Cyclo(Phe-Pro) | CAS:14705-60-3 | Manufacturer ChemFaces

Cyclo(Phe-Pro)

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Size /Price /Stock	10 mM * 1 mL in DMSO / $99.2 / In-stock
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Description:

Cyclo(Phe-Pro) inhibition of cholera toxin and toxin-coregulated pilus production correlated with reduced transcription of the virulence regulator tcpPH and was alleviated by overexpression of tcpPH.Cyclo(Phe-Pro) has been shown to inhibit cancer cell growth and induce apoptosis in HT-29 colon cancer cells.

Targets:

PARP | Caspase | NF-kB | IkB | IKK

In vitro:

Anticancer Res. 2005 Nov-Dec;25(6B):4197-202.

Caspase-3 activation and induction of PARP cleavage by cyclic dipeptide cyclo(Phe-Pro) in HT-29 cells.[Pubmed: 16309216]

Cyclo(Phe-Pro) has been shown to inhibit cancer cell growth and induce apoptosis in HT-29 colon cancer cells.
METHODS AND RESULTS:
The molecular mechanisms mediating Cyclo(Phe-Pro)-induced apoptosis in HT-29 cells were investigated. Cells were treated with 5 mM or 10 mM Cyclo(Phe-Pro) for varying times. Immunoblot analysis was used to detect poly(ADP-ribose)polymerase (PARP) cleavage. A fluorescence-based enzymatic assay was used to measure caspase-3 activity.Cyclo(Phe-Pro) (10 mM) induced time-dependent cleavage of PARP, detected as early as 8 hours post treatment. PARP cleavage was blocked by co-administration with the broad-range caspase inhibitor Z-VAD-FMK Cyclo(Phe-Pro) also induced a time-dependent increase (p < 0.01) in caspase-3 activity. This increase in activity was blocked in the presence of the caspase-3 inhibitor Ac-DEVD-CHO.
CONCLUSIONS:
These results provide evidence that Cyclo(Phe-Pro)-induced apoptosis in HT-29 cells is mediated by a caspase cascade. These findings warrant further investigation into the potential antitumour activity of Cyclo(Phe-Pro) and its related cyclic dipeptide derivatives.

In vivo:

Infect Immun. 2015 Mar;83(3):1150-61.

Cyclo(Phe-Pro) produced by the human pathogen Vibrio vulnificus inhibits host innate immune responses through the NF-κB pathway.[Pubmed: 25561711]

Cyclo(Phe-Pro) (cFP) is a secondary metabolite produced by certain bacteria and fungi. Although recent studies highlight the role of Cyclo(Phe-Pro) in cell-to-cell communication by bacteria, its role in the context of the host immune response is poorly understood. In this study, we investigated the role of Cyclo(Phe-Pro) produced by the human pathogen Vibrio vulnificus in the modulation of innate immune responses toward the pathogen.
METHODS AND RESULTS:
Cyclo(Phe-Pro) suppressed the production of proinflammatory cytokines, nitric oxide, and reactive oxygen species in a lipopolysaccharide (LPS)-stimulated monocyte/macrophage cell line and in bone marrow-derived macrophages. Specifically, Cyclo(Phe-Pro) inhibited inhibitory κB (IκB) kinase (IKK) phosphorylation, IκBα degradation, and nuclear factor κB (NF-κB) translocation to the cell nucleus, indicating that Cyclo(Phe-Pro) affects the NF-κB pathway. We searched for genes that are responsible for Cyclo(Phe-Pro) production in V. vulnificus and identified VVMO6_03017 as a causative gene. A deletion of VVMO6_03017 diminished Cyclo(Phe-Pro) production and decreased virulence in subcutaneously inoculated mice.
CONCLUSIONS:
In summary, Cyclo(Phe-Pro) produced by V. vulnificus actively suppresses the innate immune responses of the host, thereby facilitating its survival and propagation in the host environment.

Cyclo(Phe-Pro) Description

Source:	From Pantoea agglomerans
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Kinase Assay:

MBio. 2013 Aug 27;4(5):e00366-13.

Vibrio cholerae ToxR downregulates virulence factor production in response to cyclo(Phe-Pro).[Pubmed: 23982069]

