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Search Results for " opioid "

Targets Recommended: Opioid Receptor Opioid Receptor

376

抑制剂 & 化合物

19

天然产物

2

化合物库

8

重组蛋白

3

同位素标记化合物

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Cat. No.	Product Name
L2600	神经信号分子库		2540 compounds
	2540 种CNS 相关的生物活性小分子化合物的特有集合，用于高通量、高内涵筛选；
L2610	神经递质受体化合物库		1513 compounds
	1513 种与神经递质受体相关的化合物，用于高通量、高内涵筛选；

化合物库

神经信号分子库

Cat.No: L2600

Compounds: 2540

神经递质受体化合物库

Cat.No: L2610

Compounds: 1513

Cat. No.	Product Name	Target	Signaling Pathways
T12314	Opioid receptor modulator 1	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Opioid receptor modulator 1 is a modulator of opioid receptor.
T62767	Mu opioid receptor antagonist 3	Others	Others
	Mu opioid receptor antagonist 3 (compound 26) 是一种有效的、选择性的、能透过血脑屏障渗透性的μ 阿片受体 (MOR) 拮抗剂 (Ki: 0.24 nM, EC50: 0.54 nM)。Mu opioid receptor antagonist 2 对吗啡表现出明显的中枢神经系统拮抗活性，诱发戒断症状比 Naloxone 小。Mu opioid receptor antagonist 2 能够用于研究阿片类药物使用障碍 (OUD)。
T62025	μ opioid receptor agonist 2	Others	Others
	μ opioid receptor agonist 2 （Compound H-3）是一种MOR 受体激动剂，可用于疼痛及疼痛相关疾病的研究。
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)。
T4691	Asimadoline hydrochloride EMD-61753 hydrochloride,阿西马朵林盐酸盐	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Asimadoline hydrochloride (EMD-61753 hydrochloride) 是一种 κ-阿片(κ-opioid)受体激动剂，对豚鼠和人重组 κ-opioid 的 IC50值分别为 5.6 和 1.2 nM。它可改善糖尿病大鼠的异常性疼痛，具有外周抗炎作用，并有用于肠易激综合征的研究潜力。
T9459	GR103545	Others	Others
	GR103545 是 κ-阿片受体的选择性激动剂，它是一种放射性示踪剂，可以用作体内成像。
T4351	DAMGO Dagol,DAGO,RX-783006	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	DAMGO (DAGO) 是一种阿片受体激动剂，Kd 值为 3.46 nM。它能够影响啮齿动物的运动活动，可作为镇痛剂。
T79431	Mu opioid receptor antagonist 7	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Muopioid receptorantagonist 7 (compound 24) 是一种有效的CNS渗透性μOR (μ-阿片受体)拮抗剂，具有29 ± 3.0 nM的IC50。该化合物可用于研究疼痛和阿片类药物使用障碍。
T62766	Mu opioid receptor antagonist 2	Others	Others
	Mu opioid receptor antagonist 2 (compound 25) 是一种有效的、选择性的、能透过血脑屏障渗透性的μ 阿片受体 (MOR) 拮抗剂 (Ki: 0.37 nM, EC50: 0.44 nM)。Mu opioid receptor antagonist 2 对吗啡表现出明显的中枢神经系统拮抗活性，诱发戒断症状比 Naloxone 小。Mu opioid receptor antagonist 2 能够用于研究阿片类药物使用障碍 (OUD)。
T62768	Mu opioid receptor antagonist 4	Others	Others
	Mu opioid receptor antagonist 4 (compound 31) 是一种有效的、选择性的、能透过血脑屏障渗透性的μ 阿片受体 (MOR) 拮抗剂 (Ki: 0.38 nM, EC50: 0.38 nM)。Mu opioid receptor antagonist 2 对吗啡表现出明显的中枢神经系统拮抗活性，诱发戒断症状比 Naloxone 小。Mu opioid receptor antagonist 2 能够用于研究阿片类药物使用障碍 (OUD)。
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。
T62268	μ opioid receptor agonist 1	Others	Others
	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。
T61901	σ1 Receptor/μ Opioid receptor modulator 1	Others	Others
	σ1 Receptor/μ Opioid receptor modulator 1 (Compound 44) 是一种有效的σ1受体拮抗剂（Ki= 1.86 nM）和μ阿片受体激动剂（Ki=2.1 nM）。σ1 Receptor/μ Opioid receptor modulator 1 具体有效的镇痛活性，可用于神经性疼痛的研究。
T7748	Dermorphin TFA 皮啡肽三氟乙酸盐	Others; Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience; Others
	Dermorphin TFA 是在两栖类皮肤中发现的天然七肽，是 μ-阿片受体激动剂，可用于抑制神经痛。
T62673	Mu opioid receptor antagonist 5	Others	Others
