74
13
2
10
2
Cat. No. | Product Name | ||
---|---|---|---|
L9840 | 抗阿尔茨海默症化合物库 | 986 compounds | |
986 种阿尔茨海默症相关的化合物集合,可用于高通量和高内涵筛选; | |||
L2610 | 神经递质受体化合物库 | 1513 compounds | |
1513 种与神经递质受体相关的化合物,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11861 |
LM11A-31 dihydrochloride
|
Others | Others |
LM11A-31 dihydrochloride 是一种具有高血脑屏障通透性的氨基酸衍生物,能阻断 p75 介导的细胞死亡。它是一种 p75NTR(神经营养蛋白受体 p75) 非肽调节剂,是口服有效的 proNGF 拮抗剂。它可以逆转中晚期的阿尔茨海默氏病小鼠模型中的胆碱能神经突营养不良。 | |||
T0229 |
Rivastigmine
SDZ-ENA 713,卡巴拉汀,S-Rivastigmine,Exelon,利凡斯的明 |
AChE | Neuroscience |
Rivastigmine (Exelon) 是具有口服活性的、有效的、可透过血脑屏障的胆碱酯酶抑制剂,可抑制丁酰胆碱酯酶和乙酰胆碱酯酶,IC50分别为 0.037 μM 和 4.15 μM。它是一种拟副交感神经剂或胆碱能剂,用于研究轻度至中度阿尔茨海默氏型痴呆和帕金森氏病引起的痴呆。 | |||
T1628 |
Rivastigmine tartrate
SDZ-ENA 713,ENA 713,酒石酸卡巴拉汀 |
AChR; AChE | Neuroscience |
Rivastigmine tartrate (SDZ-ENA 713) 是一种具有口服活性的、可透过血脑屏障的胆碱酯酶抑制剂,能够抑制丁酰胆碱酯酶和乙酰胆碱酯酶。它是一种拟副交感神经剂或胆碱能剂,用于研究轻度至中度阿尔茨海默氏型痴呆和帕金森氏病引起的痴呆。 | |||
T0236 |
Azatadine dimaleate
马来酸阿扎他啶,SCH10649,马来酸阿扎他定,Azatadine Maleate |
5-HT Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Azatadine dimaleate (SCH10649) 是组胺和胆碱能抑制剂,IC50分别为 6.5 和 10 nM。 | |||
T34114 |
Posatirelin
BRN 6006446,Posatirelinum,BRN-6006446,RGH-2202,BRN6006446 |
AChR | Neuroscience |
Posatirelin (BRN6006446) 是一种对单胺能和胆碱能系统具有调节活性和神经营养作用的合成肽,可用于研究血管性痴呆。 | |||
T23147 |
Phaclofen
3-Amino-2-(4-chlorophenyl)propanephosphonic acid |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Phaclofen (3-Amino-2-(4-chlorophenyl)propanephosphonic acid) 是一种选择性 GABAB receptor 拮抗剂,可部分拮抗(-)-巴氯芬的镇静作用,可逆地拮抗巴氯芬或GABA对豚鼠回肠和远端结肠胆碱能抽搐反应的抑制,可用于研究神进系统疾病。 | |||
T27404 |
GAT107
GAT 107,GAT-107 |
AChR | Neuroscience |
GAT107 是一种新型有效的 α7 烟碱胆碱能受体变构激动剂和调节剂,具有抗炎活性,可逆转小鼠神经疼痛模型中的伤害感受。 | |||
T2571 |
Benactyzine hydrochloride
Neuroleptone,胃复康,盐酸贝那替嗪,Tranquilline,Amitakon |
AChR; AChE | Neuroscience |
Benactyzine hydrochloride (Neuroleptone) 是丁酰胆碱酯酶抑制剂,其Ki=0.010 mM。 | |||
T5655 |
mAChR-IN-1 hydrochloride
|
AChR | Neuroscience |
mAChR-IN-1 hydrochloride 是一种毒蕈碱胆碱能受体抑制剂,IC50值为17nM。 | |||
T10914L |
Cyclodrine
Cyclopent |
AChR | Neuroscience |
Cyclodrine (Cyclopent) 是一种胆碱能 (毒蕈碱,烟碱) 受体 (mAChR 和 nAChR) 拮抗剂。 | |||
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。 | |||
T0169 |
Nefiracetam
DM9384,奈非西坦,DZL-221 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Nefiracetam (DM9384) 是一种 GABA 能、胆碱能和单胺能神经元系统增强剂,用于治疗 Ro 5-4864 引起的抽搐。 | |||
T21439 |
Tacrine
他克林,CS 12602,Tacrinum,Tetrahydroaminocrine |
AChR | Neuroscience |
Tacrine (CS 12602) 一种间接胆碱能激动剂和中枢作用的抗胆碱酯酶。它被批准用于治疗阿尔茨海默病。 | |||
T21655 |
(±)-Acetylcarnitine chloride
Acetyl dl-carnitine chloride |
AChR | Neuroscience |
(±)-Acetylcarnitine chloride (Acetyl dl-carnitine chloride) 是一种弱胆碱能激动剂,具有神经保护作用,可用于研究神经炎。 | |||
T6707 |
Tiotropium Bromide hydrate
BA-679 BR hydrate,BA 679BR,噻托溴铵一水合物 |
