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ADL5859 HCl
Catalog No. A11072 Opioid Receptor 激动剂ADL5859 HCl是高效的选择性δ阿片受体激动剂，Ki值为0.84 nM，ED50值为20 nM。 了解更多 -
MCOPPB 3HCl
Catalog No. A10561 -
BRL 52537 HCl
Catalog No. A11210 Opioid Receptors 激动剂BRL 52537 hydrochloride是一种高度选择性和有效的κ阿片类激动剂（Ki = 0.24 nM）。比吗啡强25倍。 了解更多 -
Nalfurafine hydrochloride
Catalog No. A12579 opioid κ-selective 激动剂Nalfurafine hydrochloride是一种κ-opioid激动剂。 了解更多 -
U-69593
Catalog No. A14187 -
Alvimopan dihydrate
Catalog No. A14991 ?-opioid receptor 激动剂Alvimopan dihydrate (LY 246736,ADL 8-2698)是一种外周作用的类阿片受体（PAM-OR，IC50 = 1.7 nM）拮抗剂，可促进术后胃肠道恢复。 了解更多 -
Alvimopan monohydrate
Catalog No. A14992 ?-opioid receptor 激动剂Alvimopan monohydrate是一种外围作用的类阿片受体（PAM-OR，IC50 = 1.7 nM）拮抗剂，可促进术后肠胃的恢复。 了解更多 -
Cebranopadol (GRT-6005)
Catalog No. A12670 Opioid Receptor 激动剂Cebranopadol是一种有效的伤害感受器/孤儿蛋白FQ肽（NOP）和阿片受体激动剂。作用于人NOP，MOP，KOP 和δ-阿片肽(DOP)受体，Ki/EC50 分别为 0.9 nM/13 nM，0.7 nM/1.2 nM，2.6 nM/17 nM，18 nM/110 nM。 了解更多 -
Trimebutine maleate
Catalog No. A18115 ?- opioid receptor agonistTrimebutine Maleate is a drug with antimuscarinic and weak mu opioid agonist effects. Trimebutine Maleate modulates the calcium and potassium channels, relieves abdominal pain in patients with irritable bowel syndrome. 了解更多 -
TRV130 HCl (Oliceridine)
Catalog No. A15444 u-opioid receptor 激动剂TRV130 HCl (Oliceridine)是一种新型的μ-opioid 受体（MOR）G蛋白偏向配体。诱导强大的G蛋白信号传导（pEC50 = 8.1），效力和功效与吗啡相似，但β-arrestin募集和受体内在化作用要低得多。 了解更多 -
CYT-1010 hydrochloride
Catalog No. A21348 mu-opioid receptor agonistCYT-1010 hydrochloride is a mu-opioid receptor agonist extracted from patent WO2013173730A2, with EC50s of 13.1 nM and 0.0053 nM on beta-arrestin recruitment and inhibition of cAMP production, respectively. 了解更多 -
AR-M 1000390 hydrochloride
Catalog No. A21911 δ opioid receptor agonistAR-M 1000390 hydrochloride is an exceptionally selective, potent δ opioid receptor agonist with an EC50 of 7.2??0.9 nM for δ agonist potency. 了解更多 -
U 95666E
Catalog No. A10956 -
Rotigotine HCl
Catalog No. A11118 Dopamine Receptor 激动剂Rotigotine hydrochloride是一种多巴胺D2和D3受体激动剂。D2和D3的Ki值分别为13和0.71 nM。 了解更多 -
Pramipexole dihydrochloride monohyrate
Catalog No. A10747 Dopamine Receptor 激动剂Pramipexole dihydrochloride monohyrate是非麦角灵类的多巴胺激动剂，适用于治疗早期帕金森氏病（PD）和不安腿综合征（RLS）。 了解更多 -
B-HT 920 2HCl
Catalog No. A11341 -
Rotigotine
Catalog No. A11553 -
Naxagolide
Catalog No. A13087 -
ent Naxagolide Hydrochloride
Catalog No. A13089 dopamine D2-receptor 激动剂ent Naxagolide Hydrochloride是一种多巴胺D2受体激动剂，用于治疗锥体外系疾病。该化合物是抗帕金森病药物。 了解更多 -
Pergolide Mesylate
Catalog No. A14179 -
(+) PD 128907
Catalog No. A14376 Dopamine receptor 激动剂(+)-PD 128907 hydrochloride是一种有效的D3DR（多巴胺受体）激动剂（Ki = 2.3 nM）。 了解更多 -
Bromocriptin mesylate
Catalog No. A13705 dopamine D2 receptor 激动剂Bromocriptin mesylate是一种有效的多巴胺受体激动剂，它以最高的亲和力（Ki = 2.5 nM）与D2受体结合。 了解更多 -
Brexpiprazole
Catalog No. A13527 D2 dopamine partial 激动剂Brexpiprazole是一种新型的D2多巴胺部分激动剂研究产品，目前正在临床试验中，用于治疗抑郁症，精神分裂症和注意缺陷多动障碍（ADHD）。 了解更多 -
Dexpramipexole dihydrochloride
Catalog No. A15066 -
rac-Rotigotine Hydrochloride
Catalog No. A15217 -
UNC 9994 hydrochloride
