3,6-Anhydro-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin
Original price was: $1,795.00.$895.00Current price is: $895.00.
Catalog Number: B2027389 (100 mg)
3,6-Anhydro-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin is a structurally modified gamma-cyclodextrin derivative incorporating an intramolecular 3,6-anhydro bridge alongside carboxyethylthio functional groups. This specialized cyclic oligosaccharide derivative is designed for research in host-guest chemistry, molecular encapsulation, and targeted delivery systems. The combination of ionic carboxylate chains and structural modifications enhances its selective binding capabilities for complementary guest molecules in aqueous environments. Custom bulk amounts of this product are available upon request.
Live Chat enquiry about this product at: Live Chat.
In stock
Product Description
3,6-Anhydro-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin
Catalog number: B2027389
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: NA
Supplied as: Chemicals
Storage: −80°C
Keywords: Sugammadex Impurity A, Mono-3,6-anhydro sugammadex, 3,6-Anhydro sugammadex
References:
1. Bom, A., Bradley, M., Cameron, K., Clark, J. K., Van Egmond, J., Feilden, H., … & Zhang, M. Q. (2002). A novel concept of reversing neuromuscular block: chemical encapsulation of rocuronium bromide by a cyclodextrin-based synthetic host. Angewandte Chemie International Edition, 41(2), 265-268.
2. Adam, J. M., Bennett, D. J., Bom, A., Clark, J. K., Feilden, H., Hutchinson, E. J., … & Zhang, M. Q. (2002). Cyclodextrin-derived host molecules as reversal agents for the neuromuscular blocker rocuronium bromide. Journal of Medicinal Chemistry, 45(9), 1806-1816.
3. Gijsenbergh, F., Ramael, S., Houwing, N., & van Iersel, T. (2005). First human exposure of Org 25969, a novel agent to reverse the action of rocuronium bromide. Anesthesiology, 103(4), 695-703.
4. Nicholson, W. T., Sprung, J., & Jankowski, C. J. (2007). Sugammadex: a novel agent for the reversal of neuromuscular blockade. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 27(8), 1181-1188.
5. Suy, K., Morias, K., Cammu, G., Hans, P., van Duijnhoven, W. G., Heeringa, M., & Demeyer, I. (2007). Effective reversal of moderate rocuronium- or vecuronium-induced neuromuscular block with sugammadex, a selective relaxant binding agent. Anesthesiology, 106(2), 283-288.
6. Sacan, O., White, P. F., Tufanogullari, B., & Klein, K. (2007). Sugammadex reversal of rocuronium-induced neuromuscular block: a comparison with neostigmine. Anesthesia & Analgesia, 104(3), 569-574.
7. Puhringer, F. K., Gordon, M., Demeyer, I., Sparr, H. J., Ingimarsson, J., Klarin, B., … & van Duijnhoven, W. G. (2008). Sugammadex rapidly reverses moderate rocuronium-or vecuronium-induced neuromuscular block. Anesthesiology, 109(5), 815-822.
8. Antonik, L. J., Goldwater, D. R., Kilford, P. C., Evarts, J. B., & Shi, H. (2009). Sugammadex for reversal of neuromuscular blockade induced by rocuronium in patients with end-stage renal disease. BMC Anesthesiology, 9(1), 5.
9. Abrishami, A., Ho, J., Wong, J., Yin, L., & Chung, F. (2009). Sugammadex, a selective relaxant binding agent, for reversal of neuromuscular blockade: a systematic review and meta-analysis. Anaesthesia, 64(7), 735-743.
10. Welliver, M. (2006). New drug survey: Sugammadex sodium. AANA Journal, 74(5), 357-363.
3,6-Anhydro-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin
Products Related to 3,6-Anhydro-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin can be found at Powder
Additional Information
| Weight | 0.15 oz |
|---|---|
| Dimensions | 2 × 0.5 × 0.5 in |
Several ways to order Molecular Depot products:
1- Order online using our website’s automated shopping cart and checkout system (available 24/7).
2- Order by email: info@moleculardepot.com (we accept electronic PO, available 24/7).
3- Order by Live Chat.
4- Order by Fax: 1-858-437-9884 (available 24/7).
Â