AChR | Neuroscience |
Tiotropium Bromide hydrate (BA-679 BR hydrate) 是长效的毒蕈碱受体拮抗剂,可用于治疗慢性阻塞性气道疾病 (COPD)。 | |||
T50047 |
1-(3,4-Dihydroxyphenyl)-2-(dimethylamino)ethanone HCl
|
Others | Others |
1-(3,4-dihydroxyphenyl)-2-(dimethylamino)ethan-1-one hydrochloride 是一种胆碱能制剂,抑制胆碱代谢,从而导致大脑中乙酰胆碱水平的增加,进而增强认知功能和记忆。 | |||
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。 | |||
T21841 |
(±)-Hexanoylcarnitine chloride
DL-Hexanoylcarnitine chloride |
Others; AChE | Neuroscience; Others |
(±)-Hexanoylcarnitine chloride 是一种脂肪酸代谢产物,能将脂肪酸分解成能够被身体利用的小分子化合物。(±)-Hexanoylcarnitine chloride 可通过大鼠骨骼肌毒性特异性从而作为一种生物标志物。(±)-Hexanoylcarnitine chloride 具有胆碱能活性。 | |||
T26174 |
SAK3
SAK 3,SAK-3 |
Calcium Channel; AChR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
SAK3 是一种新型的 nAChR 活性调节剂,可增强 T 型电压门控 Ca2+ 通道 (T-VGCC) 的活性,对 Cav3.1 和 Cav3.3 T 型 Ca2+ 通道电流均有增强作用。SAK3 对人神经母细胞瘤 SH-SY5Y 细胞中东莨菪碱诱导的胆碱能功能障碍有神经保护作用。SAK3 可用于研究记忆缺陷和阿尔茨海默病。 | |||
T1281 |
Tropicamide
Ro 1-7683,托吡卡胺 |
AChR | Neuroscience |
Tropicamide (Ro 1-7683) 是一种选择性的 M4毒蕈碱乙酰胆碱受体拮抗剂,作为滴眼剂使用时,会产生短效瞳孔扩张和睫状肌麻痹。 | |||
T1568 |
Amoxapine
阿莫沙平,CL-67772 |
GlyT | Neuroscience |
Amoxapine (CL-67772) 是一种dibenzoxazepine 家族的四环抗抑郁药,常被归类为仲胺三环类抗抑郁药。 | |||
TP1902L1 |
G-Protein antagonist peptide acetate
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
G-Protein antagonist peptide acetate 是一种 substance P 相关肽,可抑制 G 蛋白与其受体的结合。G-Protein antagonist peptide acetate 竞争性和可逆性地抑制毒蕈碱型乙酰胆碱受体 M2 (M2 muscarinic receptor) 对 Gi 或 Go 的激活,并通过 β-肾上腺素受体抑制 Gs 的激活。 | |||
TP2309 |
Neurotensin TFA
NEUROTENSIN TFA,Neurotensin TFA (39379-15-2 free base),神经加压素 |
Others | Others |
Neurotensin TFA (39379-15-2 free base) 是一种内源性 13 个氨基酸的神经肽,具有显着的阿片类非依赖性镇痛作用。它在大脑中充当神经递质,在肠道中充当激素,也充当神经调节剂。由于它与多种神经递质系统如多巴胺能、血清素能、谷氨酸能、GABA 能和胆碱能系统。它具有作为人体代谢物、有丝分裂原、神经递质和创伤的作用。 | |||
T0976 |
Propoxur
残杀威,Aprocarb,Propoxure,Baygon |
AChR; Antifungal | Microbiology/Virology; Neuroscience |
Propoxur (Propoxure) 是一种氨基甲酸酯类杀虫剂,用于控制蟑螂、苍蝇、蚊子以及草坪和草坪昆虫。 | |||
T71050 |
U 80816B
|
Others | Others |
U 80816B is a cholinergic direct agonist. | |||
T70220 |
Tazomeline citrate
|
Others | Others |
Tazomeline citrate is used for alzheimer's disease treatment (Cholinergic Agonist). | |||
T34223 |
Quilostigmine
HP 290,NXX 066,NXX-066 |
Others | Others |
Quilostigmine is a cholinergic. | |||
T28742 |
Securinine mononitrate
Securinan-11-one nitrate |
Others | Others |
Securinine mononitrate is a cholinergic agent and an antagonist of gamma-aminobutyric acid A (GABAA) receptor. | |||
T22511 |
4-DAMP
|
Others | Others |
M3 cholinergic receptor antagonist | |||
T6597L |
Mosapride citrate dihydrate
GR-107719-B,Mosapride Citrate,GR 107719 B,AS 4370,AS-4370,TAK-370 |
Others | Others |
