54
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5954 |
Methyldopa hydrate
L-甲基多巴,Alpha-Methyldopa Sesquihydrate,L-(-)-α-Methyldopa hydrate,MK-351 hydrate,Methyldopa Sesquihydrate |
Dopamine Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Methyldopa hydrate (MK-351 hydrate) 是一种前药,在中枢神经系统中被代谢成 α-Methylepinephrine。它是一种 α-肾上腺素能激动剂,对α2-adrenergic receptors 有选择性。 | |||
T0342 |
Carvedilol phosphate hemihydrate
Carvedilol phosphate,BM 14190 (phosphate hemihydrate),卡维地洛磷酸盐 |
VEGFR; Others; Potassium Channel; LDL; Integrin; Gap Junction Protein; NADPH; Adrenergic Receptor; Autophagy | Angiogenesis; Autophagy; Cytoskeletal Signaling; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience; Others; Tyrosine Kinase/Adaptors |
Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) 是一种外消旋混合物,是一种非选择性β/α-1受体阻断剂,具有抗高血压活性且缺乏内在拟交感神经活性。 | |||
T12444 |
Phentolamine Analogue 1
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Phentolamine Analogue 1 是 phentolamine 类似物。其中Phentolamine 是非选择性alpha-adrenergic 拮抗剂 。 | |||
T11651 |
Indanidine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indanidine 是一种高选择性和有效性的 α-肾上腺素能激动剂,具有抗高血压活性。Indanidine 是 α-肾上腺素能拮抗剂,可以用于研究神经系统疾病。 | |||
T11894 |
Lusaperidone
R107474 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Lusaperidone (R107474) 是一种有效的α2肾上腺素受体 (adrenergic receptor) 拮抗剂,是 α (2)-肾上腺素受体的潜在放射性配体,对 α2A和α2C 具有抑制作用, Ki 值分别为0.13和0.15 nM。 | |||
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。 | |||
T26363L |
Napitane
A75200,A-75200,A 75200,ABT 200 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
napitane(A 75200)是一种新型儿茶酚胺摄取抑制剂,对α-肾上腺素能受体具有抑制作用且具有潜在的抗抑郁活性,可用于研究抑郁症。 | |||
T21371 |
Apraclonidine hydrochloride
Iopidine,ALO 2145,Apraclonidina,P-aminoclonidine,4-Aminoclonidine,Apraclonidine HCl,Apraclonidinum |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Apraclonidine hydrochloride (ALO 2145) 是一种 α2-肾上腺素能激动剂和弱的 α-1 肾上腺素能受体激动剂。 Apaclonidine hydrochloride 可降低人眼的眼内压,可用于青光眼治疗的研究。 | |||
T0279 |
Metaraminol tartrate
重酒石酸间羟胺,Metaradrine tartrate,Metaraminol bitartrate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Metaraminol tartrate (Metaradrine tartrate) 是一种 α-肾上腺素能 (α-adrenergic) 激动剂,是一种直接或间接影响肾上腺素受体的拟交感神经胺,其中 α 效应占主导地位,可作为血管加压剂。 | |||
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。 | |||
T6422 |
Brimonidine Tartrate
AGN190342 tartrate,304 tartrate,酒石酸溴莫尼定,AGN190342 (tartrate),UK 14304 (tartrate),UK14304 tartrate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Brimonidine Tartrate (AGN190342 tartrate) 是一种 alpha2 Adrenergic Receptor (alpha2-AR) 受体激动剂。 | |||
T68023L |
Tolnapersine TFA
Tolnapersine TFA(70312-00-4 Free base) |
Dopamine Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tolnapersine TFA 是混合多巴胺激动剂和α肾上腺素受体拮抗剂。 | |||
T3996 |
Dapiprazole Hydrochloride
盐酸达哌唑,Glamidolo Hydrochloride,Reversil Hydrochloride |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dapiprazole Hydrochloride (Glamidolo Hydrochloride) 是 α-adrenergic 阻断剂的药物。 | |||
T21447 |
Tolazoline
Priscol,妥拉苏林,Priscoline,Pridazole,Divascol,Vasimid,Benzalolin |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tolazoline (Benzalolin) 是一种竞争性的α-肾上腺素受体拮抗剂。 | |||
T0871 |
Noradrenaline bitartrate
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Noradrenaline bitartrate 直接作用于 α 和 β 肾上腺素能受体。它是去甲肾上腺素的酒石酸氢盐,去甲肾上腺素是一种合成苯乙胺,可模拟内源性去甲肾上腺素的拟交感神经作用。临床上,去甲肾上腺素用作外周血管收缩剂,通过其α-肾上腺素能作用导致动脉和静脉床收缩。它还被用作通过其 β-1 肾上腺素能作用介导的强效正性肌力和变时性心脏刺激剂。 | |||
T30140 |
Arotinolol hydrochloride
Arotinolol HCl |