	Mu opioid receptor antagonist 5 (compound NAP) 是一种选择性的、能够透过血脑屏障的 μ 阿片受体 (MOR) 拮抗剂 (EC50: 1.14 nM, Ki: 0.37 nM)。Mu opioid receptor antagonist 5 能够用于研究阿片类药物使用障碍 (OUD)。
T0918	Trimebutine 曲美布汀,Mebutin	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Trimebutine (Mebutin) 是阿片受体激动剂，有抗毒蕈碱活性。它是解痉剂，可调节肠道和结肠运动，并通过抗毒蕈碱和弱μ-阿片受体激动剂作用缓解腹痛。
TP1832	Gluten Exorphin C	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Gluten exorphin C 是来源于谷朊粉的阿片肽。在 GPI 和 MVD 检测中，抑制 μ 阿片和 δ 阿片活性，IC50值分别为 40 和13.5 μM。
TP1071	Nociceptin Orphanin FQ,孤菲肽	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Nociceptin (Orphanin FQ) 是一种 17 个氨基酸的多肽，是 nociceptin 受体的内源性配体，具有缓解疼痛的作用。
T1242	Alvimopan 爱维莫潘	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Alvimopan (LY 246736) 是一种选择性和竞争性 μ 阿片受体拮抗剂，IC50值为 1.7 nM。它存在于肌间和黏膜下神经元以及人体肠道固有层的免疫细胞中，可用于术后肠梗阻的研究。
T13414	ZT 52656A hydrochloride	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	ZT 52656A hydrochloride 是一种 kappa 阿片样物质的选择性激动剂，用于预防或减轻眼部疼痛。
T4386	PZM21	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	PZM21 是一种有效的选择性 μ 阿片受体激动剂，EC50值为 1.8 nM。
T4407	SR17018	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	SR17018 是一种 μ-阿片受体 (MOR) 激动剂，与 GTPγS 结合，EC50 为 97 nM。
T8992	BMS986188	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	BMS986188 是一种新型的强效选择性正向变构调节剂，用于 δ-阿片受体。
T7218	Endomorphin 2 内吗啡肽 2	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Endomorphin 2 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。
T2071	MCOPPB triHydrochloride MCOPPB trihydrochlride,MCOPPB 3HCl	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	MCOPPB triHydrochloride (MCOPPB 3HCl) 是一种伤害感受肽受体激动剂，pKi 为10.07。
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。
T5167	Cebranopadol 西博帕多,GRT6005	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Cebranopadol (GRT6005) 是镇痛 NOP 和阿片受体激动剂，对人 NOP、μ-阿片 (MOP)、κ-阿片 (KOP) 和 δ-阿片 (DOP) 受体的 Ki 值分别为 0.9、0.7、2.6 和 18 nM。
T1197	Trimebutine maleate Debridat,Polibutin,马来酸曲美布汀	Calcium Channel; Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Trimebutine maleate (Polibutin) 是一种外周 μ、δ 和 kappa 阿片受体激动剂，用作治疗慢性和急性腹痛的解痉药物。
TQ0091	LY2795050	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	LY2795050 是一种新型特异性 κ-阿片受体拮抗剂，IC50为0.72 nM。
TP1905	BW-180C (D-丙2,D-亮5)-脑啡肽,DADLE	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	BW-180C (DADLE) 是水溶性的多肽类δ-阿片受体激动剂，也对 μ-阿片受体显示活性，在体内表现出镇痛活性。
T6414	Bisacodyl 比沙可啶,Fenilaxan,Dulcolax,Brocalax	Others	Others
	Bisacodyl (Fenilaxan) 是刺激性缓泻剂，可直接作用于结肠以产生排便。它能够直接激活结肠巨噬细胞来增加 PGE2的分泌。PGE2充当旁分泌因子并减少结肠中 AQP3 的表达，抑制水从腔向血管一侧的转移，进而产生通便作用。
T26869	BMS-986122 BMS 986122	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	BMS-986122 (BMS 986122) 是选择性 μ 阿片受体正变构调节剂，可增加 β-抑制蛋白募集、腺苷酸环化酶抑制和 G 蛋白活化的作用，还增强 DAMGO 介导的 [35S]GTPγS 在小鼠脑膜中的结合。
TP1367	[D-Ala2]leucine-enkephalin (D-ALA2)-亮氨酸脑啡肽	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	[D-Ala2]leucine-enkephalin 是 δ 阿片类激动剂，是能长效抗降解的亮氨酸脑非肽，可用于研究 δ 阿片受体的信号通路。
TQ0082	Aticaprant LY-2456302,CERC-501	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Aticaprant (LY-2456302) 是一种有效的中枢渗透性 kappa-阿片受体拮抗剂，Ki 值为 0.807 nM。
T14551	Bevenopran CB-5945,ADL-5945	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
