Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1045L |
Orexin B, rat, mouse Acetate
Rat orexin B,Orexin B (mouse) Acetate,Orexin B, rat, mouse Acetate(202801-92-1 free base) |
OX Receptor | GPCR/G Protein; Neuroscience |
Orexin B, rat, mouse Acetate (Rat orexin B)(202801-92-1 free base) 是 Orexin 受体的内源性激动剂,对 OX1 和 OX2 的 Kis 分别为 420 和 36 nM。 | |||
T3177 |
Orexin 2 Receptor Agonist
OX2R |
OX Receptor | GPCR/G Protein; Neuroscience |
Orexin 2 Receptor Agonist (OX2R) 是一种选择性有效的OX2R 激动剂, EC50为23 nM。 | |||
TP1139 |
Orexin B, human
Human orexin B |
||
Orexin B, human is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2, respectively. Orexin B is a hypothalamatic neuropeptide stimulating food intake in rats. | |||
TP1045 |
Orexin B, rat, mouse
Orexin B (mouse),Rat orexin B |
||
Orexin B, rat, mouse is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2, respectively. | |||
TP1138 |
Orexin B, human TFA (205640-91-1 free base)
Orexin B, human TFA,Human orexin B TFA |
||
Orexin B, human (TFA) is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2. | |||
TP1975 |
[Ala11,D-Leu15]-Orexin B(human)
[Ala11,D-Leu15]-Orexin B |
||
Highly potent and selective OX2 receptor agonist; displays 400-fold selectivity over OX1 receptors. EC50 values are 0.13 and 52 nM for human OX2 and OX1 receptors respectively. | |||
T38139 |
Orexin receptor antagonist 2
|
||
Orexin Receptor Antagonist 2 (compound 30), characterized by its potent antagonistic activity with pKis of 7.69 and 9.78, holds promise for insomnia research[1]. | |||
TP1975L |
[Ala11,D-Leu15]-Orexin B acetate
[Ala11,D-Leu15]-Orexin B acetate (532932-99-3 Free base) |
OX Receptor | GPCR/G Protein; Neuroscience |
[Ala11,D-Leu15]-Orexin B acetate 是一种特异性 orexin-2 受体 (OX2) 激动剂,EC50 为 0.13 nM,比 OX1 (52 nM) 特异性高 400 倍。 | |||
T39561 |
Orexin 2 Receptor Agonist 2
|
||
Orexin 2 Receptor Agonist 2 (ORA-2) is a specific agonist for the orexin 2 receptor. | |||
TP1301 |
Orexin A (human, rat, mouse)
|
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Orexin A human, rat, mouse, a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A human, rat, mouse has been used to study its effect on the functioning of porcine pancreatic islets. It has also been used as an orexin receptor 1 (OX1R) agonist to study the effect of orexin systems in the effect of etonogestrel on respiratory response to prolonged metabolic acidosis. | |||
TP1550 |
Orexin A (human, rat, mouse) (TFA)
|
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Endogenous agonist at orexin receptors (Ki values are 20 and 38 nM for OX1 and OX2 receptors respectively). Stimulates feeding following central administration and may be involved in the control of sleep-wake cycle and other hypothalamic functions. | |||
TP1301L |
Orexin A (human, rat, mouse) acetate (205640-90-0 Free base)
|
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T62050 |
Orexin receptor antagonist 4
|
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Orexin receptor antagonist 4 是有效的选择性食欲素 2 受体 (OX2R) 拮抗剂。Orexin receptor antagonist 4 抑制 OX2R 和 OX1R 的 IC50分别为 4.27 nM 和295 nM。 | |||
T5503 |
IPSU
|
OX Receptor | GPCR/G Protein; Neuroscience |
IPSU 是可口服和脑渗透性的选择性OX2R 拮抗剂,pKi 值为7.85。 | |||
