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Search Results for " d1-receptors "
Targets Recommended: Dopamine Receptor 5-HT Receptor Adrenergic Receptor

28

抑制剂 & 化合物

2

重组蛋白

1

同位素标记化合物

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Cat. No. Product Name Target Signaling Pathways
T2226 Pergolide mesylate

甲磺酸培高利特,Pergolide mesylate salt,LY127809,Pergolide methanesulfonate

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor GPCR/G Protein; Neuroscience
Pergolide mesylate salt(LY127809) 是一种有效的,具有口服活性的多巴胺 D1和 D2受体激动剂,是一种 Ergoline 衍生物,可用于帕金森氏病和高泌乳素血症的研究。
T4117 Zuclopenthixol

珠氯噻醇,cis-Clopenthixol,Cisordinol,(Z)-Clopenthixol

Dopamine Receptor GPCR/G Protein; Neuroscience
Zuclopenthixol (cis-Clopenthixol) 是一种多巴胺 D1/D2受体的拮抗剂,是一种噻吨衍生物。
T67729 UCM-1306

Dopamine Receptor GPCR/G Protein; Neuroscience
UCM-1306 是具有口服活性的人多巴胺 D1 受体变构调节剂 (PAM)。UCM-1306 增加结合在人和小鼠 D1 受体的内源性多巴胺 (DA) 效应。UCM-1306可以改善运动症状,解决与长期帕金森病(PD) 相关的关键共病认知障碍。
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。
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。
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。
T23265 RS 67333 hydrochloride

RS 67333 (hydrochloride),RS 67333 HCl,盐酸RS67333

5-HT Receptor GPCR/G Protein; Neuroscience
RS 67333 hydrochloride (RO5203648) 是一种有效的、选择性的5-HT4 受体 (5-HT4R) 部分激动剂,在豚鼠纹状体中的 pKi 为 8.7。RS 67333 hydrochloride 对其他几种受体的亲和力较低,包括 5-HT1A、5-HT1D、5-HT2A、5-HT2C、多巴胺 D1、D2 和毒蕈碱 M1-M3 受体。RS 67333 hydrochloride 具有神经保护作用,可用于阿尔茨海默病研究。
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。
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。
T14767 BP 897 hydrochloride

Dopamine Receptor GPCR/G Protein; Neuroscience
BP 897 hydrochloride 是有效的部分多巴胺 D3受体激动剂和弱 D2受体拮抗剂,在多巴胺 D3 受体 (Ki=0.92 nM) 上显示出高亲和力,而在 D2 受体上显示出 70 倍的低亲和力 (Ki=61 nM)。它表现出对可卡因寻求行为的选择性抑制。
T9100 BP 897

2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]-

Dopamine Receptor GPCR/G Protein; Neuroscience
BP 897 (2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]-) 是一种有效的部分多巴胺D3受体激动剂和弱D2受体拮抗剂,在多巴胺 D3 受体(Ki=0.92 nM) 上显示出高亲和力,而在 D2 受体上显示出 70 倍的低亲和力 (Ki=61 nM)。它表现出对可卡因寻求行为的选择性抑制。
T2592 Ropinirole hydrochloride

SKF 101468 hydrochloride,SKF-101468A,Ropinirole HCl,盐酸罗匹尼罗

Dopamine Receptor GPCR/G Protein; Neuroscience
Ropinirole hydrochloride (SKF-101468A) 是D3/D2受体激动剂,对 D2受体的Ki=29 nM。它对 hD2,hD3和 hD4受体的pEC50分别为 7.4、8.4 和 6.8。它对 D1受体没有亲和力。它对帕金森氏病具有潜在的研究价值。
T0162 Quetiapine

ICI204636,Quetiapin,喹硫平

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Quetiapine (ICI204636) 是5-HT 受体激动剂和多巴胺受体拮抗剂,对人5-HT1A 的 pEC50值为 4.77,对人 D2的 pIC50值为 6.33。它用于治疗精神分裂症,以及治疗与 I 型双相情感障碍相关的急性躁狂发作。它对人 D2、HT1、5-HT2A、5-HT2C 受体具有中高等亲和力,pKi 值为 7.25、5.74、7.54和5.55。
T2546 Pimozide

R6238,匹莫奇特,匹莫齐特

Potassium Channel; Dopamine Receptor; Adrenergic Receptor; STAT GPCR/G Protein; JAK/STAT signaling; Membrane transporter/Ion channel; Neuroscience; Stem Cells
Pimozide (R6238) 是多巴胺受体拮抗剂,对多巴胺 D1、D2 和 D3 受体的 Ki 值分别为 588、1.4 和 2.5 nM。它也是STAT3和STAT5的抑制剂,对 α1 肾上腺素受体也有较高亲和性,Ki 值为 39 nM。
T30603 BT-Sch

Others Others
Bt-sch is an imaging agent based on D1 and D2 receptors of dopamine.
T29213 Zelandopam free base

