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Aristeromycin (CAS 19186-33-5)

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Application:
Aristeromycin is an antibacterial adenosine analog
CAS Number:
19186-33-5
Molecular Weight:
265.27
Molecular Formula:
C11H15N5O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Aristeromycin is a carbocyclic analogue of adenosine that exhibits antibacterial properties. Aristeromycin is derived from the nucleoside adenosine by replacing the ribose sugar with a cyclopent. Aristeromycin is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor. Aristeromycin exhibits antiviral and anticancer properties.


Aristeromycin (CAS 19186-33-5) References

  1. Highly stereoselective synthesis of aristeromycin through dihydroxylation of 4-aryl-1-azido-2-cyclopentenes.  |  Ainai, T., et al. 2004. J Org Chem. 69: 655-9. PMID: 14750788
  2. Synthesis and anti-HBV activity of α-stereoisomer of aristeromycin based analogs.  |  Kasula, M., et al. 2016. Bioorg Med Chem Lett. 26: 3945-9. PMID: 27426303
  3. Five-Membered Cyclitol Phosphate Formation by a myo-Inositol Phosphate Synthase Orthologue in the Biosynthesis of the Carbocyclic Nucleoside Antibiotic Aristeromycin.  |  Kudo, F., et al. 2016. Chembiochem. 17: 2143-2148. PMID: 27577857
  4. Aristeromycin and DZNeP cause growth inhibition of prostate cancer via induction of mir-26a.  |  Uchiyama, N., et al. 2017. Eur J Pharmacol. 812: 138-146. PMID: 28705714
  5. Coordinated Biosynthesis of the Purine Nucleoside Antibiotics Aristeromycin and Coformycin in Actinomycetes.  |  Xu, G., et al. 2018. Appl Environ Microbiol. 84: PMID: 30217843
  6. Nitrogen-Based Heterocyclic Compounds: A Promising Class of Antiviral Agents against Chikungunya Virus.  |  Santana, AC., et al. 2020. Life (Basel). 11: PMID: 33396631
  7. Synthesis and anti-HBV activity of carbocyclic nucleoside hybrids with salient features of entecavir and aristeromycin.  |  Samunuri, R., et al. 2020. RSC Med Chem. 11: 597-601. PMID: 33479662
  8. Differences in the metabolism and metabolic effects of the carbocyclic adenosine analogs, neplanocin A and aristeromycin.  |  Bennett, LL., et al. 1986. Mol Pharmacol. 29: 383-90. PMID: 3702857
  9. Interaction of ribonuclease from Aspergillus saitoi with aristeromycin and its phosphate esters.  |  Irie, M. 1971. J Biochem. 69: 965-8. PMID: 5577154
  10. Streptomyces citricolor nov. sp. and a new antibiotic, aristeromycin.  |  Kusaka, T., et al. 1968. J Antibiot (Tokyo). 21: 255-63. PMID: 5671989
  11. Induction of erythroid differentiation in leukaemic K562 cells by an S-adenosylhomocysteine hydrolase inhibitor, aristeromycin.  |  Mizutani, Y., et al. 1995. Biochem Biophys Res Commun. 207: 69-74. PMID: 7857307
  12. Effects of 4'-modified analogs of aristeromycin on the metabolism of S-adenosyl-L-homocysteine in murine L929 cells.  |  Ault-Riché, DB., et al. 1993. Mol Pharmacol. 43: 989-97. PMID: 8316227

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Aristeromycin, 5 mg

sc-233890
5 mg
$379.00