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ac-phe-nh2

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  • Inhibitors & Agonists
    9
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    2
    TargetMol | Peptide_Products
Ac-Phe-NH2
Ac-Phe NH2, Ac Phe-NH2, Ac Phe NH2
T211527376-90-1
Ac-Phe-NH2 is a non-competitive inhibitor of polyubiquitin chain elongation with a Ki value of 8 ± 1.2 mM.
  • $32
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Ac-(d-Arg)-CEH-(d-Phe)-RWC-NH2
T80121819048-44-7
Ac-DArg-c[Cys-Glu-His-DPhe-Arg-Trp-Cys]-NH2 is a synthetic cyclic octapeptide acting as a melanocortin-4 receptor (MC4R) agonist, significantly elevating heart rate and blood pressure [1].
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Troponin I (104-115)
Ac-Gly-lys-phe-lys-arg-pro-pro-leu-arg-arg-val-arg-NH2,Tni peptide (104-115)
T2490198353-69-6
Troponin I is a cardiac and skeletal muscle protein useful in the laboratory diagnosis of a heart attack. Troponin I is a part of the troponin protein complex, where it binds to actin in thin myofilaments to hold the actin-tropomyosin complex in place.
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HP 228
HP-228,Ac-Nle-gln-his-D-phe-arg-D-trp-gly-NH2,HP228
T25507109022-88-0
HP 228 is a heptapeptide by inhibits the induction of nitric oxide synthase.
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U 67827E
U-67827E, U67827E, N-Ac-Asp-tyr(So3H)-nle-gly-trp-nle-asp-phe-NH2
T26305103494-23-1
U 67827E is a long-lasting cholecystokinin agonist. It acts by decreases food intake.
  • $1,520
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IRI-426
IRI426, Ac-Arg-Pro-Asp-Val-Phe-NH2
T32192103143-78-8
IRI-426 is a bioactive chemical.
  • $1,520
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Bisnafide mesylate
T70609145124-30-7
Bisnafide is a Naphthalimide Analogue that acts as DNA intercalator and topo II inhibitor. It is also an antiangiogenic agent. Antiangiogenic agents can normalize tumor vessels and promote the delivery of cytotoxic agents to tumor sites.
  • $1,520
6-8 weeks
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Cenupatide
Ac-Arg-Aib-Arg-α(Me)Phe-NH2
TP23381006388-38-0
Cenupatide is a urokinase plasminogen activator receptor (uPAR) inhibitor. Cenupatide inhibits uPAR binding to the formyl peptide receptors (FPRs) can improve kidney lesions in a rat model of STZ-induced diabetes. Cenupatide reverted STZ-induced up-regula
  • $152
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Acetalin-2
TP2530152274-66-3
Acetalin-2, an opioid peptide with the sequence Ac-Arg-Phe-Met-Trp-Met-Arg-NH2, selectively binds to [3 H]DAMGO with a Ki value of 93.3 nM [1].
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