31
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Cat. No. | Product Name | Target | Signaling Pathways |
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T7045 |
Clonidine
Nexiclon,Catapres,Kapvay,可乐定 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Clonidine (Kapvay) 是 alpha2 肾上腺素能激动剂。 | |||
T5326 |
Sugammadex sodium
Org25969,Sugammadex (sodium),舒更葡糖钠 |
Others | Others |
Sugammadex sodium (Org25969) 是合成的 γ 环糊精衍生物,是一种新型的神经肌肉阻断逆转剂。 | |||
T0862 |
Diphenidol hydrochloride
Diphenidol HCl,盐酸地芬尼多,Difenidol hydrochloride |
Sodium Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
Diphenidol hydrochloride (Difenidol hydrochloride) 是一种非选择性的毒蕈碱 M1-M4 受体拮抗剂,具有抗心律失常活性,用作抗眩晕药和止吐药。它也是神经细胞电压门控离子通道的有效非特异性阻滞剂。 | |||
T0364L |
Dibucaine hydrochloride
Cinchocaine HCl,Dibucaine HCl,盐酸地布卡因,Cinchocaine hydrochloride |
Sodium Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
Dibucaine hydrochloride (Cinchocaine hydrochloride) 是钠通道抑制剂和有效的 SChE 抑制剂。 | |||
T0364 |
Dibucaine
地布卡因,Cinchocaine |
CaMK; Sodium Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
Dibucaine (Cinchocaine) 是钠通道抑制剂和有效的SChE 抑制剂。 | |||
T33272 |
Mefenidil
McN-2378,McN 2378 |
Others | Others |
Mefenidil (McN-2378) 是一种选择性脑血管扩张剂,在狗麻醉模型中显示出在不刺激 O2 摄取的情况下增加健康大脑中的 CBF。 | |||
T13142L |
Theodrenaline hydrochloride
Theodrenaline hydrochloride(13460-98-5 Free base) |
SARS-CoV | Microbiology/Virology |
Theodrenaline hydrochloride 是一种靶向 SARS-CoV-2 的抑制剂,可用于研究由脊髓麻醉引起的低血压。 | |||
T19658 |
Enflurane
NSC115944,Ethrane,NSC-115944,恩氟烷,Efrane,NSC 115944 |
Others | Others |
Enflurane (Efrane) 是一种挥发性麻醉剂,是 Chara australis 高电导 Ca2+ 激活的 K+ 通道的有效抑制剂。 安氟醚是通过顶空气相色谱-质谱法监测卤化挥发性麻醉剂的内标。 它可以快速调整麻醉深度,而脉搏或呼吸频率几乎没有变化。 | |||
T1198 |
Tetracaine hydrochloride
盐酸丁卡因,Amethocaine hydrochloride,Amethocalne HCl,Tetracaine HCl |
Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
Tetracaine hydrochloride (Amethocalne HCl) 是一种钙通道蛋白抑制剂,可阻断肌浆网中 Ca2+的电压敏感释放。它主要用作眼科的止痒剂和局部用药,可用于表面和脊髓麻醉。 | |||
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。 | |||
T1787 |
Levobupivacaine
|
Sodium Channel | Membrane transporter/Ion channel |
Levobupivacaine 是一种氨基酰胺类局麻药,属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。 | |||
T34753 |
Suxamethonium bromide
L.T. 1,370 I.S.,Brevidil M |
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Suxamethonium bromide can be used to cause short-term paralysis as part of general anesthesia. | |||
T21099 |
Decamethonium iodide
Decamethonium iodatum,Decamethonium diiodide,Dekamethoniumjodid |
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Decamethonium is a neuromuscular blocking agent or depolarizing muscle relaxant, and is used in anesthesia to induce paralysis. | |||
T29846 |
Alcuronium free base
Alcuronium,Alcuronum,Diallylnortoxiferine,Alcuronium kation,Alloferine |
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Alcuronium free base is a non-depolarizing skeletal muscle relaxant similar to Tubocurarine. It is used as an anesthesia adjuvant. | |||
T28591 |
Ro 48-6791
Ro-486791,Ro 486791,Ro-48-6791,Ro486791,Ro48-6791 |
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Ro 48-6791, a GABA receptor agonist, is used potentially for anesthesia. | |||
T3609 |
Dioxopromethazine
Prothanon,Dioxoprothazine,盐酸二氧丙嗪 |
Others | Others |
Dioxopromethazine (Dioxoprothazine) 是一种口服具有活性的抗组胺药,能够抑制哮喘症状。 | |||
T25637 |
Laudexium methylsulfate
Laudexium,Laudolissin methosulphate |
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Laudexium methylsulfate is a neuromuscular blocking drug or skeletal muscle relaxant. It is used adjunctively in surgical anesthesia to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. | |||
T28259 |
Org-21465
Org21465,Org 21465 |
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Org-21465, a gamma-aminobutyric acid (GABA) receptor agonist, is used potentially for the use of anesthesia. | |||
T31914 |
Gantacurium chloride
GW 280430A,AV4430A,AV 4430A,GW280430,GW 280430,GW-0430 |
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Gantacurium chloride is a benzylisoquinoline alkaloid, which may be used as an adjuvant in anesthesia. | |||
T0818L |
Decamethonium
|
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Decamethonium (Syncurine) is a depolarizing muscle relaxant or neuromuscular blocking agent, and is used in anesthesia to induce paralysis. | |||
T24690 |
Pyrromecaine HCl
