232617-15-1 Usage
Description
RibCys, also known as D-Ribose-L-cysteine, is a prodrug of L-cysteine with potential therapeutic advantages in various medical applications. It is a combination of D-ribose, a five-carbon sugar, and L-cysteine, an amino acid. This unique combination endows RibCys with properties that make it a promising candidate for treating certain health conditions.
Uses
Used in Oncology:
RibCys is used as an anti-cancer agent for the inhibition of astrocytoma cell proliferation. Astrocytoma is a type of brain cancer, and RibCys has demonstrated potential therapeutic advantages in this application, making it a valuable tool in the fight against this aggressive form of cancer.
Used in Hepatic and Renal Protection:
RibCys is used as a protective agent against acetaminophen-induced hepatic (liver) and renal (kidney) toxicity. Acetaminophen is a common pain reliever and fever reducer, but in high doses, it can cause severe damage to the liver and kidneys. RibCys has been shown to help protect these vital organs from the harmful effects of acetaminophen overdose, offering a potential therapeutic solution for those at risk of organ damage due to the use of this medication.
Check Digit Verification of cas no
The CAS Registry Mumber 232617-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,6,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 232617-15:
(8*2)+(7*3)+(6*2)+(5*6)+(4*1)+(3*7)+(2*1)+(1*5)=111
111 % 10 = 1
So 232617-15-1 is a valid CAS Registry Number.
232617-15-1Relevant articles and documents
Methods Of Preparing Thiazolidines
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Page/Page column 5-6, (2011/08/06)
The present invention provides methods of preparing thiazolidines, and in particular methods of preparing ribose-cysteine.
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.
