Cat. No. | Product Name | Target | Signaling Pathways |
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T0209 |
Loperamide hydrochloride
Loperamide HCl,R-18553 (hydrochloride),ADL 2-1294,盐酸洛哌丁胺 |
Opioid Receptor; Autophagy | Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Loperamide hydrochloride (ADL 2-1294) 是一种合成的哌啶衍生物和阿片样物质激动剂,具有止泻活性。 | |||
T38809 |
Loperamide phenyl
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Loperamide phenyl, an impurity detected in Loperamide, is an opioid receptor agonist. | |||
T33615 |
N-Desmethyl Loperamide
dLop,R20905,R-20905,R 20905 |
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N-Desmethyl Loperamide is the major metabolite of loperamide. It is also used as the precusor for radiolabelled loperamide. | |||
T25753 |
Loperamide oxide
R 58425,R58425,R-58425 |
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Loperamide oxide is a prodrug of loperamide, the effective antidiarrheal. | |||
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. | |||
T83899 |
N-didesmethyl Loperamide
R 21345 |
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N-didesmethyl Loperamide是loperamide的一个活性代谢产物,属于周围μ1-阿片受体激动剂。它能抑制孤立的豚鼠肠膜丛中由电刺激引起的收缩(IC50 = 370 nM)。N-didesmethyl Loperamide还能增强对氯喹产生抗药性的P. falciparum菌株对氯喹的敏感性(EC50 = 482 nM),同时在A-10血管平滑肌细胞中未引起毒性(IC50 = >10,000 nM)。 | |||
T70267 |
ADL 08-0011 HCl
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ADL 08-0011 is an active metabolite of the μ-opioid receptor antagonist alvimopan. It is produced from alvimopan via amide hydrolysis by gut microbiota. ADL 08-0011 is a μ-opioid receptor antagonist (Ki = 0.25 nM). It is selective for μ-opioid receptors over κ- and δ-opioid receptors (Kis = 15.8 and 31.6 nM, respectively). ADL 08-0011 inhibits endomorphin 1-induced inhibition of electrically induced contraction of isolated guinea pig ileum (pA2 = 9.4). In vivo, ADL 08-0011 (0.03-1 mg/kg) reverse... |