Vibrio cholerae is an aquatic organism that causes the severe acute diarrheal disease cholera. The ability of V. cholerae to cause disease is dependent upon the production of two critical virulence determinants, cholera toxin (CT) and the toxin-coregulated pilus (TCP). The expression of the genes that encode for CT and TCP production is under the control of a hierarchical regulatory system called the ToxR regulon, which functions to activate virulence gene expression in response to in vivo stimuli. Cyclic dipeptides have been found to be produced by numerous bacteria, yet their biological function remains unknown. V. cholerae has been shown to produce Cyclo(Phe-Pro). Previous studies in our laboratory demonstrated that Cyclo(Phe-Pro) inhibited V. cholerae virulence factor production.
METHODS AND RESULTS:
For this study, we report on the mechanism by which Cyclo(Phe-Pro) inhibited virulence factor production. We have demonstrated that exogenous Cyclo(Phe-Pro) activated the expression of leuO, a LysR-family regulator that had not been previously associated with V. cholerae virulence. Increased leuO expression repressed aphA transcription, which resulted in downregulation of the ToxR regulon and attenuated CT and TCP production. The Cyclo(Phe-Pro)-dependent induction of leuO expression was found to be dependent upon the virulence regulator ToxR. Cyclo(Phe-Pro) did not affect toxR transcription or ToxR protein levels but appeared to enhance the ToxR-dependent transcription of leuO. These results have identified leuO as a new component of the ToxR regulon and demonstrate for the first time that ToxR is capable of downregulating virulence gene expression in response to an environmental cue. IMPORTANCE: The ToxR regulon has been a focus of cholera research for more than three decades. During this time, a model has emerged wherein ToxR functions to activate the expression of Vibrio cholerae virulence factors upon host entry. V. cholerae and other enteric bacteria produce Cyclo(Phe-Pro), a cyclic dipeptide that we identified as an inhibitor of V. cholerae virulence factor production. This finding suggested that Cyclo(Phe-Pro) was a negative effector of virulence factor production and represented a molecule that could potentially be exploited for therapeutic development. In this work, we investigated the mechanism by which Cyclo(Phe-Pro) inhibited virulence factor production. We found that Cyclo(Phe-Pro) signaled through ToxR to activate the expression of leuO, a new virulence regulator that functioned to repress virulence factor production.
CONCLUSIONS:
Our results have identified a new arm of the ToxR regulon and suggest that ToxR may play a broader role in pathogenesis than previously known.

J Bacteriol. 2010 Jul;192(14):3829-32.

The cyclic dipeptide cyclo(Phe-Pro) inhibits cholera toxin and toxin-coregulated pilus production in O1 El Tor Vibrio cholerae.[Pubmed: 20453095]

Cyclo(Phe-Pro) is a cyclic dipeptide produced by multiple Vibrio species.
METHODS AND RESULTS:
In this work, we present evidence that Cyclo(Phe-Pro) inhibits the production of the virulence factors cholera toxin (CT) and toxin-coregulated pilus (TCP) in O1 El Tor Vibrio cholerae strain N16961 during growth under virulence gene-inducing conditions.
CONCLUSIONS:
The Cyclo(Phe-Pro) inhibition of CT and TCP production correlated with reduced transcription of the virulence regulator tcpPH and was alleviated by overexpression of tcpPH.

Product Name	Cyclo(Phe-Pro)
Price:	$238 / 10mg
CAS No.:	14705-60-3
Catalog No.:	CFN90271
Molecular Formula:	C₁₄H₁₆N₂O₂
Molecular Weight:	244.29 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:	From Pantoea agglomerans
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF Manual
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Antibacterial Compound Library Cytotoxic Compound Library Pro-apoptotic Compound Library Immunosuppression Compound Library Alkaloids Compound Library PARP Inhibitor Library NF-kB Inhibitor Library IKK Inhibitor Library IkB Inhibitor Library Caspase Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.0935 mL	20.4675 mL	40.935 mL	81.8699 mL	102.3374 mL
5 mM	0.8187 mL	4.0935 mL	8.187 mL	16.374 mL	20.4675 mL
10 mM	0.4093 mL	2.0467 mL	4.0935 mL	8.187 mL	10.2337 mL
50 mM	0.0819 mL	0.4093 mL	0.8187 mL	1.6374 mL	2.0467 mL
100 mM	0.0409 mL	0.2047 mL	0.4093 mL	0.8187 mL	1.0234 mL

CFN90278	Cyclo(Tyr-Phe)	5147-17-1	310.35	C₁₈H₁₈N₂O₃
CFN89034	3,6-Dibenzyl-2-hydroxy-5-methoxypyrazine	132213-65-1	306.36	C₁₉H₁₈N₂O₂
CFN96983	Emeheterone	117333-12-7	322.36	C₁₉H₁₈N₂O₃
CFN90280	Cyclo(Phe-Hpro)	1016899-94-7	260.30	C₁₄H₁₆N₂O₃
CFN90279	Cyclo(Tyr-Hpro)	813461-21-1	276.29	C₁₄H₁₆N₂O₄
CFN90277	Cyclo(Pro-Trp)	67889-75-2	283.33	C₁₆H₁₇N₃O₂
CFN96937	Demethoxyfumitremorgin C	111768-16-2	349.43	C₂₁H₂₃N₃O₂
CFN96930	Fumitremorgin C	118974-02-0	379.46	C₂₂H₂₅N₃O₃
CFN89011	Fumitremorgin B	12626-17-4	479.57	C₂₇H₃₃N₃O₅
CFN90627	Heterophyllin B	145459-19-4	778.95	C₄₀H₅₈N₈O₈