T62453 | Orexin receptor antagonist 3 | ||
Orexin receptor antagonist 3 (example 216) 是一种促食素受体 (orexin receptor) 的拮抗剂。 | |||
T75920 |
Orexin B, human TFA
|
||
Orexin B, human (TFA) 是 Orexin 受体的内源性激动剂,与 OX1和 OX2结合的 Ki 值分别为 420 和 36 nM。 | |||
T79056 |
Orexin receptor modulator-1
|
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Orexin receptormodulator-1 是一款针对食欲素受体的调节剂,主要应用于物质成瘾、惊恐障碍、焦虑、创伤后应激障碍 (PTSD)、疼痛、抑郁、季节性情感障碍、进食障碍及高血压的科研领域。 | |||
T2710 |
TCS 1102
|
OX Receptor | GPCR/G Protein; Neuroscience |
TCS 1102 是双食欲素受体拮抗剂,对 OX1和OX2受体的Ki 分别为3和 0.2 nM。 | |||
T11186 |
EMPA
|
OX Receptor | GPCR/G Protein; Neuroscience |
EMPA 是一种选择性、高亲和力和可逆的食欲素 OX2 受体拮抗剂,与人和大鼠 OX2-HEK293 膜结合,KD 值分别为 1.1 和 1.4 nM。 | |||
T75925 |
Orexin B, rat, mouse TFA
|
||
Orexin B, rat, mouse (Rat orexin B) TFA,作为一种内源性促进食欲的(Orexin receptor)激动剂,通过结合并激活两个亲密相关的孤儿G蛋白偶联受体OX1-R和OX2-R,促进食物摄入和能量消耗,并在睡眠-觉醒调节中扮演关键角色。 | |||
T73658 |
Orexin A (human, rat, mouse) (acetate)
|
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Orexin A (Hypocretin-1) (human, rat, mouse) acetate 是一种具有镇痛特性的下丘脑神经肽 (可透过血脑屏障)。Orexin A (human, rat, mouse) acetate 也是一种OX1R 激动剂,能以时间和剂量依赖性的方式诱导 SH-SY5Y 细胞BDNF 和TH 蛋白的表达。Orexin A (human, rat, mouse) acetate 可用于食欲调节、神经退行性疾病,以及调节伤害性信息传递的研究。 | |||
T1913 |
MK-3697
|
OX Receptor | GPCR/G Protein; Neuroscience |
MK3697是OX2受体的一种高效选择性拮抗剂,Ki 值为0.95nM。 | |||
T4965 |
TCS-OX2-29
|
OX Receptor | GPCR/G Protein; Neuroscience |
TCS-OX2-29 是高亲和力和选择性OX2R 拮抗剂,IC50值为 40 nM,pKI 值为 7.5。它对 OX2 的选择性比 OX1 高 250 倍以上。 | |||
T75921 |
[Ala11,D-Leu15]-Orexin B(human) TFA
|
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[Ala11,D-Leu15]-Orexin B(human) TFA为高效的orexin-2 receptor (OX2)选择性激动剂。其对OX2展现出比OX1 (52 nM) 高达400倍的较高选择性(EC50=0.13 nM)。 | |||
T2613 |
Almorexant
阿莫伦特,ACT 078573 |
OX Receptor | GPCR/G Protein; Neuroscience |
Almorexant (ACT 078573) 是一种有效的竞争性食欲素 1 受体 (OX1)/食欲素 2 受体 (OX2) 双重拮抗剂,OX1 和 OX2 的 Ki 值分别为 1.3 和 0.17 nM。 | |||
T16096 |
Filorexant
MK-6096 |
OX Receptor | GPCR/G Protein; Neuroscience |
Filorexant (MK-6096) 是一种口服有效且选择性可逆的 OX1 和 OX2 受体拮抗剂,Ki 值小于3nM。 | |||
T5498 |
SB-649868
GSK649868 |
OX Receptor | GPCR/G Protein; Neuroscience |
SB-649868 (GSK649868) 是一种有效的选择性口服活性食欲素拮抗剂,对 OX1 和 OX2 受体的 pKi 分别为 9.4 和 9.5。 | |||
T12877L |
Seltorexant
JNJ-42847922 |
OX Receptor | GPCR/G Protein; Neuroscience |
Seltorexant (JNJ-42847922) 是一种可口服,高亲和性以及选择性的 orexin-2 受体(OX2R)拮抗剂,对人和大鼠中的 OX2R 的pKi 值分别为 8.0 和 8.1。它穿过血脑屏障,迅速占据大鼠大脑中的 OX2R 结合位点。 | |||
T3722 |
MK-1064
Urokinase inhibitor 1,MK 1064 |
OX Receptor | GPCR/G Protein; Neuroscience |
MK-1064 (Urokinase inhibitor 1) 是一种选择性食欲素 2 (2-SORA)受体拮抗剂,可用于失眠患者的研究。 | |||
T6658 |
SB-408124
N-(6,8-二氟-2-甲基-4-喹啉)- N-[4-(二甲氨基)苯基]尿素 |
OX Receptor | GPCR/G Protein; Neuroscience |
SB408124 是一种 OX1 受体的非肽拮抗剂,在全细胞和膜中的 Ki 值分别为 57 和 27 nM,其选择性是 OX2 受体的 50 倍。 | |||
T6140 |
SB-334867 free base
SB334867A free base,SB-334867,SB 334867,SB334867 |
OX Receptor | GPCR/G Protein; Neuroscience |
SB-334867 free base (SB334867A free base) 是一种选择性 orexin-1(OX1) 受体拮抗剂,对 OX2有选择性,pKb 为7.4,对 5-HT2B、5-HT2C 的选择性是 100 倍,pKi 值分别为 5.4 和 5.3。它减少乙醇消耗,还抑制吗啡诱导的体内运动活动敏感性的获得。 | |||
T6155 |
Almorexant hydrochloride
ACT-078573 hydrochloride,Almorexant HCl |
OX Receptor | GPCR/G Protein; Neuroscience |