T15799	LY2940094 LY-2940094	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	LY2940094 (LY-2940094) 是一种口服有效的选择性 NOP 受体拮抗剂，可降低动物模型的自身给药酒精依赖，对 NOP 受体具有高亲和力，Ki 为 0.105 nM，和拮抗活力，Kb 为 0.166 nM。
T3996	Dapiprazole Hydrochloride 盐酸达哌唑,Glamidolo Hydrochloride,Reversil Hydrochloride	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Dapiprazole Hydrochloride (Glamidolo Hydrochloride) 是 α-adrenergic 阻断剂的药物。
T6175	ADL-5859 ADL5859 Hydrochloride,ADL5859 HCl	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	ADL-5859 (ADL5859 Hydrochloride) 是δ-阿片受体选择性激动剂，Ki 为0.8 nM，对阿片受体 κ 和 μ 具有选择性。
T14835	BTRX-335140 CYM-53093	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	BTRX-335140 (CYM-53093) 是一种有效的选择性口服活性 κ 阿片受体 (KOR) 拮抗剂，对 κOR、μOR 和 δOR 具有拮抗活性，IC50 值分别为 0.8、110 和 6500 nM。它可以很好地分布到 CNS 中，在大鼠中具有良好的体外吸收、分布、代谢、排泄和毒性以及体内药代动力学特征。
T7637	Deltorphin I Deltorphin 1,Deltorphin I(TFA),Deltorphin C	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Deltorphin I 是 δ-阿片受体的激动剂。
T7639	Deltorphin 2 Deltorphin 2(TFA),[D-Ala2]-Deltorphin II	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Deltorphin 2 ([D-Ala2]-Deltorphin II) 是一种选择性的 δ 阿片受体肽激动剂，IC50 为 1 nM。
T9833	Opiranserin hydrochloride	P2X Receptor; GlyT; 5-HT Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Opiranserin hydrochloride 是甘氨酸转运蛋白 2 型 (GlyT2) 和 5-羟色胺受体 2A (5HT2A) 的双重拮抗剂，IC50 分别为 0.86 和 1.3 μM。它显示对 rP2X3 的拮抗活性 (IC50=0.87 μM)。它正在开发为用于治疗术后疼痛的注射剂。
T5158	N-Desmethylclozapine N-去甲基氯氮平,Desmethylclozapine,Normethylclozapine,Norclozapine	Virus Protease; Dopamine Receptor; 5-HT Receptor; Opioid Receptor; AChR; Drug Metabolite	Endocrinology/Hormones; GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience
	N-Desmethylclozapine (Desmethylclozapine) 是非典型抗精神病药 Clozapine 的主要活性代谢产物。它是血清素受体亚型 5-HT2C 的拮抗剂，IC50值为7.1 nM。它也是多巴胺 D4 受体的拮抗剂和δ-阿片受体的激动剂。
T4633	Asimadoline EMD-61753,阿西马朵林	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Asimadoline (EMD-61753) 是一种 κ-阿片(κ-opioid)受体激动剂，对豚鼠和人重组 κ-opioid 的IC50值分别为 5.6 和 1.2 nM。它可改善糖尿病大鼠的异常性疼痛，具有外周抗炎作用，并有用于肠易激综合征的研究潜力。
TP2036L	DPDPE TFA (88373-73-3 free base) DPDPE TFA	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	DPDPE TFA 是选择性 δ-阿片受体激动剂肽，在体内具有镇痛作用。
T7404	Dermorphin 皮啡肽	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Dermorphin 是在两栖类皮肤中发现的天然七肽，是 μ-阿片受体激动剂，可用于抑制神经痛。
T7211	Tyr-Gly-Gly-Phe-Met-OH Methionine enkephalin,蛋氨酸脑啡肽,Met-Enkephalin,[MET5]脑啡肽	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) 是天然存在的内源性阿片肽、metenkephalin 和 zeta-和 delta-阿片受体激动剂的合成形式，是 mu-阿片受体激动剂，具有潜在的镇痛、神经调节、免疫调节、抗炎、抗肿瘤作用以及镇痛、抗抑郁和胃肠运动调节活性。
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
T6504	Flupirtine maleate Katadolon maleate,氟吡啶马来酸,马来酸氟吡汀	Potassium Channel; NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	Flupirtine maleate (Katadolon maleate) 是可透过血脑屏障的、具有口服活性的非阿片类化合物。它是间接 NMDAR 拮抗剂，可用于缓解疼痛的研究，具有神经保护特性。
T21422	Methylnaltrexone bromide Relistor,MOA-728,MOA 728,Methylnaltrexone,溴化甲基纳曲酮,MOA728	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Methylnaltrexone bromide (MOA-728) 是纳曲酮的四元衍生物，是可口服的外周作用 μ 阿片拮抗剂。它穿越血脑屏障的能力有限，可在胃肠道组织中发挥作用。

