250692-65-0
Chemical Structure
CYMAL-5, 98% (TLC)
- CAS. Nr.: 250692-65-0
- Formula:C23H42O11
- Molecular Weight:494.57
IUPAC Name: (2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-6-((5-cyclohexylpentyl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: RVTGFZGNOSKUDA-ZNGNCRBCSA-N
SMILES: OC[C@H]1O[C@@H]([C@@H]([C@H]([C@@H]1O)O)O)O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2CO)OCCCCCC3CCCCC3)O)O
Biological Activity: CYMAL-5, 98% (TLC) is a cycloalkyl aliphatic saccharide. CYMAL-5, 98% (TLC) is a glycosidic surfactant (GS) with a chiral maltose polar head group and a cyclohexyl-pentyl hydrophobic tail. CYMAL-5, 98% (TLC) is a non-ionic detergent that has a tenfold lower critical micelle concentration (CMC) in comparison with OG, and has previously been used for membrane protein extraction or crystallization of membrane proteins for X-ray crystallographic studies[1][2].
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CYMAL-5, 98% (TLC) | 99.95% | CYMAL-5, 98% (TLC) is a cycloalkyl aliphatic saccharide. CYMAL-5, 98% (TLC) is a glycosidic surfactant (GS) with a chiral maltose polar head group and a cyclohexyl-pentyl hydrophobic tail. CYMAL-5, 98% (TLC) is a non-ionic detergent that has a tenfold lower critical micelle concentration (CMC) in comparison with OG, and has previously been used for membrane protein extraction or crystallization of membrane proteins for X-ray crystallographic studies. | ||||||||||||||||||||
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-
Similarity Score 0.97
HY-142128Cymal-6 -
Similarity Score 0.90
HY-W4143902-Cyclohexylethyl-4-O-(α-D-glucopyranosyl)-β-D-glucopyranoside, 98% -
Similarity Score 0.81
HY-W040202Octyl β-D-maltopyranoside -
Similarity Score 0.81
HY-W416287Octyl 4-O-β-D-galactopyranosyl-β-D-glucopyranoside -
Similarity Score 0.80
HY-W010824n-Nonyl β-D-maltopyranoside -
Similarity Score 0.79
HY-153449Decyl α-D-maltopyranoside -
Similarity Score 0.79
HY-W040203Decyl β-D-maltopyranoside -
Similarity Score 0.79
HY-W283166n-Undecyl β-D-maltopyranoside -
Similarity Score 0.77
HY-128974N-Dodecyl-β-D-maltoside -
Explore the MedChemAI to find more analogs
References
- [1]. Ju M, et al. Enantioseparations by capillary electrophoresis using chiral glycosidic surfactants. I. Evaluation of cyclohexyl-pentyl-beta-D-maltoside surfactant. Electrophoresis. 1999;20(13):2766-2771. [Content Brief]
- [2]. Katayama H, et al. Efficient in-gel digestion procedure using 5-cyclohexyl-1-pentyl-beta-D-maltoside as an additive for gel-based membrane proteomics. Rapid Commun Mass Spectrom. 2004;18(20):2388-2394. [Content Brief]