Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1104L |
Melanin Concentrating Hormone, salmon acetate
MCH (salmon),Melanin Concentrating Hormone, salmon acetate(87218-84-6 free base) |
Others; Melanin-concentrating Hormone Receptor (MCHR) | GPCR/G Protein; Others |
Melanin Concentrating Hormone, salmon acetate (MCH (salmon))(87218-84-6 free base) 是一种 19 个氨基酸的环状肽,主要在下丘脑中表达。 | |||
TP1104 |
Melanin Concentrating Hormone, salmon
MCH (salmon) |
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Melanin Concentrating Hormone (MCH), a 19 amino acid cyclic peptide, is largely expressed in the hypothalamus. | |||
T11966 |
MCHR1 antagonist 2
|
HER; Melanin-concentrating Hormone Receptor (MCHR) | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
MCHR1 antagonist 2 是有效的黑色素聚集激素受体 1 拮抗剂,IC50为 65 nM。它也抑制hERG,在IMR-32 细胞中的IC50为 4.0 nM。 | |||
T75970 |
Melanin Concentrating Hormone, salmon TFA
|
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Melanin Concentrating Hormone, salmon TFA (MCH (salmon) TFA) 是在硬骨鱼的垂体中发现的 19 个氨基酸组成的神经肽,它调节食物摄入,能量平衡,睡眠状态和心血管系统。Melanin Concentrating Hormone, salmon TFA (MCH (salmon) TFA) 是 SLC-1/GPR24和 MCHR2的配体。 | |||
TP1102 |
MCH (salmon) TFA (87218-84-6 free base)
Melanin Concentrating Hormone, salmon TFA,MCH (salmon) TFA |
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Melanin Concentrating Hormone (MCH), a 19 amino acid cyclic peptide, is largely expressed in the hypothalamus. Melanin Concentrating Hormone is implicated in the control of general arousal and goal-orientated behaviours in mammals, and appears to be a key | |||
T8004 |
SNAP 94847 hydrochloride
|
GPR; Melanin-concentrating Hormone Receptor (MCHR) | Endocrinology/Hormones; GPCR/G Protein |
SNAP 94847 hydrochloride 是一种选择性黑色素浓缩激素受体1 拮抗剂,Ki 为 2.2 nM,具有抗抑郁样活性。它是 MCH 诱发的肌醇磷酸形成的高亲和力拮抗剂 ,pA2为 7.81。 | |||
TP1996 |
MCH(human, mouse, rat)
MCH (human, mouse, rat),黑色素聚集激酶素(MCH)( 大鼠) |
GPR; Melanin-concentrating Hormone Receptor (MCHR) | Endocrinology/Hormones; GPCR/G Protein |
MCH(human, mouse, rat) 是MCH-R 肽激动剂,对 CHO 细胞系中 MCH-2R 高度敏感,激活 MCH-1R 和 MCH-2R 的IC50 值分别为 0.3 和 1.5 nM,EC50值对分别为 3.9 和 0.1 nM。 | |||
T5406 |
SNAP 94847
SNAP-94847 |
GPR; Melanin-concentrating Hormone Receptor (MCHR) | Endocrinology/Hormones; GPCR/G Protein |
SNAP 94847 (SNAP-94847) 是一种选择性黑色素浓缩激素受体1 拮抗剂,Ki 为 2.2 nM。它具有抗焦虑和抗抑郁活性,可减少小鼠的食物摄入。 | |||
T22591 |
ATC 0175 hydrochloride
|
GPR; 5-HT Receptor; Melanin-concentrating Hormone Receptor (MCHR) | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
ATC 0175 hydrochloride 是一种具有口服活性的黑色素细胞浓缩激素1受体拮抗剂,具有强效性和选择性,ATC 0175 hydrochloride 对MCH1R、MCH2R、MCH1、5-HT2B 受体和5-HT1A 受体 具有亲和力 ,IC50分别为为13.5nM、>10,000 nM、13 nM、9.66 nM 和16.9 nM。ATC 0175 hydrochloride 在动物模型中表现出抗抑郁和抗焦虑作用。ATC0175可用于研究抑郁症和/或焦虑症。 | |||
T28902 |
T-226296
T 226296,T226296 |
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T-226296 is a antagonist of melanin concentrating hormone receptor 1 (MCHR1). | |||
T69170 | ATC0065 HCl | ||
ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist. | |||
T11965 |
MCHR1 antagonist 3
|
Others | Others |
MCHR1 antagonist 3, a potent antagonist of the melanin-concentrating hormone receptor-1 (MCHR1), is employed for the regulation of energy metabolism. | |||
T28823 |
SNAP-7941
SNAP7941 |
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SNAP-7941 is a selective antagonist of the melanin concentrating hormone receptor MCH1 with promising anxiolytic, antidepressant and anorectic effects in initial animal studies. | |||
