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6 chloropurine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    24
    TargetMol | All_Pathways
  • Cell Research
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    TargetMol | Cell_Research_Reagents
6-Chloropurine
6-Chloro-9H-purine
T747087-42-3
6-Chloropurine (6-Chloro-9H-purine) is a building block in chemical synthesis,with Antitumor activities.
  • $29
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TargetMol | Inhibitor Sale
2-Amino-6-chloropurine
T3727710310-21-1
2-Amino-6-chloropurine is a precursor in the synthesis of nucleoside analogs with antiviral activity against Epstein-Barr virus (EBV) and human herpes virus 6 (HHV-6).1 1.Qiu, Y.-L., Ksebati, M.B., Ptak, R.G., et al.(Z)- and (E)-2-((hydroxymethyl)cyclopropylidene)methyladenine and -guanine. New nucleoside analogues with a broad-spectrum antiviral activityJ. Med. Chem.41(1)10-23(1998)
  • $35
7-10 days
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9-(5(R)-C-Methyl-2,3,5-tri-O-benzoyl-D-ribofuranosyl)-6-chloropurine
T75231
9-(5(R)-C-Methyl-2,3,5-tri-O-benzoyl-D-ribofuranosyl)-6-chloropurine, a purine nucleoside analog, demonstrates broad antitumor activity, particularly against indolent lymphoid malignancies, through inhibition of DNA synthesis and induction of apoptosis. [1]
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6-Chloropurine riboside
T78265399-87-1
6-Chloropurine riboside (6-CPR) is a purine nucleoside analog that has been found to have a wide range of biological activities. It inhibits the growth of tumor cells and induces apoptosis. It has also been shown to have anti-inflammatory, antiviral and antifungal properties. It has also been found to be neuroprotective and has been used in the treatment of neurological disorders.
  • $29
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6-Chloropurine riboside-5'-triphosphate sodium
6-chloro PuTP
T83815
6-Chloropurine riboside-5'-triphosphate serves as both an inhibitor and an activator in biochemical processes. It inhibits the RNA triphosphatase mRNA-capping enzyme subunit β (Cet1; IC50 = 2 µM for the GTPase activity of the S. cerevisiae enzyme), proving its efficacy against the enzyme responsible for the capping of mRNA molecules. Additionally, it acts as a phosphorylated derivative of 6-chloropurine riboside. This compound also activates the E. coli enzyme aspartate carbamoyltransferase (EC50 = 0.76 mM), demonstrating its versatility in modulating enzyme activities. It is instrumental in the synthesis of cytokinins with anticancer properties and a photoclickable form of ATP, highlighting its applications in biochemical synthesis and potential therapeutic uses.
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3-6 months
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2-Amino-6-chloropurine-9-(2'-O-methyl)riboside
TNU0048194034-59-8
2-Amino-6-chloropurine-9-(2'-O-methyl)riboside is a Halo-nucleoside; 2'-O-Methyl nucleoside.
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7-10 days
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2-Amino-6-chloropurine -9-beta-D-(2'-deoxy-2'-fluoro)-arabinoriboside
TNU0082144924-88-9
2-Amino-6-chloropurine -9-beta-D-(2'-deoxy-2'-fluoro)-arabinoriboside is a Fluoro-modified nucleoside; Halo-nucleoside; Arabino-nucleoside.
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7-10 days
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2-Amino-6-chloropurine -9-beta-D-(2'-deoxy-3',5'-di-O-benzoyl-2'-fluoro)arabinoriboside
TNU0751118373-61-8
2-Amino-6-chloropurine -9-beta-D-(2'-deoxy-3',5'-di-O-benzoyl-2'-fluoro)arabinoriboside is a fluoro-modified nucleoside, halo-nucleoside, and arabino-nucleoside.
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7-10 days
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6-Chloropurine -9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside
TNU0753135473-15-3
6-Chloropurine -9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside is a Fluoro-modified nucleoside; Halo-nucleoside; Arabino-nucleoside.
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7-10 days
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2-Amino-6-chloropurine-9-beta-D-(2'-deoxy-3',5'-di-(O-p-toluoyl))riboside
TNU075635095-93-3
2-Amino-6-chloropurine-9-beta-D-(2'-deoxy-3',5'-di-(O-p-toluoyl))riboside is a 2'-deoxy nucleoside and halo-nucleoside.
