Molecular structure of D-Idose, CAS Number: 5978-95-0
D-Idose (CAS 5978-95-0)
Alternate Names:
Idopyranose
Application:
D-Idose is a monosaccharide component of dermatan sulfate and heparan sulfate
CAS Number:
5978-95-0
Molecular Weight:
180.16
Molecular Formula:
C6H12O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
D-Idose is a synthetic compound that can be dissolved in water and used as a substitute for heavy metals in laboratory experiments. Its mechanism of action involves binding to particular receptors in the body that trigger specific pathways to produce desired physiological or biochemical effects. Studies indicate that D-Idose can bind to estrogen and serotonin receptors, leading to the production of hormones and neurotransmitters respectively. It has also been shown to have anti-inflammatory and antioxidant properties.
D-Idose (CAS 5978-95-0) References
- Acyclic forms of [1-(13)C]aldohexoses in aqueous solution: quantitation by (13)C NMR and deuterium isotope effects on tautomeric equilibria. | Zhu, Y., et al. 2001. J Org Chem. 66: 6244-51. PMID: 11559169
- A SuperQuat glycolate aldol approach to the asymmetric synthesis of hexose monosaccharides. | Davies, SG., et al. 2005. Org Biomol Chem. 3: 348-59. PMID: 15632978
- Tandem mass spectra of ammonium adducts of monosaccharides: differentiation of diastereomers. | Madhusudanan, KP. 2006. J Mass Spectrom. 41: 1096-104. PMID: 16888745
- HPLC separation of all aldopentoses and aldohexoses on an anion-exchange stationary phase prepared from polystyrene-based copolymer and diamine: the effect of NaOH eluent concentration. | Inoue, K., et al. 2011. Molecules. 16: 5905-15. PMID: 21760572
- Dependence of pyranose ring puckering on anomeric configuration: methyl idopyranosides. | Sattelle, BM., et al. 2012. J Phys Chem B. 116: 6380-6. PMID: 22577942
- Structural features of sugars that trigger or support conidial germination in the filamentous fungus Aspergillus niger. | Hayer, K., et al. 2013. Appl Environ Microbiol. 79: 6924-31. PMID: 23995938
- Multidimensional Analysis of 16 Glucose Isomers by Ion Mobility Spectrometry. | Gaye, MM., et al. 2016. Anal Chem. 88: 2335-44. PMID: 26799269
- Acyclic forms of aldohexoses and ketohexoses in aqueous and DMSO solutions: conformational features studied using molecular dynamics simulations. | Plazinski, W., et al. 2016. Phys Chem Chem Phys. 18: 9626-35. PMID: 26996921
- Synthesis of 28a-homoselenolupanes and 28a-homoselenolupane saponins. | Sidoryk, K., et al. 2016. Org Biomol Chem. 14: 10238-10248. PMID: 27735956
- Edible vegetables as a source of aldose reductase differential inhibitors. | Balestri, F., et al. 2017. Chem Biol Interact. 276: 155-159. PMID: 28159579
- d-Idose, d-Iduronic Acid, and d-Idonic Acid from d-Glucose via Seven-Carbon Sugars. | Liu, Z., et al. 2019. Molecules. 24: PMID: 31635397
- Evaluation of the Anti-Proliferative Activity of Rare Aldohexoses against MOLT-4F and DU-145 Human Cancer Cell Line and Structure-Activity Relationship of D-Idose. | Ishiyama, H., et al. 2020. J Appl Glycosci (1999). 67: 95-101. PMID: 34354535
- Impact of Polarization on the Ring Puckering Dynamics of Hexose Monosaccharides. | J N, C. and Mallajosyula, SS. 2023. J Chem Inf Model. 63: 208-223. PMID: 36475659
- Synthesis of 3-deoxy-2-octulosonic acid derivatives and characterisation of their 3-deoxyoctitols. | Krülle, T., et al. 1994. Carbohydr Res. 254: 141-56. PMID: 8180981
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
D-Idose, 50 mg | sc-285368 | 50 mg | $312.00 | |||
D-Idose, 100 mg | sc-285368A | 100 mg | $516.00 |