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Results for "

phe

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    3267
    TargetMol | Inhibitors_Agonists
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    TargetMol | Inhibitors_Agonists
Fmoc-N-Me-Phe-OH
Fmoc-N-methyl-L-phenylalanine
T591677128-73-5
Fmoc-N-Me-Phe-OH (Fmoc-N-methyl-L-phenylalanine) is a Malaria Parasite inhibitor.
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H-Phe-Phe-OH
T80372577-40-4
H-Phe-Phe-OH is a dipeptide composed of two phenylalanine (an essential amino acid and precursor to tyrosine) units linked together.
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Fmoc-Phe(4-CN)-OH
T9059173963-93-4
Fmoc-Phe(4-CN)-OH is an N-Fmoc protected phenylalanine derivative and potentially useful synthetic intermediate
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N-Formyl-Met-Leu-Phe
fMLP, N-Formyl-MLF
T709159880-97-6
N-Formyl-Met-Leu-Phe (N-Formyl-MLF) (fMLF) is a synthetic peptide that acts as an agonist at formyl peptide receptors (FPR; Ki = 0.8 pM).
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Gly-Phe β-naphthylamide acetate
Gly-Phe β-naphthylamide acetate(21438-66-4 Free base)
T41308L
Gly-Phe β-naphthylamide acetate is the substrate of Cathepsin C and can be used for research on the function of cathepsin C, intralysosomal hydrolysis and lysosomal membrane permeability.
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Phe-Met-Arg-Phe Like Peptide acetate
Pqdpflrfamide acetate, Phe-Met-Arg-Phe Like Peptide acetate(98495-35-3 free base)
TP1057L
Phe-Met-Arg-Phe Like Peptide acetate (Pqdpflrfamide acetate) is a FMRF-like peptide from visceral and somatic muscles of the snail Helix aspersa. FMRF (Phe-Met-Arg-Phe) is a neuropeptide peptide consisting of 4 amino acid residues.
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Boc-Gly-Gly-Phe-Gly-OH acetate
Boc-Gly-Gly-Phe-Gly-OH acetate(187794-49-6 free base), GGFG acetate
TP1159L
Boc-Gly-Gly-Phe-Gly-OH acetate (GGFG acetate) is a self-assembly of N- and C-protected tetrapeptide.
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N-Formyl-Met-Leu-Phe-Lys
fMLFK
TP116867247-11-4
N-Formyl-Met-Leu-Phe-Lys (fMLFK) is a peptide that acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM for FPR1, 6.7 μM for FPR2, and 0.88 μM for FPR2-D2817.32G. This chemotactic peptide binds specifically to receptors on leukocyte membranes and its uptake can contribute to the quantitative assessment of neutrophils in localized inflammatory processes, independent of associated edema formation or microcirculatory compromise.
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γ-Glu-Phe TFA(7432-24-8 free base)
γ-Glu-Phe TFA(7432-24-8,FREE)
TP1266
γ-Glu-Phe TFA(7432-24-8 free base) is a dipeptide composed of gamma-glutamate and phenylalanine and is a proteolytic breakdown product of larger proteins. It is probably formed by transpeptidation between glutathione and the corresponding amino acid, catalyzed by gamma-glutamyl transpeptidase.
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Gly-Phe-Arg acetate(121822-47-7 free base)
TP1861L
Gly-Phe-Arg acetate is a superpotent synthetic tripeptide mimics of the mud-crab pumping pheromone.
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Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA
T10920199807-33-5
Arg-Gly-Asp-D-Phe-Val (TFA) has anti-tumor activity and is an inhibitor of integrin αvβ3.
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3-6 months
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H-D-Phe-Pip-Arg-pNA
S-2238, S2238, S 2238
T3446264815-81-2
S 2238 is a chromogenic substrate for thrombin that is used in amidolytic assay.
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H-4-Nitro-Phe-OEt . HCl
T3703258816-66-3
H-4-Nitro-Phe-OEt . HCl is an alanine derivative.
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7-10 days
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Cyclo(L-Phe-L-Val)
T3747635590-86-4
Cyclo(L-Phe-L-Val) is a metabolite of the sponge bacterium Pseudoalteromonas sp. NJ6-3-1, capable of autoinducing the production of antibacterial substances active against S. aureus at low cell density. It induces neurite outgrowth and branching of chick cortical neurons in vitro at concentrations of 16 and 32 μM, increases phosphorylation of the PI3K substrate Akt, and this induction can be blocked by the PI3K inhibitor LY294002. Additionally, it enhances axon sprouting of calcitonin gene-related protein positive (CGRP+) primary afferents in the spinal cord post-crush injury and of serotonin neurons in the uninjured spinal cord. Cyclo(L-Phe-L-Val) is also a bitter taste component of cocoa and roasted coffee.
