Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8557 |
N-terminally acetylated Leu-enkephalin
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
N-terminally acetylated Leu-enkephalin 是一种五氨基酸内源性肽,可作为阿片受体激动剂。N-末端乙酰化 Leu-脑啡肽是 Leu-脑啡肽的 N-末端乙酰化形式。 | |||
T22752L |
(D-Ser2)-Leu-Enkephalin-Thr
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
(D-Ser2)-Leu-Enkephalin-Thr 是阿片受体的 delta 选择性药物,具有镇痛作用。 | |||
T7173 |
[Leu5]-Enkephalin
亮氨酸脑啡肽,Leucine enkephalin,Leucyl-enkephalin,Leu-enkephalin |
Opioid Receptor; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience |
[Leu5]-Enkephalin (Leu-enkephalin) 是一种参与伤害感受的内源性神经肽,是 δ-阿片和 μ-阿片受体的激动剂,Ki 值分别为 4.0 和 3.4 nM | |||
T7665 |
[Leu5]-Enkephalin TFA(58822-25-6(free bas))
Leu-enkephalin,Leucine enkephalin,Leucyl-enkephalin |
Opioid Receptor; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience |
[Leu5]-Enkephalin TFA(58822-25-6(free bas)) (Leucyl-enkephalin) 是最有效的 δ 受体。 | |||
T7173L |
[Leu5]-Enkephalin acetate(58822-25-6 free base)
亮氨酸脑啡肽,Leucine enkephalin,Leu-enkephalin,Leucyl-enkephalin |
Opioid Receptor; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience |
[Leu5]-Enkephalin acetate(58822-25-6 free base) 是一种参与伤害感受的内源性神经肽,是 δ-opioid 和 μ-opioid 受体的激动剂(Kis 分别为 4.0 和 3.4 nM) | |||
TP1113L |
[Leu5]-Enkephalin, amide acetate
[Leu5]-Enkephalin, amide acetate(60117-24-0 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
[Leu5]-Enkephalin, amide acetate 是一种 δ 阿片受体激动剂。 | |||
T31631 |
Enkephalin-leu, ala(2)-ser(6)-
DALES,2-Ala-6-ser-leu-enkephalin |
||
Enkephalin-leu, ala(2)-ser(6)- is an active compound at the delta (non-complexed) opioid receptor. | |||
TP1252 |
N-terminally acetylated Leu-enkephalin acetate
Ac-L-Tyr-Gly-Gly-L-Phe-D-Leu-COOH,N-terminally acetylated Leu-enkephalin |
||
N-terminally acetylated Leu-enkephalin is the N-terminally acetylated form of Leu-enkephalin. | |||
T8991 |
BMS986187
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
BMS986187 是一种有效的δ-阿片受体选择性正变构调节剂 (PAM),其 EC50= 0.03 μM,pKB= 6.02 (~1 μM)。BMS986187 对 μ 受体无明显 PAM 活性 (EC50=3 μM)。 | |||
T25302 |
Deltakephalin
DTLET,Enkephalin leu, thr(2)-thr(6)- |
||
Deltakephalin is a synthetic, potent specific opiate delta receptors agonist. | |||
T20435L |
Leuphasyl TFA
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Leuphasyl TFA 是一种酰胺肽,一种 δ-阿片受体激动剂,是一种抗降解的长效 Leu-脑啡肽类似物,用于研究 δ 阿片受体的信号通路。 它 是一种有效的长效 Leu-脑啡肽类似物,可抵抗酶促降解。 | |||
T27878 |
LY 164929
LY-164929,LY164929 |
||
LY 164929 is a highly selective ligand for the lower affinity [3H]D-Ala2-D-Leu-5-enkephalin binding site. | |||
T83504 |
[D-Ala2] Leu-Enkephalinamide
|
||
[D-Ala2] Leu-Enkephalinamide,一种脑啡肽类似物,展现出优异的角膜通透性及镇痛效果,适用于眼部疾病研究。 | |||
T61095 |
SCH-42354
|
||
SCH-42354 is a potent, orally active inhibitor of neutral endopeptidase (NEP), serving as the active form of the prodrug SCH-42495. By inhibiting NEP hydrolysis, SCH-42354 enhances the activity of atrial natriuretic peptide (ANP) and prevents the hydrolysis of leu-enkephalin and ANF with IC50 values of 8.3 nM and 10.0 nM, respectively. Furthermore, SCH-42354 exhibits antihypertensive activity [1] [2]. |