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Search Results for " 2-methyl adenosine "

20

Compounds

Cat No. Product Name Synonyms Targets
TN7208 2-Methyladenosine 2-methyl adenosine Others
2-Methyladenosine (2-methyl adenosine) is a marine derived natural products found in Family Tethyidae.
TNU0419 2’-Deoxy-N6-methyl adenosine
Nucleoside Derivatives - N-Methylated nucleosides; Drugs and Inhibitors; antitumor and differentiation agent bacterial nucleoside; methylated adduct of DNA, antimalarial agent
T75033 Adenosine-2-carboxy methyl amide
Adenosine-2-carboxy methyl amide, a purine nucleoside analogue, exhibits broad antitumor activity against indolent lymphoid malignancies through mechanisms including DNA synthesis inhibition and apoptosis induction.[1]
TNU1524 2-(3-Methyl-n-butylidenehydrazino) adenosine
2-(3-Methyl-n-butylidenehydrazino) adenosine is a Nucleoside Derivative - 2-Modified purine nucleoside.
TNU0297 Adenosine-2-carboxylic acid methyl ester
Adenosine-2-carboxylic acid methyl ester is a Nucleoside Derivative - 2-Modified purine nucleoside.
TNU0554 N1-Methyl-2’-beta-C-methyl   adenosine
N1-Methyl-2'-beta-C-methyl adenosine is a Nucleoside Derivative - 2'-Modified nucleoside; N-Methylated alkylated nucleoside.
T75056 N1-Methyl-2’-beta-C-methyl adenosine
N1-Methyl-2’-beta-C-methyl adenosine, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include DNA synthesis inhibition and ind...
TNU0587 8-Chloro-2’-O-methyl   adenosine
Nucleoside Derivatives - Halo-nucleosides, 8-Modified purine nucleosides, 2’-modified nucleosides
TNU0559 N1-Methyl-2’-O-(2-methoxyethyl)   adenosine
N1-Methyl-2'-O-(2-methoxyethyl) adenosine is a Nucleoside Derivative - 2'-Modified nucleoside, N-Methylated/ alkylated nucleoside.
T75061 N1-Methyl-2’-O-(2-methoxyethyl) adenosine
N1-Methyl-2’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor effects, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthe...
TNU0560 N6-Methyl-2’-O-(2-methoxyethyl)   adenosine
N6-Methyl-2'-O-(2-methoxyethyl) adenosine is a Nucleoside Derivative - 2'-Modified nucleoside, 6-Modified purine nucleoside.
T75062 N6-Methyl-2’-O-(2-methoxyethyl) adenosine
N6-Methyl-2’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synth...
TNU0462 N6-(3-Methoxybenzyl)-2’-C-methyl adenosine
N6-(3-Methoxybenzyl)-2'-C-methyl adenosine is a Nucleoside Derivative - 6-Modified purine nucleoside; 2'-Modified nucleoside.
TNU0458 N6-(3-Trifluoromethylbenzyl)-2’-C-methyl adenosine
N6-(3-Trifluoromethylbenzyl)-2'-C-methyl adenosine is a Nucleoside Derivative - 6-Modified purine nucleoside; 2'-Modified nucleoside.
TNU0564 N6-Methyl-3’-O-(2-methoxyethyl)   adenosine
N6-Methyl-3'-O-(2-methoxyethyl) adenosine is a Nucleoside Derivative - 3'-Modified nucleoside, 6-Modified purine nucleoside.
TNU0563 N1-Methyl-3’-O-(2-methoxyethyl)   adenosine
N1-Methyl-3'-O-(2-methoxyethyl) adenosine is a Nucleoside Derivative - 3'-Modified nucleoside, N-Methylated/ alkylated nucleoside.
T75063 N1-Methyl-3’-O-(2-methoxyethyl) adenosine
N1-Methyl-3’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies. Its anticancer mechanisms primarily involve the inhibition of DNA synthesis...
TNU0585 N6-Methyl-2’-beta-C-ethynyl   adenosine
N6-Methyl-2'-beta-C-ethynyl adenosine is a Nucleoside Derivative - 2'-Modified nucleoside, 6-Modified purine nucleoside.
TNU0463 N6-(4-Methoxybenzyl)-2’-C-methyl adenosine
N6-(4-Methoxybenzyl)-2'-C-methyl adenosine is a Nucleoside Derivative - 6-Modified purine nucleoside; 2'-Modified nucleoside.
T75069 N6-Methyl-2’-beta-C-ethynyl adenosine
N6-Methyl-2’-beta-C-ethynyl adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibit...
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