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Cat. No.	Product Name	Target	Signaling Pathways
T62268	μ opioid receptor agonist 1
	μ opioid receptor agonist 1 （Compound H-1a）是一种光学纯的氧杂环取代吡咯并吡唑衍生物，也是一种 MOR 受体激动剂，能够用于研究疼痛及疼痛相关疾病。
T38193L	β-Endorphin (1-27) (human) acetate β-Endorphin (1-27) (human) acetate(76622-84-9 Free base)	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	β-Endorphin (1-27) (human) acetate 存在于大脑垂体和下丘脑中，具有镇痛活性。 β-Endorphin (1-27) (human) acetate 是一种阿片受体激动剂，对 μ-阿片受体和 δ-阿片受体具有较好的亲和力。
TQ0267	Endomorphin 1 内吗啡肽 1,Endomorphin-1	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Endomorphin 1 是一种高亲和力和选择性的 μ-阿片受体激动剂，对 kappa3 结合位点具有合理的亲和力，Ki 为 20 到 30 nM 之间。
TP1885L1	[(pF)Phe4]Nociceptin(1-13)NH2 acetate	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	[(pF)Phe4]Nociceptin(1-13)NH2 acetate 是一种选择性 NOP 受体激动剂，pKi 为 10.68，pEC50 为 9.31。 [(pF)Phe4]Nociceptin(1-13)NH2 acetate 对 δ、κ 和 μ 阿片受体具有高选择性（>3000 倍）。
TP1882L1	Orphanin FQ(1-11) acetate(178249-41-7 free base)	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Orphanin FQ(1-11) acetate(178249-41-7 free base) 含有 Nociceptin 氨基酸 1-11 的肽片段。 ORL1/KOR-3 受体的强效激动剂 (Ki = 55 nM)；对阿片受体无亲和力，包括 μ、δ、κ1 和 κ3 受体 (Ki >1000 nM)。在 CD-1 小鼠中显示镇痛特性。
T79060	MOR agonist-1	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	MOR agonist-1为一种针对MOR（μ-opioid receptor）的激动剂，展现出优秀的镇痛效果，适用于疼痛及其相关疾病的研究应用。
T76439	DALDA acetate
	DALDA acetate 是一种强效和高选择性μ-opioid receptor 激动剂，其Ki 为 1.69 nM。DALDA acetate 具有抗痛和呼吸作用。
T37199	Bilaid C
	Bilaid C is a tetrapeptide μ-opioid receptor agonist (Ki= 210 nM in HEK293 cell membranes expressing the human receptor) that has been found inPenicillium.1It inhibits forskolin-induced cAMP accumulation by 77% in HEK293 cells expressing the human μ-opioid receptor when used at a concentration of 10 μM. Bilaid C induces inward rectifying potassium channel (Kir) currents in rat locus coeruleus slices that endogenously express high levels of the μ-opioid receptor (EC50= 4.2 μM). 1.Dekan, Z., Siana...
T80086	DALDA TFA	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	DALDA TFA作为一种μ-opioid受体激动剂，展现出高效能及高选择性，其Ki值达1.69 nM。此化合物主要表现为镇痛效应及对呼吸的作用。
T9669	EST73502 hydrochloride
	EST73502 hydrochloride 是一种选择性的，具有口服活性和血脑屏障渗透性的 μ-opioid 受体 (μ-opioid receptor/MOR) 激动剂和 σ1 受体(σ1R) 拮抗剂，对 MOR 和 σ1R 作用的Ki 值分别为 64 nM 和 118 nM。EST73502 hydrochloride 可用于缓解疼痛研究。
T75919	PL-017 TFA
	PL-017 TFA 是高效、选择性的 μ 阿片受体(μopioid receptor)激动剂，具有 5.5 nM 对125I-FK 33,824 与 μ 位点结合的 IC50 值。该化合物在大鼠中展现出持久且可逆的缓解疼痛效果。
T72423	Endomorphin 1 acetate
	Endomorphin 1 acetate，一种高度选择性的，高亲和力的μ-opioid 受体激动剂 (Ki: 1.11 nM)，对 kappa3结合位点具有高亲和力，Ki 值为 20 到 30 nM 之间。Endomorphin 1 acetate 具有镇痛特性。
T79430	μ opioid receptor agonist 3	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	μopioid receptor agonist3 (compound 20) 是高效的μOR激动剂，其EC50 值为0.87 nM。该化合物在疼痛和神经精神适应症研究中具备潜在应用价值。
T76285	β-Endorphin (6-31), human β-EP (6-31), human	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	β-Endorphin是一种内源性阿片类神经肽，作为opioid receptor激动剂，主要与μ-阿片受体发生作用。该肽在中枢和周围神经系统特定神经元中表达，是人类体内三种内啡肽之一。β-Endorphin在减轻压力、维护生理平衡及调控神经系统的疼痛感知中发挥作用。
T69537	Difelikefalin HCl
	Difelikefalin HCl is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Difelikefalin HCl is selective for KOR over the μ-opioid receptor (MOR; EC50 = >1 µM in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07...
TP1882	Orphanin FQ(1-11) Orphanin FQ (1-11)
	Orphanin FQ(1-11) is a peptide fragment containing amino acids 1-11 of Nociceptin. Orphanin FQ(1-11) is a potent agonist of the ORL1/KOR-3 receptor (Ki = 55 nM) and displays no affinity for opioid receptors, including μ, δ, κ1 and κ3 receptors (Ki >1000 nM). Orphanin FQ(1-11) displays analgesic properties in CD-1 mice.
T69530	Difelikefalin TFA
	Difelikefalin TFA is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Difelikefalin TFA is selective for KOR over the μ-opioid receptor (MOR; EC50 = >1 µM in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07...
TP1986	[Arg14,Lys15]Nociceptin
	Highly potent and selective NOP receptor agonist (EC50 = 1 nM). Displays > 875-fold selectivity over opioid receptors (IC50 values are 0.32, 280, > 10000 and 1500 for NOP, μ, δ and κ receptors respectively). Longer lasting and 30-fold more potent than noc
T37483	Difelikefalin (trifluoroacetate salt)
	Difelikefalin is a κ-opioid receptor (KOR) agonist.1It activates KOR in HEK293 cells expressing the human receptor (EC50= 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50= 0.048 nM). Difelikefalin is selective for KOR over the μ-opioid receptor (MOR; EC50= >1 μM in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07 and 0.05 m...
T75896	[Arg14,Lys15]Nociceptin TFA
	[Arg14,Lys15]Nociceptin TFA 是一种高效、选择性的 NOP (ORL1; OP4)受体激动剂，EC50为 1 nM。[Arg14,Lys15]Nociceptin TFA 对阿片受体具有较高的选择性，对 NOP、μ、δ 和 κ 受体的 IC50值分别为 0.32、280、>10000 和 1500 nM。
T36722	Deltorphin II (trifluoroacetate salt)
	Deltorphin II is a peptide agonist of δ2-opioid receptors.1,2It is selective for δ-opioid receptors over μ- and κ-opioid receptors in radioligand bindings assays (Kis = 0.0033, >1, and >1 μM, respectively) and induces [35S]GTPγS binding in mouse brain membrane preparations (EC50= 0.034 μM). Deltorphin II (0.12 mg/kg) decreases the infarction zone:risk zone ratio in a rat model of myocardial ischemia-reperfusion injury induced by coronary occlusion, an effect that can be reversed by the δ2-opioid...

