首页 工具
登录
购物车

搜索结果

Search Results for " α2-adrenoceptor "

33

抑制剂 & 化合物

6

天然产物

如果没找到您满意的产品或者您对产品有其他要求,可以联系我们专业顾问为您提供针对性的合理建议。     QQ咨询       网站留言咨询

提交您的定制咨询

点击图片重新获取验证码
Cat. No. Product Name Target Signaling Pathways
T12643 (R)-Terazosin

(R)-特拉唑嗪,盐酸特拉唑嗪

Adrenergic Receptor GPCR/G Protein; Neuroscience
(R)-Terazosin 是一种 Terazosin 的活性 R 型对映体, 是 α1-肾上腺素受体拮抗剂,对 α1a,α1b 和α1d-肾上腺素受体的Ki 分别为 6.51 nM,1.01 nM 和 1.97 nM。
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。
T0137 Mirtazapine

米氮平,6-Azamianserin,Org3770

Dopamine Receptor; 5-HT Receptor; Opioid Receptor; Adrenergic Receptor; Histamine Receptor Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience
Mirtazapine (6-Azamianserin) 是一种有效的具有口服活性的去甲肾上腺素能和特异性血清素能抗抑郁剂 (NaSSA)。它也是一种5-HT2、5-HT3、组胺 H1 受体和 α2-肾上腺素受体拮抗剂,pKi 值分别为 8.05、8.1、9.3 和 6.95。
T11015 Midaglizole hydrochloride

(±)-DG5128,(±)-DG5128 hydrochloride,DG5128 hydrochloride,DG5128

Adrenergic Receptor GPCR/G Protein; Neuroscience
Midaglizole hydrochloride ((±)-DG5128) (DG5128) 是有效的 α2-肾上腺素受体拮抗剂。Midaglizole hydrochloride (DG5128) 对 α2-肾上腺素能受体的亲和力 (pKi= 6.28) 比 α1-肾上腺素能受体高 7.4 倍。
T21957 Guanabenz hydrochloride

NE56490

Adrenergic Receptor GPCR/G Protein; Neuroscience
Guanabenz hydrochloride (NE56490) 是一种具有降血压作用的口服活性 α2-肾上腺素受体激动剂。
T14490 Talipexole dihydrochloride

Domnin,盐酸他利克索,B-HT 920 dihydrochloride

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor GPCR/G Protein; Neuroscience
Talipexole dihydrochloride (Domnin) 是一种多巴胺 D2 受体激动剂、α2-肾上腺素受体激动剂和 5-HT3 受体拮抗剂,有抗帕金森病活性。
T23397 ST 91

Others; Adrenergic Receptor GPCR/G Protein; Neuroscience; Others
ST-91 是一种 α2-肾上腺素能受体激动剂,具有混合的 α-肾上腺素能受体类型/亚型选择特征。
T4526 Piperoxan hydrochloride

dl-Piperoxan hydrochloride,盐酸哌罗克生,Benodaine hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
Piperoxan hydrochloride (Benodaine hydrochloride) 是第一代抗组胺剂,是一种 α2肾上腺素受体拮抗剂。
T9762 Upidosin

SB-216469,SB 216469,Rec 15-2739,Recordati 15/2739

Adrenergic Receptor GPCR/G Protein; Neuroscience
Upidosin (SB-216469) 是一种有效的、选择性的α1-肾上腺素受体拮抗剂,α1a 亚型Ki=0.34nM,α1b 亚型Ki=3.9nM,β1d 亚型Ki=1.5nM,γ2-肾上腺素受体Ki=33.3nM。
T21787L Azepexole hydrochloride

4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1)

Adrenergic Receptor GPCR/G Protein; Neuroscience
Azepexole hydrochloride (4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1)) 是一种具有麻醉作用的强效α2-肾上腺素受体激动剂。
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。
T5105 1-(2-Pyridyl)piperazine

1-(2-吡啶基)哌嗪,NSC13778

Adrenergic Receptor GPCR/G Protein; Neuroscience
1-(2-Pyridyl)piperazine (NSC-13778) 是一种选择性的 α2-肾上腺素受体拮抗剂。它显示出交感神经活性。它也是 Azaperone 的代谢物。
T77565 Fluparoxan hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
Fluparoxan hydrochloride 是一种高度选择性和有效的α2-肾上腺素受体拮抗剂,可用于预防、改善或治疗神经发育障碍和神经退行性疾病。
T21911 Rilmenidine hemifumarate

