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Cat. No. | Product Name | Target | Signaling Pathways |
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TP1087 |
Substance P
Neurokinin P,P物质 |
Endogenous Metabolite; Neurokinin receptor | GPCR/G Protein; Metabolism; Neuroscience |
Substance P (Neurokinin P) 是一种神经肽,其内源性受体是神经激肽1受体,在中枢神经系统中作为神经递质和神经调节剂。 | |||
T7554 |
Substance P (7-11)
Substance P 7-11(TFA) |
Others; Neurokinin receptor | GPCR/G Protein; Neuroscience; Others |
Substance P (7-11) (Substance P 7-11(TFA)) 是神经肽物质P 的C-末端片段,可引起细胞内钙浓度的增加。 | |||
TP2155 |
Substance P TFA
Neurokinin P TFA |
Others | Others |
Substance P TFA (Neurokinin P TFA) is a neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS, targeting the neurokinin 1 receptor (NK1-receptor, NK1R). | |||
T7828 |
[Sar9,Met(O2)11]-Substance P
Bhsar-sp,NA,精氨酰-脯氨酰-赖氨酰-脯氨酰-谷氨酰-谷氨酰-苯丙氨酰-苯丙氨酰-SAR-亮氨酸-蛋氨酸[O2]-胺 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
[Sar9,Met(O2)11]-Substance P (NA) 是选择性速激肽NK1受体激动剂。 | |||
T6905 |
Netupitant
Ro 67-31898/000,奈妥吡坦,CID 6451149 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Netupitant (CID 6451149) 是一种高效选择性、可口服的神经激肽 1 受体 (NK1) 拮抗剂,具有止吐作用,在 CHO 细胞中对 hNK1的 Ki 值为 0.95 nM。 | |||
T7396 |
Substance P(1-7)
Substance P 1-7 |
Others; Neurokinin receptor | GPCR/G Protein; Neuroscience; Others |
Substance P(1-7) (Substance P 1-7) 是神经肽P 物质的片段,可对孤束核产生抑制和缓和作用,具有抗炎、抗伤害和抗痛觉过敏的作用。 | |||
T1790 |
Fosaprepitant dimeglumine
福沙匹坦二甲葡胺,L785298,福沙吡坦二甲葡胺,MK-0517,Fosaprepitant dimeglumine salt |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Fosaprepitant dimeglumine (MK-0517) 是 Aprepitant 的前药。它是一种神经激肽 1 受体拮抗剂,可用于预防化疗引起的恶心呕吐。 | |||
T68068L |
(R)-CJ 11974
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
T25616 |
Lanepitant 2HCl
LY303870 dihydrochloride,LY 303870 dihydrochloride,LY-303870 dihydrochloride,Lanepitant dihydrochloride |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Lanepitant 2HCl 是一种非肽类神经激肽-1 受体拮抗剂,具有镇痛和抗炎活性。Lanepitant 2HCl 抑制 P 物质与神经激肽-1 受体的结合,抑制神经源性炎症和疼痛传递,可用于研究偏头痛等疼痛性神经病变类疾病。 | |||
T1743 |
Aprepitant
MK-869,MK-0869,阿瑞匹坦,L-754030,Aprepitant` |
HIV Protease; Antibacterial; Antibiotic; Neurokinin receptor | GPCR/G Protein; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Aprepitant (Aprepitant`) 是选择性和高亲和力的神经激肽1受体拮抗剂,Kd 值为86 pM。 | |||
T7209 |
Maropitant
马罗匹坦,马罗皮坦 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Maropitant 是一种可口服的选择性神经激肽受体拮抗剂,通过阻止催吐中心与化学感受器触发区中 P 物质的结合而起作用,有预防呕吐作用。 | |||
T3716 |
Rolapitant
罗拉吡坦,SCH619734,罗拉匹坦 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Rolapitant (SCH619734) 是一种高效选择性具有口服活性的神经激肽 1 受体抑制剂,Ki 值为0.66 nM。 | |||
T76427 |
(D-Pro2,D-Trp6,8,Nle10)-Neurokinin B
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(D-Pro2,D-Trp6,8,Nle10)-Neurokinin B 是 Neurokinin B(Neurokinin Receptor) 的竞争性拮抗剂,pA2 为 5.5,对 Substance P 或 Neurokinin A 没有影响。 | |||
T13306L2 | Vapreotide diacetate | ||
Vapreotide diacetate is a synthetic analog of somatostatin. It has analgesic activity most likely mediated through the blockade of the neurokinin-1 receptor (NK1R), the substance P (SP)-preferring receptor. | |||
T76429 |
Neurokinin Receptor (393-407), rat
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Neurokinin Receptor(393-407), rat (SPR393–407) 是一段属于大鼠神经激肽1受体(NK1R)的特定肽。它与P物质(SP)结合后,通过内吞作用迅速被NK1R内化,并循环至质膜。此化合物主要应用于神经源性炎症研究领域。 | |||
T37110 |
Biotin-Substance P
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Biotin-Substance P 在中枢神经系统中作为神经递质和神经调节剂。神经激肽1受体 (neurokinin 1 receptor,NK1R)是 Biotin-Substance P 的内源性受体。 | |||
T76405 |
[D-Trp2,7,9] Substance P
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[D-Trp2,7,9] Substance P 是一种速激肽 (Neurokinin Receptor) 拮抗剂,对 NK-1、NK-2和 NK-3受体的 Ki 值分别为 1 μM、1.3 μM 和 ~9 μM。 | |||
T71935 |
WIN 66306
