Product Name :
1,2-O-Isopropylidene-α-D-glucofuranose (CAS 18549-40-1)

Synonym :
Monoacetone glucose

Application :
1,2-O-Isopropylidene-α-D-glucofuranose is a derivative of glucofuranose

CAS:
18549-40-1

Purity:

Molecular Weight:
220.22

Formula :
C9H16O6

Physical state:
Solid

solubility :
Soluble in water (50 mg/ml).

Shipping Condition :
Store at 4° C

Melting point:
159-160° C (lit.)

SMILES:
CC1(O[C@@H]2[C@H]([C@H](O[C@@H]2O1)C(CO)O)O)C

References:
:Noninvasive evaluation of liver metabolism by 2H and 13C NMR isotopomer analysis of human urine. | Burgess, SC., et al. 2003. Anal Biochem. 312: 228-34. PMID: 12531210Sources of plasma glucose by automated Bayesian analysis of 2H NMR spectra. | Merritt, M., et al. 2003. Magn Reson Med. 50: 659-63. PMID: 14523948Glucose production, gluconeogenesis, and hepatic tricarboxylic acid cycle fluxes measured by nuclear magnetic resonance analysis of a single glucose derivative.Bromo-PEG3-C2-acid structure | Jin, ES.91103-37-6 Price , et al.PMID:33693607 2004. Anal Biochem. 327: 149-55. PMID: 15051530Glucose production pathways by 2H and 13C NMR in patients with HIV-associated lipoatrophy. | Weis, BC., et al. 2004. Magn Reson Med. 51: 649-54. PMID: 15065235Comparison of [3,4-13C2]glucose to [6,6-2H2]glucose as a tracer for glucose turnover by nuclear magnetic resonance. | Jin, ES., et al. 2005. Magn Reson Med. 53: 1479-83. PMID: 15906303Effects of insulin and cytosolic redox state on glucose production pathways in the isolated perfused mouse liver measured by integrated 2H and 13C NMR. | Hausler, N., et al. 2006. Biochem J. 394: 465-73. PMID: 16288601Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment. | Delgado, TC., et al. 2008. Magn Reson Med. 60: 517-23. PMID: 18727053Quantifying endogenous glucose production and contributing source fluxes from a single 2H NMR spectrum. | Nunes, PM. and Jones, JG. 2009. Magn Reson Med. 62: 802-7. PMID: 19488990Low level toxicity and antitumor activity of butyric mono- and polyester monosaccharide derivates in mice. | Pouillart, P., et al. 1990. J Biol Regul Homeost Agents. 4: 135-41. PMID: 2096598Controlled curing of adhesive complex coacervates with reversible periodate carbohydrate complexes. | Shao, H., et al. 2011. J Biomed Mater Res A. 97: 46-51. PMID: 21308985Scaling-up the synthesis of myristate glucose ester catalyzed by a CALB-displaying Pichia pastoris whole-cell biocatalyst. | Guo, D., et al. 2015. Enzyme Microb Technol. 75-76: 30-6. PMID: 26047913Intramolecular 13C analysis of tree rings provides multiple plant ecophysiology signals covering decades. | Wieloch, T., et al. 2018. Sci Rep. 8: 5048. PMID: 29567963Synthesis, antiproliferative activity and SAR analysis of (−)-cleistenolide and analogues. | Benedeković, G., et al. 2020. Eur J Med Chem. 202: 112597. PMID: 32653698Metabolomic and phenotypic implications of the application of fertilization products containing microcontaminants in lettuce (Lactuca sativa). | Matamoros, V., et al. 2021. Sci Rep. 11: 9701. PMID: 33958645Global CO2 fertilization of Sphagnum peat mosses via suppression of photorespiration during the twentieth century. | Serk, H., et al. 2021. Sci Rep. 11: 24517. PMID: 34972838