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N-Boc-Phe-Leu-Phe-Leu-Phe (Synonyms: Boc-FLFLF)

Katalog-Nr.GC36706 Copy One-Click Copy Product Info

N-Boc-Phe-Leu-Phe-Leu-Phe (Boc-FLFLF) ist ein Antagonist des Formylpeptidrezeptors 1 (FPR1), der die Schmerzwirkung verstÄrkt und die antinozizeptive AktivitÄt von Annexin hemmt.

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N-Boc-Phe-Leu-Phe-Leu-Phe Chemische Struktur

Cas No.: 148182-34-7

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Sample solution is provided at 25 µL, 10mM.



Description of N-Boc-Phe-Leu-Phe-Leu-Phe

N-Boc-Phe-Leu-Phe-Leu-Phe is an antagonist of formyl peptide receptor (FPR) 1, with the apparent dissociation constant KD of 230nM[1]. N-Boc-Phe-Leu-Phe-Leu-Phe inhibits neutrophil chemotaxis induced by FPR1, and suppresses the production of superoxide[2]. N-Boc-Phe-Leu-Phe-Leu-Phe has been widely used as a model compound to develop a series of derivatives and is employed as a positron emission tomography imaging agent[1,3].

In vitro, N-Boc-Phe-Leu-Phe-Leu-Phe treatment at 120μM for 48h inhibited VEGF-A165-mediated human umbilical vein endothelial cell (HUVEC) proliferation and blocked the activation of the downstream secondary signaling mediators EKR1/2 and AKT[4]. Treatment of rat conjunctival goblet cells with N-Boc-Phe-Leu-Phe-Leu-Phe (0.1mM) for 30 minutes would affect the intracellular calcium ion concentration regulated by Maresin 2 and reduce the response of lipoxin (LX) A4[5].

In, vivo, N-Boc-Phe-Leu-Phe-Leu-Phe treatment via intraperitoneal injections (1mg/kg) twice a week for 8 weeks significantly inhibited the anti-fibrotic effect of Ac2-26 in mice with liver fibrosis and promoted liver inflammation induced by CCl4[6]. Intraperitoneal injection of N-Boc-Phe-Leu-Phe-Leu-Phe (1μl; 10mM) every other day for 6 consecutive days can block the renal injury repair effect of BML-111 in the diabetic mouse model[7].

References:
[1] Hayashi R, Kitajima T, Mizuguchi H, et al. Development of potent antagonists for formyl peptide receptor 1 based on Boc-Phe-D-Leu-Phe-D-Leu-Phe-OH[J]. Bioorganic & Medicinal Chemistry, 2014, 22(15): 3824-3828.
[2] Stenfeldt A L, Karlsson J, Wennerås C, et al. Cyclosporin H, Boc-MLF and Boc-FLFLF are antagonists that preferentially inhibit activity triggered through the formyl peptide receptor[J]. Inflammation, 2007, 30(6): 224-229.
[3] Dalpiaz A, Ferretti M E, Vertuani G, et al. C-and N-terminal residue effect on peptide derivatives' antagonism toward the formyl-peptide receptor[J]. European journal of pharmacology, 2002, 436(3): 187-196.
[4] Nawaz I M, Chiodelli P, Rezzola S, et al. N-tert-butyloxycarbonyl-Phe-Leu-Phe-Leu-Phe (BOC2) inhibits the angiogenic activity of heparin-binding growth factors[J]. Angiogenesis, 2018, 21(1): 47-59.
[5] Olsen M V, Lyngstadaas A V, Bair J A, et al. Signaling pathways used by the specialized pro-resolving mediator maresin 2 regulate goblet cell function: Comparison with maresin 1[J]. International journal of molecular sciences, 2022, 23(11): 6233.
[6] Fan J H, Luo N, Liu G F, et al. Mechanism of annexin A1/N-formylpeptide receptor regulation of macrophage function to inhibit hepatic stellate cell activation through Wnt/β-catenin pathway[J]. World Journal of Gastroenterology, 2023, 29(22): 3422.
[7] Hao H, Xie F, Xu F, et al. LipoxinA4 analog BML-111 protects podocytes cultured in high-glucose medium against oxidative injury via activating Nrf2 pathway[J]. International Immunopharmacology, 2022, 111: 109170.

