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  3. FSVVPSPK

FSVVPSPK is an orally active peptide. FSVVPSPK exerts significant anti-adipogenic, antioxidant and anti-inflammatory effects in vitro and in vivo, mainly through activating the HO-1/Nrf2 pathway. FSVVPSPK can be used in research related to obesity and metabolic disorders.

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

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FSVVPSPK

FSVVPSPK Chemical Structure

CAS No. : 2016043-82-4

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Description

FSVVPSPK is an orally active peptide. FSVVPSPK exerts significant anti-adipogenic, antioxidant and anti-inflammatory effects in vitro and in vivo, mainly through activating the HO-1/Nrf2 pathway. FSVVPSPK can be used in research related to obesity and metabolic disorders[1].

IC50 & Target[1]

IL-6

 

IL-1β

 

HO-1

 

PPARγ

 

In Vitro

FSVVPSPK (10-100 μM; 48 h) exhibits no significant cytotoxicity against BMMSC cells, but inhibits intracellular reactive oxygen species (ROS) production[1].
FSVVPSPK (10-100 μM; 7 days) inhibits adipogenic differentiation of BMMSCs by downregulating adipogenic transcription factors, suppressing lipogenic enzyme activity and enhancing lipolysis, with a maximum inhibitory rate of 55.72% on lipid accumulation after treatment at 100 μM for 7 days[1].
FSVVPSPK (10-100 μM; 2-3 days) upregulates the expression of HO-1 in the cytoplasm and Nrf2 in the nucleus of BMMSCs[1].
FSVVPSPK (10-100 μM; 7 days) inhibits the production of pro-inflammatory cytokines (IL-6, IL-1β, TNF-α) in BMMSCs[1].

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

Western Blot Analysis[1]

Cell Line: BMMSCs
Concentration: 10, 50 and 100 μM
Incubation Time: 7 d
Result: Suppressed the expression of adipogenic transcription factors (PPARγ, SREBP-1, C/EBPα) and adipocyte protein 2 (aP2).
Inhibited lipogenic enzymes (FAS, LPL).
Upregulated lipolysis-related p-HSL.

Western Blot Analysis[1]

Cell Line: BMMSCs
Concentration: 10, 50 and100 μM
Incubation Time: 3 d (HO-1); 2 d (Nrf2)
Result: Elevated HO-1 expression in the BMMSCs cytoplasm.
Increased Nrf2 expression within the cell nucleus.
In Vivo

FSVVPSPK (1-10 mg/kg; p.o.; once daily; for 15 consecutive weeks) improves obesity, oxidative stress and inflammation in high-fat diet-induced obese mice[1].

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

Animal Model: C57BL/6 (male, 6 weeks old, HFD-induced obesity model)[1]
Dosage: 1, 10 mg/kg body weight
Administration: p.o.; daily; 15 weeks
Result: Reduced body weight gain, fat percentage and adipose tissue weight.
Decreased subcutaneous adipose tissue adipocyte size to levels.
Suppressed protein expression of adipogenic transcription factors (PPARγ, SREBP-1, C/EBPα) and lipogenic enzymes (LPL, FAS, aP2), and increased expression of p-HSL and p-AMPK in subcutaneous adipose tissue.
Reduced fasting blood glucose, total cholesterol, LDL, and triglycerides, and increased HDL.
Reduced serum proinflammatory cytokines (IL-6, IL-1β, TNFα), and increased serum antioxidant enzyme activities (CAT, SOD, GPx).
Activated Nrf2 and HO-1 in subcutaneous adipose tissue.
Molecular Weight

860.01

Formula

C41H65N9O11

CAS No.
Sequence

Phe-Ser-Val-Val-Pro-Ser-Pro-Lys

Sequence Shortening

FSVVPSPK

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    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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FSVVPSPK
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HY-P11608
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