Rilmenidine (hemifumarate),S-3341 hemifumarate

Apoptosis; Imidazoline Receptor Apoptosis; Neuroscience
Rilmenidine hemifumarate (S-3341 hemifumarate) 是一种新型且具有口服活性和选择性 的 I1咪唑啉受体 (I1 imidazoline receptor) 和α2肾上腺素受体激动剂,可诱导自噬 ,调节白血病细胞增殖,刺激促凋亡蛋白 Bax,诱导人白血病 K562 细胞线粒体通路的紊乱和凋亡。
T1247 Clonidine hydrochloride

Clonidine HCl,Catapres,盐酸可乐定

Adrenergic Receptor GPCR/G Protein; Neuroscience
Clonidine hydrochloride (Catapres) 是一种α2-adrenoceptor 激动剂,是一种抗高血压药。
T0115 Idazoxan hydrochloride

RX 781094,盐酸咪唑克生

Adrenergic Receptor; Imidazoline Receptor GPCR/G Protein; Neuroscience
Idazoxan hydrochloride (RX 781094) 是一种 α2-肾上腺素受体拮抗剂,改善帕金森氏病、L-DOPA 引起的运动障碍和实验性帕金森病的运动症状。它也是咪唑啉受体拮抗剂,可竞争性拮抗唑啉样药物的中枢性降压作用。
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。
T23366 SKF 86466 hydrochloride

Others Others
α2-adrenoceptor antagonist
T22760 Efaroxan hydrochloride

Others Others
α2 adrenoceptor antagonist and imidazoline I1 receptor ligand
T22861 Imiloxan hydrochloride

Others Others
α2-adrenoceptor antagonist
T6765 Atipamezole hydrochloride

阿替美唑盐酸盐,MPV-1248 hydrochloride,Antisedan

Adrenergic Receptor GPCR/G Protein; Neuroscience
Atipamezole hydrochloride (MPV-1248 hydrochloride) 是一种 α2-肾上腺素受体拮抗剂,Ki=1.6 nM。
T6766 Atipamezole

Antisedan,阿替美唑,MPV 1248

Adrenergic Receptor GPCR/G Protein; Neuroscience
Atipamezole (Antisedan) 是 α2-肾上腺素受体拮抗剂,Ki=1.6 nM。
T69367 Azepexole

Azepexole is a selective α2-adrenoceptor agonist that exhibits greater than 300-fold selectivity for the α2-adrenoceptor over the α1-adrenoceptor.
T79641 (±)-N-Methylcoclaurine

Adrenergic Receptor GPCR/G Protein; Neuroscience
(±)-N-Methylcoclaurine为选择性α2-肾上腺素受体拮抗剂。
T28631 RX821002

RX-821002,RX 821002

RX821002 is a potent and selective antagonist of α2-adrenoceptor with low affinity for imidazoline sites. RX821002 displays selectivity for the α2D over the α2A subtypes (pKd values are 9.7 and 8.2 respectively).
T27321 Fipamezole HCl

MPV1730,JP1730,MPV-1730,MPV 1730,JP 1730,JP-1730

Fipamezole HCl, a α2-adrenoceptor antagonist, is used potentially for the treatment of dyskinesia associated with Parkinson's disease.
T70155 Fenoldopam hydrochloride

Fenoldopam hydrochloride is a selective D1-like dopamine receptor partial agonist. It acts as a vasodilator in vivo and does not readily cross the blood-brain barrier. Fenoldopam HCl is also an α2-adrenoceptor antagonist in vitro.
T68098 Midaglizole

(±)-DG5128 free base,DG5128 free base,(±)-DG5128 free base ; DG5128 free base

Midaglizole ((±)-DG5128 free base, DG5128 free base) 是一种有效的α2-adrenoceptor 拮抗剂。Midaglizole 是一种降血糖药。Midaglizole 在具有升高血压并降低血糖水平的作用。
T60304 (E)-Guanabenz

(E)-Guanabenz ((E)-Wy-8678) 是一种具有口服活性的中枢α2-肾上腺素受体 (α2-adrenoceptor)激动剂。(E)-Guanabenz 具有抗高血压活性,通过刺激中枢 α2- 肾上腺素受体,并减少交感神经向外周的净流出而起作用。(E)-Guanabenz z 也直接结合并抑制 GADD34,具有神经保护活性。(E)-Guanabenz 可用于研究高血压和帕金森病。
T21492 Medetomidine

