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39

抑制剂 & 化合物

6

天然产物

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Cat. No. Product Name Target Signaling Pathways
T0287 Hexamethonium Bromide

Gangliostat,溴化六甲铵,Simpatoblock,六甲溴铵,Hexamethonium Dibromide

Apoptosis; Dopamine Receptor; AChR Apoptosis; GPCR/G Protein; Neuroscience
Hexamethonium Bromide (Hexamethonium Dibromide) 是神经节中神经元型烟碱型 AChR 的特异性拮抗剂。在自发性高血压动物模型中,它能降低其交感神经活动和血压。
T28540 Ripisartan

UP 269-6,UP-2696,UP 2696,UP-269-6,UP269-6

RAAS Endocrinology/Hormones
Ripisartan (UP-269-6) 是一种强效的特异性血管紧张素 II 受体拮抗剂,对血管紧张素 II 介导的交感神经性心动过速反应有抑制作用。
T12160 N6-Cyclohexyladenosine

CHA,A1受体促进剂

Adenosine Receptor GPCR/G Protein; Neuroscience
N6-Cyclohexyladenosine (CHA) 是一种选择性腺苷 A1 受体激动剂,EC50 为 8.2 nM。
T68095 Losulazine

Dopamine Receptor; Norepinephrine GPCR/G Protein; Neuroscience
Losulazine 是一种新型的降压化合物。其确切的作用机制尚未确定,但其降压作用取决于完整的、功能性交感神经系统的存在。
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。
TP1618L PACAP-38 (31-38), human, mouse, rat acetate

PACAP-38 (31-38), human, mouse, rat acetate(138764-85-9 Free base)

PACAP GPCR/G Protein
PACAP-38 (31-38), human, mouse, rat acetate 是 PAC1 受体的激活剂。PACAP-38 (31-38), human, mouse, rat acetate 对交感神经元 NPY 和儿茶酚胺的产生具有强效、有效和持续的刺激作用,可用于神经营养和神经保护研究。
T22963 McN-A 343

AChR Neuroscience
McN-A 343作为选择性M1 muscarinic激动剂, 以其刺激交感神经节中muscarinic传导的能力而闻名。在溃疡性结肠炎的实验模型中,它已被发现能有效减轻炎症和氧化应激。
T20344 Acetylcholine bromide

Others Others
Acetylcholine bromide 是乙酰胆碱的溴化物盐。它是一种神经递质,存在于神经肌肉接头、自主神经节、副交感神经效应器接头、交感神经效应器接头的一个子集以及中枢神经系统的许多部位。
T29548 Acetabuton

Aceperone

Acetabuton is an alpha-adrenergic blocker and a hemodynamic and sympathetic drug.
T68634 Wy 26392

Wy 26392 is an alpha 2 adrenoceptors antagonist that increase central sympathetic tone and blood pressure in low doses.
T24603 PD-34799-SA

PD 34799-SA,PD34799-SA

PD-34799-SA is an effective inhibitor of vasoconstrictor responses to sympathetic nerve stimulation.
T68397 Xamoterol fumarate

Xamoterol fumarate is a selective beta-1-adrenergic partial agonist. Because it is a partial agonist, it acts as an agonist when sympathetic activity is low and as an antagonist when sympathetic activity is high. It reduces myocardial ischemia and improves ventricular function in patients with mild to moderate heart failure. In patients with severe heart failure it has been shown to produce benefits in systolic and diastolic function.
T68190 Carmoxirole (free base)

Carmoxirole (free base) is a dopamine D2 receptor agonist with limited central activity that modulates sympathetic activation and subsequently reduces pre-load and afterload in animals. It was shown, that carmoxirole induced beneficial effects on hemodynamic and neurohumoral parameters in heart failure. In addition, experimental evidence showed that carmoxirole lowered blood pressure in various models of hypertension mainly or exclusively through inhibition of noradrenaline release from sympathe...
TP1618 PACAP-38 (31-38), human, mouse, rat

PACAP-38 (31-38), human, mouse, rat demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production.
TP1414 PACAP-38 (31-38), human, mouse, rat TFA

PACAP-38 (31-38), human, mouse, rat (TFA) demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal.
T9097L Guanadrel Sulfate

CL 1388R,U 28288D,CHEBI:5556,Hylorel,Hyloride

Guanadrel Sulfate is a postganglionic adrenergic blocking agent. The uptake of guanadrel and storage in sympathetic neurons occurs via the norepinephrine pump or transporter.
T70269 Hexamethonium chloride dihydrate

Hexamethonium chloride dihydrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant.
TP1619 PACAP-38 (16-38), human, mouse, rat

PACAP-38 (16-38), human, mouse, rat demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production.
T24032 Ephedrine levulinate

