Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4369 |
SCH-23390 hydrochloride
R-(+)-SCH23390 hydrochloride |
Potassium Channel; Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
SCH-23390 hydrochloride (R-(+)-SCH23390 hydrochloride) 是一种选择性多巴胺 D1样受体拮抗剂,对 D1和 D5受体的Ki 分别为 0.2 和 0.3 nM。它还抑制 G 蛋白偶联的内向整流钾通道,IC50为 268 nM。它与5-HT2和5-HT1C 受体具有高亲和力,是人5-HT2C 受体激动剂,Ki 为 9.3 nM。 | |||
T12865 |
SCH-23390 maleate
R-(+)-SCH-23390 maleate |
Potassium Channel; Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
SCH-23390 maleate (R-(+)-SCH-23390 maleate) 是多巴胺D1样受体选择性拮抗剂,与D1和D5受体结合的Ki 分别为 0.2 nM 和 0.3 nM。它也是人5-HT2C 受体激动剂,Ki 为 9.3 nM。它与5-HT2和5-HT1C 受体具有高亲和力。它还抑制 G 蛋白偶联的内向整流钾通道,IC50为 268 nM。 | |||
T23066 |
NGD 94-1
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
NGD 94-1 是一种选择性的 D4 受体拮抗剂,对D4受体的亲和力为3 nM,而对D1、D2、D3和D5受体的亲和力大于2 pM。NGD 94-1 可用研究认知障碍等精神性疾病。 | |||
T6988 |
SKF 38393 hydrochloride
(±)-SKF-38393 hydrochloride,SKF-38393A,SKF38393 HCl |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
SKF 38393 hydrochloride (SKF38393 HCl) 是选择性的多巴胺 D1 受体激动剂,IC50=110 nM。 | |||
T60835 |
SKF83959
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
SKF83959 是苯并氮平类化合物,是一种具有选择性和有效性的多巴胺D1受体部分激动剂,对大鼠D1,D5,D2和D3受体的Ki 值分别为 1.18, 7.56, 920 和 399 nM。SKF83959 是 sigma (σ)-1受体的有效变构调节剂,可改善认知功能障碍,用于研究抑郁症和阿尔茨海默病。 | |||
T16999 |
Tavapadon
PF-6649751,CVL-751 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Tavapadon (CVL-751) 是一种具有口服活性,高选择性的多巴胺 D1/D5受体部分激动剂,它可有效促进运动并减少残疾,对帕金森氏病具有潜在的应用价值。 | |||
T28167 |
NGB 2904
NGB2904 HCl,NGB-2904,NGB2904 |
Others; Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
NGB 2904 是一种具有口服活性的、选择性的多巴胺(DA) D3受体拮抗剂,可用于具可卡因成瘾。 | |||
T22921 |
LE 300
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
LE 300 是选择性多巴胺 D1 样受体拮抗剂,作用于人多巴胺 D1 和 D5 受体的Kis 分别为 1.9 nM 和 7.5 nM。在大鼠尾动脉实验中,它作用于5-HT2A 受体的pA2 为 8.32。 | |||
T31602 |
Ecopipam
Sch-39166,UNII-0X748O646K,Sch 39166 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Ecopipam (UNII-0X748O646K) 是一种有效的、选择性、具有口服活性的多巴胺 D1/D5 受体拮抗剂,Ki 值分别为 1.2 nM 和 2.0 nM。Ecopipam 对 D2、D4、5-HT 和 α2a 受体 (Ki=0.98,5.52,0.08 和 0.73 μM) 显示出超过 40 倍的选择性。Ecopipam 可用于精神分裂症、可卡因成瘾和肥胖症的研究。 | |||
T5397 |
A-381393
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
A-381393 是选择性、可透过血脑屏障的多巴胺 D4受体拮抗剂,对人多巴胺 D4.4,D4.2和 D4.7受体的 Ki 分别为 1.5,1.9 和 1.6 nM,选择性是对 D1,D2,D3,D5多巴胺受体的 2700 多倍,对 5-HT2A 的选择性适中,Ki=370 nM。 | |||
T7834 |
ABT-724
2 - [(4-吡啶-2-基哌嗪-1-基)甲基]-1H-苯并咪唑 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
ABT-724 是高度选择性的多巴胺D4受体激动剂,对人多巴胺D4受体的EC50=12.4 nM。它是大鼠D4(EC50为 14.3 nM) 和雪貂D4受体 (EC50为 23.2 nM) 的有效部分激动剂,对多巴胺 D1,D2,D3或 D5受体没有影响。它可用于勃起功能障碍的研究,并具有较少的副作用。 | |||
T19342 |
Glycerol phenylbutyrate-D5
HPN-100-D5 |
Sigma receptor | GPCR/G Protein |
Glycerol phenylbutyrate-D5 is a deuterium-labeled Glycerol phenylbutyrate. Glycerol phenylbutyrate is a sigma-2 (σ2) receptor ligand (pKi: 8.02). | |||
T16893 |
SKF-82958
Chloro-AP,(±)-SKF 82958 |
Others | Others |
SKF 82958 is a D1/D5 receptor full agonist. | |||
T16892 |
SKF-82958 hydrobromide
(±)-SKF 82958 hydrobromide,Chloro-APB hydrobromide |
Others | Others |
SKF-82958 hydrobromide is a D1/D5 receptor full agonist. | |||
T13463L |
Dihydrexidine
DAR-0100 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Dihydrexidine is a full efficacy D1-like dopamine receptor (D1/D5) agonist (IC50: 10 nM for D1 receptor). It also shows potent antiparkinsonian activity. | |||
T13076 |
Tamoxifen-d5
ICI 47699-d5,(Z)-Tamoxifen-d5,trans-Tamoxifen-d5 |
HSP | Cytoskeletal Signaling; Metabolism |