Medetomidine(Domtor)是一种有效的、高选择性的、具有口服活性的α2肾上腺素受体激动剂,对α2和α1肾上腺素受体的 Ki 值分别为1.08 nM 和1750 nM。
T60548 Guanoxabenz hydrochloride

Guanoxabenz (Hydroxyguanabenz) hydrochloride 是 α2 肾上腺素能受体的激动剂,Ki 值为 4000 nM,对 α2A 肾上腺素受体完全激活形式的Ki 值为 40 nM。
T16759 Ritanserin

利坦丝林,R 55667

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Ritanserin (R 55667) 是一种长效、高效、相对选择性、可口服的5-HT2受体拮抗剂,IC50值为 0.9 nM。
T23396 ST1936

ST 1936 oxalate

5-HT Receptor GPCR/G Protein; Neuroscience
ST1936 (ST 1936 oxalate) 是一种具有选择性和高效性的 5-HT6 受体激动剂,抑制人 5-HT6、5-HT7 和 5-HT2B 受体,通过完全激活克隆的人 5-HT6 受体来刺激 cAMP、Ca2+、ERK1/2 和 Fyn 激酶。

化合物

(R)-Terazosin
Cat.No: T12643
Synonym: (R)-特拉唑嗪,盐酸特拉唑嗪
Target: Adrenergic Receptor
Medetomidine hydrochloride
Cat.No: T6579
Synonym: MPV785,Medetomidine HCl,Domitor
Target: Adrenergic Receptor
Mirtazapine
Cat.No: T0137
Synonym: 米氮平,6-Azamianserin,Org3770
Target: Dopamine Receptor, 5-HT Receptor, Opioid Receptor, Adrenergic Receptor, Histamine Receptor
Midaglizole hydrochloride
Cat.No: T11015
Synonym: (±)-DG5128,(±)-DG5128 hydrochloride,DG5128 hydrochloride,DG5128
Target: Adrenergic Receptor
Guanabenz hydrochloride
Cat.No: T21957
Synonym: NE56490
Target: Adrenergic Receptor
Talipexole dihydrochloride
Cat.No: T14490
Synonym: Domnin,盐酸他利克索,B-HT 920 dihydrochloride
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor
ST 91
Cat.No: T23397
Synonym:
Target: Others, Adrenergic Receptor
Piperoxan hydrochloride
Cat.No: T4526
Synonym: dl-Piperoxan hydrochloride,盐酸哌罗克生,Benodaine hydrochloride
Target: Adrenergic Receptor
Upidosin
Cat.No: T9762
Synonym: SB-216469,SB 216469,Rec 15-2739,Recordati 15/2739
Target: Adrenergic Receptor
Azepexole hydrochloride
Cat.No: T21787L
Synonym: 4H-Oxazolo[4,5-d]azepin-2-amine, 6-ethyl-5,6,7,8-tetrahydro-, hydrochloride (1:1)
Target: Adrenergic Receptor
Dexmedetomidine hydrochloride
Cat.No: T6466
Synonym: Precedex,(+)-Medetomidine hydrochloride,(S)-Medetomidine hydrochloride,盐酸右美托咪定,Dexmedetomidine HCl
Target: Adrenergic Receptor
1-(2-Pyridyl)piperazine
Cat.No: T5105
Synonym: 1-(2-吡啶基)哌嗪,NSC13778
Target: Adrenergic Receptor
Fluparoxan hydrochloride
Cat.No: T77565
Synonym:
Target: Adrenergic Receptor
Rilmenidine hemifumarate
Cat.No: T21911
Synonym: Rilmenidine (hemifumarate),S-3341 hemifumarate
Target: Apoptosis, Imidazoline Receptor
Clonidine hydrochloride
Cat.No: T1247
Synonym: Clonidine HCl,Catapres,盐酸可乐定
Target: Adrenergic Receptor
Idazoxan hydrochloride
Cat.No: T0115
Synonym: RX 781094,盐酸咪唑克生
Target: Adrenergic Receptor, Imidazoline Receptor
Dexmedetomidine
Cat.No: T2524
Synonym:
Target: Adrenergic Receptor
SKF 86466 hydrochloride
Cat.No: T23366
Synonym:
Target: Others
Efaroxan hydrochloride
Cat.No: T22760
Synonym:
Target: Others
Imiloxan hydrochloride
Cat.No: T22861
Synonym:
Target: Others
Atipamezole hydrochloride
Cat.No: T6765
Synonym: 阿替美唑盐酸盐,MPV-1248 hydrochloride,Antisedan
Target: Adrenergic Receptor
Atipamezole
Cat.No: T6766
Synonym: Antisedan,阿替美唑,MPV 1248
Target: Adrenergic Receptor
Azepexole
Cat.No: T69367
Synonym:
Target:
(±)-N-Methylcoclaurine
Cat.No: T79641
Synonym:
Target: Adrenergic Receptor
RX821002
Cat.No: T28631
Synonym: RX-821002,RX 821002
Target:
Fipamezole HCl
Cat.No: T27321
Synonym: MPV1730,JP1730,MPV-1730,MPV 1730,JP 1730,JP-1730
Target:
Fenoldopam hydrochloride
Cat.No: T70155
Synonym:
Target:
Midaglizole
Cat.No: T68098
Synonym: (±)-DG5128 free base,DG5128 free base,(±)-DG5128 free base ; DG5128 free base
Target:
(E)-Guanabenz
Cat.No: T60304
Synonym:
Target:
Medetomidine
Cat.No: T21492
Synonym:
Target:
Guanoxabenz hydrochloride
Cat.No: T60548
Synonym:
Target:
Ritanserin
Cat.No: T16759
Synonym: 利坦丝林,R 55667
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor, Histamine Receptor
ST1936
Cat.No: T23396
Synonym: ST 1936 oxalate
Target: 5-HT Receptor
Cat. No. Product Name Target Signaling Pathways
T3158 Harmane

