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Results for "

5'-amino-5'-deoxyadenosine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7
    TargetMol | All_Pathways
  • Cell Research
    3
    TargetMol | Cell_Research_Reagents
  • Reference Standards
    1
    TargetMol | Standard_Products
5'-Amino-5'-deoxyadenosine
Nsc 238990, NH2dAdo, 5'Amino5'deoxyadenosine, 5' Amino 5' deoxyadenosine
T2101714365-44-7
5'-Amino-5'-deoxyadenosine (NH2dAdo) is an adenosine kinase inhibitor targeting malignant tumors of the inert lymphatic system with antitumor and anticancer effects. Its mechanism is mediated by the inhibition of DNA synthesis and induction of apoptosis.
  • $108
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Anisodine hydrobromide
T2101876822-34-9
Anisodine hydrobromide is an inhibitor of adenosine kinase.
  • $1,520
6-8 weeks
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2'-NH2-ATP
2'-NH2-ATP, 2'-Amino-2'-deoxyadenosine-5'-triphosphate
T4069661468-88-0
2'-NH2-ATP (2'-Amino-2'-deoxyadenosine-5'-triphosphate) is an adenosine derivative that functions as a weak competitive inhibitor of ATP, with a K i value of 2.3 mM, and is used in nucleic acid labeling.
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Anisodine hydrobromide (Standard)
TMSM-310576822-34-9
Anisodine hydrobromide (Standard) is a reference standard for research and analysis in studies involving Anisodine hydrobromide. 5'-Amino-5'-deoxyadenosine is an inhibitor of adenosine kinase.
  • $756
7-10 days
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7-CH-dADP trisodium
7-Deaza-2'-deoxyadenosine-5'-O-diphosphate trisodium
TSW-01108
7-CH-dADP (7-Deaza-2'-deoxyadenosine-5'-O-diphosphate) trisodium is a derivative of the nucleotide ADP, formed by the removal of hydroxyl and amino groups.
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2'-Amino-2'deoxyadenosine-5'-O-diphosphate sodium
2'-NH2-ADP sodium
TSW-01128
2'-Amino-2'-deoxyadenosine-5'-O-diphosphate (2'-NH2-ADP) sodium is an amine-modified nucleotide, serving as a structural analog of the purine nucleotide ADP.
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3'-Amino-3'-deoxyadenosine-5'-O-diphosphate sodium
TSW-01152
3'-Amino-3'-deoxyadenosine-5'-O-diphosphate sodium is an amine-modified nucleotide that can be utilized in the synthesis of other active compounds. Its coumarin-labeled derivative exhibits significant fluorescence changes when interacting with myosin, effectively mimicking the function of natural ADP.
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