Almorexant hydrochloride (ACT-078573 hydrochloride) 是一种有效的竞争性食欲素 1 受体(OX1)/食欲素 2 受体 (OX2) 双重拮抗剂,OX1 和 OX2 的 Ki 值分别为 1.3 和 0.17 nM。 | |||
T26559 |
ACT-462206
|
OX Receptor | GPCR/G Protein; Neuroscience |
ACT-462206 是一种可口服且可穿过血脑屏障的Orexin 1/Orexin 2 受体拮抗剂。ACT-462206 具有高效性,可用于研究睡眠和焦虑。 | |||
T39229 |
YNT-185
|
OX Receptor | GPCR/G Protein; Neuroscience |
YNT-185 is a nonpeptide, selective agonist of the orexin type-2 receptor (OX2R), demonstrating EC50 values of 0.028 μM and 2.75 μM for OX2R and OX1R, respectively. Furthermore, YNT-185 effectively alleviates symptoms of narcolepsy-cataplexy in mouse models. | |||
T67782 |
Daridorexant hydrochloride
Nemorexant hydrochloride,Quviviq |
OX Receptor | GPCR/G Protein; Neuroscience |
Daridorexant hydrochloride (Nemorexant hydrochloride) 是一种新型的双Orexin 受体拮抗剂。Daridorexant hydrochloride 可用于失眠研究。 | |||
TP1973L |
OXA (17-33) acetate
|
OX Receptor | GPCR/G Protein; Neuroscience |
OXA (17-33) acetate 是一种比 OX2 (EC50 = 187 nM) 更有效的 orexin-1 受体 (OX1, EC50 = 8.29 nM)) 激动剂。 | |||
T5500 |
DORA-22
|
OX Receptor | GPCR/G Protein; Neuroscience |
DORA-22 是一种双食欲素受体拮抗剂,可改善轻度压力引起的失眠,对记忆的影响很小。 | |||
T28060 |
MK-8133
|
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MK-8133 is an antagonist of orexin-2 selective receptor with favorable development properties. | |||
T39560 |
Danavorexton
|
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Danavorexton is an orexin receptor agonist. | |||
T69715 |
ORN-0829 hydrate
|
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ORN-0829 hydrate is a potent dual orexin 1/2 receptor antagonist for the treatment of insomnia. | |||
T24013 |
DORA 42
DORA42,DORA-42 |
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DORA 42 is a dual antagonist of the orexin receptor OX1R and OX2R. | |||
T62370 |
Nivasorexant
|
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Nivasorexant 是一种食欲素受体 (orexin receptor) 的有效拮抗剂。 | |||
T11477 | GSK1059865 | Others | Others |
GSK1059865 is a potent antagonist of the orexin 1 receptor. | |||
T4965L |
TCS-OX2-29 HCl
TCSOX 229,TCS-OX229,TCS OX229,TCS OX2 29,TCSOX-229,TCSOX229 |
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TCS-OX2-29 is a selective orexin-2 receptor antagonist (IC50 = 40 nM), which plays an important role in pain modulation. | |||
T39808 | Firazorexton | ||
Firazorexton is a potent orexin type 2 receptor (OX2R) agonist. | |||
T69858 | RTIOX-372 | ||
RTIOX-372 is a potent and selective orexin-1 receptor antagonist. | |||
T70332 |
JNJ-61393215
|
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JNJ-61393215 is a novel selective orexin-1 receptor (OX1R) antagonist. | |||
T75922 |
OXA(17-33) TFA
|
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OXA(17-33) TFA,一种高效且选择性的orexin-1 receptor (OX1)激动剂,其对OX1 (EC50=8.29 nM) 的选择性是对OX2 (187 nM) 的23倍。 | |||
TP1973 |
OXA(17-33)
OXA (17-33) |
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Potent and selective peptide orexin OX1 receptor agonist (EC50 values are 8.29 and 187 nM for OX1 and OX2 receptors respectively). Truncated form of orexin A. | |||
T39807 |
Suntinorexton
|
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Suntinorexton, a heterocyclic compound, is a selective agonist of orexin type 2 receptors. |