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。 | |||
TP2309 |
NEUROTENSIN TFA (39379-15-2 free base)
Pyr-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH TFA(55508-42-4 free base),NEUROTENSIN TFA,神经加压素 |
Others | Others |
Neurotensin TFA (39379-15-2 free base) 是一种内源性 13 个氨基酸的神经肽,具有显着的阿片类非依赖性镇痛作用。它在大脑中充当神经递质,在肠道中充当激素,也充当神经调节剂。由于它与多种神经递质系统如多巴胺能、血清素能、谷氨酸能、GABA 能和胆碱能系统。它具有作为人体代谢物、有丝分裂原、神经递质和创伤的作用。 | |||
T38807L |
[Lys8, Lys9]-Neurotensin (8-13) acetate
|
Neurotensin Receptor | GPCR/G Protein |
[Lys8, Lys9]-Neurotensin (8-13) acetate 是一种神经降压素类似物,通过激活 G 蛋白偶联受体 NTS1 和 NTS2 发挥镇痛作用,hNTS1 和 hNTS2 受体的 Ki 值分别为 0.33 nM 和 0.95 nM。 | |||
T7617L |
Neurotensin(8-13) 3TFA(60482-95-3(free base))
|
Neurotensin Receptor | GPCR/G Protein |
Neurotensin(8-13) 3TFA(60482-95-3(free base)) 是神经降压素 (NT) 片段,神经降压素 (8-13) 导致细胞表面 NT1 受体 (NTR1) 密度降低。 | |||
T40850 |
[D-Trp11]-Neurotensin
[D-Trp11]-Neurotensin |
||
[D-Trp11]-Neurotensin is a compound that functions as a selective antagonist of Neurotensin (NT) in perfused rat hearts, while exhibiting full agonist properties in guinea pig atria and rat stomach strips. Additionally, this compound can inhibit hypotension induced by NT. | |||
T38807 |
[Lys8, Lys9]-Neurotensin (8-13)
JMV438,[Lys8, Lys9]-Neurotensin (8-13) |
||
[Lys8, Lys9]-Neurotensin (8-13) (JMV438) is a Neurotensin analog that elicits analgesic effects by activating the G protein-coupled receptors NTS1 and NTS2. The compound has K i values of 0.33 nM and 0.95 nM for hNTS1 and hNTS2 receptors, respectively. | |||
T33656 |
Neurotensin (1-6)
|
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Neurotensin (1-6) affects dopamine release from striatum. | |||
TP2393 |
Neurotensin-related hexapeptide
Lant-6 |
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Neurotensin-related hexapeptide exists in retinal ganglion cells and in their central projections in pigeons and may be utilized as a neuroactive substance by the central terminals of numerous retinal ganglion cells in birds. | |||
T76572 |
Acetyl neurotensin (8-13)
|
||
Acetyl neurotensin (8-13) 是神经降压素类似物,具有完全结合和药理活性。 | |||
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。 | |||
T8657 |
KYP-2047
|
Others | Others |
KYP-2047 是一种非常有效的选择性脯氨酰寡肽酶 (POP) 抑制剂。 | |||
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。 | |||
T7615 |
Xenopsin
爪蟾肽,Xenopsin(2TFA) |
Others | Others |
Xenopsin (Xenopsin(2TFA)) 是一种神经降压素样八肽,来自于非洲爪蟾皮肤,能够抑制胃泌素刺激的胃酸分泌。 | |||
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。 | |||
T7615L |
Xenopsin 2TFA(51827-01-1(free base)
|
Others | Others |
Xenopsin 2TFA(51827-01-1(free base) 是一种以前从两栖动物皮肤中分离出来的神经降压素样八肽。 | |||
TP1116L |
Kinetensin acetate(103131-69-7 free base)
Kinetensin (human) acetate |
Neurotensin Receptor | GPCR/G Protein |
Kinetensin acetate(103131-69-7 free base) 是从经胃蛋白酶处理的人血浆中分离出来的。它是一种神经降压素样肽。 | |||
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。 | |||
TP2209L |
Xenin 8 acetate
Xenin 8 acetate (117442-28-1 Free base) |
IGF-1R | Tyrosine Kinase/Adaptors |
Xenin 8 acetate 是神经降压素/异视素家族中 Xenin 的生物活性片段。 Xenin 8 acetate 增强精氨酸诱导的胰岛素释放(40%)并增强胰高血糖素对精氨酸(60%)和卡巴胆碱(50%)的反应。 | |||
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). | |||
TP2462 |
Magaratensin
Asp-lys-arg-pro-tyr-ile-leu-his-glu |
