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Reveromycin A

Cell cycle inhibitor
 
ALX-380-216-MC01 0.1 mg 193.00 USD
 
ALX-380-216-MC25 0.25 mg 447.00 USD
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Antibiotic. Dominant analog of the reveromycin complex. Inhibitor of the mitogenic activity of epidermal growth factor (EGF). G1 phase cell cycle inhibitor, selectively inhibiting isoleucyl-tRNA synthetase. Displays antiproliferative as well as potent antifungal activity. Induces apoptosis in osteoclasts thus inhibiting bone resorption.

Product Specification

Formula:C36H52O11
 
MW:660.8
 
Source:Isolated from Streptomyces sp. MST-AS5344.
 
CAS:134615-37-5
 
Formulation:Lyophilized.
 
Purity:≥99% (HPLC)
 
Appearance:White to tan solid.
 
Solubility:Soluble in ethyl acetate, 100% ethanol, methanol, dimethyl formamide or DMSO.
 
Shipping:Ambient
 
Long Term Storage:-20°C
 
380-216
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380-216

Product Literature References

Molecular pathogenesis and its therapeutic modalities of lung cancer metastasis to bone: S. Sone and S. Yano; Cancer Metastasis Rev. 26, 685 (2007), Abstract;
Regulation of osteoclast polarization: N. Takahashi, et al.; Odontology 95, 1 (2007), (Review), Abstract;
Reveromycin A, an agent for osteoporosis, inhibits bone resorption by inducing apoptosis specifically in osteoclasts: J.T. Woo, et al.; PNAS 103, 4729 (2006), Abstract; Full Text
Reveromycin A inhibits osteolytic bone metastasis of small-cell lung cancer cells, SBC-5, through an antiosteoclastic activity: H. Muguruma, et al.; Clin. Cancer Res. 11, 8822 (2005), Abstract; Full Text
Chemical modification of reveromycin A and its biological activities: T. Shimizu, et al.; Bioorg. Med. Chem. Lett. 12, 3363 (2002), Abstract;
Identification of Saccharomyces cerevisiae isoleucyl-tRNA synthetase as a target of the G1-specific inhibitor Reveromycin A: Y. Miyamoto, et al.; J. Biol. Chem. 277, 28810 (2002), Abstract; Full Text
Reveromycins, new inhibitors of eukaryotic cell growth. I. Producing organism, fermentation, isolation and physico-chemical properties: H. Takahashi, et al.; J. Antibiot. (Tokyo) 45, 1409 (1992), Abstract;
Reveromycins, new inhibitors of eukaryotic cell growth. II. Biological activities: H. Takahashi, et al.; J. Antibiot. (Tokyo) 45, 1414 (1992), Abstract;

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For Research Use Only. Not for use in diagnostic procedures.
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