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Opioid Receptor

Opioid Receptor

Opioid receptors belong to the large superfamily of seven transmembrane-spanning (7TM) G protein-coupled receptors (GPCRs). As a class, GPCRs are of fundamental physiological importance mediating the actions of the majority of known neurotransmitters and hormones.
TargetMol
1 2 3 4 5 6 7
Cat. No. Product Name CAS No. Purity Chemical Structure
T76285 β-Endorphin (6-31), human
化合物 β-Endorphin (6-31), human
77761-27-4 98%
TargetMol Chemical Structure β-Endorphin (6-31), human
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。
TN3368 Akuammigine
化合物 TN3368
642-17-1 98%
TargetMol Chemical Structure Akuammigine
Akuammigine has in vitro antimalarial activity. Akuammigine competitively antagonizes the effect of noradrenaline on postsynaptic alpha-adrenoceptors, yielding p...
T7306 Valorphin
化合物Valorphin
144313-54-2 98%
TargetMol Chemical Structure Valorphin
Valorphin (Valorphin TFAsalt) 是内源性血红蛋白 β 链第 33-39 位氨基酸残基,具有阿片类镇痛活性,与大鼠 mu-阿片受体结合,IC50 为 14 nM。它有抗肿瘤活性,也可用于缓解疼痛的研究。
T12169 Naltrindole hydrochloride
纳曲吲哚盐酸盐
111469-81-9 98%
TargetMol Chemical Structure Naltrindole hydrochloride
Naltrindole hydrochloride 是一种选择性的非肽类 δ 阿片受体拮抗剂 (Ki = 0.02 nM)。
TN3367 Akuammidine
化合物 TN3367
639-36-1 98%
TargetMol Chemical Structure Akuammidine
Akuammidine shows anti-inflammatory and anti-asthmatic properties, it has opioid analgesic activity, it shows a preference for mu-opioid binding sites with Ki va...
T13438 (R,S)-Ivosidenib
化合物 T13438
2070009-31-1 98%
TargetMol Chemical Structure (R,S)-Ivosidenib
(R,S)-Ivosidenib is the less active enantiomer of Ivosidenib .
T12314 Opioid receptor modulator 1
化合物 T12314
77514-44-4 98%
TargetMol Chemical Structure Opioid receptor modulator 1
Opioid receptor modulator 1 is a modulator of opioid receptor.
T15165 DPI-3290
化合物 T15165
182417-73-8 98%
TargetMol Chemical Structure DPI-3290
DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent antinocicepti...
T27934 LY255582
化合物LY255582
119193-09-8 98%
TargetMol Chemical Structure LY255582
LY255582 是一种具有选择性的中枢活性阿片受体拮抗剂,对 mu、delta 和 kappa 受体具有高亲和力 ,Ki 分别为 0.4 nM、5.2、2.0 nM。LY255582 可以抑制饮食相关的中脑边缘多巴胺水平的增加,并减少食物摄入的消耗。LY255582 常用于对肥胖的研究。LY255582是用于阿片受体介...
T11478L GSK1521498 free base
化合物 T11478L
1007573-18-3 98%
TargetMol Chemical Structure GSK1521498 free base
GSK1521498 free base is a potent and selective antagonist of the μ-opioid receptor. GSK1521498 free base also has the potential for disorders of compulsive consu...
T11198 Endomorphin 2 TFA
内吗啡肽 2 三氟乙酸盐
1276124-00-5 98%
TargetMol Chemical Structure Endomorphin 2 TFA
Endomorphin 2 TFA, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. a high affinity, highly selective agonist of the...
