γ-Rubromycin

  • BVT-0007-M0011 mg INQ
  • BVT-0007-M0055 mg INQ
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MSDS

Additional Information

Properties
Formula C26H18O12
MW 522.4
CAS 27267-71-6
Source/Host Isolated from Streptomyces sp.
Purity ≥98% (HPLC)
Appearance Red powder.
Solubility Soluble in methylene chloride, DMSO or methanol.
Identity Determined by 1H-NMR.
Origin Manufactured by BioViotica.
InChi Key CKLKRRFSZZUFKT-UHFFFAOYSA-N
Product Type Chemical
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light when in solution.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
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Product Description

  • Antibiotic.
  • HIV-1 reverse transcriptase and human telomerase inhibitor.
  • Antibacterial.
  • Cytostatically active against different tumor cell lines.

Product References

  1. Rubromycins. 3. The constitution of alpha-rubromycin, beta-rubromycin, gamma-rubromycin, and gamma-iso-rubromycin: H. Brockmann & A. Zeeck; Chem. Ber. 103, 170 (1970)
  2. Inhibition of human immunodeficiency virus-1 reverse transcriptase activity by rubromycins: competitive interaction at the template.primer site: M.E. Goldman, et al.; Mol. Pharmacol. 38, 20 (1990)
  3. Inhibition of human telomerase by rubromycins: implication of spiroketal system of the compounds as an active moiety: T. Ueno, et al.; Biochemistry 39, 5995 (2000)
  4. Rubromycins: Structurally intriguing, biologically valuable, synthetically challenging antitumour antibiotics: M. Brasholz, et al.; Eur. J. Org. Chem. 3801 (2007)
  5. Total synthesis of (+/-)-gamma-rubromycin on the basis of two aromatic Pummerer-type reactions: S. Akai, et al.; Angew. Chem. Int. Ed. 46, 7458 (2007)
  6. An efficient formal synthesis of the human telomerase inhibitor (+/-)-gamma-rubromycin: D.C. Rathwell, et al.; Angew. Chem. Int. Ed. 48, 7996 (2009)
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