    7-10 days
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    (Rac)-Z-Phe-Phe-FMK
    Cathepsin L-IN-2
    T38469108005-94-3
    (Rac)-Z-Phe-Phe-FMK (Cathepsin L-IN-2) is a cathepsin L inhibitor that inhibits the tendency of β-amyloid to induce apoptotic changes .
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    7-10 days
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    H-D-Phe-Pip-Arg-pNA acetate
    H-D-Phe-Pip-Arg-pNA acetate,S-2238 acetate
    T38542115388-96-0
    H-D-Phe-Pip-Arg-pNA (S-2238) acetate is a chromogenic substrate based on the N-terminal fragment of the A alpha chain of fibrinogen, the physiological target of thrombin. As a specific indicator of thrombin activity, it is utilized to quantify thrombin. This assay ensures high sensitivity, accuracy, and ease of execution.
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    7-10 days
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    H-D-Phe-Pip-Arg-pNA hydrochloride
    S-2238 hydrochloride,H-D-Phe-Pip-Arg-pNA hydrochloride
    T39066160192-34-7
    H-D-Phe-Pip-Arg-pNA hydrochloride, a chromogenic substrate, mimics the N-terminal segment of the A alpha chain of fibrinogen, the native substrate of thrombin. It is specific to thrombin and is used for quantifying antithrombin-heparin cofactor (AT-III), enabling a sensitive, accurate, and straightforward AT-III assay.
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    7-10 days
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    Pro-Phe-Phe
    T39128164257-32-3
    Pro-Phe-Phe, a highly aggregation-prone tripeptide composed of natural amino acids, exhibits the formation of distinctive helical-like sheets that engage in aromatic dry interfaces. This property makes Pro-Phe-Phe an excellent candidate for the development of modular super-helical self-assembling nanostructures.
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    Hyp-Phe-Phe
    T401572493080-84-3
    Hyp-Phe-Phe is a tripeptide known for its strong aromatic interactions between the Phe rings, leading to helical-like sheet formation and a cross helical architecture. Notably, Hyp-Phe-Phe exhibits excellent shear piezoelectricity properties, making it a valuable candidate for piezoelectric materials.
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    Mc-Gly-Gly-Phe-Gly-PAB-OH
    Mc-GGFG-PAB-OH, Mc-Gly-Gly-Phe-Gly-PAB-OH
    T402572632342-05-1
    Mc-Gly-Gly-Phe-Gly-PAB-OH, also known as Mc-GGFG-PAB-OH, is a cleavable ADC linker used specifically in the synthesis of antibody-drug conjugates (ADCs).
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    H-D-Phe-Pip-Arg-pNA dihydrochloride
    S-2238 dihydrochloride, H-D-Phe-Pip-Arg-pNA dihydrochloride
    T4071162354-65-8
    H-D-Phe-Pip-Arg-pNA dihydrochloride (S-2238 dihydrochloride), a chromogenic substrate, mimics the N-terminal fragment of the A alpha chain of fibrinogen, the native substrate of thrombin. Specifically designed for thrombin detection, it is employed for quantifying antithrombin-heparin cofactor (AT-III) and is characterized by its sensitivity, accuracy, and ease of implementation.
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    {Boc}-Phe-Leu-Phe-Leu-Phe
    T4076866556-73-8
    {Boc}-Phe-Leu-Phe-Leu-Phe ({Boc}-FLFLF) is a selective antagonist of the formyl peptide receptor (FPR) family, effectively inhibiting receptor activity in response to formyl peptides.
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    H-Tyr-Phe-OH
    L-Tyrosyl-L-phenylalanine
    T6093517355-11-2
    H-Tyr-Phe-OH(L-Tyrosyl-L-phenylalanine) is a dipeptide polypeptide composed of tyrosine and phenylalanine that inhibits the activity of the angiotensin-converting enzyme (ACE) and has oral activity. It can be used as a biomarker for the study of thyroid nodules and also exhibits xanthine oxidase inhibitory (uric acid lowering) activity and acts as a regulator of IL-8 production by neutrophil-like cells.
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    7-10 days
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    Fmoc-Phe-Thr(psi(Me,Me)pro)-OH
    T644511196703-48-6
    Fmoc-Phe-Thr(psi(Me,Me)pro)-OH is an essential organic compound for life sciences research, catalog number T64451, CAS number 1196703-48-6.
      7-10 days
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