5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Arotinolol hydrochloride(Arotinolol HCl) 是一种非选择性的 α/β-肾上腺素受体 (α/β-adrenergic receptor ) 阻滞剂。Arotinolol hydrochloride 对放射性配体 125I-ICYP 与 5HT1B-羟色胺受体能结合有抑制作用。Arotinolol hydrochloride 是一种抗高血压和抗肥胖试剂,可改善大鼠主动脉僵硬,研究肥胖相关疾病。 | |||
T8738 |
LUN42518 HCl 47142-51-8(free base)
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
LUN42518 HCl 47142-51-8(free base) 是酚妥拉明的类似物。酚妥拉明是一种非选择性的α-肾上腺素能拮抗剂。 | |||
T83965 |
Tamsolusin Hydrochloride
YM 12617,LY-253352 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tamsolusin Hydrochloride (YM 12617) 是一种高选择性α-1A肾上腺素受体拮抗剂,可用于治疗良性前列腺肥大。 | |||
T6703 |
Tetrahydrozoline hydrochloride
Murine Plus,盐酸四氢萘咪唑,Tetryzoline hydrochloride,Tyzine,Tetrahydrozoline HCl,盐酸四氢唑林 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tetrahydrozoline hydrochloride (Murine Plus) 是一种咪唑啉的衍生物,是一种 α-肾上腺素能 (α-adrenergic) 激动剂,能引起血管收缩,常用于研究鼻充血、结膜充血。 | |||
T10003 |
α1 adrenoceptor-MO-1
|
Others | Others |
α1 adrenoceptor-MO-1(S 对映体)对α1肾上腺素受体具有亲和力,具有抗α-肾上腺素能和镇痛作用。α1 adrenoceptor-MO-1比R 对映体更具活性。 | |||
T22029 |
AL 34662
|
5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
AL 34662 是一种具有选择性和高效性的 5-HT2A 受体激动剂,对大鼠和人 5-HT2 受体的IC50 分别为 0.77 nM 和 1.5 nM。AL 34662 还是一种亲和力较低的 α-1D 肾上腺素能激动剂,EC50 值为 0.4 μM。AL 34662 可用于降低眼压。 | |||
T21445 |
Naphazoline
AK-Con,Naphcon-a,Clear Eyes,All Clear,萘甲唑林 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Naphazoline (Naphcon-a) 是一种具有显着 α 肾上腺素能活性的拟交感神经化合物。 萘甲唑啉可用作血管收缩剂,当应用于粘膜时可快速减少肿胀。 | |||
T26778L |
Besipirdine hydrochloride
HP 749 hydrochloride,Besipirdine hydrochloride(119257-34-0 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Besipirdine hydrochloride 是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine hydrochloride 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine hydrochloride 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。 | |||
T1158 |
Phenoxybenzamine hydrochloride
苯氧苯札明,NCI-c01661,NSC 37448,盐酸酚苄明,Phenoxybenzamine HCl |
CaMK; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Phenoxybenzamine hydrochloride (NCI-c01661) 是一种选择性的 α-adrenoceptor 和 calmodulin 的抑制剂,是常用的抗高血压药。 | |||
T10952 |
Dabuzalgron
达布扎琼,Ro 115-1240 |
Apoptosis; Adrenergic Receptor | Apoptosis; GPCR/G Protein; Neuroscience |
Dabuzalgron (Ro 115-1240) 是一种口服活性选择性 α-1A 肾上腺素受体激动剂,用于治疗尿失禁。它通过维持线粒体功能来预防多柔比星引起的心脏毒性。 | |||
T0397 |
Tetrahydrozoline
四氢唑林,四氢唑啉,Tetryzolin,Tetryzoline |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tetrahydrozoline (Tetryzoline) 是一种咪唑啉的衍生物,是一种 α-肾上腺素能 (α-adrenergic) 激动剂,能引起血管收缩,广泛用于研究鼻充血、结膜充血。 | |||
T26778 |
Besipirdine
HP 749 free base,P-867493,P867493,HP 749,HP749,P 867493 |
Sodium Channel; Adrenergic Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Besipirdine (HP 749 free base)是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。 | |||
T5389 |
Volinanserin
M 100907,MDL100907,氟利色林 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Volinanserin (MDL100907) 是选择性的5-HT2受体拮抗剂,Ki 值为 0.36 nM,可用于精神疾病的研究。它对 5-HT2 受体的选择性比 5-HT1c、α-1 肾上腺素能受体和 σ 受体高 300 倍。 | |||
T0210L |
Tamsulosin
LY253351 free base,HSDB7744,(R)-(-)-YM12617 free base,Harnal-D,Flowmax,HSDB 7744,HSDB-7744 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tamsulosin ((R)-(-)-YM12617 free base) 是一种肾上腺素能受体α 1A 拮抗剂,用于良性前列腺增生(BPH)的治疗。Tansulosin 用于治疗排尿困难,这是前列腺肥大的一种常见症状。Tansulosin 和其他被称为α受体阻滞剂的药物通过放松膀胱颈部肌肉和前列腺本身的肌肉纤维来发挥作用,使其更容易排尿。 | |||
T1050 |
Prazosin hydrochloride
Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress |
Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy | Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂,可降低外周阻力并放松血管平滑肌。 它可用于研究高血压和酒精使用障碍。 它是一种合成哌嗪衍生物,具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3,IC50分别为 1.8 和 13 μM 。 | |||
