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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
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。
T77374	Ontuxizumab MORAb-004	Others	Others
	Ontuxizumab (MORAb-004) 是一种靶向内髓酸的单克隆抗体，具有抗肿瘤作用。Ontuxizumab 是一种有效的 IgG1/κ 抗内皮素 (TEM-1 或 CD248) 的单克隆抗体，可用于治疗转移性黑色素瘤。
T69475	Dinalbuphine sebacate
	Dinalbuphine sebacate is a long-lasting prodrug of nalbuphine, acting as a moderate-efficacy partial agonist or antagonist of the μ-opioid receptor and as a high-efficacy partial agonist of the κ-opioid receptor.
T81297	Renvistobart
	Renvistobart为针对[Homo sapiens(含Ig结构域及ITIM、VSIG9、VSTM3的T细胞免疫受体)]的Homo sapiens IgG1-κ型单克隆抗体。
T40510	Ac-RYYRWK-NH2 TFA Ac-RYYRWK-NH2 TFA
	Ac-RYYRWK-NH2 is a highly effective and specific partial agonist for the nociceptin receptor (NOP). It demonstrates a remarkable affinity for rat cortical membranes ORL1, with [3H]Ac-RYYRWK-NH2 exhibiting a Kd value of 0.071 nM. However, it shows negligible affinity towards μ-, κ-, or δ-opioid receptors.
T71491	Enadoline (Free Base)
	Enadoline (Free Base) is a kappa-opioid receptor agonist; PD 129290 (CAM 570; CI 977) is the S,S(-)-enantiomer; PD 129289 (CAM 569) is the corresponding R,R(+)-enantiomer. In human studies, it produced visual distortions and feelings of dissociation, reminiscent of the effects of salvinorin A. It was studied as a potential analgesic, but abandoned because of the dose-limiting effects of dysphoria, which could be expected from a κ-opioid agonist. There was mention of its potential in treating com...
T72696	UCK2 Inhibitor-3
	UCK2 Inhibitor-3是一款UCK2 (尿苷胞苷激酶2)的非竞争性抑制剂，其IC50值为16.6 μM。该化合物能在一定程度上补偿因感染或快速分裂的细胞中DHODH (二氢旋酸脱氢酶)功能的缺失，有效地挽救尿苷。此外，UCK2 Inhibitor-3还能抑制DNA聚合酶η和κ，其IC50值分别为56 μM和16 μM。

化合物

Synonym: MORAb-004

Target: Others

Dinalbuphine sebacate

Synonym: Ac-RYYRWK-NH2 TFA

Target:

Enadoline (Free Base)

Cat. No.	Product Name	Target	Signaling Pathways
T83913	Mitraciliatine
	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。