15
2
Cat. No. | Product Name | Target | Signaling Pathways |
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T2524 |
Dexmedetomidine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dexmedetomidine 是选择性、具有口服活性的 α2 肾上腺素能受体激动剂,Ki=1.08 nM。它对 α1 肾上腺素受体显示出 1620 倍的选择性。它具有抗焦虑活性,可用于研究促进睡眠和缓解疼痛。 | |||
T6579 |
Medetomidine hydrochloride
MPV785,Medetomidine HCl,Domitor |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Medetomidine hydrochloride (MPV785) 是一种 α2 肾上腺素受体激动剂,能够作用于α2和α1肾上腺素受体,其Ki 分别为1.08 nM 和1750 nM。 | |||
T2150 |
Guanfacine hydrochloride
盐酸胍法辛,Tenex,Intuniv,Guanfacine |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Guanfacine hydrochloride (Intuniv) 是一种 α2A 肾上腺素受体激动剂,Kd=31 nM,具有抗高血压作用。 | |||
T1180 |
Blonanserin
布南色林,AD-5423 |
Dopamine Receptor; Sigma receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Blonanserin (AD-5423) 是一种有效的5-HT2A 和多巴胺 D2 受体拮抗剂,Ki 为 0.812 和 0.142 nM,是一种非典型的抗精神病试剂。 | |||
T6466 |
Dexmedetomidine hydrochloride
Precedex,(+)-Medetomidine hydrochloride,(S)-Medetomidine hydrochloride,盐酸右美托咪定,Dexmedetomidine HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dexmedetomidine hydrochloride (Precedex) 是一种有效的、选择性的、具有口服活性的 α2 肾上腺素能受体 (α2-adrenoceptor) 激动剂,Ki=1.08 nM。它对 α1 肾上腺素受体显示出 1620 倍的选择性。它具有抗焦虑作用,可用于研究促进安定和缓解疼痛。 | |||
T21390 |
Fexofenadine
Carboxyterfenadine,Telfast,非索非那定,MDL 16.455,Allegra |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Fexofenadine (Carboxyterfenadine) 是一种抗组胺药物,用于治疗过敏症状,如鼻塞、花粉热和荨麻疹。与第一代抗组胺药相比,它通过血脑屏障并引起镇静的能力较差。 | |||
T2335 |
Ebastine
Ebastel,依巴斯汀,LAS-W 090,Ebastin,Kestine,RP64305 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ebastine (Kestine) 是一种可口服的组胺 H1 受体拮抗剂,用于过敏性鼻炎的症状和慢性特发性荨麻疹的研究。 | |||
T1240 |
Flumazenil
Ro 15-1788,氟马西尼 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Flumazenil (Ro 15-1788) 是一种有竞争性的GABAA 受体拮抗剂,以剂量依赖的方式逆转苯二氮卓类药物诱导的作用,包括镇静、精神运动缺陷、健忘和换气不足。 | |||
T28378 |
PF-0713
PF 0713,PF713 |
||
PF 0713, a GABAA receptor agonist, is used as an intravenous sedative-hypnotic for general anaesthesia, ICU sedation, procedural sedation, chemotherapy. | |||
T29008 |
Triclofos Sodium
SCH-10159,SCH 10159,SCH10159 |
||
Triclofos Sodium is used to treat insomnia and used for sedation. | |||
T72240 |
Romifidine hydrochloride
|
||
Romifidine hydrochloride,一种α2肾上腺素受体激动剂,在体内具有显著的镇定效果。 | |||
T29227 |
ZK-91296
ZK 91296,ZK91296 |
||
ZK-91296 is a GABA receptor agonist. ZK 91296 can reduce anxiety in animals at doses well below those causing sedation. ZK 91296 may possess pharmacological selectivity for a particular type of BZ receptor interaction, perhaps including topographic as wel | |||
T60297 |
Triclofos
|
||
Triclofos 是一种有效的口服活性的镇静剂。Triclofos 在体内可迅速水解成 trichloroethanol (TCEOH) 和磷酸一钠,有助于镇静。 | |||
T41183 |
Helianorphin-19
|
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Helianorphin-19 is a high affinity, potent and selective κ-opioid receptor (KOR) agonist (Ki = 25 nM; EC50= 45 nM). Helianorphin-19 exhibits approximately 200-fold selectivity for KOR over μ and δ-opioid receptors.In vivoHelianorphin-19 shows potent peripheral analgesic efficacy in a mouse model of visceral pain without affecting motor coordination/sedation. | |||
T60943 |
Tiapride
|
||
Tiapride 是一种非典型的抗精神病剂,不会引起强直性昏厥和镇静。Tiapride 是多巴胺 D2受体的选择性拮抗剂,其对 D1;D2;D3;D4 受体的 IC50值分别为 1440、45.8、>100 和 11.7 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2800 |
L-Theanine
L-茶氨酸,左旋茶氨酸 |
Apoptosis; Others | Apoptosis; Others |
L-Theanine 是一种存在于绿茶叶片中的非蛋白氨基酸物质,能阻断大脑中谷氨酸与谷氨酸受体结合,具有神经保护和抗氧化活性。 它通过口服能抑制皮层神经元兴奋从而产生抗应激作用。 | |||
TN4519 |
Mesuaxanthone A
胡桐,海棠木 |
Others | Others |
Mesuaxanthone A and mesuaxanthone B are two yellow pigments.They produce varying degrees of C.N.S. depression characterised by ptosis, sedation, decreased spontaneous motor activity, loss of muscle tone, potentiation of pentobarbitone sleeping time and et |