects in the treatment of various metabolic disorders. This chemical has been studied for its anti-diabetic and anti-inflammatory properties, and it has shown promising results in preclinical studies. Additionally, it has been investigated for its potential use in the development of new pharmaceutical drugs for the treatment of diabetes and other related conditions.
Uses
Used in Pharmaceutical Industry:
(1R)-1-C-(4-Carboxythiazolidin-2-yl)-L-arabinitol is used as a potential therapeutic agent for the treatment of various metabolic disorders, particularly diabetes and related conditions. Its anti-diabetic and anti-inflammatory properties make it a promising candidate for the development of new pharmaceutical drugs.
Used in Research and Development:
(1R)-1-C-(4-Carboxythiazolidin-2-yl)-L-arabinitol is used in preclinical studies to investigate its potential therapeutic effects and to further understand its anti-diabetic and anti-inflammatory properties. This research can contribute to the development of new treatments and therapies for metabolic disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 85504-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85504-89:
(7*8)+(6*5)+(5*5)+(4*0)+(3*4)+(2*8)+(1*9)=148
148 % 10 = 8
So 85504-89-8 is a valid CAS Registry Number.
85504-89-8Relevant articles and documents
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.