YM-435,YM435,MYD-37,MYD37,Zelandopam

Others Others
Zelandopam is a dopamine D1 agonist. Zelandopam is a potent stimulant of pancreatic exocrine secretion by acting on DA D1 receptors of the pancreas in dogs. Intravenous administration of Zelandopam produces renal vasodilating and diuretic/natriuretic effe
T4117L2 Zuclopenthixol dihydrochloride

Others Others
Zuclopenthixol dihydrochloride is an D1 and D2 dopamine receptors antagonist.
T68963 alpha-Clopenthixol dihydrochloride

Others Others
alpha-Clopenthixol dihydrochloride is a thioxanthene with therapeutic actions similar to the phenothiazine antipsychotics. It is an antagonist at D1 and D2 dopamine receptors.
TQ0315 Tandospirone

坦度螺酮,SM-3997

5-HT Receptor GPCR/G Protein; Neuroscience
Tandospirone (SM-3997) is a selective partial agonist of 5-HT1A receptor (Ki: 27 nM) that displays selectivity over SR-2, SR-1C, α1, α2, D1 and D2 receptors (Kis: 1300-41000 nM).
T68193 Clopenthixol

Others Others
Clopenthixol is a thioxanthene with therapeutic actions similar to the phenothiazine antipsychotics. It is an antagonist at D1 and D2 dopamine receptors.
T35307 Zicronapine

Lu-31130,Lu31-130,Lu 31130,Lu 31-130,Lu31130,Lu-31-130

Others Others
Zicronapine( LU 31-130) is an atypical antipsychotic. Zicronapine has monoaminergic activity and multi-receptor properties. It has shown effective antagonism against dopamine D1, D2, and serotonin 5HT2A receptors in vitro and in vivo.
T41014 MLS1082

Others Others
MLS1082 is a pyrimidone-derived compound that acts as a positive allosteric modulator of D1-like dopamine receptors. It exhibits an EC 50 value of 123 nM for stimulating G protein signaling in response to dopamine activation.
T69103 Clopenthixol decanoate

Others Others
Clopenthixol decanoate is a thioxanthene with therapeutic actions similar to the phenothiazine antipsychotics. It is an antagonist at D1 and D2 dopamine receptors.
T84445 (−)-Apomorphine (hydrochloride hydrate)

Others Others
(−)-Apomorphine, a non-selective dopamine receptor agonist, demonstrates pKi values of 6.43 (D1), 7.08 (D2L), 7.59 (D3), 8.36 (D4), and 7.83 (D5) for human recombinant receptors. It induces biphasic effects on locomotor activity and possesses anti-Parkinsonian and neuroprotective properties.[1,2,3,4]
T73823 DETQ

Others Others
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。
T60418 Ropinirole

Others Others
Ropinirole (SKF 101468) 是一种选择性 D2 样家族受体激动剂,但它对 D1 受体没有亲和力。 它是一种具有口服活性的有效 D3/D2 受体激动剂,对 D2 受体的 Ki 为 29 nM,对 hD2、hD3 和 hD4 受体的 pEC50 分别为 7.4、8.4 和 6.8。Ropinirole 具有治疗帕金森氏病的研究潜力。
T74668 Zicronapine fumarate

Others Others
Zicronapine (Lu 31-130) fumarate 是抗精神病药,主要通过拮抗多巴胺D1/D2受体和5-HT2A受体发挥作用,在动物模型中显示出显著的前认知效果,展现出治疗多种神经和精神疾病的可能性。
T83776 Dopamine D3 Receptor Agonist 13a

Dopamine D3 受体激动剂13a是一种Dopamine D3 受体激动剂。该化合物选择性地与Dopamine D3 受体结合,相较于Dopamine D1、D2和D4受体(Kis = 0.14、4,600、2.85和756 nM,分别)具有更高的亲和力,并且还能与血清素(5-HT)受体亚型5-HT1A、5-HT2A、5-HT2B和5-HT2C(Kis = 6、54、1.47和252 nM,分别)结合;然而,它是Dopamine D2受体的部分激动剂(EC50 = 2.26 nM,在G蛋白招募分析中)并且作为Dopamine D3受体的拮抗剂(IC50 = 4.62 nM)。在大鼠身上,当剂量为3 mg/kg时,Dopamine D3 受体激动剂13a能减少可卡因自我给药。