化合物

μ opioid receptor agonist 1

Cat.No: T62268

β-Endorphin (1-27) (human) acetate

Cat.No: T38193L

Synonym: β-Endorphin (1-27) (human) acetate(76622-84-9 Free base)

Target: Opioid Receptor

Cat.No: TQ0267

Synonym: 内吗啡肽 1,Endomorphin-1

Target: Opioid Receptor

[(pF)Phe4]Nociceptin(1-13)NH2 acetate

Cat.No: TP1885L1

Target: Opioid Receptor

Orphanin FQ(1-11) acetate(178249-41-7 free base)

Cat.No: TP1882L1

Target: Opioid Receptor

MOR agonist-1

Cat.No: T79060

Target: Opioid Receptor

Cat.No: T76439

Cat.No: T37199

Cat.No: T80086

Target: Opioid Receptor

EST73502 hydrochloride

Cat.No: T9669

Cat.No: T75919

Endomorphin 1 acetate

Cat.No: T72423

μ opioid receptor agonist 3

Cat.No: T79430

Target: Opioid Receptor

β-Endorphin (6-31), human

Cat.No: T76285

Synonym: β-EP (6-31), human

Target: Opioid Receptor

Difelikefalin HCl

Cat.No: T69537

Orphanin FQ(1-11)

Cat.No: TP1882

Synonym: Orphanin FQ (1-11)

Difelikefalin TFA

Cat.No: T69530

[Arg14,Lys15]Nociceptin

Cat.No: TP1986

Difelikefalin (trifluoroacetate salt)

Cat.No: T37483

[Arg14,Lys15]Nociceptin TFA

Cat.No: T75896

Deltorphin II (trifluoroacetate salt)

Cat.No: T36722

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