228579-27-9
Chemical Structure
Cymal-6
Synonym(s): Cyclohexyl-hexyl-β-D-maltoside
- No. CAS: 228579-27-9
- Formula:C24H44O11
- Molecular Weight:508.60
IUPAC Name: (2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-6-((6-cyclohexylhexyl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: WUCWJXGMSXTDAV-QKMCSOCLSA-N
SMILES: OC[C@@H](O[C@H]([C@@H]([C@H]1O)O)OCCCCCCC2CCCCC2)[C@H]1O[C@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO
Biological Activity: Cymal-6 (Cyclohexyl-hexyl-β-D-maltoside) is a potent TEM-1 beta-lactamase inhibitor with an Ki value of 40.05 µM. Cymal-6 (Cyclohexyl-hexyl-β-D-maltoside) can be used as glycosidic surfactant[1][2].
| Referencia número | Nombre del producto | Pureza | Descripciòn | Pricing | |||||||||||||||||||
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Cymal-6 | 99.67% | Cymal-6 (Cyclohexyl-hexyl-β-D-maltoside) is a potent TEM-1 beta-lactamase inhibitor with an Ki value of 40.05 µM. Cymal-6 (Cyclohexyl-hexyl-β-D-maltoside) can be used as glycosidic surfactant. | ||||||||||||||||||||
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Similarity Score 0.97
HY-123622CYMAL-5, 98% (TLC) -
Similarity Score 0.89
HY-W4143902-Cyclohexylethyl-4-O-(α-D-glucopyranosyl)-β-D-glucopyranoside, 98% -
Similarity Score 0.83
HY-W040202Octyl β-D-maltopyranoside -
Similarity Score 0.83
HY-W416287Octyl 4-O-β-D-galactopyranosyl-β-D-glucopyranoside -
Similarity Score 0.82
HY-W010824n-Nonyl β-D-maltopyranoside -
Similarity Score 0.81
HY-153449Decyl α-D-maltopyranoside -
Similarity Score 0.81
HY-W040203Decyl β-D-maltopyranoside -
Similarity Score 0.80
HY-W283166n-Undecyl β-D-maltopyranoside -
Similarity Score 0.79
HY-128974N-Dodecyl-β-D-maltoside -
Explore the MedChemAI to find more analogs
References
- [1]. Avci FG, et al. Targeting a hidden site on class A beta-lactamases. J Mol Graph Model. 2018 Sep;84:125-133. [Content Brief]
- [2]. Ju M, et al. Enantioseparations by capillary electrophoresis using chiral glycosidic surfactants. II. Comparisonof chiral cyclohexyl-alkyl-β-D-maltoside surfactant. Journal of Liquid Chromatography & Related Technologies. 2000, 23(1):35-45.