Mosapride Citrate is a 5-HT4 receptor agonist used to stimulate gastrointestinal motility via acetylcholine. Mosapride Citrate facilitates acetylcholine release from the enteric cholinergic neurons. | |||
T71531 |
Metamizil hydrochloride
|
Others | Others |
Metamizil hydrochloride is a cholinolytic agent -- an agent that blocks the transmission of excitation from cholinergic nerve fibers -- and an antagonist of the mediator acetylcholine. | |||
T33634 |
Neopterin, L-erythro-
Neopterin, L-(-)-,L-Neopterin,L-Erythro-neopterin |
Others | Others |
Neopterin, L-erythro- can be used as a cholinergic receptor. | |||
T34750 |
Sut 8701
Sut8701,Sut-8701 |
Others | Others |
Sut 8701 is a cholecystokinin analog that prevents cholinergic degeneration in the rat cerebral cortex following basal forebrain lesioning and can slow down the degenerative processes in Alzheimer's disease. | |||
T22593 |
Azatadine
|
Others | Others |
Azatadine is histamine and cholinergic inhibitor (IC50: 6.5 nM and 10 nM, respectively). | |||
T22435 |
Tacrine hydrochloride
四氢氨基吖啶,盐酸他克林,Tacrine HCl |
Others | Others |
Tacrine is a indirect cholinergic agonist and centrally acting anticholinesterase. Tacrine hydrochloride hydrate is an inhibitor of acetyl (AChE) and butyryl-cholinestrase (BChE) with IC50s of 31 nM and 25.6 nM, respectively. | |||
T26553 |
Aclatonium Napadisilate
Acaltonium napadisilate |
Others | Others |
Aclatonium Napadisilate, a cholinergic agonist, has been shown to stimulates endocrine and exocrine pancreatic secretion. | |||
T15743 |
Levomepromazine
Methotrimeprazine |
Others | Others |
Methotrimeprazine is an orally available neuroleptic agent. It is commonly used to relieve nausea and vomiting in palliative care settings. Levomepromazine has antagonist actions at multiple neurotransmitter receptor sites, including cholinergic, dopamine | |||
T29203 |
Zanapezil fumarate
TAK 147,TAK147,TAK-147 |
Others | Others |
Zanapezil is an acetylcholinesterase (AChE) inhibitor. Zanapezil increases choline acetyltransferase activity in cultured rat septal cholinergic neurons. | |||
T69234 |
Piperilate HCl
|
Others | Others |
Piperilate HCl is an antispasmodic, antimuscarinic agent. It is a muscarinic cholinergic receptor antagonist. | |||
T5476 |
mAChr-in-1
|
AChR | Neuroscience |
mAChR-IN-1 是一种毒蕈碱胆碱能受体拮抗剂,IC50为17 nM。 | |||
T10224 |
ABT-418 hydrochloride
|
Others | Others |
ABT-418 hydrochloride is a selective agonist of nAChRs with cognitive enhancing and anxiolytic activities. It activates cholinergic channel and can be used for the research of Alzheimer's disease. | |||
T20522 |
Acetylcholine perchlorate
AI351678,AI3-51678,AI3 51678 |
Others | Others |