化合物

Pergolide mesylate
Cat.No: T2226
Synonym: 甲磺酸培高利特,Pergolide mesylate salt,LY127809,Pergolide methanesulfonate
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor
Zuclopenthixol
Cat.No: T4117
Synonym: 珠氯噻醇,cis-Clopenthixol,Cisordinol,(Z)-Clopenthixol
Target: Dopamine Receptor
UCM-1306
Cat.No: T67729
Synonym:
Target: Dopamine Receptor
LE 300
Cat.No: T22921
Synonym:
Target: Dopamine Receptor, 5-HT Receptor
Rotigotine Hydrochloride
Cat.No: T21446
Synonym: Rotigotine (Hydrochloride),N 0923,N-0924,Rotigotine HCl,盐酸罗替戈汀,N-0923,罗替戈汀盐酸盐
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor
Chlorprothixene hydrochloride
Cat.No: T0074L
Synonym: NSC 78193,Minithixen,泰尔登盐酸盐,Truxal hydrochloride,盐酸氯普噻吨,NSC 56379,NSC 169899,Minithixen hydrochloride
Target: Dopamine Receptor, 5-HT Receptor, Antibacterial, AChR, Histamine Receptor
RS 67333 hydrochloride
Cat.No: T23265
Synonym: RS 67333 (hydrochloride),RS 67333 HCl,盐酸RS67333
Target: 5-HT Receptor
SKF83959
Cat.No: T60835
Synonym:
Target: Dopamine Receptor
NGB 2904
Cat.No: T28167
Synonym: NGB2904 HCl,NGB-2904,NGB2904
Target: Others, Dopamine Receptor, 5-HT Receptor
BP 897 hydrochloride
Cat.No: T14767
Synonym:
Target: Dopamine Receptor
BP 897
Cat.No: T9100
Synonym: 2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]-
Target: Dopamine Receptor
Ropinirole hydrochloride
Cat.No: T2592
Synonym: SKF 101468 hydrochloride,SKF-101468A,Ropinirole HCl,盐酸罗匹尼罗
Target: Dopamine Receptor
Quetiapine
Cat.No: T0162
Synonym: ICI204636,Quetiapin,喹硫平
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor, AChR, Histamine Receptor
Pimozide
Cat.No: T2546
Synonym: R6238,匹莫奇特,匹莫齐特
Target: Potassium Channel, Dopamine Receptor, Adrenergic Receptor, STAT
BT-Sch
Cat.No: T30603
Synonym:
Target: Others
Zelandopam free base
Cat.No: T29213
Synonym: YM-435,YM435,MYD-37,MYD37,Zelandopam
Target: Others
Zuclopenthixol dihydrochloride
Cat.No: T4117L2
Synonym:
Target: Others
alpha-Clopenthixol dihydrochloride
Cat.No: T68963
Synonym:
Target: Others
Tandospirone
Cat.No: TQ0315
Synonym: 坦度螺酮,SM-3997
Target: 5-HT Receptor
Clopenthixol
Cat.No: T68193
Synonym:
Target: Others
Zicronapine
Cat.No: T35307
Synonym: Lu-31130,Lu31-130,Lu 31130,Lu 31-130,Lu31130,Lu-31-130
Target: Others
MLS1082
Cat.No: T41014
Synonym:
Target: Others
Clopenthixol decanoate
Cat.No: T69103
Synonym:
Target: Others
(−)-Apomorphine (hydrochloride hydrate)
Cat.No: T84445
Synonym:
Target: Others
DETQ
Cat.No: T73823
Synonym:
Target: Others
Ropinirole
Cat.No: T60418
Synonym:
Target: Others
Zicronapine fumarate
Cat.No: T74668
Synonym:
Target: Others
Dopamine D3 Receptor Agonist 13a
Cat.No: T83776
Synonym:
Target:
Cat. No. Product Name Species Expression System
TMPY-00150 IGF2/IGF-II Protein, Human, Recombinant

PP9974,胰岛素样生长因子,C11orf43,IGF-II,insulin-like growth factor 2

Human P. pastoris (Yeast)
Insulin-like growth factor 2 (IGF-2/IGF-II) is a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumor, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. IGF-2/IGF-II is a mediator of prolactin-induced alveologenesis; prolactin, IGF-2, and cyclin D1, all of which are overexpressed in br...
TMPY-04270 GPR133 Protein, Human, Recombinant (His)

PGR25,GPR133

Human HEK293 Cells
ADGRD1 (Adhesion G Protein-Coupled Receptor D1, also known as GPR133) is a Protein Coding gene. 4 alternatively spliced human isoforms have been reported. ADGRD1, an orphan member of the adhesion family of G-protein-coupled receptors, is a critical regulator of the response to hypoxia and tumor growth in Glioblastoma (GBM). ADGRD1 represents a novel molecular target in GBM and possibly other malignancies where hypoxia is fundamental to pathogenesis. Variations in the ADGRD1 locus are linked with...

重组蛋白

IGF2/IGF-II Protein, Human, Recombinant
Cat.No: TMPY-00150
Species: Human
Expression System: P. pastoris (Yeast)
GPR133 Protein, Human, Recombinant (His)
Cat.No: TMPY-04270
Species: Human
Expression System: HEK293 Cells
Cat. No. Product Name Target Signaling Pathways
TMIJ-0242 Tandospirone-d8

Tandospirone-d8 是 Tandospirone 的氘代化合物。Tandospirone 的 CAS 号为 87760-53-0。

同位素标记化合物

Tandospirone-d8
Cat.No: TMIJ-0242
Synonym:
Target:
TargetMol Loading
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