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WIN 66306 is a cyclic heptapeptide antagonist of neurokinin-1 (NK1) and NK2 receptors originally isolated from A. flavipes. It binds to NK1 and NK2 receptors and inhibits contractions induced by substance P in isolated guinea pig ileum in a concentration-dependent manner. | |||
T76406 |
[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11)
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[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) 为高效的神经激肽 NK1 拮抗剂,能够有效抑制金蛋白 P 物质 (GPSP) 与 P 物质 (SP) 的活性。 | |||
T81077 |
Substance P(1-4)
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Substance P(1-4)为一有效的神经激肽受体(NK-R)拮抗剂,具有调节正常造血功能并抑制内源性红细胞集落(EEC)形成的能力。 | |||
T38276 |
Benzomalvin C
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Benzomalvin C is a weak antagonist of the neurokinin-1 (NK1) receptor inhibiting binding of substance P by 46% when used at 100 μg/ml in vitro. It is also a weak inhibitor of indolamine 2,3-dioxygenase (IDO) with an IC50 value of 130 μM for recombinant IDO. It was isolated from Penicillium and contains an epoxide group at C-19 and C-20, which is not present in benzomalvins A, B, or E. | |||
T76477 |
[His11]Substance P
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[His11]Substance P 是 Substance P (Substance P ) 的类似物。Substance P (Neurokinin P) 是一种神经肽,在中枢神经系统中作为神经递质和神经调节剂。 | |||
T76476 |
[Gly11] Substance P
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[Gly11] Substance P 是 Substance P (Substance P ) 的类似物。Substance P (Neurokinin P) 是一种神经肽,在中枢神经系统中作为神经递质和神经调节剂。 | |||
T68371 |
Rolapitant hydrochloride hydrate
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Rolapitant, also known as SCH-619734, is an orally bioavailable, centrally-acting, selective, neurokinin 1 receptor (NK1-receptor) antagonist with potential antiemetic activity. Upon oral administration, rolapitant competitively binds to and blocks the activity of the NK1-receptor in the central nervous system, thereby inhibiting the binding of the endogenous ligand, substance P (SP). This may prevent both SP-induced emesis and chemotherapy-induced nausea and vomiting (CINV). The interaction of ... | |||
T76404 |
[Glp5,(Me)Phe8,Sar9] Substance P (5-11)
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[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) 是一种 Substance P 类似物,在大鼠大脑中对神经激肽 1 受体 (NK1R) 的作用与 Substance P 大致相等,但作用时间大大延长。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 能选择性地激活大鼠大脑间脑和中脑皮层的多巴胺代谢。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 还可增加大鼠运动活性,诱导成瘾剂寻求行为的恢复。 | |||
T70456 |
Nolpitantium Free Base
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Nolpitantium Free Base is a highly selective nonpeptide antagonist of neurokinin-1 (NK1) receptor. Nolpitantium potently, selectively and competitively inhibited substance P binding to NK1 receptors from various animal species, including humans. In vitro, it was a potent antagonist in functional assays for NK1 receptors such as [Sar9, Met(O2)11]substance P-induced endothelium-dependent relaxation of rabbit pulmonary artery and contraction of guinea-pig ileum. Up to 1 mkM, Nolpitantium had no eff... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T38033 | Benzomalvin B | ||
Benzomalvin B is a fungal metabolite originally isolated from Penicillium. It acts as an antagonist of neurokinin-1 (NK1) receptors, inhibiting binding of substance P by 24% in vitro when used at a concentration of 100 μg/ml. | |||
T71833 |
Acetylaszonalenin
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Acetylaszonalenin is a fungal metabolite that has been found in A. flavipes.1 It acts as an antagonist of neurokinin-1 (NK1) receptors, inhibiting binding of substance P with a Ki value of 170 μM. |