Protocol of N-Boc-Phe-Leu-Phe-Leu-Phe

Cell experiment [1]:

Cell lines

Human umbilical vein endothelial cells (HUVECs)

Preparation Method

HUVECs were cultured on a plate coated with porcine gelatin, in M199 medium supplemented with 20% FCS, endothelial cell growth factor (10μg/mL) and porcine heparin (100μg/mL). The cells were cultured in a humidified 37°C incubator with 5% CO2. The medium was changed every 2-3 days until the cells reached confluence. HUVECs were seeded at a density of 1.7 × 104 cells/cm2 and incubated under serum starvation conditions overnight. Then, in the presence of 2.5% FCS, the cells were treated with 30ng/mL VEGF-A165 and increasing concentrations of N-Boc-Phe-Leu-Phe-Leu-Phe (0, 3, 7.5, 15, 30, 60, and 120μM) to stimulate the cells. After 48 hours, the cells were counted using a fluorescence counter.

Reaction Conditions

0, 3, 7.5, 15, 30, 60, and 120μM; 48h

Applications

N-Boc-Phe-Leu-Phe-Leu-Phe treatment significantly inhibited VEGF-A165-mediated HUVEC proliferation in a dose-dependent manner.
Animal experiment [2]:

Animal models

C57BL/6 mice

Preparation Method

Six to eight-week-old C57BL/6 mice (weighing 18-25g) were raised in a constant temperature and humidity room with a 12-hour day-night cycle. Thirty-two mice were randomly divided into four subgroups, with eight mice in each group: the control group, the CCl4-induced liver fibrosis group, the liver fibrosis + Ac2-26 group, and the liver fibrosis + Ac2-26 + N-Boc-Phe-Leu-Phe-Leu-Phe-Leu-Phe group. The control group mice were intraperitoneally injected with olive oil, and the other three subgroups were intraperitoneally injected twice a week with 20% CCl4 (500mL) and CCl4 + Ac2-26 at 1mg/kg, with or without N-Boc-Phe-Leu-Phe-Leu-Phe-Leu-Phe at 1mg/kg. At 8 weeks after injection, the mice were anesthetized with pentobarbital sodium (50mg/kg intravenous injection) and liver tissue samples were collected for analysis.

Dosage form

1mg/kg twice a week for 8 weeks; i.p.

Applications

N-Boc-Phe-Leu-Phe-Leu-Phe-Leu-Phe treatment inhibited the anti-liver fibrosis effect of Ac2-26 and promoted the liver inflammation induced by CCl4 in mice.

References:
[1] Nawaz I M, Chiodelli P, Rezzola S, et al. N-tert-butyloxycarbonyl-Phe-Leu-Phe-Leu-Phe (BOC2) inhibits the angiogenic activity of heparin-binding growth factors[J]. Angiogenesis, 2018, 21(1): 47-59.
[2] Fan J H, Luo N, Liu G F, et al. Mechanism of annexin A1/N-formylpeptide receptor regulation of macrophage function to inhibit hepatic stellate cell activation through Wnt/?-catenin pathway[J]. World Journal of Gastroenterology, 2023, 29(22): 3422.

Chemical Properties of N-Boc-Phe-Leu-Phe-Leu-Phe

Cas No. 148182-34-7 SDF
Überlieferungen Boc-FLFLF
Formula C44H59N5O8 M.Wt 785.97
Löslichkeit Water: < 0.1 mg/mL (insoluble) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of N-Boc-Phe-Leu-Phe-Leu-Phe

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.2723 mL 6.3616 mL 12.7231 mL
5 mM 254.5 μL 1.2723 mL 2.5446 mL
10 mM 127.2 μL 636.2 μL 1.2723 mL
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