Tamoxifen-d5 is a deuterium labeled Tamoxifen. Tamoxifen is a selective modulator of estrogen receptor (SERM). Tamoxifen is a potent activator of Hsp90 and enhances the Hsp90 molecular chaperone ATPase activity. | |||
T10440 |
Azilsartan-d5
TAK-536 D5 |
Others | Others |
Azilsartan (TAK-536) D5 is the deuterium-labeled Azilsartan. Azilsartan is a specific antagonist of the angiotensin II type 1 receptor. | |||
T10558 |
Blonanserin D5
AD-5423 D5 |
Others | Others |
Blonanserin D5 is a deuterium-labeled Blonanserin. Blonanserin (AD-5423) is a dopamine D2/5-HT2 receptor antagonist with an atypical antipsychotic effect. | |||
T12973 |
Solifenacin D5 hydrochloride
|
Others | Others |
Solifenacin D5 hydrochloride is a deuterium labeled Solifenacin hydrochloride. Solifenacin hydrochloride is an antagonist of muscarinic receptor(pKis of 7.6, 6.9 and 8.0 for M1, M2 and M3 receptors, respectively). | |||
T67921 |
Retinoic acid-d5
all-trans-Retinoic acid-d5,Isotretinoin-d5,Vitamin A acid-d5,Accutane-d5,ATRA-d5 |
Retinoid Receptor | Metabolism |
Retinoic acid-d5 (Vitamin A acid-d5)是视黄酸的氘标记形式。视黄酸是一种天然的RAR 核受体激动剂, 对 RARα/β/γ 的 IC50 为 14 nM,与 PPARβ/δ 结合的Kd 为 17 nM。视黄酸是维生素a 的代谢物,在细胞生长、分化和器官发育中起着重要作用。视黄酸通过激活视黄酸受体α作为转录因子Nrf2的抑制剂来发挥作用。 | |||
T0074L |
Chlorprothixene hydrochloride
NSC 78193,Minithixen,泰尔登盐酸盐,Truxal hydrochloride,盐酸氯普噻吨,NSC 56379,NSC 169899,Minithixen hydrochloride |
Dopamine Receptor; 5-HT Receptor; Antibacterial; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Chlorprothixene hydrochloride (Truxal hydrochloride) 是一种多巴胺和组胺受体拮抗剂,具有抗精神病作用,高亲和力地结合人 D1,D2,D3,D5,H1 受体,Ki 分别为 18 nM,2.96 nM,4.56 nM,9 nM 和 3.75 nM。 | |||
T73823 |
DETQ
|
||
DETQ是一种具有选择性、变构性和口服活性的多巴胺D1受体增强剂。在表达人类D1受体的HEK293细胞中,通过增加cAMP水平发挥作用,其EC50为5.8nM,Kb为26nM。DETQ对大鼠和小鼠的D1受体效力降低约30倍,对人类D5受体则无活性。 | |||
T6647 |
Rotigotine-
Neupro,N-0923,罗替戈汀,N-0437,SPM 962 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Rotigotine (N-0923) 是多巴胺受体激动剂,是5-HT1A receptor 的部分激动剂,以及α2B-肾上腺素受体的拮抗剂,用于治疗帕金森病和不宁腿综合征。 | |||
T70035 |
Tasimelteon-d5
|
||
Tasimelteon-d5 is intended for use as an internal standard for the quantification of tasimelteon by GC- or LC-MS. Tasimelteon is a melatonin (MT) receptor agonist. It selectively binds MT1 and MT2 receptors over a panel of 160 additional receptors and enzymes at 10 µM. Tasimelteon inhibits forskolin-induced cAMP accumulation with EC50 values of 0.79 and 1 nM in NIH3T3 cells expressing the MT1 or MT2 receptor, respectively. Formulations containing tasimelteon have been used in the treatment of no... | |||
T21446 |
Rotigotine Hydrochloride
Rotigotine (Hydrochloride),N 0923,N-0924,Rotigotine HCl,盐酸罗替戈汀,N-0923,罗替戈汀盐酸盐 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Rotigotine Hydrochloride (N-0924) 是多巴胺受体激动剂,是5-HT1A 受体的部分激动剂,以及α2B-肾上腺素受体的拮抗剂,具有抗帕金森病活性。 | |||
T70313 | Indoxyl Sulfate-d5 potassium salt | ||
Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver. Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay). ... | |||
T23364 |
SKF 83959 hydrobromide
|
Others | Others |
SKF 83959 hydrobromide is a Dopamine D1-like receptor partial agonist. | |||
T23381 | Spiperone hydrochloride | Others | Others |
5-HT2A serotonin and selective D2-like dopamine receptor antagonist | |||
T12676 |
(Rac)-Rotigotine hydrochloride
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
(Rac)-Rotigotine hydrochloride is a racemate of Rotigotine. Rotigotine is a full agonist of dopamine receptor, a partial the 5-HT1A receptor agonist. | |||
T22858 |
Iloperidone hydrochloride
|
Others | Others |
Iloperidone hydrochloride is a D(2)/5-HT(2) receptor antagonist. It is also an atypical antipsychotic for the treatment of schizophrenia symptoms. |