Loturine,Harman,Aribine,哈尔满碱

Adrenergic Receptor; Monoamine Oxidase; Imidazoline Receptor GPCR/G Protein; Neuroscience
Harmane (Loturine) 是一种在咖啡和烟草烟雾中发现的 β-咔啉生物碱,是有效的神经毒素,可引起严重的动作震颤和精神病学表现。它还是选择性的单胺氧化酶抑制剂,具有致突变作用,对 MAO A/B 的 IC50值分别为 0.5 和 5 μM。
TN7042 N-methyltyramine

Adrenergic Receptor GPCR/G Protein; Neuroscience
N-methyltyramine 是一种从豆科植物大叶相思中分离出的生物碱,是一种 α2-肾上腺素受体拮抗剂,通过酶促肾上腺素合成调节肾上腺素能受体,可用于研究肠道疾病。
TN1015 Meranzin

Adrenergic Receptor; Immunology/Inflammation related GPCR/G Protein; Immunology/Inflammation; Neuroscience
Meranzin 是从传统中药 Chaihu-Shugan-San (CSS) 中的生物活性化合物,是从紫茉莉叶中分离出的,能够调节共有的 α2-肾上腺素受体,并参与 AMPA-ERK1/2-BDNF 信号传导。它有潜在的预防动脉粥样硬化和抑郁症合并症。
T4429 Rauwolscine hydrochloride

Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride

Adrenergic Receptor GPCR/G Protein; Neuroscience
Rauwolscine hydrochloride (Isoyohimbine hydrochloride) 是一种高选择性的 α2 adrenergic 受体拮抗剂,Ki=12 nM。
TN2267 Tetrahydroalstonine

Adrenergic Receptor GPCR/G Protein; Neuroscience
Tetrahydroalstonine 是从 Rhazya stricta 的果实中提取出来的吲哚类生物碱,是一种具有选择性的 α2-肾上腺素受体拮抗剂。Tetrahydroalstonine 在Rauwolfia tetraphylla 中表现出抗精神病活性。
TCS2185 Yohimbine

Adrenergic Receptor GPCR/G Protein; Neuroscience
Yohimbine 是一种有效的、相对非选择性的α2 - 肾上腺素能受体拮抗剂,IC50=0.6μM。

天然产物

Harmane
Cat.No: T3158
Synonym: Loturine,Harman,Aribine,哈尔满碱
Target: Adrenergic Receptor, Monoamine Oxidase, Imidazoline Receptor
N-methyltyramine
Cat.No: TN7042
Synonym:
Target: Adrenergic Receptor
Meranzin
Cat.No: TN1015
Synonym:
Target: Adrenergic Receptor, Immunology/Inflammation related
Rauwolscine hydrochloride
Cat.No: T4429
Synonym: Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride
Target: Adrenergic Receptor
Tetrahydroalstonine
Cat.No: TN2267
Synonym:
Target: Adrenergic Receptor
Yohimbine
Cat.No: TCS2185
Synonym:
Target: Adrenergic Receptor
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