化合物

Opioid receptor modulator 1

Cat.No: T12314

Target: Opioid Receptor

Mu opioid receptor antagonist 3

Cat.No: T62767

Target: Others

μ opioid receptor agonist 2

Cat.No: T62025

Target: Others

Cat.No: T8991

Target: Opioid Receptor

Asimadoline hydrochloride

Cat.No: T4691

Synonym: EMD-61753 hydrochloride,阿西马朵林盐酸盐

Target: Opioid Receptor

Cat.No: T9459

Target: Others

Cat.No: T4351

Synonym: Dagol,DAGO,RX-783006

Target: Opioid Receptor

Mu opioid receptor antagonist 7

Cat.No: T79431

Target: Opioid Receptor

Mu opioid receptor antagonist 2

Cat.No: T62766

Target: Others

Mu opioid receptor antagonist 4

Cat.No: T62768

Target: Others

μ opioid receptor agonist 3

Cat.No: T79430

Target: Opioid Receptor

μ opioid receptor agonist 1

Cat.No: T62268

Target: Others

σ1 Receptor/μ Opioid receptor modulator 1

Cat.No: T61901

Target: Others

Cat.No: T7748

Synonym: 皮啡肽三氟乙酸盐

Target: Others, Opioid Receptor

Mu opioid receptor antagonist 5

Cat.No: T62673

Target: Others

Cat.No: T0918

Synonym: 曲美布汀,Mebutin

Target: Opioid Receptor

Gluten Exorphin C

Cat.No: TP1832

Target: Opioid Receptor

Cat.No: TP1071

Synonym: Orphanin FQ,孤菲肽

Target: Opioid Receptor

Cat.No: T1242

Synonym: 爱维莫潘

Target: Opioid Receptor

ZT 52656A hydrochloride

Cat.No: T13414

Target: Opioid Receptor

Cat.No: T4386

Target: Opioid Receptor

Cat.No: T4407

Target: Opioid Receptor

Cat.No: T8992

Target: Opioid Receptor

Cat.No: T7218

Synonym: 内吗啡肽 2

Target: Opioid Receptor

MCOPPB triHydrochloride

Cat.No: T2071

Synonym: MCOPPB trihydrochlride,MCOPPB 3HCl

Target: Opioid Receptor

Cat.No: TQ0267

Synonym: 内吗啡肽 1,Endomorphin-1

Target: Opioid Receptor

Cat.No: T5167

Synonym: 西博帕多,GRT6005

Target: Opioid Receptor

Trimebutine maleate

Cat.No: T1197

Synonym: Debridat,Polibutin,马来酸曲美布汀

Target: Calcium Channel, Opioid Receptor

Cat.No: TQ0091

Target: Opioid Receptor

Cat.No: TP1905

Synonym: (D-丙2,D-亮5)-脑啡肽,DADLE

Target: Opioid Receptor

Cat.No: T6414

Synonym: 比沙可啶,Fenilaxan,Dulcolax,Brocalax

Target: Others

Cat.No: T26869

Synonym: BMS 986122

Target: Opioid Receptor

[D-Ala2]leucine-enkephalin

Cat.No: TP1367

Synonym: (D-ALA2)-亮氨酸脑啡肽

Target: Opioid Receptor

Cat.No: TQ0082

Synonym: LY-2456302,CERC-501

Target: Opioid Receptor

Cat.No: T14551

Synonym: CB-5945,ADL-5945

Target: Opioid Receptor

Cat.No: T15799

Synonym: LY-2940094

Target: Opioid Receptor

Dapiprazole Hydrochloride

Cat.No: T3996

Synonym: 盐酸达哌唑,Glamidolo Hydrochloride,Reversil Hydrochloride

Target: Adrenergic Receptor

Cat.No: T6175

Synonym: ADL5859 Hydrochloride,ADL5859 HCl

Target: Opioid Receptor

Cat.No: T14835

Synonym: CYM-53093

Target: Opioid Receptor

Cat.No: T7637

Synonym: Deltorphin 1,Deltorphin I(TFA),Deltorphin C

Target: Opioid Receptor

Cat.No: T7639

Synonym: Deltorphin 2(TFA),[D-Ala2]-Deltorphin II

Target: Opioid Receptor

Opiranserin hydrochloride

Cat.No: T9833

Target: P2X Receptor, GlyT, 5-HT Receptor

N-Desmethylclozapine

Cat.No: T5158

Synonym: N-去甲基氯氮平,Desmethylclozapine,Normethylclozapine,Norclozapine

Target: Virus Protease, Dopamine Receptor, 5-HT Receptor, Opioid Receptor, AChR, Drug Metabolite

Cat.No: T4633

Synonym: EMD-61753,阿西马朵林

Target: Opioid Receptor

DPDPE TFA (88373-73-3 free base)

