19916-77-9

2′-Deoxy-N-methylguanosine Chemical Structure
19916-77-9

Chemical Structure

2′-Deoxy-N-methylguanosine

  • CAS No.: 19916-77-9
  • Formula:C11H15N5O4
  • Molecular Weight:281.27

IUPAC Name: 9-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-(methylamino)-1,9-dihydro-6H-purin-6-one

InChIKey: XEZUVZDXOQPEKT-RRKCRQDMSA-N

SMILES: O[C@H]1C[C@H](N2C(N=C(NC)NC3=O)=C3N=C2)O[C@@H]1CO

Biological Activity: 2’-Deoxy-N2-methylguanosine, DNA adduct is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

Cat. No. Product Name Purity Description Pricing
HY-154406
2′-Deoxy-N-methylguanosine 99.82% 2’-Deoxy-N2-methylguanosine, DNA adduct is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
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HY-111647R
N2-Methylguanosine (Standard) ≥98% N2-Methylguanosine (Standard) is the analytical standard of N2-Methylguanosine (HY-111647). This product is intended for research and analytical applications. N2-Methylguanosine is a commonly modified nucleoside in rRNA and tRNA, with specific distributions in both E. coli rRNA and eukaryotic tRNA. N2-Methylguanosine can be found in urine. N2-Methylguanosine affects the structure and stability of RNA.
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HY-154392
2-Chloro-2’-deoxy inosine 2-Chloro-2’-deoxy inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
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HY-154407
2’-Deoxy-N2,N2-dimethylguanosine 2’-Deoxy-N2,N2-dimethylguanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
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HY-154428
2'-Deoxy-N2-isopropyl guanosine 2’-Deoxy-N2-isopropyl guanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
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HY-154429
2'-Deoxy-N2,N2-diethyl guanosine 2’-Deoxy-N2,N2-diethyl guanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
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HY-17563R
2'-Deoxyguanosine (Standard) 99.21% 2'-Deoxyguanosine (Standard) is the analytical standard of 2'-Deoxyguanosine. This product is intended for research and analytical applications. 2’-Deoxyguanosine (Deoxyguanosine) is a purine nucleoside with a variety of biological activities. 2’-Deoxyguanosine can induce DNA division in mouse thymus cells. 2’-Deoxyguanosine is a potent cell division inhibitor in plant cells. In Vitro: 2'-Deoxyguanosine inhibits the clonal growth of HL-60 and K562 leukemia cells with IC50 values of 50 and 80 μM, respectively.
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HY-17563S1
2'-Deoxyguanosine-13C10,15N5 2'-Deoxyguanosine-13C10,15N5 (Deoxyguanosine-13C10,15N5; Guanine deoxyriboside-13C10,15N5) is a 13C- and 15N-labeled 2'-Deoxyguanosine (HY-17563).
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HY-17563S2
2'-Deoxyguanosine-13C10 99.8% 2'-Deoxyguanosine-13C10 (Deoxyguanosine-13C10; Guanine deoxyriboside-13C10) is 13C-labeled 2'-Deoxyguanosine (HY-17563). 2'-Deoxyguanosine (Deoxyguanosine) is deoxyguanosine.
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HY-17563S4
2'-Deoxyguanosine-15N5 99.80% 2'-Deoxyguanosine-15N5 (Deoxyguanosine-15N5; Guanine deoxyriboside-15N5) is 15N labeled 2'-Deoxyguanosine (HY-17563). 2'-Deoxyguanosine (Deoxyguanosine) is deoxyguanosine.
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HY-D0185
2'-Deoxyguanosine monohydrate 99.70% 2'-Deoxyguanosine monohydrate is a nucleoside composed of guanine and 2'-deoxyribose, and it is one of the basic structural units of DNA. The oxidation products of 2'-Deoxyguanosine monohydrate may participate in DNA damage, which in turn may affect gene expression or induce cancer.
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References