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Cat. No. | Product Name | Target | Signaling Pathways |
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T1097 |
Loratadine
氯雷他定,SCH 29851,Loratidine |
Influenza Virus; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Loratadine (SCH 29851) 是一种组胺 H1受体反向激动剂,IC50>32 μM。它抑制炎症介质的免疫释放,具有抗登革热病毒的活性。 | |||
T70306 |
Loratadine N-oxide
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Loratadine N-oxide is a metabolite of the histamine H1 receptor inverse agonist loratadine. | |||
T20814 |
Loratadine specified impurity F
11-Fluoro dihydroloratadine |
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Loratadine specified impurity F is a fluorinated analog of Loratadine. | |||
T20815 |
4-Chloroloratadine
4-Chloro loratadine,Loratadine specified impurity C |
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4-Chloroloratadine is an impurity of Loratadine, a nonsedating-type histamine H1-receptor. | |||
T20816 |
Isoloratadine
Iso loratadine,Loratadine specified impurity E |
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Isoloratadine is a Loratadine impurity. It is an isomer of Loratadine used for the preparation of ureas and tricyclic amides, it is also useful for inhibition of G-protein function and treatment of proliferative diseases. | |||
T70305 | Zoledronate trisodium hydrate | ||
Zoledronate trisodium is a Bone Resorption Inhibitor and Osteoporosis Therapy Adjunct | |||
T65952 | N-Methyl Desloratadine | ||
N-Methyl Desloratadine 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T65952,CAS号为 38092-89-6。 | |||
T36618 |
Rupatadine
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Rupatadine (UR-12592) is a potent dual PAF/H1 antagonist with Ki of 0.55/0.1 uM(rabbit platelet membranes/guinea pig cerebellum membranes).IC50 value:Target: PAF/H1 antagonistin vitro: Rupatadine competitively inhibited histamine-induced guinea pig ileum contraction (pA2 = 9.29 +/- 0.06) without affecting contraction induced by ACh, serotonin or leukotriene D4 (LTD4). It also competitively inhibited PAF-induced platelet aggregation in washed rabbit platelets (WRP) (pA2 = 6.68 +/- 0.08) and in hu... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T2520 |
Desloratadine
Sch34117,地氯雷他定,NSC 675447 |
Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Desloratadine (Sch34117) 是非镇静H1抗组胺药 Loratadine 的主要口服代谢物,可减少对支气管平滑肌、毛细血管和胃肠道平滑肌中 H1 受体的典型组胺能作用,包括血管舒张、支气管收缩、血管通透性增加、疼痛、瘙痒和胃肠道平滑肌的痉挛性收缩。它是一种选择性H1受体拮抗剂,具有抗过敏和抗炎活性。 |