Catalog No. A16087 dopamine D2 receptor 激动剂UNC 9994 hydrochloride，独特的，β-arrestin偏向的功能选择性多巴胺D2受体（D2R）激动剂（Ki值为30 nM；在ε-arrestin-2募集试验中EC50值为50 nM），在体内具有抗精神病活性。UNC9994在野生型小鼠中显着抑制了PCP诱导的超运动，而在Δr-arrestin-2基因敲除小鼠中这种作用被完全消除。 了解更多 -
Nalmefene hydrochloride
Catalog No. A13843 dopamine receptor 激动剂Nalmefene hydrochloride是opioid receptor拮抗剂。 了解更多 -
SKF38393 HCl
Catalog No. A15839 -
PF-06256142
Catalog No. A18872 D1 receptor agonistPF-06256142 is a potent and selective orthosteric agonist of the D1 receptor, with D1 EC50=30 nM and D1 binding Ki = 12 nM. 了解更多 -
Quinagolide hydrochloride
Catalog No. A18038 dopamine D2 receptor agonistQuinagolide hydrochloride is a selective dopamine D2 receptor agonist, also is a prolactin inhibitor. 了解更多 -
Pardoprunox hydrochloride
Catalog No. A21624 partial dopamine D2 and D3 receptor agonistPardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist. 了解更多 -
SKF-82958 hydrobromide
Catalog No. A21763 D1/D5 receptor full agonistSKF-82958 hydrobromide is a D1/D5 receptor full agonist. 了解更多 -
Dihydrexidine
Catalog No. A21949 D1-like dopamine receptor (D1/D5) agonistDihydrexidine (DAR-0100) is a high potent, selective and full efficacy D1-like dopamine receptor (D1/D5) agonist with an IC50 of 10 nM for D1 receptor. Dihydrexidine exhibits potent antiparkinsonian activity. 了解更多 -
Ro 10-5824 dihydrochloride
Catalog No. A21986 dopamine D4 receptor partial agonistRo 10-5824 dihydrochloride is a selective dopamine D4 receptor partial agonist, with Ki of 5.2 nM. 了解更多 -
Cariprazine
Catalog No. A21202 D3 receptor and D2 receptor partial agonistCariprazine is a novel antipsychotic drug candidate that exhibits high affinity for the D3 (Ki=0.085 nM) and D2 (Ki=0.49 nM) receptors, and moderate affinity for the 5-HT1A receptor (Ki=2.6 nM). 了解更多 -
Immethridine hydrobromide
Catalog No. A13641 histamine H3 receptor 激动剂Immethridine hydrobromide是一种强而高选择性的组胺H3受体激动剂（pEC50 = 9.74），其选择性是H4受体的300倍（pKi值分别为9.07和6.61）。 了解更多 -
Pitolisant hydrochloride
Catalog No. A15213 Nonimidazole inverse 激动剂Pitolisant hydrochloride是一种在重组人H3受体（Ki = 0.16 nM）处新颖，有效且选择性的壬二唑反向激动剂。 了解更多 -
Pitolisant oxalate
Catalog No. A15214 Nonimidazole inverse 激动剂Pitolisant oxalate是一种在重组人H3受体上的新型，有效且选择性的壬咪唑反向激动剂（Ki = 0.16 nM）。 了解更多 -
Lidocaine hydrochloride
Catalog No. A16132 -
H4 Receptor antagonist 1
Catalog No. A18929 histamine H4 receptor inverse agonistH4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist, with an IC50 of 19 nM. 了解更多 -
Synephrine (Oxedrine)
Catalog No. A10882 -
Salbutamol sulfate (Albuterol)
Catalog No. A10819 Adrenergic Receptor 激动剂Salbutamol sulfate (Albuterol)是一种短效β2肾上腺素能受体激动剂。 了解更多 -
Phenylephrine HCl
Catalog No. A11666 α1-adrenergic receptor 激动剂Phenylephrine HCl是一种选择性的α1肾上腺素能受体激动剂，主要用作减充血剂，扩张瞳孔和增加血压的药物。 了解更多 -
Isoprenaline HCl
Catalog No. A10484 β adrenoceptor 激动剂Isoprenaline HCl或isoproterenol是非选择性β肾上腺素能激动剂，在结构上类似于肾上腺素。 了解更多 -
Detomidine hydrochloride
Catalog No. A10298 Adrenergic Receptor 激动剂Detomidine hydrochloride是具有镇痛作用的镇静剂。α2-肾上腺素能激动剂产生剂量依赖性的镇静和镇痛作用，并通过激活α2儿茶酚胺受体介导，从而引起负反馈反应，从而减少兴奋性神经递质的产生。 了解更多
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