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7-10 days
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2-Amino-6-chloropurine-9-beta-D-(2'-deoxy)riboside
TNU0757120595-72-4
2-Amino-6-chloropurine-9-beta-D-(2'-deoxy)riboside is a 2'-deoxy nucleoside and halo-nucleoside.
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7-10 days
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9-(2'-O-Acetyl-5'-O-benzoyl-3'-deoxy-beta-D-ribofuranosyl)-6-chloropurine
TNU09811347118-41-5
9-(2'-O-Acetyl-5'-O-benzoyl-3'-deoxy-beta-D-ribofuranosyl)-6-chloropurine is a Nucleoside Derivative used as a 3'-Deoxy nucleoside, Halo-nucleoside, scaffold, and template.
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7-10 days
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9-(5(R)-C-Methyl-2,3,5-tri-O-benzoyl-b-D-ribofuranosyl)-6-chloropurine
TNU0992
9-(5(R)-C-Methyl-2,3,5-tri-O-benzoyl-b-D-ribofuranosyl)-6-chloropurine is a useful organic compound for research related to life sciences and the catalog number is TNU0992.
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7-10 days
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(S)-9-(2,3-Dihydroxypropyl)-2-amino-6-chloropurine
TNU1436885322-01-0
(S)-9-(2,3-Dihydroxypropyl)-2-amino-6-chloropurine is a Nucleoside Derivative - Acyclic nucleoside.
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7-10 days
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9-(2,5-Di-O-benzoyl-2-C-beta-ethynyl-beta-D-ribofuranosyl)-6-chloropurine
TNU1616
9-(2,5-Di-O-benzoyl-2-C-beta-ethynyl-beta-D-ribofuranosyl)-6-chloropurine is a useful organic compound for research related to life sciences and the catalog number is TNU1616.
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7-10 days
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9-(2,3-Di-O-acetyl-6-O-benzoyl-5-deoxy-D-ribo-exofuranoyl)-6-chloropurine
TNU1673
9-(2,3-Di-O-acetyl-6-O-benzoyl-5-deoxy-D-ribo-exofuranoyl)-6-chloropurine is an organic compound useful for life sciences research (catalog number: TNU1673).
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7-10 days
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2-Amino-6-chloropurine-9-(2'-O-propargyl)riboside
TNU02062095417-35-7
Nucleoside Derivatives - 2'-Modified nucleosides, Halo-nucleosides; Scaffolds and Templates
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7-10 days
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2-Amino-6-chloropurine-3',5'-di-O-acetyl-2'-deoxyriboside
TNU071969992-11-6
Nucleoside - 2'-deoxy nucleoside; halo nucleoside
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7-10 days
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9-(2'-O-Acetyl-5'-O-benzoyl-3'-O-methyl-beta-D-ribofuranosyl)-6-chloropurine
TNU07322072145-46-9
Nucleosides - 3'-O-methyl nucleoside; halo-nucleoside
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7-10 days
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9-(2-O-Acetyl-5-O-toluyl-3-deoxy-3-fluoro-beta-D-ribofuranosyl)-2-amino-6-chloropurine
TNU07691612192-25-2
Fluoro-modified nucleoside; Halo-nucleoside
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7-10 days
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6-Chloroguanineriboside
TNU00232004-07-1
6-Chloroguanineriboside is a Halo nucleoside.
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7-10 days
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2′,3′,5′-Tri-O-acetyl-6-chloroguanosine
TNU078716321-99-6
2',3',5'-Tri-O-acetyl-6-chloroguanosine is a Halo-nucleoside.
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7-10 days
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3,5-O-Ditoluoyl 6-chloropurine-9-β-D-deoxyriboside
TNU142691713-46-1
3,5-O-Ditoluoyl 6-chloropurine-9-β-D-deoxyriboside is a nucleoside derivative classified under other modified nucleosides.
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7-10 days
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6-chloro-purine-9-b-D-(2-O-acetyl-3,5-di-O-benzoyl)xylo-furanoside
TNU1002132370-61-7
Nucleoside Derivatives - Xylo-nucleoside; Halo-nucleoside; Scaffolds and Templates
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7-10 days
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