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Magaratensin is a neurotensin-related peptide related to the skin of Rana margarate. | |||
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. | |||
T75711 |
Contulakin G
|
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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。 | |||
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 | |||
T72410 | Sortilin antagonist 1 | ||
Sortilin antagonist 1 是一种 sortilin 拮抗剂,抑制神经紧张素 (NTS) 与 Sortilin 结合的 IC50值为 20 nM。NTS 是 sortilin 配体。Sortilin antagonist 1 可用于神经疾病的研究。 | |||
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. | |||
TP2209 |
Xenin-8
|
Others | Others |
neurotensin-like peptide that modulate pancreatic insulin and glucagon secretion/effects | |||
T24279 |
L 156903
L-156903,L156903 |
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L 156903 is a bioactive chemical. It also inhibits the binding of neurotensin to brain tissue. | |||
TP1116 |
Kinetensin
Kinetensin (human) |
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Kinetensin is a neurotensin-like peptide. | |||
TP1085 |
Neuromedin N
Neuromedin N (rat, mouse, porcine, canine) |
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Neuromedin N is a neuropeptide derived from the same precursor polypeptide as neurotensin, and with similar but subtly distinct expression and effects. | |||
T13530 | AF40431 | Others | Others |
AF40431 is the first reported small-molecule ligand of sortilin (IC50: 4.4 µM; Kd: 0.7 µM). AF40431 is bound in the neurotensin-binding site of sortilin. | |||
TP2012 |
JMV 449
|
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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 | |||
TP1482 |
Xenopsin TFA (51827-01-1 free base)
Xenopsin TFA |
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Xenopsin TFA is a neurotensin-like octapeptide derived from the skin of xenopus xenopus.Xenopsin TFA is an inhibitor of tetrachloroside to stimulate gastric acid secretion. | |||
T78954 |
hNTS1R agonist-1
|
Neurotensin Receptor | GPCR/G Protein |
hNTS1R agonist-1 (Compound 10)为能穿透血脑屏障的hNTS1R全激动剂(Ki:6.9 nM)。它能提升帕金森病(PD)模型小鼠的运动能力及记忆。作为一种Neurotensin(8-13)类似物,hNTS1R agonist-1同时具有神经保护作用。 | |||
T82647 |
Cyanine5 NHS ester bromide
|
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Cyanine5 NHS ester bromide 是用于标记肽、蛋白质和寡核苷酸氨基的活性染料。作为菁染料,该化合物特别适用于通过精氨酸残基对神经紧张素 (8-13) 进行荧光标记。 | |||
T80765 |
Xenopsin TFA
|
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Xenopsin TFA是一种神经降压素样八肽,源自非洲爪蟾皮肤。该化合物能够抑制胃泌素刺激的胃酸分泌。 | |||
T80766 |
Xenin-8 TFA
|
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Xenin-8 TFA为Xenin的C端八肽段,同时是其生物活性片段。该化合物隶属于神经降压素/xenopsin家族多肽中。它能激发基础胰岛素的分泌并剂量依赖性地加强胰岛素对葡萄糖反应(EC50=0.16 nM)。 | |||
T70039 | BIM-46174 | ||
BIM-46174 is a New Inhibitor of the Heterotrimeric Gα/Gβγ Protein Complex. BIM-46174 acts as a selective inhibitor of heterotrimeric G-protein complex. BIM-46174 prevents the heterotrimeric G-protein signaling linked to several GPCRs mediating (a) cyclic AMP generation (Gαs), (b) calcium release (Gαq), and (c) cancer cell invasion by Wnt-2 frizzled receptors and high-affinity neurotensin receptors (Gαo/i and Gαq). BIM-46174 inhibits the growth of a large panel of human cancer cell lines, includ... | |||
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。 |