1-methyladenosine

1-Methyladenosine (M1A) belongs to the class of organic compounds known as purine nucleosides.

1-Methyladenosine-D3 is the hydrochloride salt form of deuterium-labeled 1-Methyladenosine. This compound is a modification of RNA that serves as a biomarker for tumors, with elevated levels in the body linked to cancer development. Upon methylation, 1-Methyladenosine (T7571) upregulates the expression of PPARδ, regulates cholesterol metabolism, and activates the Hedgehog signaling pathway, thereby driving the onset of liver tumors.

1-Methyladenosine-D is the deuterated form of 1-Methyladenosine. This compound is an RNA modification and serves as a tumor marker, with elevated levels in the body linked to cancer development. Methylated 1-Methyladenosine (T7571) can promote liver tumor development by upregulating PPARδ expression, regulating cholesterol metabolism, and activating the Hedgehog signaling pathway.

1-Methyladenosine-D3 hydrochloride is the deuterium-labeled hydrochloride salt form of 1-Methyladenosine. This compound is known as an RNA modification and serves as a tumor marker, as elevated levels in the body are associated with cancer development. Post-methylation, 1-Methyladenosine can drive liver tumor formation by upregulating PPARδ expression, regulating cholesterol metabolism, and activating the Hedgehog signaling pathway.

1-Methyladenosine-d3hydroiodide (N1-Methyladenosine-d3hydroiodide) is the deuterium-labeled version of 1-Methyladenosine (hydroiodide).

Nucleoside Derivatives - N-Alkylated nucleosides; 2'-Modified nucleosides; Naturally modified ribo-nucloesides

3'-Deoxy-N1-methyladenosine is a Nucleoside Derivative - 3'-Modified nucleoside, N-Methylated/ alkylated nucleoside;3'-Deoxy nucleoside.

YTH-IN-1 is an inhibitor of the five YTH structural domains in the human YTHDF1, YTHDF2, YTHDF3, YTHDC1, and YTHDC2 proteins.The YTH family of proteins is an N 6-methyladenosine (m6A) reader that plays an important regulatory role in gene expression.

FTO-IN-8, also known as FTO-43, is an inhibitor of N6-methyladenosine demethylase FTO (fat mass- and obesity-associated protein). It exhibits an IC50 value of 5.5 μM and displays anti-cancer cell proliferative activity [1].

2'-O-Methyladenosine 5'-monophosphate triethyl ammonium is an adenosine analog that primarily functions as a smooth muscle vasodilator and has demonstrated potential in inhibiting cancer progression. Its notable products include adenosine phosphate, Acadesine, Clofarabine, Fludarabine phosphate, and Vidarabine [1].

2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine is an adenosine analog, known for primarily acting as a smooth muscle vasodilator and for inhibiting cancer progression. Its popular products include adenosine phosphate, Acadesine, Clofarabine, Fludarabine phosphate, and Vidarabine [1].