Bumecaine hydrochloride,Pyrromecaine |
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Pyrromecaine is a local anesthetic used for surface anesthesia. Pyromecaine has a wide spectrum of antiarrhythmic action, exerts a favorable effect on the contractility of the left ventricle, and on the myocardial blood flow following the ligation of the | |||
T31296 |
Decamethonium chloride
Decamethylenebis(trimethylammonium chloride),Decamethonium dichloride |
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Decamethonium is a depolarizing muscle relaxant or neuromuscular blocking agent,[1] and is used in anesthesia to induce paralysis. | |||
T25636 |
Laudexium
Laudexium ion,Laudexium cation |
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Laudexium is a neuromuscular blocking drug or skeletal muscle relaxant in the category of non-depolarizing neuromuscular-blocking drugs. It is used adjunctively in surgical anesthesia to facilitate endotracheal intubation and to provide skeletal muscle re | |||
T33638 |
Neostigmine Iodide
SB 24,SB24,TL1321,TL 1321,TL-1321,SB-24 |
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Neostigmine Iodide is a parasympathic compound used as a reversible acetylcholinesterase inhibitor to improve muscle tone in patients with myasthenia gravis and in routine anesthesia to reverse the effects of non-depolarizing muscle relaxants such as rocu | |||
T83124 |
Amylocaine
|
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Amylocaine为一种酯类局部麻醉药,能在给药部位附近产生可逆性麻木,主要应用于脊柱麻醉。 | |||
T82146 |
Hydroxydione
|
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Hydroxydione展现全身麻醉效应,作为一种神经活性类固醇,适用于麻醉研究。 | |||
T0029 |
Procaine
Duracaine,Spinocaine,普鲁卡因,Novocaine,Vitamin H3,奴夫卡因 |
Histone Demethylase; DNA/RNA Synthesis; Sodium Channel | Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel |
Procaine (Vitamin H3) 是DNA 脱甲基剂,是一种酯类局部麻醉剂。它起效缓慢,作用持续时间短,主要用于浸润麻醉、周围神经阻滞和脊髓阻滞。 | |||
T37702 |
Pancuronium (bromide hydrate)
|
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Pancuronium is an aminosteroid antagonist of muscle-type nicotinic acetylcholine receptors (nAChRs) with an IC50value of 14.8 nM using patch clamp electrophysiology in BOSC23 cells expressing mouse nAChRs.1It acts as a non-depolarizing neuromuscular blocking agent.2Pancuronium enhances anesthesia induced by isoflurane , reducing immobilization with an ED50value of 1.62 μg/kg.3 1.Liu, M., and Dilger, J.P.Site selectivity of competitive antagonists for the mouse adult muscle nicotinic acetylcholin... | |||
T33287 |
Mephentermine Sulfate
sulfuric acid,MLS002153976,N,2-dimethyl-1-phenylpropan-2-amine,AC1NWAW7,Mephentermine sodium |
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Mephentermine sulfate is a cardiac stimulant, before as a stimulant in psychiatry, has been used as a treatment for low blood pressure. Mephentermine sulfate is a sympathomimetic agent with specificity for alpha-1 adrenergic receptors. It is used to maint | |||
T80638 |
Glycinexylidide
GX |
MEK | MAPK |
Glycinexylidide (GX) 是一种 Lidocaine 的活性代谢物。作为有效的局部麻醉药,Lidocaine 可以通过阻断复杂电压依赖性的钠通道来发挥作用。此外,它还能抑制胃癌细胞生长、迁移和侵袭。GX 显示出在麻醉、癌症治疗和心血管疾病研究中的应用潜力。 | |||
T69598 |
Isoproterenol-d7 HCl
|
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Isoproterenol-d7 is intended for use as an internal standard for the quantification of isoproterenol by GC- or LC-MS. Isoproterenol is an agonist of β1- and β2-adrenergic receptors (β1- and β2-ARs; Kis = 224 and 458 nM, respectively). It is selective for β1- and β2-ARs over β3-ARs (Ki = 1,570 nM). Isoproterenol inhibits contractions in isolated field-stimulated rat vas deferens (EC50 = 45.6 nM). In vivo, isoproterenol (0.33 mg/kg) decreases blood pressure and increases water intake in nephrectom... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0012 |
Cinchonine
LA40221,(8R,9S)-Cinchonine,奎宁树,辛可宁 |
Apoptosis; P-gp; Parasite | Apoptosis; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Cinchonine (LA40221) 是金鸡纳树皮中的一种天然产物。它可激活内质网应激诱导的人肝癌细胞凋亡。它是一种酰胺类局部麻醉剂。 | |||
T5734 |
(+)-BORNEOL
d-Borneol,(+)-冰片 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
(+)-BORNEOL (d-Borneol) 是一种天然的双环单萜,在中药中用于镇痛和麻醉;增强 GABA 受体活性,EC50 为 248 μM。 | |||
Fr16605 |
Lupinine
鲁冰花,羽扇豆碱 |
AChR; AChE | Neuroscience |
Lupinine 是一种能够抵消乙醇麻醉的生物碱。 Lupinine 是一种 AChE 和 BChE 抑制剂和潜在的 CD69 激活剂,存在于 Loranthus、Calia 和 Lupinus 物种中。它还可以抑制肝素。 |