1. Signaling Pathways
  2. GPCR/G Protein
    Neuronal Signaling
  3. Neurotensin Receptor

Neurotensin Receptor (神经降压素受体)

The neuropeptide neurotensin (NT) exerts central actionsthat include hypothermia, analgesia, and a number of effects that involve the modulation of nigrostriatal and mesocortico-limbic dopaminergic pathways. The two neurotensin receptor subtypes known to date, NTR1 and NTR2, belong to the family of G-protein-coupled receptors with seven putative transmembrane domains (TM). The NTR1 has high affinity for neurotensin, whereas the NTR2 has lower affinity for the peptide and is selectively recognized by levocabastine, an anti-histamine H1 receptor antagonist. These receptors have widespread, though not identical, central and peripheral distributions and exhibit distinct ontogenic profiles.

It is notably reported that NTR1 activation results in significant antinociception but also causes marked hypotension and hypothermia. In sharp contrast, NTR2 has emerged as an important pain target because NTR2-selective analogues exhibit potent analgesic activity in both acute and chronic pain conditions in dose-dependent analgesic effects without inducing drop in blood pressure or body temperature.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-14277
    Levocabastine Antagonist
    Levocabastine (R 50547) 是一种强效选择性组胺 H1 受体拮抗剂。Levocabastine 也是一种选择性、高亲和力的神经降压素受体亚型 2 (NTR2) 拮抗剂,对 mNTR2 的 Ki 值为 17 nM。Levocabastine 可作为 VLA-4 拮抗剂,干扰过敏性结膜炎 (AC) 结膜嗜酸性粒细胞的浸润。
    Levocabastine
  • HY-P0066
    Contulakin G Agonist
    Contulakin G 是一种 O-糖基化无脊椎动物神经紧张素。Contulakin-G 是一种较弱的神经紧张素受体 (neurotensin receptor) 激动剂。Contulakin G 还是一种有效的镇痛剂。
    Contulakin G
  • HY-P3057
    [D-Trp11]-Neurotensin Modulator
    [D-Trp11]-Neurotensin 是 Neurotensin (NT) 的类似物,在灌注的大鼠心脏中是 NT 的选择性拮抗剂,但在豚鼠心房和大鼠胃条中起完全激动剂的作用。[D-Trp11]-Neurotensin 可抑制 NT 引起的低血压。
    [D-Trp11]-Neurotensin
  • HY-153688
    SORT-PGRN interaction inhibitor 3 Inhibitor
    SORT-PGRN interaction inhibitor 3 (Compound 13) 是一种 SORT-PGRN 相互作用抑制剂 (IC50: 0.17 μM)。SORT-PGRN interaction inhibitor 3 可用于神经退行性疾病的研究。
    SORT-PGRN interaction inhibitor 3
  • HY-P4223
    Acetyl neurotensin (8-13)
    Acetyl neurotensin (8-13) 是最短的神经降压素类似物,具有完全结合和药理活性。
    Acetyl neurotensin (8-13)
  • HY-149941
    hNTS1R agonist-1 Agonist
    hNTS1R agonist-1 (Compound 10) 是一种可穿透大脑屏障的 hNTS1R 完全激动剂 (Ki: 6.9 nM)。hNTS1R agonist-1 可增强帕金森病 (PD) 小鼠的运动功能和记忆力。hNTS1R agonist-1 是一种 Neurotensin(8-13) 类似物,是一种神经保护剂。
    hNTS1R agonist-1
  • HY-14551B
    (S)-Osanetant Antagonist 99.25%
    (S)-Osanetant 是 Osanetant 的S对映体。Osanetant (SR142801) 是一种选择性的 NK3 受体拮抗剂。Osanetant 有抗焦虑和抗抑郁的作用,并被研究用于精神分裂症。
    (S)-Osanetant
  • HY-P1256
    JMV 449 Agonist
    JMV 449 是一种有效的神经降压素受体 (neurotensin receptor) 激动剂。JMV 449 显示抑制 [125I]-neurotensin 与新生小鼠脑结合的 IC50 为 0.15 nM,对收缩豚鼠回肠的 EC50 为 1.9 nM。JMV 449 对小鼠具有高效、持久的降温和缓解疼痛作用。
    JMV 449
目录号 产品名 / 同用名 应用 反应物种