Cat.No: TP2036L

Synonym: DPDPE TFA

Target: Opioid Receptor

Cat.No: T7404

Synonym: 皮啡肽

Target: Opioid Receptor

Tyr-Gly-Gly-Phe-Met-OH

Cat.No: T7211

Synonym: Methionine enkephalin,蛋氨酸脑啡肽,Met-Enkephalin,[MET5]脑啡肽

Target: Opioid Receptor

[Leu5]-Enkephalin

Cat.No: T7173

Synonym: 亮氨酸脑啡肽,Leucine enkephalin,Leucyl-enkephalin,Leu-enkephalin

Target: Opioid Receptor, Endogenous Metabolite

Flupirtine maleate

Cat.No: T6504

Synonym: Katadolon maleate,氟吡啶马来酸,马来酸氟吡汀

Target: Potassium Channel, NMDAR, iGluR

Methylnaltrexone bromide

Cat.No: T21422

Synonym: Relistor,MOA-728,MOA 728,Methylnaltrexone,溴化甲基纳曲酮,MOA728

Target: Opioid Receptor

Cat. No.	Product Name	Target	Signaling Pathways
T6S1010	Allomatrine 槐定碱,别苦参碱	Others	Others
	Allomatrine 是一种来源槐花树皮的生物碱。它能够激活 κ-阿片受体，进而产生缓解疼痛的作用。
T5S0581	Sec-O-Glucosylhamaudol 亥茅酚苷,Hamaudol 3-glucoside	Others; Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience; Others
	Sec-O-Glucosylhamaudol (Hamaudol 3-glucoside) 是从滨海前胡中分离得到的一种天然产物，能够降低 μ 阿片受体的蛋白水平，可用于缓解疼痛的研究。它通过调节脂多糖刺激的 RAW264.7 细胞系中的 p38 丝裂原活化蛋白激酶具有抗炎作用。
T2726	Sinomenine Cucoline,Kukoline,青藤碱	Apoptosis; Others; NF-κB; Opioid Receptor; Autophagy	Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; NF-κB; Others
	Sinomenine (Kukoline) 是来自汉防己的一种生物碱，是 μ 阿片受体激活剂，也是NF-κB 活化的阻断剂。
T5S2360	Corydaline Corydalin,紫堇碱,延胡索甲素,(+)-Corydaline	P450; Virus Protease; Opioid Receptor; AChE	Endocrinology/Hormones; GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience
	Corydaline (Corydalin) 是从 Corydalis yanhusuo 提取的一种异喹啉生物碱，是一种新型促动力植物药的主要活性成分之一。它促进胃排空和小肠转运，促进胃的调节，具有抗乙酰胆碱酯酶、抗过敏和镇痛活性。
T2921	Sinomenine hydrochloride 盐酸青藤碱,Sabianine A hydrochloride,Cucoline hydrochloride,Kukoline hydrochloride	Apoptosis; NF-κB; Opioid Receptor; Autophagy	Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; NF-κB
	Sinomenine hydrochloride (Kukoline hydrochloride) 是来自汉防己的一种生物碱，是NF-κB 活化的阻断剂。Sinomenine 也是一种 μ 阿片受体激活剂。
T2870	Matrine Vegard,苦参碱,Matridin-15-one,Matrinium,α-Matrine,(+)-Matrine	Mitophagy; Ferroptosis; Opioid Receptor; Autophagy	Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Matrine (Vegard) 是一种从槐属植物中分离出来的生物碱，可作为一种κ阿片受体激动剂，有抗肿瘤活性。
T2S2362	Dehydrocorydaline nitrate 去氢延胡索甲素硝酸盐,硝酸脱氢紫堇碱	BCL; Others; PARP; p38 MAPK; Caspase; Parasite; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Others; Proteases/Proteasome
	Dehydrocorydaline nitrate 是生物碱。Dehydrocorydaline 调节 Bax，Bcl-2蛋白表达，激活 caspase-7，caspase-8，并使 PARP 失活。它能增强 p38 MAPK 活化，具有抗炎、抗癌、抗疟疾等功效。
TN1308	6-Hydroxyflavanone	Others; Lipoxygenase; COX; GABA Receptor	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; Others
	6-Hydroxyflavanone 是从菖蒲叶中提取分离，通过靶向环氧合酶-2（COX-2），5-脂氧合酶（5-LOX）以及阿片类药物和 GABA-A 受体从而具有抗炎和抗神经性疼痛活性。6-Hydroxyflavanone 在链脲佐菌素诱导的糖尿病神经病变模型中具有抗伤害感受特性。
T5S0754	Isoquercetin 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷	NF-κB; Wnt/beta-catenin; NO Synthase	Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; Stem Cells
	Isoquercetin (3-Glucosylquercetin) 是天然存在的多酚，具有抗氧化，抗增殖和抗炎特性。它通过调节核因子-κB 转录调节系统调节一氧化氮合酶 2 的表达。它通过 Nrf2/ARE 抗氧化剂信号传导途径减轻乙醇诱导的肝毒性，氧化应激和炎症反应。它具有高生物利用度和低毒性，是预防糖尿病妊娠出生缺陷的有希望的候选药物。