T26677 |
ATC0175
ATC 0175,ATC-0175 |
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ATC0175 is a melanin-concentrating hormone receptor 1 antagonist with oral activity. | |||
T26676 |
ATC0065
ATC 0065,ATC-0065 |
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ATC0065 is a melanin-concentrating hormone receptor 1 antagonist with oral activity. | |||
T16293 | NGD-4715 | Others | Others |
NGD-4715 is a selective and orally active antagonist of melanin-concentrating hormone receptor 1. | |||
T26703 |
AZ13483342
AZ-13483342,AZ 13483342 |
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AZ13483342 is an antagonist of the melanin concentrating hormone receptor 1 (MCH1) with a potential diabetes therapeutic activity. | |||
T16852 |
SB-568849
|
Others | Others |
SB-568849 is a melanin-concentrating hormone receptor 1 antagonist (pKi: 7.7). | |||
T10173 | MCHR1 antagonist 1 | Others | Others |
MCHR1 antagonist 1 is a selective antagonist of melanin-concentrating hormone-1 (MCH1) receptor (Kb: 1 nM, Ki: 4 nM at human MCH1). | |||
T23719 | AMG-076 | ||
AMG-076 is an antagonist of melanin-concentrating hormone receptor 1. It also reduced hERG inhibition. | |||
T14372 |
AZD1979
|
Others | Others |
AZD1979 is an antagonist of Melanin-concentrating hormone receptor 1 (MCHr1) (IC50: 12 nM). | |||
T15450 |
GW-803430
GW-3430 |
Others | Others |
GW-803430 is a potent and selective antagonist of melanin-concentrating hormone receptor 1 (MCH R1) (pIC50: 9.3). GW-803430 is orally active in an animal model of obesity. | |||
T11964 | MCH-1 antagonist 1 | P450 | Metabolism |
MCH-1 antagonist 1 also inhibits CYP3A4 (IC50: 10μM).MCH-1 antagonist 1 is a potent melanin concentrating hormone (MCH-1) antagonist (Ki: 2.6 nM). | |||
T7749 | ALB-127158 | ||
ALB-127158(a) 是一种有效的选择性黑色素浓缩激素 1 (MCH1) 受体拮抗剂,可能是炎症性肠病 (IBD) 的潜在治疗方法 | |||
T82140 |
Hypertrehalosemic neuropeptide (Nauphoeta cinerea)
|
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Hypertrehalosemic neuropeptide (Nauphoeta cinerea) 属于脂动激素/红色素浓缩激素 (AKH/RPCH) 家族,具有促进海藻糖合成的功能。 | |||
TP1997 |
[Ala17]-MCH
|
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Potent melanin-concentrating hormone (MCH) receptor agonist (EC50 values are 17 and 54 nM at MCH1 and MCH2 receptors respectively). Displays some selectivity towards MCH1 over MCH2 (Ki values are 0.16 and 34 nM respectively). | |||
T76640 |
hMCH-1R antagonist 1
|
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hMCH-1R antagonist 1 (Compound 30)为高效且具有选择性的hMCHR1拮抗剂,KB值仅为3.6 nM。它与hMCHR1和hMCHR2的结合能力强,IC50值分别为65 nM与49 nM,主要用于代谢研究领域。 | |||
T81319 |
Quizalofop-P
|
Acetyl-CoA Carboxylase | Metabolism |
Quizalofop-P被杂草通过茎叶吸收,能在植株内实现向上和向下的双向运输,并在顶端和分生区域累积,通过抑制脂肪酸合成,进而导致杂草死亡。此外,Quizalofop-P对禾本科杂草与双子叶作物具有显著的选择性。 | |||
T64692 |
AMY-101 acetate
|
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Complement component C3 plays a particularly versatile role in this process by keeping the cascade alert, acting as a point of convergence of activation pathways, fueling the amplification of the complement response, exerting direct effector functions, and helping to coordinate downstream immune responses[3]. In C3-/- mice alcohol-induced liver steatosis is absent or strongly reduced after chronic or acute alcohol exposure. This suggests that the complement system and its component C3 contribute... |