Acetylcholine perchlorate is the perchlorate salt of acetylcholine. Acetylcholine, an endogenous neurotransmitter at cholinergic synapses, could amplify the action potential of the sarcolemma following by inducing muscle contractions. | |||
T21464 |
Methiocarb
Mercaptodimethur,Mesurol |
Others | Others |
Methiocarb, a carbamate pesticide, is used as an insecticide, acaricide, bird repellent, and molluscicide. Methiocarb stimulates cholinergic by inhibiting reversibly acetylcholinesterase activity, making methiocarb a potent neurotoxin. | |||
T20131 |
Cevimeline hydrochloride
盐酸西维美林,Cevimeline HCl,Evoxac |
Others | Others |
Cevimeline HCl is an agonist of cholinergic that binds to muscarinic receptors. Muscarinic agonists in sufficient dosage can enhance the secretion of exocrine glands, such as salivary and sweat glands. | |||
T32833 |
Lobeline, (+)-
(+)-Lobeline |
Others | Others |
Lobeline, (+)- is an alkaloid that has actions similar to nicotine on nicotinic cholinergic receptors but is less potent. It has been proposed for a variety of therapeutic uses including in respiratory disorders, peripheral vascular disorders, insomnia, a | |||
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 | |||
T10914 |
Cyclodrine hydrochloride
|
AChR | Neuroscience |
Cyclodrine hydrochloride 是一种胆毒蕈碱受体(mAChR)和烟碱受体(nAChR)双重拮抗剂,可以用于研究神经系统相关疾病。 | |||
T78109 |
(Ala13)-Apelin-13 TFA
|
Others | Others |
'(Ala13)-Apelin-13 TFA' 为高效的APJ受体拮抗剂,能够通过迷走神经胆碱能通路抑制胃动力。 | |||
T8443L |
MCI-225 hydrochloride hydrate
AA-10021,AA10021,MCI225,DDP-225,AA-10025,AA-10026 |
Others | Others |
MCI-225 is a norepinephrine reuptake/5-HT3/5-HT reuptake inhibitor. MCI-225 could be effective in the treatment of senile dementia of the Alzheimer type, which is accompanied with both deficit in the BF-cortex cholinergic neuron and cerebral glucose hypom | |||
T76130 |
Acetylcholinesterase
|
Others | Others |
Acetylcholinesterase(ACHE; EC 3.1.1.7), 即乙酰胆碱酯酶,是一种胆碱能酶,主要存在于神经肌肉接头和胆碱能类型的化学突触中,常用于生化研究。Acetylcholinesterase 可以催化乙酰胆碱和其他一些充当神经递质的胆碱酯分解或水解为乙酸和胆碱。Acetylcholinesterase 主要作用是终止突触之间的神经元传递和信号传导,以防止 ACh 扩散和附近受体的激活。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3026 |
(-)-Huperzine A
HupA,石杉碱,Huperzine A,石杉碱甲 |
Apoptosis; AChR; AChE; iGluR | Apoptosis; Membrane transporter/Ion channel; Neuroscience |
(-)-Huperzine A (HupA) 是从中国梅花苔中分离得到的一种生物碱,具有神经保护活性。它是高特异性可逆的,具有血脑屏障渗透性的一种乙酰胆碱酯酶抑制剂, 其IC50值为 82 nM。 它也是 N-甲基-D-天冬氨酸受体的非竞争性拮抗剂,可研究神经退行性疾病,如阿尔茨海默病。 | |||
T3767 |
Polygalacic acid
Virgaureagenin G,毛果一枝黄花皂苷元G,远志酸 |
MMP; AChR; AChE | Neuroscience; Proteases/Proteasome |
Polygalacic acid (Virgaureagenin G) 是一种从远志 Polygala tenuifolia Willd 根中分离出来的三萜,可抑制 MMP 表达。它对认知障碍有显著的神经保护作用,PA 通过抑制乙酰胆碱酯酶活性,增加胆碱乙酰转移酶活性,提高海马和额皮质中的乙酰胆碱水平来提高胆碱能系统反应性。 它可以用于骨关节炎相关研究。 | |||
T6S0109 |
Sipeimine
Kashmirine,西贝母碱,Imperialine,西贝碱 |
Others | Others |
Sipeimine (Kashmirine) 是一种天然产物,从平贝母中分离得到。 | |||