T1577 |
Midodrine hydrochloride
Pro-Amatine,盐酸米多君 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Midodrine hydrochloride (Pro-Amatine) 通过去甘氨酸反应转化为其活性代谢物 desglymidodrine。Desglymidodrine 选择性地结合并激活小动脉和静脉血管系统的 α-1-肾上腺素能受体。这会导致平滑肌收缩并导致血压升高。 Desglymidodrine 在血脑屏障中的扩散很差,因此与对中枢神经系统的影响无关。Midodrine hydrochloride 是 midodrine 的盐酸盐形式,是一种直接作用的前药和拟交感神经药,具有抗低血压特性。 | |||
T61495 |
Medroxalol
|
||
Medroxalol (RMI81968) is an orally active adrenergic receptor antagonist that effectively blocks both α- and β-adrenergic receptors, effectively producing antihypertensive and vasodilating effects [1]. | |||
T13211 |
Tropodifene
Tropaphen |
Others | Others |
Tropodifene is an inhibitor of the α-Adrenergic receptor. | |||
T30589 |
Brl 41992
Brl41992,Brl-41992 |
||
Brl 41992 is selective for adrenergic α-2A receptor. | |||
T25301 |
Deiodoamiodarone
Amiodarone hydrochloride impurity A,Dideiodo Amiodarone |
||
Deiodoamiodarone is an intermediate of amiodarone. Amiodarone is an α/β-adrenergic receptor antagonist and coronary vasodilator. | |||
T31022 |
CP 59430
CP-59430,CP59430 |
||
CP 59430 is an azide analogue of prazosin. Prazosin is a highly selective α 1-adrenergic receptor antagonist. | |||
T1158L |
Phenoxybenzamine
NSC-37448,A688,NSC 37448,NSC37448,A-688 |
||
Phenoxybenzamine is an α-1 adrenergic receptor antagonist. Phenoxybenzamine may exert a neuroprotective effect by reducing neuroinflammation after traumatic brain injury. | |||
T69031 |
Cirazoline (free base)
|
||
Cirazoline (free base) is a full agonist at the α1A adrenergic receptor, a partial agonist at both the α1B and α1D adrenergic receptors, and a nonselective antagonist to the α₂ adrenergic receptor. It is believed that this combination of properties could make cirazoline an effective vasoconstricting agent. | |||
T60834 |
Phentolamine hydrochloride
|
||
Phentolamine hydrochloride | |||
T69381 | Dechloro perphenazine | ||
Dechloro perphenazine is the dechlorinated analogue of Perphenazine (P291100), an D2 dopamine receptor antagonist; α-adrenergic receptor antagonist and σ-receptor agonist. | |||
T69094 |
α-hydroxy Metoprolol
|
||
α-hydroxy Metoprolol is an active metabolite of the β1-adrenergic receptor blocker metoprolol. It is formed via metabolism of metoprolol by the cytochrome P450 (CYP) isoform CYP2D6. | |||
T10371 | Arotinolol | 5-HT Receptor | GPCR/G Protein; Neuroscience |
Arotinolol is a nonselective α/β-adrenergic receptor blocker and a vasodilating β-blocker. Arotinolol also shows potency for inhibiting the binding of the radioligand 125I-ICYP to 5HT1B-serotonergic receptor sites. It is an antihypertensive agent. | |||
T69341 | Tramazoline hydrochloride | ||
Tramazoline hydrochloride is commonly used in nasal spray as a nasal decongestant by acting as an α-adrenergic receptor agonist that inhibits secretion of nasal mucus. | |||
T69151 |
Adrenaline sulfate
|
||
Adrenaline sulfate 是一种由肾上腺髓质分泌的口服活性激素。Adrenaline sulfate 是一种 α-adrenergic 和 β-adrenergic 受体激动剂。Adrenaline sulfate 可用于治疗过敏反应。Adrenaline sulfate 具有心脏骤停研究潜力[4]。 | |||
T60425 | Tetrahydrozoline nitrate | ||
Tetrahydrozoline (Tetryzoline) nitrate 是咪唑啉的衍生物。它是一种引起血管收缩的α-肾上腺素能 (α-adrenergic) 激动剂。Tetrahydrozoline 广泛用于鼻充血和结膜充血的研究。 | |||
T32656 |
Lerimazoline
ST-71,Trimizoline,Trimazoline,ST 71,ST71 |
||
Lerimazoline(Trimazoline, Trimizoline, ST-71) is used in the form of tramazoline hydrochloride in nasal decongestant preparations. It is used to inhibits the secretion of nasal mucus as an α-adrenergic receptor agonist. | |||
