Molecular structure of Heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin Heptasodium Salt, CAS Number: 201346-23-8
Heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin Heptasodium Salt (CAS 201346-23-8)
Application:
Heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin Heptasodium Salt is An anthrax lethal toxin inhibitor.
CAS Number:
201346-23-8
Molecular Weight:
2045.67
Molecular Formula:
C56H91Na7O56S7
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Anthrax lethal toxin inhibitor and -Cyclodextrin derivative
Heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin Heptasodium Salt (CAS 201346-23-8) References
- Toxins of Bacillus anthracis. | Brossier, F. and Mock, M. 2001. Toxicon. 39: 1747-55. PMID: 11595637
- Enantiomeric separation of basic compounds using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin in combination with potassium camphorsulfonate in nonaqueous capillary electrophoresis: optimization by means of an experimental design. | Servais, AC., et al. 2004. Electrophoresis. 25: 2701-10. PMID: 15352001
- Influence of the nature of the electrolyte on the chiral separation of basic compounds in nonaqueous capillary electrophoresis using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin. | Servais, AC., et al. 2005. J Chromatogr A. 1068: 143-50. PMID: 15844552
- Nonaqueous capillary electrophoresis method for the enantiomeric purity determination of S-timolol using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin: validation using the accuracy profile strategy and estimation of uncertainty. | Marini, RD., et al. 2006. J Chromatogr A. 1120: 102-11. PMID: 16643932
- Enantiomeric separation of omeprazole and its metabolite 5-hydroxyomeprazole using non-aqueous capillary electrophoresis. | Olsson, J., et al. 2006. J Chromatogr A. 1129: 291-5. PMID: 16854427
- Nonaqueous electrokinetic chromatography-electrospray ionization mass spectrometry using anionic cyclodextrins. | Mol, R., et al. 2007. J Chromatogr A. 1159: 51-7. PMID: 17543975
- Chiral separation of four phenothiazines by nonaqueous capillary electrophoresis and quality by design-based method development for quantification of dextromepromazine as chiral impurity of levomepromazine. | Niedermeier, S. and Scriba, GKE. 2020. J Chromatogr A. 1624: 461232. PMID: 32540073
- Macrophages are sensitive to anthrax lethal toxin through an acid-dependent process. | Friedlander, AM. 1986. J Biol Chem. 261: 7123-6. PMID: 3711080
- The channel formed in planar lipid bilayers by the protective antigen component of anthrax toxin. | Finkelstein, A. 1994. Toxicology. 87: 29-41. PMID: 7512762
- Identification of residues lining the anthrax protective antigen channel. | Benson, EL., et al. 1998. Biochemistry. 37: 3941-8. PMID: 9521715
Inhibitor of:
Anthrax.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Heptakis(2,3-di-O-methyl-6-O-sulfo)-β-cyclodextrin Heptasodium Salt, 5 mg | sc-207730 | 5 mg | $360.00 |