TN1236 |
3',4',7-Trihydroxyisoflavone
|
MAPK; JNK | MAPK |
3',4',7-Trihydroxyisoflavone 是大豆异黄酮大豆苷元衍生物,是 Cot (Tpl2/MAP3K8) 和 MKK4 抑制剂,具有抗癌、抗血管生成和自由基清除特性。3',4',7-Trihydroxyisoflavone 通过调节小鼠胆碱能功能和BDNF信号通路增强记忆作用,可改善因内源性或外源性糖皮质激素而受损的皮肤屏障功能,可用于研究特应性皮炎。 | |||
T1221 |
Acetylcholine chloride
ACh chloride,Pilofrin,氯化乙酰胆碱 |
Calcium Channel; Endogenous Metabolite; AChR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Acetylcholine chloride (Pilofrin) 是一种神经递质,是胆碱能激动剂,通过刺激烟碱乙酰胆碱受体调节多巴胺能神经元活性,在体外抑制 p53 突变肽的聚集。 | |||
T0375 |
Atropine
DL-Hyoscyamine,阿托品,Tropine tropate,颠茄碱 |
Endogenous Metabolite; AChR | Metabolism; Neuroscience |
Atropine (DL-Hyoscyamine) 是竞争性的毒蕈碱乙酰胆碱受体拮抗剂,有抗近视效果。它是一种从颠茄植物中分离出来的天然生物碱,可阻断乙酰胆碱对心率和收缩力的抑制作用。 | |||
T9113 |
Myristicin
Myristicine,肉豆蔻醚 |
IL Receptor; Anti-infection; BCL; P450; PARP; 5-HT Receptor; Caspase; GABA Receptor; NO Synthase | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Myristicin (Myristicine) 是一种在香料和伞形植物中发现的天然产物。肉豆蔻素具有抗胆碱能、抗菌和肝保护作用,还具有抗炎作用,其通过钙途径抑制dsrna 刺激的巨噬细胞中的NO、细胞因子、趋化因子和生长因子。Myristicin 可以诱导细胞凋亡,其特征是改变线粒体膜电位、细胞色素c 释放、Caspase-3激活、parp 切割和DNA 断裂。 | |||
T1437 |
D-Panthenol
D-泛醇,D-Pantothenyl alcohol,Ilopan,Dexpanthenol,Pantothenol |
Endogenous Metabolite | Metabolism |
D-Panthenol (D-Pantothenyl alcohol) 是 D-pantothenic acid 和胆碱能剂的酒精类似物。D-Panthenol 作为乙酰化反应所必需的辅酶A的前体,参与乙酰胆碱的合成。虽然 D-Panthenol 作用的确切机制尚不清楚,但它可能增强乙酰胆碱的作用。D-Panthenol 作用于胃肠道,增加下肠蠕动。它也适用于局部皮肤,以缓解瘙痒和促进愈合。 | |||
T4S0969 |
Obtusifolin
决明蒽醌,决明蒽醌;美决明子素 |
Antioxidant; NF-κB | NF-κB; oxidation-reduction |
Obtusifolin 是分离自决明子的种子中,能够抑制NF-kB 通路,调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。 | |||
T2S2363 |
Corydine
|
IL Receptor; Antifection | Immunology/Inflammation; Microbiology/Virology |
Corydine is the adrenolytic and weak cholinergic agent, it shows antimicrobial, and antineoplastic activities. Corydine shows irritant and respiratory stimulant and CNS depressant activities. Injected intravenously in rabbits corydine produced an initial | |||
T22357 |
Lobeline sulfate
硫酸山梗菜碱,Lobelin sulphate |
Others | Others |
Lobelin sulphate is an alkaloid that has actions similar to nicotine on nicotinic cholinergic receptors but is less potent. It has a variety of therapeutic uses including in insomnia, and smoking cessation, peripheral vascular disorders, respiratory disor | |||
TN3472 | Axillaridine A | Others | Others |
Axillaridine A is a new cholinesterase inhibitors, it may act as potential leads in the discovery of clinically useful inhibitors for nervous-system disorders, particularly by reducing memory deficiency in Alzheimer's disease patients by potentiating and | |||
T81072 |
Suffruticosol A
