CAS 2096-10-8
:2-Aminoadenosine
Description:
2-Aminoadenosine is a purine nucleoside derivative characterized by the presence of an amino group at the 2-position of the adenine moiety. Its molecular formula is C10H13N5O3, and it features a ribose sugar linked to the adenine base. This compound is known for its role in various biochemical processes, particularly in cellular signaling and metabolism. It can act as a modulator of adenosine receptors, influencing physiological functions such as neurotransmission and immune responses. 2-Aminoadenosine is also studied for its potential therapeutic applications, including its effects on cancer and neurodegenerative diseases. The compound is typically soluble in water and exhibits stability under physiological conditions, making it relevant for in vitro and in vivo studies. Its CAS number, 2096-10-8, is a unique identifier that facilitates the tracking and research of this substance in scientific literature and databases. Overall, 2-Aminoadenosine is a significant molecule in biochemistry, with implications for both fundamental research and clinical applications.
Formula:C10H14N6O4
InChI:InChI=1S/C10H14N6O4/c11-7-4-8(15-10(12)14-7)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H4,11,12,14,15)/t3-,5-,6-,9-/m1/s1
InChI key:InChIKey=ZDTFMPXQUSBYRL-UUOKFMHZSA-N
SMILES:NC1=C2C(N(C=N2)[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)=NC(N)=N1
Synonyms:- (2R,3R,4S,5R)-2-(2,6-Diamino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydro-3,4-furandiol
- 2,6-Diamino-9-β-<span class="text-smallcaps">D</span>-ribofuranosylpurine
- 2,6-Diaminonebularine
- 2,6-Diaminopurine Riboside
- 2,6-Diaminopurine ribonucleoside
- 2,6-Diaminopurinosine
- 2-(2,6-Diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
- 5-(2,6-Diaminopurin-9-yl)-2-(hydroxymethyl)oxolane-3,4-diol
- 9-(β-D-Ribofuranosyl)-9H-purin-2,6-diamin
- 9-pentofuranosyl-9H-purine-2,6-diamine
- 9-β-Ribosyl-2,6-diaminopurine
- 9H-Purine, 2,6-diamino-9-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
- 9H-Purine-2,6-diamine, 9-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
- 9H-Purine-2,6-diamine, 9-β-D-ribofuranosyl-
- Adenosine, 2-amino-
- NSC 7363
- 9H-Purine, 2,6-diamino-9-β-D-ribofuranosyl-
- 2-Aminoadenosine
- (2R,3R,4S,5R)-2-(2,6-Diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
- 2-AMINOADENOSINE HPLC98+%
- See more synonyms
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Found 12 products.
2-Aminoadenosine
CAS:Formula:C10H14N6O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:282.262-Aminoadenosine, 97%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C10H14N6O4Purity:97%Color and Shape:Powder, WhiteMolecular weight:282.26Ref: IN-DA002KBV
1g25.00€5g25.00€10g26.00€25g50.00€5kgTo inquire100g112.00€10kgTo inquire25kgTo inquire2,6-Diaminopurine-riboside
CAS:<p>2,6-Diaminopurine-riboside</p>Purity:98%Molecular weight:336.73g/mol2-Aminoadenosine
CAS:<p>2-Aminoadenosine is a Nucleoside Derivative - 2-Modified purine nucleoside.</p>Formula:C10H14N6O4Color and Shape:SolidMolecular weight:282.262-Aminoadenosine
CAS:<p>2-Aminoadenosine is a synthetic nucleoside analog of adenosine in which the purine base is 2,6-diaminopurine, featuring an additional amino group at the C2 position. This modification enhances hydrogen bonding potential and alters base-pairing specificity, allowing it to form three hydrogen bonds with uracil or thymine, in contrast to adenine's two. As a result, 2-aminoadenosine has been studied for its impact on nucleic acid stability, replication fidelity, and enzymatic recognition. It has also shown potential in antiviral and anticancer research due to its ability to disrupt normal RNA and DNA metabolism.</p>Formula:C10H14N6O4Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:282.26 g/mol2-Amino Adenosine
CAS:Controlled Product<p>Applications A nucleoside analog as inhibitor or substrate of adenosine kinase from M. tuberculosis.<br>References Barrow, E., et al.: J. Antimicrob. Chemother., 252, 801 (2003), Long, M., et al.: J. Bacteriol., 185, 6548 (2003), Yadav, V., et al.: J. Med. Chem., 47, 1987 (2004),<br></p>Formula:C10H14N6O4Color and Shape:NeatMolecular weight:282.26










