Review



fmoc protected phe analogs  (Chem Impex International)


Bioz Verified Symbol Chem Impex International is a verified supplier
Bioz Manufacturer Symbol Chem Impex International manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 95
      Buy from Supplier

    Structured Review

    Chem Impex International fmoc protected phe analogs
    Fmoc Protected Phe Analogs, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pm39969055-415-12-18?v=Chem+Impex+International
    Average 95 stars, based on 4 article reviews
    fmoc protected phe analogs - by Bioz Stars, 2026-07
    95/100 stars

    Images



    Similar Products

    fmoc protected phe analogs  (Chem Impex International)
    95
    Chem Impex International fmoc protected phe analogs
    Fmoc Protected Phe Analogs, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pm39969055-415-12-18?v=Chem+Impex+International
    Average 95 stars, based on 1 article reviews
    fmoc protected phe analogs - by Bioz Stars, 2026-07
    95/100 stars
    		  Buy from Supplier
    prrp analog p52 palm srthr hs nle ei rtpdi npawy asrgi rpvgr phe pno2 amide  (Gyros Protein Technologies)
    96
    Gyros Protein Technologies prrp analog p52 palm srthr hs nle ei rtpdi npawy asrgi rpvgr phe pno2 amide
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    Prrp Analog P52 Palm Srthr Hs Nle Ei Rtpdi Npawy Asrgi Rpvgr Phe Pno2 Amide, supplied by Gyros Protein Technologies, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pmc11773474-74-2-17?v=Gyros+Protein+Technologies
    Average 96 stars, based on 1 article reviews
    prrp analog p52 palm srthr hs nle ei rtpdi npawy asrgi rpvgr phe pno2 amide - by Bioz Stars, 2026-07
    96/100 stars
    		  Buy from Supplier
    phe analogs  (Chem Impex International)
    95
    Chem Impex International phe analogs
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    Phe Analogs, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pmc11837044-340-13-18?v=Chem+Impex+International
    Average 95 stars, based on 1 article reviews
    phe analogs - by Bioz Stars, 2026-07
    95/100 stars
    		  Buy from Supplier
    somatostatin analog d phe cys tyr d trp arg thr pen thr nh2 ctap  (Tocris)
    94
    Tocris somatostatin analog d phe cys tyr d trp arg thr pen thr nh2 ctap
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    Somatostatin Analog D Phe Cys Tyr D Trp Arg Thr Pen Thr Nh2 Ctap, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/10__1523_slash_eneuro__0524___23__2024-69-1-8?v=Tocris
    Average 94 stars, based on 1 article reviews
    somatostatin analog d phe cys tyr d trp arg thr pen thr nh2 ctap - by Bioz Stars, 2026-07
    94/100 stars
    		  Buy from Supplier
    n-terminal dota-conjugated gastrin analog pp-f11n (dota-( d glu) -ala-tyr-gly-trp-nle-asp-phe  (PSL GmbH)
    90
    PSL GmbH n-terminal dota-conjugated gastrin analog pp-f11n (dota-( d glu) -ala-tyr-gly-trp-nle-asp-phe
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    N Terminal Dota Conjugated Gastrin Analog Pp F11n (Dota ( D Glu) Ala Tyr Gly Trp Nle Asp Phe, supplied by PSL GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pmc10241010-51-13-24?v=PSL+GmbH
    Average 90 stars, based on 1 article reviews
    n-terminal dota-conjugated gastrin analog pp-f11n (dota-( d glu) -ala-tyr-gly-trp-nle-asp-phe - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier
    prelude  (Gyros Protein Technologies)
    96
    Gyros Protein Technologies prelude
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    Prelude, supplied by Gyros Protein Technologies, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/gyros+protein+technologies___pps-110c?v=Gyros+Protein+Technologies
    Average 96 stars, based on 1 article reviews
    prelude - by Bioz Stars, 2026-07
    96/100 stars
    		  Buy from Supplier
    at1002 analog (arg-arg-arg-gly-gly-phe-cys-ile-gly-arg-leu)  (Peptide Institute)
    90
    Peptide Institute at1002 analog (arg-arg-arg-gly-gly-phe-cys-ile-gly-arg-leu)
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    At1002 Analog (Arg Arg Arg Gly Gly Phe Cys Ile Gly Arg Leu), supplied by Peptide Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pm33905867-64-1-35?v=Peptide+Institute
    Average 90 stars, based on 1 article reviews
    at1002 analog (arg-arg-arg-gly-gly-phe-cys-ile-gly-arg-leu) - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier
    enkephalin analog, tyr-d-ala-gly-(nme)phe-gly-ol (damgo)  (Bachem)
    90
    Bachem enkephalin analog, tyr-d-ala-gly-(nme)phe-gly-ol (damgo)
    <t>p52</t> suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.
    Enkephalin Analog, Tyr D Ala Gly (Nme)phe Gly Ol (Damgo), supplied by Bachem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phe+analogs/pmc07957511-149-9-14?v=Bachem
    Average 90 stars, based on 1 article reviews
    enkephalin analog, tyr-d-ala-gly-(nme)phe-gly-ol (damgo) - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    p52 suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.