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Suffruticosol A是一种从P. lactiflora种子中分离得到的神经保护剂,能够逆转由Scopolamine诱导的细胞神经退行性损伤。该化合物还能改善海马体胆碱能缺陷并部分增强BDNF信号传导,从而在Scopolamine诱导模型中显示出改善神经功能的作用,可恢复小鼠记忆与认知行为。 |
Cat. No. | Product Name | Species | Expression System |
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TMPY-02286 |
Influenza A H1N1 (A/Puerto Rico/8/34/Mount Sinai) Matrix protein 1/M1 Protein (His)
cholinergic receptor, muscarinic 1 |
H1N1 | E. coli |
Influenza A H1N1 (A/Puerto Rico/8/34/Mount Sinai) Matrix protein 1/M1 Protein (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 29.3 kDa and the accession number is B4UPA8. | |||
TMPY-00498 |
Influenza A H3N2 (A/Aichi/2/1968) Matrix protein 1/M1 Protein (His)
cholinergic receptor, muscarinic 1 |
H3N2 | E. coli |
Influenza A H3N2 (A/Aichi/2/1968) Matrix protein 1/M1 Protein (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 30 kDa and the accession number is I6SGW5. | |||
TMPY-00554 |
CHRNB3 Protein, Human, Recombinant (His)
cholinergic receptor, nicotinic, beta 3 (neuronal),... |
Human | HEK293 Cells |
Cholinergic nicotinic receptor (CHRN) gene family has been known to mediate the highly additive effects of nicotine in the body, and implicated nicotine dependence (ND) and related phenotypes. Cigarette smoking is protective in Parkinson's disease (PD), possibly because of nicotine action on brain nicotinic-acetylcholine receptors. The beta3 nicotinic-acetylcholine receptor subunit (encoded by CHRNB3) is depleted in the striatum of PD patients and associated with nicotine dependence. CHRNB3 Prot... | |||
TMPY-00496 |
Influenza A H1N1 (A/Brevig Mission/1/1918) Matrix protein 1/M1 Protein (His)
cholinergic receptor, muscarinic 1 |
H1N1 | E. coli |
Influenza A H1N1 (A/Brevig Mission/1/1918) Matrix protein 1/M1 Protein (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 30 kDa and the accession number is Q8BAC3.1. | |||
TMPY-03844 |
Influenza A H7N9 (A/Anhui/1/2013) Matrix protein 1/M1 Protein (His)
cholinergic receptor, muscarinic 1 |
H7N9 | E. coli |
Influenza A H7N9 (A/Anhui/1/2013) Matrix protein 1/M1 Protein (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 28.5 kDa. | |||
TMPY-04195 |
CHRNB3 Protein, Human, Recombinant (hFc)
cholinergic receptor, nicotinic, β 3 (neuronal), |
Human | HEK293 Cells |
Cholinergic nicotinic receptor (CHRN) gene family has been known to mediate the highly additive effects of nicotine in the body, and implicated nicotine dependence (ND) and related phenotypes. Cigarette smoking is protective in Parkinson's disease (PD), possibly because of nicotine action on brain nicotinic-acetylcholine receptors. The beta3 nicotinic-acetylcholine receptor subunit (encoded by CHRNB3) is depleted in the striatum of PD patients and associated with nicotine dependence. CHRNB3 Prot... | |||
TMPY-04321 |