L-Ephedrine levulinate

Ephedrine levulinate is an alkaloid. Ephedrine acts as an agonist at alpha- and beta-adrenergic receptors and indirectly causes the release of norepinephrine from sympathetic neurons.
T68714 Iobenguane I 131

Iobenguane I 131 is a guanidine analog with specific affinity for tissues of the sympathetic nervous system and related tumors. The radiolabeled forms are used as antineoplastic agents and radioactive imaging agents. MIBG serves as a neuron-blocking agent which has a strong affinity for, and retention in, the adrenal medulla and also inhibits ADP-ribosyltransferase.
TP1490 Proadrenomedullin (1-20), human

Endogenous peptide agonist of Mas related GPR X2 (MRGPRX2, EC50 = 251 nM). Also a noncompetitive nicotinic cholinergic antagonist. Inhibits nicotine-stimulated catecholamine secretion from PC12 cells in vitro, and from sympathetic nerve endings and adrena
T69161 Hexamethonium bromide dihydrate

Hexamethonium bromide dihydrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant.
T68645 Hexamethonium monotartrate

Hexamethonium monotartrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant.
TP1609 Angiotensin II (1-4), human

Angiotensin II is a potent direct vasoconstrictor, causing arteries and veins to constrict, so leading to an increase in blood pressure. Angiotensin also potentiates the release of norepinephrine by a direct action on postganglionic sympathetic fibers.
T15455 RGH-5526

GYKI-11679

Others Others
RGH-5526是一种新型的抗高血压药。它引起下丘脑去甲肾上腺素(NA)周转(利用)增加,下丘脑去甲肾上腺素能神经元活性的增加可能导致外周交感神经活性的降低,从而显著降低血压。
T68807 Azelnidipine, (R)-

Azelnidipine, (R)-, is an L-type calcium channel blocker (CCB). Studies have shown that in patients with hypertension (HT) and heart failure preserved ejection fraction (HFpEF), azelnidipine improved the severity of HF and cardiac sympathetic nerve activity compared with cilnidipine, an N-type CCB (Cat#326734).
TP1144 Corticotropin-releasing factor (human)

Human corticotropin-releasing factor,Human CRF,Corticotropin-releasing factor human

Corticotropin-releasing factor human (Human CRF; Human corticotropin-releasing factor) is an immunomodulatory neuropeptide that acts to release ACTH from the anterior pituitary and stimulates the sympathetic nervous system and adrenal medulla. Functions b
T50109 Guanethidine

Guanethidine 于1959年合成,被认为可以通过干扰神经节后交感神经纤维中的化学递质物质的代谢来降低血压。
T37373 4-hydroxy-3-Methoxyphenylglycol (piperazine salt)

4-hydroxy-3-Methoxyphenylglycol (piperazine salt) is a metabolite of norepinephrine derived in part by deamination of normetanephrine or by O-methylation of dihydroxyphenylglycol after cellular uptake of either intermediate. It is released into the blood and cerebrospinal fluid and has been used as a biochemical index of recent sympathetic nervous system activity.
T68806 Azelnidipine, (S)-

Azelnidipine, (S)-, is an L-type calcium channel blocker (CCB). Studies have shown that in patients with hypertension (HT) and heart failure preserved ejection fraction (HFpEF), azelnidipine improved the severity of HF and cardiac sympathetic nerve activity compared with cilnidipine, an N-type CCB (Cat#326734).
T25912 Oxypyrronium bromide

L.D. 3055,Immetropan,LD 3055,LD3055,LD-3055

Oxypyrronium bromide 一种含有季铵的抗胆碱能和解痉剂。在动物模型中,它抑制胃运动、迷走神经刺激或乙酰胆碱静脉注射引起的低血压;鼓索神经刺激引起的流涎和节前颈交感神经刺激引起收缩。
T68811 Trimetaphan camsilate

Trimetaphan camsilate is a drug that counteracts cholinergic transmission at the ganglion type of nicotinic receptors of the autonomic ganglia and therefore blocks both the sympathetic nervous system and the parasympathetic nervous system. It acts as a non-depolarizing competitive antagonist at the nicotinic acetylcholine receptor, is short-acting, and is given intravenously.
T80080 PAMP-12 (unmodified) (TFA)

PAMP-12 (unmodified) TFA 作为MRGPRX2 (MrgX2)激动剂,展现出高效性(EC50=20-50 nM)。该化合物为内源性肽,能够通过抑制交感神经末梢及肾上腺嗜铬细胞中的儿茶酚胺释放来诱发低血压。
T78027 PAMP-12 (unmodified)

