CAS 14365-44-7
:5'-AMINOADENOSINE
Description:
5'-Aminoadenosine, with the CAS number 14365-44-7, is a purine nucleoside that consists of an adenine base attached to a ribose sugar with an amino group at the 5' position. This compound is characterized by its role in various biochemical processes, particularly in cellular metabolism and signaling pathways. It is a derivative of adenosine, which is a crucial molecule in energy transfer and signal transduction in cells. The presence of the amino group can influence its interaction with enzymes and receptors, potentially affecting its biological activity. 5'-Aminoadenosine is soluble in water and exhibits polar characteristics due to its hydroxyl groups and amino group, making it interact well with other polar molecules. Its structural features allow it to participate in the synthesis of nucleotides and nucleic acids, contributing to cellular functions such as protein synthesis and energy metabolism. Overall, 5'-Aminoadenosine is significant in biochemical research and may have implications in therapeutic applications.
Formula:C10H14N6O3
InChI:InChI=1/C10H14N6O3/c11-1-4-6(17)7(18)10(19-4)16-3-15-5-8(12)13-2-14-9(5)16/h2-4,6-7,10,17-18H,1,11H2,(H2,12,13,14)
SMILES:C(C1C(C(C(n2cnc3c(N)ncnc23)O1)O)O)N
Synonyms:- 5'-Nh-Ado
- 5’-Amino-5’-Deoxyadenosine
- 5'-Amino-5'-Deoxy-D-Adenosine
- 9-(5-amino-5-deoxypentofuranosyl)-9H-purin-6-amine
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Found 5 products.
5'-Amino-5'-deoxyadenosine
CAS:Formula:C10H14N6O3Purity:92%Color and Shape:SolidMolecular weight:266.25665''-Amino-5''-deoxyadenosine
CAS:Formula:C10H14N6O3Purity:≥ 98.0% (HPLC)Color and Shape:White powderMolecular weight:266.265'-Amino-5'-deoxyadenosine
CAS:<p>5'-Amino-5'-deoxyadenosine (NH2dAdo) is an adenosine kinase inhibitor targeting malignant tumors of the inert lymphatic system with antitumor and anticancer</p>Formula:C10H14N6O3Purity:95.55%Color and Shape:SolidMolecular weight:266.265'-Amino-5'-deoxyadenosine hydrochloride
CAS:<p>5'-Amino-5'-deoxyadenosine hydrochloride (5'-ADeA) is a nucleotide that is synthesized from ribose 5-phosphate and adenosine monophosphate. It has been shown to have potential as a biomarker for skin cancer. The synthesis of 5'-ADeA is catalyzed by the enzyme caffeic acid 4-monooxygenase, which converts caffeic acid into 5'-ADeA. This reaction requires molecular oxygen, NADPH, and iron ions. The activity of this enzyme can be inhibited by sodium carbonate or basic fibroblast growth factor (bFGF). This drug has been shown to have anti-inflammatory effects in vivo.</p>Formula:C10H14N6O3Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:266.26 g/mol




