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Results for "

substance p (7 11)

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Peptide Products
    4
    TargetMol | Peptide_Products
  • Substance P (7-11)
    Substance P
    T755451165-05-0
    Substance P (7-11) (Substance P 7-11(TFA)) is a C-terminal fragment of Substance P .
    • $39
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  • Substance P (7-11) acetate
    Substance P (7-11) acetate (51165-05-0 free base)
    T7554L1
    Substance P (7-11) acetate is a specific fragment of the neuropeptide Substance P, acting as a neurotransmitter and neuromodulator in the central nervous system, with its endogenous receptor being neurokinin 1 (NK1R), making it useful for neurophysiological and pharmacological research.
    • $41
    In Stock
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  • [Tyr6,D-Phe7,D-His9]-Substance P (6-11)
    TP2810145194-26-9
    [Tyr6,D-Phe7,D-His9]-Substance P (6-11) is a tachykinin NK1 receptor antagonist that can counteract histamine-induced hyperalgesia.
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  • [D-Arg1,D-Trp5,7,9,Leu11]-Substance P
    TP4199122481-75-8
    [D-Arg1,D-Trp5,7,9,Leu11]-Substance P is a potent inhibitor of small cell lung cancer (SCLC) cell growth. As a neuropeptide antagonist, [D-Arg1,D-Trp5,7,9,Leu11]-Substance P effectively blocks colony formation stimulated by multiple neuropeptides such as vasopressin and bradykinin. It inhibits Ca2+ mobilization and mitogen-activated protein kinase activation induced by vasopressin or bradykinin. [D-Arg1,D-Trp5,7,9,Leu11]-Substance P also suppresses the growth of H-69 xenografts in nude mice.
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  • YM49598
    YM-49598, YM 49598
    T29186738575-62-7
    YM49598 is a tachykinin receptor antagonist. YM49598 exhibited high binding affinities at NK(1) (pK(i) = 9.09 +/- 0.02) and NK(2) (pK(i) = 9.94 +/- 0.03) receptors, respectively. YM49598 was almost inactive but produced a potent inhibition (IC(50) = 11 +/
    • $1,820
    8-10 weeks
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  • [Sar9] Substance P acetate(77128-75-7 free base)
    TP1862L
    [Sar9]-Substance P acetate is one of NK-1 receptor agonist. The action of SP on progesterone metabolism was mimicked by the rNK1-specific agonist [Sar-9,Met(O2)11]-SP.
    • $54
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