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28585-51-5

28585-51-5 structure
28585-51-5 structure
  • Name: 2-Thiothymidine
  • Chemical Name: 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-sulfanylidenepyrimidin-4-one
  • CAS Number: 28585-51-5
  • Molecular Formula: C10H14N2O4S
  • Molecular Weight: 258.29
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
  • Create Date: 2018-07-15 16:17:55
  • Modify Date: 2026-07-16 14:27:57
  • 2-Thiothymidine 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 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-sulfanylidenepyrimidin-4-one
Synonyms 1-((2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
2-THIOTHYMIDINE
1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-4-one
2-thiothymidine
2-Thio-desoxythymidin
Thymidine,2-thio
Thymidine, 2-thio
2'-deoxy-5-methyl-2-thiouridine
1-(2-Deoxy-b-D-erythro-pentofuranosyl)-5-methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone
1-[(2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-sulfanylidenyrimidin-4-one
2-Thio-2'-deoxythymidine
2-Thiothymidin
Description 2-Thiothymidine 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]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.  

Density 1.52 g/cm3
Molecular Formula C10H14N2O4S
Molecular Weight 258.29
Exact Mass 258.06700
PSA 119.57000
Index of Refraction 1.672

~%

28585-51-5 structure

28585-51-5

Literature: Hatano, Akihiko; Kurosu, Masayuki; Yonaha, Susumu; Okada, Munehiro; Uehara, Sanae Organic and Biomolecular Chemistry, 2013 , vol. 11, # 40 p. 6900 - 6905

~59%

28585-51-5 structure

28585-51-5

Literature: Hatano, Akihiko; Harano, Aiko; Kirihara, Masayuki Chemistry Letters, 2006 , vol. 35, # 2 p. 232 - 233
Precursor  2

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