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  3. 23-epi-26-Deoxyactein

23-epi-26-Deoxyactein  (Synonyms: 27-Deoxyactein)

Cat. No.: HY-139058 Purity: 99.45%
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23-epi-26-Deoxyactein is a natural and orally active anti-obesity and anti-cancer compound.

For research use only. We do not sell to patients.

23-epi-26-Deoxyactein Chemical Structure

23-epi-26-Deoxyactein Chemical Structure

CAS No. : 501938-01-8

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Based on 1 publication(s) in Google Scholar

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Description

23-epi-26-Deoxyactein is a natural and orally active anti-obesity and anti-cancer compound[1][2][3].

In Vitro

23-epi-26-Deoxyactein (DA :10 μM and 20 μM) inhibits 3T3-L1 adipogenesis through down-regulating the expression of C/ebpα, C/ebpβ, and Pparγ, which are the critical adipogenic transcription factors[1].
23-epi-26-Deoxyactein (DA) promotes mitochondrial biogenesis in pancreatic β-cells preventing methylglyoxal-induced oxidative cell damage and protects osteoblasts against Antimycin A-induced cell damage[2].
23-epi-26-Deoxyactein (DA) inhibits growth of the MCF7 human breast cancer cells and induces cell cycle arrest at G1 (IC50 of 21μM)[3].
23-epi-26-Deoxyactein (0.1-1 μM) protects osteoblasts against Antimycin A-induced cell damage[4].

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

Cell Differentiation Assay[1]

Cell Line: 3T3-L1 preadipocytes.
Concentration: 0-50 μM.
Incubation Time: 8 days.
Result: 10 μM DA inhibited the adipogenesis of 3T3-L1 preadipocytes mainly at the early stage of differentiation.
In Vivo

23-epi-26-Deoxyactein (DA: 5 and 10 mg/kg/d) significantly lowers body weight gain, fat mass, and liver weight in HFD-fed mice. 23-epi-26-Deoxyactein (DA) also reduces insulin resistance and serum lipoprotein levels in HFD-fed mice[1].
23-epi-26-Deoxyactein (DA) promotes adipocyte lipolysis in mice through activating the AMPK signaling and SIRT1-FOXO1 pathway[1].

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

Animal Model: Diet induced obesity in C57BL/6 mice[1].
Dosage: 1-10 mg/kg.
Administration: Orally, daily for 12 weeks.
Result: Lowered body weight gain, fat mass, and liver weight.
5 mg/kg/d DA significantly improved HFD-induced glucose intolerance.
Molecular Weight

660.83

Formula

C37H56O10

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C[C@]([C@]12C)(C[C@@](O[C@]([C@@](O3)([H])[C@@]43C)(OC4)C5)([H])[C@]2([H])[C@@H]5C)[C@@](CC6)([H])[C@@]7(C[C@H]1OC(C)=O)[C@]([C@]6([H])C8(C)C)(CC[C@@H]8O[C@H](OC[C@H]9O)[C@@H]([C@H]9O)O)C7

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Purity & Documentation

Purity: 99.45%

References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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23-epi-26-Deoxyactein
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