T1242 Alvimopan
爱维莫潘
156053-89-3 99.97%
TargetMol Chemical Structure Alvimopan
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。
TQ0082 Aticaprant
化合物Aticaprant
1174130-61-0 99.93%
TargetMol Chemical Structure Aticaprant
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。
TP1813L Dynorphin A 1-10 acetate(79994-24-4 free base)
化合物Dynorphin A 1-10 acetate
TP1813L 99.93%
TargetMol Chemical Structure Dynorphin A 1-10 acetate(79994-24-4 free base)
Dynorphin A 1-10 acetate(79994-24-4 free base) 是一种内源性 opioid 样物质神经肽,与 κ-opioid 样物质受体的细胞外环 2 结合。 Dynorphin A (1-10) 还阻断 NMDA 激活的电流,IC50 为 42.0 μM。
TP2322L Beta-Neoendorphin acetate(77739-21-0 free base)
化合物beta-Neoendorphin acetate
78658-39-6 99.91%
TargetMol Chemical Structure beta-Neoendorphin acetate(77739-21-0 free base)
beta-Neoendorphin acetate(77739-21-0 free base) 是 κ-opioid 受体的激动剂
TP1082L Neuropeptide AF (human) acetate
神经肽AF(人类)醋酸盐
99.89%
TargetMol Chemical Structure Neuropeptide AF (human) acetate
Neuropeptide AF (human) acetate (Neuropeptide AF (human) acetate (192387-38-5 Free base)) 属于抗阿片类神经肽,是 Neuropeptide AF (human) 衍生物,可调节脂肪细胞代谢。
T2726 Sinomenine
青藤碱
115-53-7 99.89%
TargetMol Chemical Structure Sinomenine
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。
T0478 Progesterone
孕酮
57-83-0 99.89%
TargetMol Chemical Structure Progesterone
Progesterone (Pregn-4-ene-3,20-dione) 是类固醇激素,能够调节月经周期。
T21422 Methylnaltrexone bromide
溴化甲基纳曲酮
73232-52-7 99.88%
TargetMol Chemical Structure Methylnaltrexone bromide
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。
T2071 MCOPPB triHydrochloride
化合物MCOPPB trihydrochlride
1108147-88-1 99.88%
TargetMol Chemical Structure MCOPPB triHydrochloride
MCOPPB triHydrochloride (MCOPPB 3HCl) 是一种伤害感受肽受体激动剂,pKi 为10.07。
β-Endorphin (6-31), human
T76285
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。
Akuammigine
TN3368
Akuammigine has in vitro antimalarial activity. Akuammigine competitively antagonizes the effect of noradrenaline on postsynaptic alpha-adrenoceptors, yielding p...
Valorphin
T7306
Valorphin (Valorphin TFAsalt) 是内源性血红蛋白 β 链第 33-39 位氨基酸残基,具有阿片类镇痛活性,与大鼠 mu-阿片受体结合,IC50 为 14 nM。它有抗肿瘤活性,也可用于缓解疼痛的研究。
Naltrindole hydrochloride
T12169
Naltrindole hydrochloride 是一种选择性的非肽类 δ 阿片受体拮抗剂 (Ki = 0.02 nM)。
Akuammidine
TN3367
Akuammidine shows anti-inflammatory and anti-asthmatic properties, it has opioid analgesic activity, it shows a preference for mu-opioid binding sites with Ki va...
(R,S)-Ivosidenib
T13438
(R,S)-Ivosidenib is the less active enantiomer of Ivosidenib .
Opioid receptor modulator 1
T12314
Opioid receptor modulator 1 is a modulator of opioid receptor.
DPI-3290
T15165
DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent antinocicepti...
LY255582
T27934
LY255582 是一种具有选择性的中枢活性阿片受体拮抗剂,对 mu、delta 和 kappa 受体具有高亲和力 ,Ki 分别为 0.4 nM、5.2、2.0 nM。LY255582 可以抑制饮食相关的中脑边缘多巴胺水平的增加,并减少食物摄入的消耗。LY255582 常用于对肥胖的研究。LY255582是用于阿片受体介...
GSK1521498 free base
T11478L
GSK1521498 free base is a potent and selective antagonist of the μ-opioid receptor. GSK1521498 free base also has the potential for disorders of compulsive consu...
Endomorphin 2 TFA
T11198
Endomorphin 2 TFA, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. a high affinity, highly selective agonist of the...
Alvimopan
T1242
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。
Aticaprant
TQ0082
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。
Dynorphin A 1-10 acetate(79994-24-4 free base)
TP1813L
Dynorphin A 1-10 acetate(79994-24-4 free base) 是一种内源性 opioid 样物质神经肽,与 κ-opioid 样物质受体的细胞外环 2 结合。 Dynorphin A (1-10) 还阻断 NMDA 激活的电流,IC50 为 42.0 μM。
beta-Neoendorphin acetate(77739-21-0 free base)
TP2322L
beta-Neoendorphin acetate(77739-21-0 free base) 是 κ-opioid 受体的激动剂
Neuropeptide AF (human) acetate
TP1082L
Neuropeptide AF (human) acetate (Neuropeptide AF (human) acetate (192387-38-5 Free base)) 属于抗阿片类神经肽,是 Neuropeptide AF (human) 衍生物,可调节脂肪细胞代谢。
Sinomenine
T2726
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。
Progesterone
T0478
Progesterone (Pregn-4-ene-3,20-dione) 是类固醇激素,能够调节月经周期。
Methylnaltrexone bromide
T21422
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。
MCOPPB triHydrochloride
T2071
MCOPPB triHydrochloride (MCOPPB 3HCl) 是一种伤害感受肽受体激动剂,pKi 为10.07。
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TargetMol Loading
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