CHRNA5 Protein, Human, Recombinant (His)
cholinergic receptor, nicotinic, α5 (neuronal),... |
Human | HEK293 Cells |
Genetic variation in the cluster on chromosome 15, encoding the nicotinic acetylcholine receptor subunits (CHRNA5-CHRNA3-CHRNB4), has shown strong associations with tobacco consumption and an additional risk increase in smoking-related diseases such as chronic obstructive pulmonary disease (COPD), peripheral artery disease and lung cancer. CHRNA5 may influence susceptibility to lung cancer among Han smokers. Genetic variation in nicotinic receptor alpha 5 (CHRNA5) has been associated with increa... | |||
TMPH-01085 |
CHAT Protein, Human, Recombinant (His)
CHAT,Choline O-acetyltransferase,ChAT,CHOACTase,Choline acet... |
Human | E. coli |
Catalyzes the reversible synthesis of acetylcholine (ACh) from acetyl CoA and choline at cholinergic synapses. CHAT Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 72.7 kDa and the accession number is P28329. | |||
TMPY-01742 |
Acetylcholinesterase Protein, Mouse, Recombinant (His)
Acre,Chrne,acetylcholinesterase (Yt blood group) |
Mouse | HEK293 Cells |
Acetylcholinesterase, also known as ACHE, is an enzyme that degrades (through its hydrolytic activity) the neurotransmitter acetylcholine, producing choline and an acetate group. Acetylcholinesterase plays a crucial role in nerve impulse transmission at cholinergic synapses by rapid hydrolysis of the neurotransmitter acetylcholine (ACh). ACHE appears to be a potential therapeutic target at muscle injuries including organophosphate myopathy. It is an externally oriented membrane-bound enzyme and ... | |||
TMPH-02669 |
GJA1 Protein, Mouse, Recombinant (His & Myc)
Gap junction 43 kDa heart protein,Gja1,Gap junction alpha-1 ... |
Mouse | Baculovirus Insect Cells |
Gap junction protein that acts as a regulator of bladder capacity. A gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. Negative regulator of bladder functional capacity: acts by enhancing intercellular electrical and chemical transmission, thus sensitizing bladder muscles to cholinergic neural stimuli and causing them to contract. May play a role in cell growth inhibi... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T11273 |
Fenpiverinium D3 bromide
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Others | Others |
Fenpiverinium bromide has anti-cholinergic and anti-spasmodic effects.Fenpiverinium D3 bromide is a deuterium labeled Fenpiverinium bromide. | |||
TMID-0258 |
(±)-Atropine-d3 (N-methyl-d3)
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(±)-Atropine-d3 (N-methyl-d3) 是 (±)-Atropine 的氘代化合物。(±)-Atropine 的 CAS 号为 51-55-8。Atropine 是竞争性的毒蕈碱乙酰胆碱受体拮抗剂,有抗近视效果。它是一种从颠茄植物中分离出来的天然生物碱,可阻断乙酰胆碱对心率和收缩力的抑制作用。 |