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  3. Sucrose dilaurate

Sucrose dilaurate acts as an emulsifier, dispersant and stabilizer. Sucrose dilaurate reduces the release of HMGB1 from UVB-irradiated keratinocytes. Sucrose dilaurate inhibits melanogenesis and decreases bilirubin levels. Sucrose dilaurate induces autophagy in human epidermal keratinocytes, thereby reducing carboxymethyl lysine (CML) levels. Sucrose dilaurate reduces the secretion of insulin-like growth factor-binding protein 3 (IGFBP3) and nerve growth factor (NGF) by senescent keratinocytes. Sucrose dilaurate is investigated as an emulsifier, dispersant or stabilizer in the cosmetics, food and pharmaceutical industries.

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Sucrose dilaurate

Sucrose dilaurate Chemical Structure

CAS No. : 25915-57-5

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Description

Sucrose dilaurate acts as an emulsifier, dispersant and stabilizer. Sucrose dilaurate reduces the release of HMGB1 from UVB-irradiated keratinocytes. Sucrose dilaurate inhibits melanogenesis and decreases bilirubin levels. Sucrose dilaurate induces autophagy in human epidermal keratinocytes, thereby reducing carboxymethyl lysine (CML) levels. Sucrose dilaurate reduces the secretion of insulin-like growth factor-binding protein 3 (IGFBP3) and nerve growth factor (NGF) by senescent keratinocytes. Sucrose dilaurate is investigated as an emulsifier, dispersant or stabilizer in the cosmetics, food and pharmaceutical industries[1][2][3][4].

In Vitro

Sucrose dilaurate (as a component of the SDL combination, a mixture of Sucrose dilaurate and sucrose dilaurate at a ratio of approximately 6:4) significantly reduces bilirubin levels when incubated in a cell-free system, inhibits hydrogen peroxide-induced bilirubin production in human tKC keratinocytes, decreases intracellular bilirubin levels in HaCaT keratinocytes, and reduces skin-bound bilirubin levels in human skin sections[2].
Sucrose dilaurate (0.005%; 24 h) significantly induces autophagosome formation in neonatal human epidermal keratinocytes[3].
Sucrose dilaurate (0.01%; 24 h) significantly reduces CML levels in glyceraldehyde-glycosylated neonatal human epidermal keratinocytes[3].
Sucrose dilaurate (0.001%; 72 h) significantly inhibits the release of IGFBP3 and NGF from doxorubicin-induced senescent HaCaT keratinocytes[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

ELISA Assay[4]

Cell Line: doxorubicin-induced senescent HaCaT keratinocytes
Concentration: 0.001%
Incubation Time: 72 h
Result: Significantly suppressed the release of IGFBP3 from senescent HaCaT keratinocytes to levels similar to those released by normal keratinocytes.
Significantly suppressed the release of NGF from senescent HaCaT keratinocytes.
Molecular Weight

706.90

Formula

C36H66O13

CAS No.
SMILES

O=C(CCCCCCCCCCC)OC[C@]1(O[C@@H]([C@H]([C@@H]1OC(CCCCCCCCCCC)=O)O)CO)O[C@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO

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Sucrose dilaurate
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HY-182824
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