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4338-48-1

4338-48-1 structure
4338-48-1 structure
  • Name: N6-(2-Hydroxyethyl)adenosine
  • Chemical Name: (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
  • CAS Number: 4338-48-1
  • Molecular Formula: C12H17N5O5
  • Molecular Weight: 311.29
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
  • Create Date: 2018-06-16 17:23:33
  • Modify Date: 2024-01-09 10:14:23
  • N6-(2-Hydroxyethyl)adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

Name (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
Synonyms (2R,3R,4S,5R)-2-[6-(2-hydroxyethylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol
Description N6-(2-Hydroxyethyl)adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog
References

[1]. Man S, et al. Potential and promising anticancer drugs from adenosine and its analogs. Drug Discov Today. 2021 Jun;26(6):1490-1500.  

[2]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.  

Density 1.88g/cm3
Boiling Point 725.8ºC at 760 mmHg
Melting Point 194-195ºC
Molecular Formula C12H17N5O5
Molecular Weight 311.29
Flash Point 392.7ºC
Exact Mass 311.12300
PSA 145.78000
Index of Refraction 1.806
Hazard Codes Xi

~94%

4338-48-1 structure

4338-48-1

Literature: Fujii, Tozo; Saito, Tohru; Terahara, Norihiko Chemical & Pharmaceutical Bulletin, 1986 , vol. 34, # 3 p. 1094 - 1107

~50%

4338-48-1 structure

4338-48-1

Literature: Fujii, Tozo; Saito, Tohru; Terahara, Norihiko Chemical & Pharmaceutical Bulletin, 1986 , vol. 34, # 3 p. 1094 - 1107