T0348 |
Labetalol hydrochloride
盐酸拉贝洛尔,Sch-15719W,AH-5158 hydrochloride,Labetalol HCl,柳胺苄心定 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Labetalol hydrochloride (Sch-15719W) 是混合的α/β肾上腺素能拮抗剂,可用于研究高血压。 | |||
T70979 | Sunepitron Free Base | ||
Sunepitron Free Base is a combined 5-HT1A receptor agonist and α₂-adrenergic receptor antagonist. It was previously under development by Pfizer for the treatment of depression and anxiety. It made it to phase III clinical trials before being discontinued. | |||
T26920 |
Bucindolol hydrochloride
MJ 131051,Bucindolol HCl,MJ131051,MJ-13105-1,MJ-131051 |
||
Bucindolol is a beta-adrenergic receptor antagonist. Bucindolol is a fourth-generation β-blocker. Bucindolol prevented new-onset AF; β₁ and α(2c) polymorphisms predicted therapeutic response; and the 47% of patients who were β₁389 Arg homozygotes had an e | |||
T15701 |
Methyldopa hydrochloride
L-(-)-α-Methyldopa hydrochloride,MK-351 hydrochloride |
Others | Others |
L-(-)-α-Methyldopa hydrochloride is an alpha-adrenergic agonist psychoactive drug. It is used as a sympatholytic or antihypertensive. Methyldopa has a dual mechanism of action. It is a competitive inhibitor of the enzyme DOPA decarboxylase, which converts |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1287 |
Synephrine
辛弗林,Oxedrine |
Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Synephrine (Oxedrine) 是来自 Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂,是一种生物碱。它也是一种拟交感神经化合物,能够用于减肥。 | |||
T6688 |
Synephrine hydrochloride
辛弗林盐酸盐,Oxedrine hydrochloride,Synephrine HCl |
Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Synephrine hydrochloride (Oxedrine hydrochloride) 是一种来自Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂的生物碱,也是一种拟交感神经化合物,能够用于减肥。 | |||
T0505 |
Methyldopa
L-(-)-α-Methyldopa,MK-351,甲基多巴 |
Dopamine Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
L-(-)-α-Methyldopa (MK-351) 是一种前药,在中枢神经系统中被代谢成 α-Methylepinephrine。它是 α-肾上腺素能激动剂,对 α2- adrenergic receptors 有选择性。 | |||
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。 | |||
T5S2059 |
Glaucine
|
Calcium Channel; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; PDE | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience |
Glaucine 是从海罂粟中分离的一种生物碱,具有镇咳、抗炎和支气管扩张作用。它是具有口服活性的磷酸二酯酶 4 选择性抑制剂。它还是非选择性的 α-肾上腺素受体拮抗剂,具有抗氧化和抗病毒活性。 | |||
T1680 |
Tolazoline hydrochloride
Imidaline hydrochloride,苯甲唑啉盐酸盐,Imidaline (hydrochloride),Benzidazol hydrochloride,Tolazoline HCl,NSC35110 (hydrochloride) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tolazoline hydrochloride (NSC35110(hydrochloride)) 是一种 α 肾上腺素受体抑制剂。 | |||
TN1465 |
Cannabigerol
|
NOS; 5-HT Receptor; ROS | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cannabigerol 是一种植物大麻素,是一种高亲和力 α2-肾上腺素能受体激动剂、中度亲和力 5-HT1A 受体拮抗剂和低亲和力 CB1/CB2受体拮抗剂。它可降低眼压,有潜力治疗青光眼。 | |||
T2142 |
Yohimbine hydrochloride
盐酸育亨宾,Antagonil,Yohimbine HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Yohimbine hydrochloride (Antagonil) 是一种植物生物碱,具有 α-2-肾上腺素能阻断活性。它被用作散瞳药和治疗勃起功能障碍。 | |||
T75425 |
Synephrine hemitartrate
|
||
Synephrine (Oxedrine) hemitartrate,一种生物碱,是一种来自Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂。Synephrine hemitartrate 是一种拟交感神经化合物,可用于减肥。 | |||
TN2001 |
Oblongine
|
Others | Others |
Oblongine chloride may have potential haemodynamic effects, it can cause a dose-dependent reduction of systolic and diastolic blood pressure, and that these effects are not mediated by α²-adrenergic receptor stimulation. |