Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1310 |
Neurotensin
|
Neurotensin Receptor | GPCR/G Protein |
Neurotensin 是一种 13 个氨基酸的神经肽,参与调节促黄体激素和催乳素的释放,并与多巴胺能系统有显着的相互作用。它作为细胞有丝分裂原,作用于各种结肠直肠癌和胰腺癌。 | |||
T7617 |
Neurotensin(8-13)
神经降压素(8-13),Neurotensin(8-13)(3TFA) |
Neurotensin Receptor | GPCR/G Protein |
Neurotensin(8-13) 是神经降压素的活性片段,可导致细胞表面 NT1 受体 (NTR1) 密度降低。 | |||
TQ0086 |
AF38469
AF-38469 |
Neurotensin Receptor | GPCR/G Protein |
AF38469 是一种新型、特异性和可口服的Sortilin 抑制剂,IC50值为 330 nM。 | |||
T16860 |
SBI-553
|
Neurotensin Receptor | GPCR/G Protein |
SBI-553 是能透过血脑屏障的NTR1的别构抑制剂,EC50值为 0.34 μM。 | |||
T9044 |
SORT-PGRN interaction inhibitor 1
|
Neurotensin Receptor | GPCR/G Protein |
SORT-PGRN interaction inhibitor 1 是一种 sortilin-progranulin 相互作用抑制剂,IC50为 2 μM。 | |||
T11861 |
LM11A-31 dihydrochloride
|
Others | Others |
LM11A-31 dihydrochloride 是一种具有高血脑屏障通透性的氨基酸衍生物,能阻断 p75 介导的细胞死亡。它是一种 p75NTR(神经营养蛋白受体 p75) 非肽调节剂,是口服有效的 proNGF 拮抗剂。它可以逆转中晚期的阿尔茨海默氏病小鼠模型中的胆碱能神经突营养不良。 | |||
T23386 |
SR 142948
|
Neurotensin Receptor | GPCR/G Protein |
SR 142948 是一种神经降压素 (NT) 受体拮抗剂。 | |||
TQ0075 |
ML314
|
Neurotensin Receptor | GPCR/G Protein |
ML314 是一种具有脑渗透性非肽 β-抑制素偏向神经降压素 NTR1 受体激动剂(EC50:1.9 μM),是一种用于甲基苯丙胺滥用的偏向神经降压素受体配体,抑制 NTR2 和 GPR35。 | |||
T28217 |
NTRC-844
NTRC 844,NTRC844 |
Neurotensin Receptor | GPCR/G Protein |
NTRC-844 是一种具有选择性的大鼠神经紧张素受体 2 型(NTS2)拮抗剂,在动物疼痛模型中显示出镇痛活性。 | |||
TP1085L |
Neuromedin N acetate(92169-45-4 free base)
Neuromedin N (rat, mouse, porcine, canine) acetate |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Neuromedin N acetate(92169-45-4 free base) 是一种神经肽,其衍生自与神经降压素相同的前体多肽,具有相似但略有不同的表达和作用。Neuromedin N 是多巴胺 D2 受体激动剂与大鼠新纹状体膜结合的有效调节剂。 | |||
T37529 |
TC NTR1 17
|
||
Non-peptide neurotensin receptor 1 (NTS1) partial agonist (EC50 <15.6 nM and Emax = 63% of neurotensin response in Ca2+ mobilization assay). Exhibits over 50-fold selectivity for NTS1 over NTS2 and GPR35. Hershberger et al (2014) Imidazole-derived agonists for the neurotensin 1 receptor. Bioorg.Med.Chem.Lett. 24 262 PMID:24332089 | |||
T16034 |
Meclinertant
SR 48692 |
Others | Others |
Meclinertant is an effective, selective, nonpeptide, and orally active neurotensin receptor 1 (NTS1) antagonist. Meclinertant competitively antagonizes neurotensin-induced intracellular Ca2+ mobilization (pA2 : 8.13), in human colon carcinoma (HT-29) cell | |||
T16358 |
NTRC-824
|
Others | Others |
NTRC-824 is >150-fold selectivity for NTS2 over NTS1 (Ki >30 μM). NTRC-824 is an effective, selective, and neurotensin-like nonpeptide neurotensin receptor type 2 (NTS2) antagonist (IC50: 38 nM and a Ki : 202 nM). | |||
T75711 |
Contulakin G
|
||
Contulakin G为O-糖基化无脊椎动物神经紧张素,作为较弱的神经紧张素受体(neurotensin receptor)激动剂,并具有有效的镇痛作用。 | |||
T70271 | PD-149163 | ||
PD-149163 is a selective, brain penetrating Neurotensin NTR1 receptor agonist. Neurotensin agonists block the pre-pulse inhibition deficits produced by a 5-HT2A and an α1 agonist. As a result, PD-149163 shows pro-cognitive, anti-psychotic and anxiolytic effects. | |||
T32700 |
Levocabastine
Livostin,Bilina |
||
Levocarbastine is a second-generation H1 receptor antagonist for allergic conjunctivitis. It also acts as a potent selective antagonist for the neurotensin receptor NTS2 and is the first drug to be used to characterize different neurotensin subtypes. | |||
T75868 | JMV 449 acetate | ||
JMV 449 acetate 是一种有效的神经降压素受体 (neurotensin receptor) 激动剂。JMV 449 acetate 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 acetate 对小鼠具有高效、持久的降温和缓解疼痛作用。 | |||
T28845 |
SR142948A HCl
SR142948A,SR 142948A,SR-142948A,SR142948A hydrochloride |
||
SR 142948A is a non-peptide antagonist of neurotensin receptor. SR 142948A affects the expression of c-Fos and has properties of antipsychotic agent. SR 142948A blocks hypothermia and analgesia induced by neurotensin. It blocks the increase in the concent | |||
TP2012 |
JMV 449
|
||
Potent, metabolically stable neurotensin receptor agonist peptide (IC50 = 0.15 nM for inhibition of [125I]-NT binding to neonatal mouse brain; EC50 = 1.9 nM for contraction of guinea pig ileum). Produces long-lasting hypothermic, neuroprotective and analg | |||
T73677 | SR 142948 dihydrochloride | ||
SR 142948 dihydrochloride是一种口服活性高、选择性强的非肽类神经降压素受体(NT)拮抗剂,其在h-NTR1-CHO细胞、HT-29细胞和成年大鼠脑中IC50分别为1.19 nM、0.32 nM、3.96 nM。在HT-29细胞中,该化合物能够有效拮抗NT诱导的肌醇单磷酸盐形成,IC50为3.9 nM。此外,SR 142948 dihydrochloride在体内能够阻断NT诱导的体温下降、镇痛和转向行为,且具有良好的血脑屏障通透性,适用于精神疾病研究。 |