T3417	Amentoflavone Didemethyl-ginkgetin,穗花杉双黄酮,Amenthoflavone,3',8''-Biapigenin	Apoptosis; P450; Phospholipase; Reactive Oxygen Species; Opioid Receptor; COX; Antibacterial; RSV; Antifungal	Apoptosis; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB
	Amentoflavone (3',8''-Biapigenin) 是一种具有很多生物活性的双黄酮类天然产物，有抗炎、抗氧化和神经保护等作用。
T27534	Herkinorin BF3DNCA methyl ester	Others	Others
	Herkinorin is an opioid analgesic and an analogue of the natural product Salvinorin A. herkinorin is a μ-opioid agonist with more than 100x higher μ-opioid affinity and 50x lower κ-opioid affinity compared to Salvinorin A. Herkinorin is a semi-synthetic c
TN3367	Akuammidine	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Akuammidine shows anti-inflammatory and anti-asthmatic properties, it has opioid analgesic activity, it shows a preference for mu-opioid binding sites with Ki values of 0.6, 2.4 and 8.6 microM at mu-, delta- and kappa-opioid binding sites, respectively.
T76027	β-Endorphin, equine TFA	Others	Others
	β-Endorphin, equine TFA，是具备强效亲和力于μ和δ阿片受体(μ/δ opioid receptors)的内源性阿片类多肽，主要功能包括止痛。
TN1890	Lupeol acetate	Others; TNF; NOS	Apoptosis; Immunology/Inflammation; Others
	Lupeol acetate possesses antinociceptive, antifertility, and anti-inflammatory properties, the effect probably involves the opioid system, as indicated by the complete blockade of the opioid antagonist naloxone.
T13433	β-Endorphin, human	Others	Others
	β-Endorphin, human, a prominent endogenous peptide, existing in the hypophysis cerebri and hypothalamus,and is an agonist of opioid receptor.
TN3368	Akuammigine	Opioid Receptor; Adrenergic Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Akuammigine has in vitro antimalarial activity. Akuammigine competitively antagonizes the effect of noradrenaline on postsynaptic alpha-adrenoceptors, yielding pA2 values of 4.68. Akuammidine also shows a preference for mu-opioid binding sites with Ki val
TN4613	(-)-N-methylcoclaurine N-Methylcoclaurine	Others	Others
	N-Methylcoclaurine shows binding affinities for the ĸ opioid receptor with the equilibrium dissociation constant (Ki) value of 0.9 ± 0.1 uM. N-methylcoclaurine also shows promising butyrylcholinesterase inhibition activities, with the IC50 value of 1
T83913	Mitraciliatine	Others	Others
	Mitraciliatine是一种在M. speciosa（泰国称为Kratom）中发现的生物碱，是μ-阿片受体（MOR）部分激动剂和κ-阿片受体（KOR）激动剂。该化合物对MOR和KOR具有选择性，与δ-阿片受体（DOR; EC50s分别为228, 218, 和 >1,000 nM，针对小鼠受体在GTPγS结合实验中的表现）。Mitraciliatine（100 nmol/动物，脑室内注射）在小鼠的热水尾部缩回实验中延长了撤回潜伏期，这一效果可以通过敲除MOR而非KOR来逆转。与吗啡不同，Mitraciliatine不会诱发过度活动或呼吸抑制。
TN4064	Flavoglaucin	Phosphatase; IL Receptor; TNF; NOS; NF-κB; COX; Nrf2; Prostaglandin Receptor; Autophagy	Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB
	Flavoglaucin exhibits significant inhibitory effects on PTP1B, the IC50 value of 13.4, micrometer; it also shows good binding affinity for human opioid or cannabinoid receptors. Flavoglaucin appears to be an antitumor promoter, it also has anti-inflammato

