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抑制剂&激动剂
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TargetMol产品目录中 "u 27"的结果
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TargetMol产品目录中 "

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  • 抑制剂&激动剂
    6
    TargetMol | Inhibitors_Agonists
  • 重组蛋白
    1
    TargetMol | Recombinant_Protein
  • 多肽产品
    2
    TargetMol | Peptide_Products
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    19
    TargetMol | Antibody_Products
  • U 27391
    U-27391,U27391
    T26304106314-87-8
    U 27391 is a metalloproteinase inhibitor. It acts by inhibits the action of human recombinant interleukin-1beta and glycosaminoglycan synthesis.
    • ¥ 10600
    6-8周
    规格
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  • RU 27849
    RU-27849,RU27849
    T3443177963-70-3
    RU 27849 is used to study the binding of tryptamine recognition sites.
    • ¥ 10600
    6-8周
    规格
    数量
  • PNU-271965E
    PNU271965E
    T34101646064-41-7
    PNU-271965E is a bio-active chemical.
    • ¥ 10600
    待询
    规格
    数量
  • Melan-A/MART-1 analog
    [Leu27]-Melan-A, MART-1 (26-35)
    T81825204060-45-7
    [Leu27]-Melan-A, MART-1 (26-35)是一种具有改良的HLA-A*0201结合能力和增强的免疫原性及抗原性的生物活性肽。该类似物在第27位的Leu替换了Ala,与原生Melan-A (26-35)相比表现出更佳的性能。当序列N端为谷氨酰胺(Q)或谷氨酸(E)时,肽可能会自发形成焦谷氨酰(pGlu)。Q或E到pGlu的转化是自然发生的,pGlu的疏水性γ-内酰胺环被认为可增强针对胃肠道蛋白酶的抵抗力,使得含pGlu的肽成为这类肽的正常子集,在HPLC分析中通常作为评估肽纯度的一部分。
    • 待询
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  • Acetyl-(D-Phe2,Lys15,Arg16,Leu27)-VIP (1-7)-GRF (8-27)
    T83195202463-00-1
    Acetyl-(D-Phe2,Lys15,Arg16,Leu27)-VIP (1-7)-GRF (8-27),是一种血管活性肠肽,起到VIP1受体拮抗剂的作用。
    • 待询
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  • Neuromedin U-23 (rat) (trifluoroacetate salt)
    T35597
    Neuromedin U-23 (NMU-23) is a neuropeptide involved in diverse biological processes, including smooth muscle contraction, energy homeostasis, and nociception.1It is an agonist of neuromedin-U receptor 1 (NMUR1; EC50= 0.17 nM for the human receptor in a calcium mobilization assay using HEK293 cells) and NMUR2 (EC50= ~1.4-2 nM for arachidonic acid release in CHO cells expressing the human receptor).2,3NMU-23 (1 μM) induces contractions in isolated rat colon smooth muscle strips.4It decreases body weight and food intake and increases core body temperature in mice when administered at a dose of 36 μg/animal.5Intrathecal administration of NMU-23 decreases the mechanical pain threshold in the von Frey test in rats.6 1.Mitchell, J.D., Maguire, J.J., and Davenport, A.P.Emerging pharmacology and physiology of neuromedin U and the structurally related peptide neuromedin SBr. J. Pharmacol.158(1)87-103(2009) 2.Szekeres, P.G., Muir, A.I., Spinage, L.D., et al.Neuromedin U is a potent agonist at the orphan G protein-coupled receptor FM3J. Biol. Chem.275(27)20247-20250(2000) 3.Hosoya, M., Moriya, T., Kawamata, Y., et al.Identification and functional characterization of a novel subtype of neuromedin U receptorJ. Biol. Chem.275(38)29528-29532(2000) 4.Brighton, P.J., Wise, A., Dass, N.B., et al.Paradoxical behavior of neuromedin U in isolated smooth muscle cells and intact tissueJ. Pharmacol. Exp. Ther.325(1)154-164(2008) 5.Peier, A., Kosinski, J., Cox-York, K., et al.The antiobesity effects of centrally administered neuromedin U and neuromedin S are mediated predominantly by the neuromedin U receptor 2 (NMUR2)Endocrinology150(7)3101-3109(2009) 6.Yu, X.H., Cao, C.Q., Mennicken, F., et al.Pro-nociceptive effects of neuromedin U in ratNeuroscience120(2)467-474(2003)
    • 待估
    35日内发货
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    数量