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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1406 |
Amantadine hydrochloride
盐酸金刚烷胺,1-adamantanamine HCl,1-Adamantanamine hydrochloride,Symmetrel,CI-719,Amantadine HCl,1-Adamantylamine hydrochloride |
Dopamine Receptor; Influenza Virus | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Amantadine hydrochloride (CI-719) 是一种抗病毒药物,用于预防或对症治疗甲型流感和帕金森病。它阻断质子流通过 M2 离子通道,从而阻止病毒 RNA 释放到感染细胞的细胞质中。 | |||
T1406L |
Amantadine sulfate
1-Adamantanamine Sulfate |
||
Amantadine is used both as an antiviral and an anti-parkinsonian drug. Amantadine is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release, and blocks dopamine reuptake. The drug has many effects in the brain, including the rel | |||
T0645 |
N-(1-Adamantyl)acetamide
|
Others | Others |
N-(1-Adamantyl)acetamide 用作合成amantadine hydrochloride 的中间体。 | |||
T1443 |
Memantine hydrochloride
3,5-二甲基金刚胺盐酸盐,盐酸美金刚,Namenda,Memantine HCl,D-145 (hydrochloride) |
P450; GluR; NMDAR; Autophagy; iGluR | Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Memantine hydrochloride (Memantine HCl) 是一种具有一些多巴胺能作用的金刚烷胺衍生物,是一种温和的 NMDA 受体非竞争性拮抗剂,能够抑制 CYP2B6 和 CYP2D6。它可作为抗帕金森剂。 | |||
T20993 |
Memantine
|
Others | Others |
Memantine 是口服具有活性的、非竞争性的N-甲基-D-天冬氨酸受体拮抗剂,可用于研究中重度阿尔茨海默病。 | |||
T13209 |
Tromantadine
|
HSV | Microbiology/Virology |
Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication). | |||
T24428 |
M090
M 090,M-090 |
||
M090 is a potent inhibitor against amantadine-resistant viruses, including the 2009 H1N1 pandemic strains and oseltamivir-resistant viruses. | |||
T13209L | Tromantadine hydrochloride | HSV | Microbiology/Virology |
Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication). | |||
T38145 | Eltoprazine | ||
Eltoprazine(DU28853) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor.IC50 value:Target: 5-HT1A/1B agonist; 5-HT2C antagonistin vitro: The binding of [3H]eltoprazine to whole tissue sections was saturable and revealed an apparent dissociation constant (Kd) of 11 nM. Specific [3H]eltoprazine binding was completely displaced by 5-HT; conversely, unlabelled eltoprazine reduced [3H]5-HT binding to the levels of no... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7060 |
Amantadine
1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine |
Others | Others |
Amantadine (1-Aminoadamantane) 是抗病毒药物,也是是 NMDA 型谷氨酸受体的弱拮抗剂,能促进高多巴胺的释放,并阻断多巴胺的再摄取。 |