天然产物

Cat.No: T6S1010

Synonym: 槐定碱,别苦参碱

Target: Others

Sec-O-Glucosylhamaudol

Cat.No: T5S0581

Synonym: 亥茅酚苷,Hamaudol 3-glucoside

Target: Others, Opioid Receptor

Cat.No: T2726

Synonym: Cucoline,Kukoline,青藤碱

Target: Apoptosis, Others, NF-κB, Opioid Receptor, Autophagy

Cat.No: T5S2360

Synonym: Corydalin,紫堇碱,延胡索甲素,(+)-Corydaline

Target: P450, Virus Protease, Opioid Receptor, AChE

Sinomenine hydrochloride

Cat.No: T2921

Synonym: 盐酸青藤碱,Sabianine A hydrochloride,Cucoline hydrochloride,Kukoline hydrochloride

Target: Apoptosis, NF-κB, Opioid Receptor, Autophagy

Cat.No: T2870

Synonym: Vegard,苦参碱,Matridin-15-one,Matrinium,α-Matrine,(+)-Matrine

Target: Mitophagy, Ferroptosis, Opioid Receptor, Autophagy

Dehydrocorydaline nitrate

Cat.No: T2S2362

Synonym: 去氢延胡索甲素硝酸盐,硝酸脱氢紫堇碱

Target: BCL, Others, PARP, p38 MAPK, Caspase, Parasite, Autophagy

6-Hydroxyflavanone

Cat.No: TN1308

Target: Others, Lipoxygenase, COX, GABA Receptor

Cat.No: T5S0754

Synonym: 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷

Target: NF-κB, Wnt/beta-catenin, NO Synthase

Cat.No: T3417

Synonym: Didemethyl-ginkgetin,穗花杉双黄酮,Amenthoflavone,3',8''-Biapigenin

Target: Apoptosis, P450, Phospholipase, Reactive Oxygen Species, Opioid Receptor, COX, Antibacterial, RSV, Antifungal

Cat.No: T27534

Synonym: BF3DNCA methyl ester

Target: Others

Cat.No: TN3367

Target: Opioid Receptor

β-Endorphin, equine TFA

Cat.No: T76027

Target: Others

Cat.No: TN1890

Target: Others, TNF, NOS

β-Endorphin, human

Cat.No: T13433

Target: Others

Cat.No: TN3368

Target: Opioid Receptor, Adrenergic Receptor

(-)-N-methylcoclaurine

Cat.No: TN4613

Synonym: N-Methylcoclaurine

Target: Others

Cat.No: T83913

Target: Others

Cat.No: TN4064

Target: Phosphatase, IL Receptor, TNF, NOS, NF-κB, COX, Nrf2, Prostaglandin Receptor, Autophagy

