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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0053 |
Hydroxyzine Pamoate
Hydroxyzine embonate,双羟萘酸羟嗪,Bobsule,Equipose |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine Pamoate (Bobsule) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。 | |||
T2200 |
Hydroxyzine dihydrochloride
Hydroxyzine 2HCl,盐酸羟嗪 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine dihydrochloride (Hydroxyzine 2HCl) 是一种苯二氮卓抗组胺剂,是可口服的组胺 H1 受体和血清素拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它还可以作为止吐剂和镇静剂,有缓解焦虑和紧张的作用。 | |||
T5495 |
Decloxizine dihydrochloride
盐酸去氯羟嗪,UCB 1402 dihydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Decloxizine dihydrochloride (UCB 1402 dihydrochloride) 是组胺 1 受体拮抗剂。 | |||
T22713 |
Decloxizine
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Decloxizine 是一种组胺受体H1拮抗剂。 | |||
T11591 |
Hydroxyzine D4
羟嗪 D4 |
Others | Others |
Hydroxyzine D4 is a deuterium-labeled variation of Hydroxyzine, a chemical compound known for its anticholinergic, anxiolytic, and analgesic properties. It is classified as a heterocyclic histamine H1-receptor antagonist. | |||
T0217L |
(+)-Dropropizine
(+)-Dropropizine,左羟丙哌嗪 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
(+)-Dropropizine 可以抑制组胺受体,抗过敏,并通过调节参与咳嗽反射的神经肽和干扰感觉神经末梢的刺激激活来减少咳嗽。 | |||
T20711 |
Hemipyocyanine
1-羟基吩嗪,528-71-2 |
Amylase | Metabolism |
Hemipyocyanine (528-71-2) 是一种 α-淀粉酶抑制剂。 | |||
T18912 |
ADHP
10-乙酰基-3,7-二羟基吩嗪,10-Acetyl-3,7-dihydroxyphenoxazine |
Others | Others |
ADHP (10-Acetyl-3,7-dihydroxyphenoxazine) 是荧光过氧化物酶底物,其λex=530 nm,λem=590 nm。 | |||
T0217 |
Levodropropizine
(S)-(-)-Dropropizine,左羟丙哌嗪,DF-526 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levodropropizine ((S)-(-)-Dropropizine) 是一种组胺受体抑制剂,可用作外周镇咳药。 | |||
T0452 |
Dropropizine
(±)-Dropropizine,UCB-196,羟丙哌嗪,UCB-1967 |
Others | Others |
Dropropizine (UCB-1967) 是外周镇咳剂,能够作用于外周受体及其传入导体,发挥抑制咳嗽反射的作用。 | |||
T6420 |
BMS-707035
N-[(4-氟苯基)甲基1,6-二氢-5-羟基-1-甲基-6-氧代-2-(四氢-1,1-二氧-2H-1,2-噻嗪-2-基)-4-嘧啶甲酰胺 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
BMS707035是一种 HIV-1 整合酶抑制剂,IC50为15 nM。 | |||
T23134 |
Resorufin pentyl ether
7-羟基吩噁嗪酮二戊醚,Pentoxyresorufin |
Others | Others |
fluorometric cytochrome P450 substrate | |||
T68141 |
Seganserin
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Seganserin 是一种非选择性5-羟色胺2-HT 受体拮抗剂,可逆转了氟西汀和喹帕嗪对黄体酮诱导的食欲亢进,抑郁和痛觉的抑制作用,逆转氟西汀和喹帕嗪诱导的抗抑郁和镇痛作用。 | |||
T0089 |
Cetirizine dihydrochloride
盐酸西替利嗪,P071,UCB P071,Cetirizine DiHCl |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cetirizine dihydrochloride (UCB P071) 是羟嗪的羧化代谢物,是特异性口服有效的 H1 受体长效拮抗剂。它标记抗过敏特性,抑制过敏反应期间嗜酸性粒细胞趋化,可有效治疗过敏性鼻炎、确诊荨麻疹和花粉诱发的哮喘。 | |||
T73981 | Deschloro Cetirizine dihydrochloride | ||
Deschloro Cetirizine Dihydrochloride 为 Cetirizine 杂质(impurity)。Cetirizine 属于第二代抗组胺药,作为羟嗪羧化代谢物,它表现为特异性、口服活性的长效组胺 H1 受体(histamine H1-receptor)拮抗剂。 | |||
T73933 |
Cetirizine methyl ester
|
||
Cetirizine methyl ester 是Cetirizine 的杂质。Cetirizine 是羟嗪的羧化代谢物,是第二代抗组胺剂。Cetirizine 是一种特异的、具有口服活性的 H1 受体 (histamine H1-receptor) 的长效拮抗剂。 | |||
T73962 | Cetirizine Impurity C dihydrochloride | ||
Cetirizine Impurity C dihydrochloride 为Cetirizine杂质之一,属于羟嗪的羧化代谢物,是第二代抗组胺剂中的一个。其为具有特异性且口服有效的H1受体(histamine H1-receptor)长效拮抗剂。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20884 |
Hydroxyzine
Hydroxyzine free base,羟嗪 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine (Hydroxyzine free base) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。 |