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inhibitory and anti-HIV effects on leukemia L1210 cells Oxanosine

Date:July 03 2020Web Page No:520045

Oxanosine isolated from the culture broth of Streptomyces capreolus MG265-CF3 was reported as a novel nucleoside. The structure of oxanosine is similar to guanine, a nucleobase, with the nitrogen (N) next to the carbonyl group changs to oxygen (O), and the sugar has the same ribose structure as RNA by X-ray analysis 1). Even in recent years, studies on oxanosine derivatives have been reported 2).

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Oxanosine (Inhibitor for GMP synthetase and inosine monophosphate (IMP) dehydrogenase)

Specification

CAS#80394-72-5
Molecular FormulaC10H12N4O6
Molecular Weight284.227
SourceStreptomyces capreolus MG265-CF3
Purity> 98% (HPLC)
SolubilitySoluble in H2O, MeOH, DMSO
Insoluble in CHCl3

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Application Note

  • Antibacterial activity against Eschericia.coli K-12.3)
  • Cell growth inhibitory activity against HeLa cells (IC50:32 μg/ml).3)
  • Inhibits proliferation of mouse leukemia L1210 cells (Ki:7.4×10-4 M).3)
  • Competitive inhibitor of GMP synthetase (Ki:7.4×10-4 M).4)
  • Induces a reversion toward the normal phenotype of K-ras-transformed rat kidney cells.5)
  • Inhibits HIV-1 replication against CEM cells and U937 cells (EC50:7.0 μg/ml(CEM), EC50:27 μg/ml(U937)).6)
  • Oxanosine alone did not affect HIV replication in HIV-infected H9 cells up to 100 μg/ml, in contrast, the compound showed concentration-dependent inhibition of HIV (1~100 μg/ml) without cytotoxicity in the presence of 2′, 3′-dideoxyinosine.7)

* Biological activity of the product was not verified. The values shown above were cited from the references.


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Reference

  1. Nakamura, H. et al., J. Antibiot., 34(9), 1219-1221(1981). [PMID:7328061]
  2. Yu, R. et al., Chem. Res. Toxicol., 32(3), 456-466(2019). [PMID:30746940]
  3. Shimada, N. et al., J. Antibiot., 34(9), 1216-1218(1981). [PMID:7328060]
  4. Yagisawa, N. et al., J. Antibiot., 35(6), 755-759(1982). [PMID:6288649]
  5. Itoh, O. et al., Cancer Res., 49(4), 996-1000(1989). [PMID:2643467]
  6. Saito, Y. et al., J. Antibiot., 53(3), 309-313(2000). [PMID:10819305]
  7. Nakamura, M. et al., Biomed. Pharmacother., 59(1-2), 47-50(2005). [PMID:15740935]

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[Date : May 19 2026 00:10]

Detail Product Name Product Code Supplier Size Price
Oxanosine, Antitumor, GMP Synthase Inhibitor
DatasheetThis may not be the latest data sheet.
00762 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 284.23 Purity : > 98% (HPLC) Molecular Formula : C10H12N4O6 Solubility : Soluble in H2O, Methanol, and DMSO, Insoluble in CHCl3. Inhibitory activity of leukemia L210 : IC50=1.0 μg/ml, Competitive inhibitory activity of GMP synthase : Ki=7.4x10-4 M. Oxanosine was isolated from culture broth of Streptomyces capreolus MG265-CF3 and was reported as a novel nucleoside. It was also reported that this compound has an inhibitory activity of HIV replication and leukemia L1210 cell growth.
Storage -20°C CAS 80394-72-5
Link

Bioactive Compounds

[Date : May 19 2026 00:10]

Oxanosine, Antitumor, GMP Synthase Inhibitor


  • Product Code: 00762
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 284.23 Purity : > 98% (HPLC) Molecular Formula : C10H12N4O6 Solubility : Soluble in H2O, Methanol, and DMSO, Insoluble in CHCl3. Inhibitory activity of leukemia L210 : IC50=1.0 μg/ml, Competitive inhibitory activity of GMP synthase : Ki=7.4x10-4 M. Oxanosine was isolated from culture broth of Streptomyces capreolus MG265-CF3 and was reported as a novel nucleoside. It was also reported that this compound has an inhibitory activity of HIV replication and leukemia L1210 cell growth.
Storage -20°C CAS 80394-72-5
Link

Bioactive Compounds

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