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Thymidine glycol monophosphate (TgMP) is a modified nucleoside monophosphate that results from the oxidation of thymidine, a DNA base. It is formed when thymidine undergoes a chemical reaction with reactive oxygen species, such as hydroxyl radicals, leading to the addition of two hydroxyl groups to the 5,6-double bond of the pyrimidine ring. This modification can cause mispairing during DNA replication, potentially leading to mutations. TgMP is considered a biomarker of oxidative DNA damage and is studied for its role in various diseases, including cancer, as well as in the context of aging and environmental stressors.

6168-31-6

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6168-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6168-31-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6168-31:
(6*6)+(5*1)+(4*6)+(3*8)+(2*3)+(1*1)=96
96 % 10 = 6
So 6168-31-6 is a valid CAS Registry Number.

6168-31-6Downstream Products

6168-31-6Relevant academic research and scientific papers

Thymidine radical formation via one-electron transfer oxidation photoinduced by pterin: Mechanism and products characterization

Serrano, Mariana P.,Vignoni, Mariana,Lorente, Carolina,Vicendo, Patricia,Oliveros, Esther,Thomas, Andrés H.

, p. 418 - 431 (2016)

UV-A radiation (320-400 nm), recognized as a class I carcinogen, induces damage to the DNA molecule and its components through different mechanisms. Pterin derivatives are involved in various biological functions, including enzymatic processes, and it has been demonstrated that oxidized pterins may act as photosensitizers. In particular, they accumulate in the skin of patients suffering from vitiligo, a chronic depigmentation disorder. We have investigated the ability of pterin (Ptr), the parent compound of oxidized pterins, to photosensitize the degradation of the pyrimidine nucleotide thymidine 5′-monophosphate (dTMP) in aqueous solutions under UV-A irradiation. Although thymine is less reactive than purine nucleobases, our results showed that Ptr is able to photoinduce the degradation of dTMP and that the process is initiated by an electron transfer from the nucleotide to the triplet excited state of Ptr. In the presence of molecular oxygen, the photochemical process leads to the oxidation of dTMP, whereas Ptr is not consumed. In the absence of oxygen, both compounds are consumed to yield a product in which the pterin moiety is covalently linked to the thymine. This compound retains some of the spectroscopic properties of Ptr, such as absorbance in the UV-A region and fluorescence properties.

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