PAMP-12 (unmodified)为有效的MRGPRX2 (MrgX2)激动剂,其EC50值为20-50 nM。作为内源性肽,它能够通过抑制交感神经末梢和肾上腺嗜铬细胞的儿茶酚胺分泌来引发低血压。
T76539 Insulin-like growth factor II

Insulin-like growth factor II (IGF-2)为人血清中主要生长激素,对神经突生长具有许可性和直接作用,同时增强交感与感觉神经元的生存能力。
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。
T20886 Atomoxetine

Tomoxetine,HSDB7352,HSDB-7352,HSDB 7352

Norepinephrine Neuroscience
Atomoxetine (HSDB 7352) 是一种选择性去甲肾上腺素抑制剂,它可能通过增加外周交感神经元中的去甲肾上腺素浓度而导致血压升高 。Atomoxetine 是突触前去 Norepinephrativev 转运体的高度选择性拮抗剂,对其他去甲肾上腺素受体或其他神经递质转运体或受体几乎或没有亲和力,但对5-羟色胺转运体的亲和力较弱。、 Atomoxetine 选择性地抑制去甲肾上腺素的再摄取,可用于治疗患有多动症和慢性抽搐的青少年。
T74142 Angiotensin II human TFA

Angiotensin II human (Angiotensin II) TFA 作为肾素/血管紧张素系统中关键的生物活性肽,扮演着血管收缩剂的角色并在调节人体血压中发挥中心作用。其主要通过与 G 蛋白偶联受体 (GPCRs)、血管紧张素 II 1型受体 (AT1R) 和血管紧张素 II 2型受体 (AT2R) 的相互作用来介导效应,包括刺激交感神经系统、增加醛固酮的生物合成和肾脏功能。此外,Angiotensin II human TFA 促进血管平滑肌细胞的生长和 I 型及 III 型胶原在成纤维细胞中的合成,导致血管壁与心肌增厚及纤维化,并诱导细胞凋亡。还通过LOX-1依赖的氧化还原敏感路径诱导内皮细胞中的毛细血管形成。
T36729 Urotensin II (goby) (trifluoroacetate salt)

Urotensin II is a peptide vasoconstrictor and agonist of the urotensin (UT) receptor (Ki= 2.06 nM for the human recombinant receptor expressed in HEK293 cells).1It stimulates intracellular calcium mobilization in HEK293 cells expressing human and rat UT (EC50s = 0.47 and 0.78 nM, respectively) but decreases intracellular calcium concentration in goby (G. mirabilis) enterocytes when used at a concentration of 500 nM.2Urotensin II (20 mU/ml) stimulates active sodium and chloride absorption across ...