    Journal: Molecular Metabolism

    Article Title: Roles for Prlhr /GPR10 and Npffr2 /GPR74 in feeding responses to PrRP

    doi: 10.1016/j.molmet.2024.102093

    Figure Lengend Snippet: p52 suppress food intake independently of GPR10 and GPR74 expression in mice . A. Wild-type mice were treated with vehicle, liraglutide (dose) or the indicated concentration of p52 at the onset of the dark cycle and food intake was monitored over the subsequent 4 h (n = 8 per group). B Wild-type (WT) (n = 7), 10KO (n = 9), 74KO (n = 5), and 10/74KO (n = 5) mice were treated with vehicle or p52 (5 mg/kg) at the onset of the dark cycle and food intake was monitored over the subsequent 4 h. All graphs: Shown is mean ± SEM. One-way ANOVA, Dunnett's multiple comparisons test and unpaired t-test were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.

    Article Snippet: The long-acting PrRP analog p52 (Palm-SRTHR HS-Nle-EI RTPDI NPAWY ASRGI RPVGR Phe(pNO2)-amide) was synthesized on a Prelude (Gyros Protein Technologies) by automated synthesis using the Fmoc/ t Bu protocol, purified by reversed-phase HPLC and characterized by single quadrupolar LC/MS using a Waters Mass Lynx 3100 platform.

    Techniques: Expressing, Concentration Assay

    p52, but not NTS PrlhOX or the activation of NTS Prlh neurons, suppresses locomotor activity in mice . A. Locomotor activity in wild-type mice treated with vehicle and p52 (n = 12, 5 mg/kg IP), respectively. B. Locomotor activity in Prlh Cre (n = 6; Ctrl-WT) and NTS PrlhOX (n = 7, PrlhOX-WT) mice. C. Locomotor activity in control mice (Ctrl; n = 9) and NTS Prlh−Dq mice (Dq; n = 3) treated with either saline or CNO (1 mg/kg IP) twice daily. All graphs: Shown is mean beam breaks per hour ± SEM for the light cycle, the dark cycle, and averaged over the entire 24-hour day. Multiple paired t-tests, Holm-Šídák method and Šídák-Bonferroni method were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.

    Journal: Molecular Metabolism

    Article Title: Roles for Prlhr /GPR10 and Npffr2 /GPR74 in feeding responses to PrRP

    doi: 10.1016/j.molmet.2024.102093

    Figure Lengend Snippet: p52, but not NTS PrlhOX or the activation of NTS Prlh neurons, suppresses locomotor activity in mice . A. Locomotor activity in wild-type mice treated with vehicle and p52 (n = 12, 5 mg/kg IP), respectively. B. Locomotor activity in Prlh Cre (n = 6; Ctrl-WT) and NTS PrlhOX (n = 7, PrlhOX-WT) mice. C. Locomotor activity in control mice (Ctrl; n = 9) and NTS Prlh−Dq mice (Dq; n = 3) treated with either saline or CNO (1 mg/kg IP) twice daily. All graphs: Shown is mean beam breaks per hour ± SEM for the light cycle, the dark cycle, and averaged over the entire 24-hour day. Multiple paired t-tests, Holm-Šídák method and Šídák-Bonferroni method were used; p values are shown for significant comparisons. ∗: p < 0.05, ∗∗: p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗: p < 0.0001.

    Article Snippet: The long-acting PrRP analog p52 (Palm-SRTHR HS-Nle-EI RTPDI NPAWY ASRGI RPVGR Phe(pNO2)-amide) was synthesized on a Prelude (Gyros Protein Technologies) by automated synthesis using the Fmoc/ t Bu protocol, purified by reversed-phase HPLC and characterized by single quadrupolar LC/MS using a Waters Mass Lynx 3100 platform.

    Techniques: Activation Assay, Activity Assay, Control, Saline