mch

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。

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。

Melanin Concentrating Hormone (MCH), a 19 amino acid cyclic peptide, is largely expressed in the hypothalamus.

Neuropeptide EI, rat acetate(125934-45-4 free base) 在不同的行为范例中显示功能性 MCH 拮抗剂和 MSH 激动剂活性。

[Ala17]-MCH TFA 是一种 MCH 的类似物，是 MCHR1的配体 (Ki=0.16 nM) 选择性优于对 MCHR2的 (Ki=34 nM)。Eu3+螯合标记 [Ala17]-MCH 对 MCHR1(Kd=0.37 nM) 亲和性高，而对 MCHR2的亲和性低。

MCH (human, mouse, rat) TFA 是一种有效的 MCH-R 的肽激动剂，与 MCH1R 和 MCH2R 结合的 IC50值分别为 0.3 nM 和 1.5 nM。MCH (human, mouse, rat) 对 CHO 细胞系中 MCH-2R 高度敏感，通过 FLIPR 监测细胞内钙动员，显示出功能性激活 MCH-1R 和 MCH-2R 的EC50值对分别为 3.9 nM 和 0.1 nM。

(Phe13,Tyr19)-MCH (human, mouse, rat) 作为一种高效的 SLC-1 与 S643b 受体配体，可充当这两种受体的激动剂。

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

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).

[Ala17]-MCH acetate 是 MCHR1 的选择性配体，Ki 为 0.16 nM，Kd 为 0.37 nM（Eu3+ 螯合物标记）。 [Ala17]-MCH acetate 对 MCHR2 具有选择性，Ki 为 34 nM。

Ac-hMCH(6-16)-NH2 shows non-selective agonist activity towards both MCH-1R and MCH-2R, which are human MCH receptors in the brain. The compound effectively binds to and activates these receptors, with IC 50 values of 0.16 nM and 2.7 nM for MCH-1R and MCH-2R, respectively.

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。

AY 77 (Unk-Cha-Chg-NH2)是一种有效的、具有选择性的 PAR2激动剂。AY 77对 Ca2+和 ERK1/2信号显示出选择性(Ca2+释放的ec50值为40 nM, ERK1/2磷酸化的ec50值为2 μM)。AY 77能够促进人乳腺癌细胞的体外迁移。

Lysozyme from chicken egg white (Lysozyme) 是一种存在于鸡蛋清中的杀菌酶，它溶解革兰氏阳性菌。

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。

Displays functional MCH-antagonist and MSH-agonist activity in different behavioral paradigms.

Caloxin 2A1 TFA 是一种新型 PM Ca2+ 泵抑制剂， 抑制人红细胞渗漏鬼中的 Ca2+-Mg2+-ATP 酶，抑制 Ca2+ 依赖性形成 140-kDa 酸稳定的酰基磷酸盐。

Boc-LRR-AMC TFA 是一种荧光蛋白酶底物，可检测 26S 蛋白酶体或 20S 蛋白酶核心的胰蛋白酶样活性。

The ω-3 polyunsaturated fatty acids (PUFAs) found in fish oils provide cardiovascular benefits. Docosahexaenoic acid (DHA), a C22:6 PUFA, is the most abundant ω-3 fatty acid in neural tissues, especially in the retina and brain. It can be synthesized from other dietary ω-3 PUFAs or taken as a nutritional supplement. Docosahexaenoyl glycine consists of DHA with glycine attached at its carboxy terminus.

aliotoxin是神经BK型肽基的抑制剂，对Kv通道和钙激活的钾通道能产生特异性抑制。Kaliotoxin对细胞膜电位和神经元兴奋性的调控具有研究意义。其产品编号为 T37808，CAS号为 145199-73-1

OSK-1 is a potent potassium channel blocker belonging to the α-KTx3 toxins. It exhibits IC50 values of 0.6 nM, 5.4 nM, and 0.014 nM for Kv1.1, Kv1.2, and Kv1.3 channels, respectively. Additionally, OSK-1 acts as a moderate blocker of the calcium-activated KCa3.1 channel, with an IC50 of 225 nM. Consequently, OSK-1 finds application as an immunosuppressive drug.

N-Methyl-L-leucin ((S)-4-Methyl-2-(methylamino)pentanoic acid) 是一种新型钙通道拮抗剂，可用于研究疼痛。

H-D-Allo-Ile-OH能够抑制3[H] gabapentin结合电压依赖性L型钙通道，可用于研究神经和精神疾病。

Leconotide is a calcium channel blocker and antihyperalgesia agent; isolated from the venom of the cone snail, Conus catus.