化合物

Hexamethonium Bromide
Cat.No: T0287
Synonym: Gangliostat,溴化六甲铵,Simpatoblock,六甲溴铵,Hexamethonium Dibromide
Target: Apoptosis, Dopamine Receptor, AChR
Ripisartan
Cat.No: T28540
Synonym: UP 269-6,UP-2696,UP 2696,UP-269-6,UP269-6
Target: RAAS
N6-Cyclohexyladenosine
Cat.No: T12160
Synonym: CHA,A1受体促进剂
Target: Adenosine Receptor
Losulazine
Cat.No: T68095
Synonym:
Target: Dopamine Receptor, Norepinephrine
Methyldopa hydrate
Cat.No: T5954
Synonym: L-甲基多巴,Alpha-Methyldopa Sesquihydrate,L-(-)-α-Methyldopa hydrate,MK-351 hydrate,Methyldopa Sesquihydrate
Target: Dopamine Receptor, Adrenergic Receptor
PACAP-38 (31-38), human, mouse, rat acetate
Cat.No: TP1618L
Synonym: PACAP-38 (31-38), human, mouse, rat acetate(138764-85-9 Free base)
Target: PACAP
McN-A 343
Cat.No: T22963
Synonym:
Target: AChR
Acetylcholine bromide
Cat.No: T20344
Synonym:
Target: Others
Acetabuton
Cat.No: T29548
Synonym: Aceperone
Target:
Wy 26392
Cat.No: T68634
Synonym:
Target:
PD-34799-SA
Cat.No: T24603
Synonym: PD 34799-SA,PD34799-SA
Target:
Xamoterol fumarate
Cat.No: T68397
Synonym:
Target:
Carmoxirole (free base)
Cat.No: T68190
Synonym:
Target:
PACAP-38 (31-38), human, mouse, rat
Cat.No: TP1618
Synonym:
Target:
PACAP-38 (31-38), human, mouse, rat TFA
Cat.No: TP1414
Synonym:
Target:
Guanadrel Sulfate
Cat.No: T9097L
Synonym: CL 1388R,U 28288D,CHEBI:5556,Hylorel,Hyloride
Target:
Hexamethonium chloride dihydrate
Cat.No: T70269
Synonym:
Target:
PACAP-38 (16-38), human, mouse, rat
Cat.No: TP1619
Synonym:
Target:
Ephedrine levulinate
Cat.No: T24032
Synonym: L-Ephedrine levulinate
Target:
Iobenguane I 131
Cat.No: T68714
Synonym:
Target:
Proadrenomedullin (1-20), human
Cat.No: TP1490
Synonym:
Target:
Hexamethonium bromide dihydrate
Cat.No: T69161
Synonym:
Target:
Hexamethonium monotartrate
Cat.No: T68645
Synonym:
Target:
Angiotensin II (1-4), human
Cat.No: TP1609
Synonym:
Target:
RGH-5526
Cat.No: T15455
Synonym: GYKI-11679
Target: Others
Azelnidipine, (R)-
Cat.No: T68807
Synonym:
Target:
Corticotropin-releasing factor (human)
Cat.No: TP1144
Synonym: Human corticotropin-releasing factor,Human CRF,Corticotropin-releasing factor human
Target:
Guanethidine
Cat.No: T50109
Synonym:
Target:
4-hydroxy-3-Methoxyphenylglycol (piperazine salt)
Cat.No: T37373
Synonym:
Target:
Azelnidipine, (S)-
Cat.No: T68806
Synonym:
Target:
Oxypyrronium bromide
Cat.No: T25912
Synonym: L.D. 3055,Immetropan,LD 3055,LD3055,LD-3055
Target:
Trimetaphan camsilate
Cat.No: T68811
Synonym:
Target:
PAMP-12 (unmodified) (TFA)
Cat.No: T80080
Synonym:
Target:
PAMP-12 (unmodified)
Cat.No: T78027
Synonym:
Target:
Insulin-like growth factor II
Cat.No: T76539
Synonym:
Target:
(E)-Guanabenz
Cat.No: T60304
Synonym:
Target:
Atomoxetine
Cat.No: T20886
Synonym: Tomoxetine,HSDB7352,HSDB-7352,HSDB 7352
Target: Norepinephrine
Angiotensin II human TFA
Cat.No: T74142
Synonym:
Target:
Urotensin II (goby) (trifluoroacetate salt)
Cat.No: T36729
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T6751 Acetylcholine iodide

Acetylcolina

Others Others
Acetylcholine iodide (Acetylcolina) 是一种在中枢和外周神经系统中常见的神经递质。
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。
T7040 Angiotensin II human

DRVYIHPF,Angiotensin II,Hypertensin II,血管紧张素Ⅱ,Ang II,血管紧张素II

Apoptosis; RAAS Apoptosis; Endocrinology/Hormones
Angiotensin II human (Ang II) 是一种生物活性肽,一种血管收缩剂。Angiotensin II 可以与 AT1R 和 AT2R 相互作用,调节人类血压,刺激交感神经,增加醛固酮生物合成和肾脏活动。
T3S2259 Methyl eugenol

4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚

GABA Receptor Membrane transporter/Ion channel; Neuroscience
Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物,存在于植物叶子、果实、根茎中,当植物相应的部位因食草动物进食而受损时,就会释放。它可用于消灭雄性东方果蝇。
T2S1727 Lycorenine

Antifection Microbiology/Virology
Lycorenine may produce a decrease in blood pressure as the result of alpha-adrenergic blockade in conjunction with the reduction of the spontaneous sympathetic nerve activity, and produce bradycardia by modifying vagal activity. The development of tachyph
T20173 Noradrenaline tartrate

NSC 169106,NSC-169106,l-Noradrenaline d-bitartrate,NSC169106,Norepinephrine bitartrate

Norepinephrine bitartrate is a precursor of epinephrine. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers and of the diffuse projection system in the brain arising from the locus ceruleus.

天然产物

Acetylcholine iodide
Cat.No: T6751
Synonym: Acetylcolina
Target: Others
Synephrine
Cat.No: T1287
Synonym: 辛弗林,Oxedrine
Target: Endogenous Metabolite, Adrenergic Receptor
Angiotensin II human
Cat.No: T7040
Synonym: DRVYIHPF,Angiotensin II,Hypertensin II,血管紧张素Ⅱ,Ang II,血管紧张素II
Target: Apoptosis, RAAS
Methyl eugenol
Cat.No: T3S2259
Synonym: 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚
Target: GABA Receptor
Lycorenine
Cat.No: T2S1727
Synonym:
Target: Antifection
Noradrenaline tartrate
Cat.No: T20173
Synonym: NSC 169106,NSC-169106,l-Noradrenaline d-bitartrate,NSC169106,Norepinephrine bitartrate
Target:
TargetMol Loading
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