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-01719	OPRM1 Protein, Human, Recombinant (His) Mu opioid receptor,OPRM1,Mu opiate receptor,Mu-type...	Human	E. coli
	OPRM1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 47.6 kDa and the accession number is P35372.
TMPY-04733	OPCML Protein, Rat, Recombinant (hFc) opioid binding protein/cell adhesion molecule-like	Rat	HEK293 Cells
	OPCML Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 59 kDa and the accession number is P32736-1.
TMPY-00893	OPCML Protein, Human, Recombinant (His) OPCM,IGLON1,OBCAM,opioid binding protein/cell adhes...	Human	HEK293 Cells
	OPCML Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 34 kDa and the accession number is A8K0Y0.
TMPY-03818	OPCML Protein, Mouse, Recombinant (His) opioid binding protein/cell adhesion molecule-like,...	Mouse	HEK293 Cells
	OPCML Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 32.7 kDa and the accession number is Q6DFY2.
TMPJ-00737	PDYN Protein, Human, Recombinant (His) PDYN,ADCA,Big Dyn,Dynorphin B,PENKB,SCA23	Human	HEK293 Cells
	Proenkephalin-B(PDYN), belongs to the opioid neuropeptide precursor family. The N-terminal domain contains 6 conserved cysteines thought to be involved in disulfide bonding and/or processing. Leu-enkephalins, which is a type of Proenkephalin-B, compete with and mimic the effects of opiate drugs. They play a role in a number of physiologic functions, including pain perception and responses to stress. Dynorphin peptides differentially regulate the kappa opioid receptor. Dynorphin A has a typical o...
TMPH-02020	RGS17 Protein, Human, Recombinant (GST) Regulator of G-protein signaling 17,RGS17	Human	E. coli
	Regulates G protein-coupled receptor signaling cascades, including signaling via muscarinic acetylcholine receptor CHRM2 and dopamine receptor DRD2. Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound form. Binds selectively to GNAZ and GNAI2 subunits, accelerates their GTPase activity and regulates their signaling activities. Negatively regulates mu-opioid receptor-mediated activation of the G-proteins. R...
TMPY-04121	NAGA Protein, Human, Recombinant (His) D22S674,N-acetylgalactosaminidase, α-,N-acetylgalactosaminid...	Human	HEK293 Cells
	NAGA (Alpha-N-Acetylgalactosaminidase) is a Protein Coding gene. NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. It belongs to the glycosyl hydrolase 27 family. The antinociceptive effect of NAGA may involve the participation of endogenous opioid peptides and endogenous catecholamines. Normal alpha-NAGA is synthesized as a 52 kDa precursor which matures to a 49 kDa species through phosphorylation and car...
TMPJ-00513	LTF Protein, Human, Recombinant (His) Lactoferroxin-A,Talalactoferrin,LTF,Lactotransferrin,Lactofe...	Human	HEK293 Cells
	Lactotransferrin is a member of the transferrin family that transfer iron to the cells and control the level of free iron in the blood and external secretions. Lactotransferrin is a secreted protein and contains two transferrin-like domains. Lactotransferrin can be cleaved into the following four chains: Kaliocin-1, Lactoferroxin-A, Lactoferroxin-B, and Lactoferroxin-C. Lactoferroxin A, Lactoferroxin B, and Lactoferroxin C have opioid antagonist activity. Lactoferroxin A shows preference for mu-...

重组蛋白

OPRM1 Protein, Human, Recombinant (His)

Cat.No: TMPH-01719

Species: Human

Expression System: E. coli

OPCML Protein, Rat, Recombinant (hFc)

Cat.No: TMPY-04733

Species: Rat

Expression System: HEK293 Cells

OPCML Protein, Human, Recombinant (His)

Cat.No: TMPY-00893

Species: Human

Expression System: HEK293 Cells

OPCML Protein, Mouse, Recombinant (His)

Cat.No: TMPY-03818

Species: Mouse

Expression System: HEK293 Cells

PDYN Protein, Human, Recombinant (His)

Cat.No: TMPJ-00737

Species: Human

Expression System: HEK293 Cells

RGS17 Protein, Human, Recombinant (GST)

Cat.No: TMPH-02020

Species: Human

Expression System: E. coli

NAGA Protein, Human, Recombinant (His)

Cat.No: TMPY-04121

Species: Human

Expression System: HEK293 Cells

LTF Protein, Human, Recombinant (His)

Cat.No: TMPJ-00513

Species: Human

Expression System: HEK293 Cells

Cat. No.	Product Name	Target	Signaling Pathways
T11867	Loperamide-d6 hydrochloride R-18553 D6 hydrochloride	Others	Others
	Loperamide D6 hydrochloride, a deuterium-labeled variant of Loperamide hydrochloride, acts as an opioid receptor agonist utilized for diarrhea treatment.
T10181	6-beta-Naloxol D5 hydrochloride 6β-Naloxol D5 hydrochloride	Others	Others
	6-beta-Naloxol D5 hydrochloride is a deuterium-labeled opioid antagonist, closely related to naloxone, that serves as an effective compound in the field of chemical research.
TMIJ-0213	Naloxone-d5 HCl
	Naloxone-d5 HCl 是 Naloxone HCl 的氘代化合物。Naloxone HCl 的 CAS 号为 357-08-4。Naloxone hydrochloride 是一种特异性、没有激动剂活性的opiate拮抗剂。它是 mu、delta 和 kappa 阿片受体的竞争性拮抗剂。

同位素标记化合物

Loperamide-d6 hydrochloride

Cat.No: T11867

Synonym: R-18553 D6 hydrochloride

Target: Others

6-beta-Naloxol D5 hydrochloride

Cat.No: T10181

Synonym: 6β-Naloxol D5 hydrochloride

Target: Others

Naloxone-d5 HCl

Cat.No: TMIJ-0213

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