47
15
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0322 |
Fipexide
|
Dopamine Receptor; AChR | GPCR/G Protein; Neuroscience |
Fipexide 是对氯苯乙酸衍生物,是哌嗪化学类的精神活性药物,作为促智药物,有用于老年痴呆的研究潜力。它可降低了纹状体腺苷酸环化酶的活性,通过多巴胺能神经传递对认知表现出积极的作用。 | |||
T9989 |
AChE-IN-27
|
Others | Others |
AChE-IN-27是一种用于高通量测定的小分子。 | |||
T14991 |
CMS-121
CMS121 |
Acetyl-CoA Carboxylase | Metabolism |
CMS-121 是喹诺酮衍生物,对乙酰辅酶 A 羧化酶 1 具有抑制作用,具有口服活性。CMS-121具有保护 HT22 细胞免受缺血和氧化损伤的活性,EC50分别为7 nM 和200 nM。CMS-121具有强大的抗炎,抗氧化,神经保护和肾保护作用。 | |||
T26526 |
Abt-288
ABT 288,ABT288 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
ABT-288 是一种具有选择性和高效性的 H3 拮抗剂,可用于治疗轻度至中度阿尔茨海默氏痴呆。 | |||
T31175 |
Dabelotine
UNII-6RY56RB98P |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dabelotine (UNII-6RY56RB98P) 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T19812 |
Propentofylline
HWA-285,Karsivan,Propentophylline,Hextol,HWA 285,HWA285 |
PDE | Metabolism |
Propentofylline (Hextol) 是一种甲基黄嘌呤衍生物,具有神经保护、抗增殖和抗炎活性,可增强的突触腺苷信号传导,可用于研究阿尔茨海默病、血管性痴呆、认知障碍、痴呆和慢性疼痛。 | |||
T31592 |
E6801
E 6801,E-6801 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
E6801是一种新型选择性5-HT6受体激动剂,具有广泛的生物活性。E6801可用于研究痴呆、帕金森病、抑郁症、肥胖症癫痫,焦虑等多种疾病。 | |||
T25226 |
Ceronapril
Ceronaprilum,SQ 29852,SQ-29852,SQ29852 |
RAAS | Endocrinology/Hormones |
Ceronapril (SQ 29852) 是一种具有口服活性和高效性的血管紧张素转换酶 (ACE) 抑制剂(IC50 : 36 nM),可用于研究痴呆和高血压。 | |||
T7525 |
Didox
3,4-二羟基苯甲羟肟酸,NSC-324360 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Didox (NSC-324360) 是一种合成的核糖核苷酸还原酶抑制剂,可降低患有痴呆症的 HIV 患者大脑中氧化损伤标志物的水平。 | |||
T27795 |
Landipirdine
RO 5025181,RO5025181,SYN-120,SYN120,RO-5025181,SYN 120 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Landipirdine (RO-5025181) 是一种选择性 5-HT6R 拮抗剂,可用于研究痴呆等中枢神经系统疾病。 | |||
T11949 |
Masupirdine mesylate
SUVN-502 mesylate,SVN-502 mesylate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Masupirdine mesylate (SUVN-502 mesylate) 是一种具有选择性且可穿越血脑屏障的 5-HT6 受体拮抗剂。Masupirdine mesylate 可用于研究阿尔茨海默病和痴呆等神经系统疾病。 | |||
T61807 |
5-HT6/7 antagonist 1
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT6/7 antagonist 1是一种 5-HT6/7/2A 和 D2 受体双重拮抗剂,可用于研究痴呆和阿尔兹海默症。 | |||
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。 | |||
T7041 |
Donepezil
E2020,Donepezilo,Aricept,多奈哌齐 |
AChE | Neuroscience |
Donepezil (Aricept) 是一种AChE 抑制剂,对牛 AChE 和人 AChE 的IC50分别为 8.12 nM 和 11.6 nM。 | |||
T67941 |
PDE5-IN-9
|
||
PDE5-IN-9对Phosphodiesterase PDE1c 具有抑制作用,可用来治疗高血压、心力衰竭、心肌梗塞、肾衰竭、哮喘、支气管炎和痴呆。 | |||
T21556 |
Hydroxytacrine maleate
Velnacrine maleate,HP 029 maleate |
AChE | Neuroscience |
Hydroxytacrine maleate (Velnacrine maleate) 是一种胆碱酯酶(cholinesterase) 抑制剂,可增强啮齿动物的记忆力,可用于研究阿尔茨海默型老年性痴呆(SDAT)。 | |||
T9832 |
(Rac)-EC5026
Urea, N-[3-fluoro-4-(trifluoromethoxy)phenyl]-N'-[1-(2-methyl-1-oxobutyl)-4-piperidinyl]- |
Epoxide Hydrolase | Metabolism |
(Rac)-EC5026 ((Rac)-BPN-19186) 是一种有效的可溶性环氧水解酶 (sEH) 哌啶抑制剂,Ki 值为 0.06 nM。(Rac)-EC5026 可用于帕金森氏病和路易体痴呆 (DLB) 的研究。 | |||
T77054 |
Lecanemab
BAN-2401 |
Beta Amyloid | Neuroscience |
Lecanemab (BAN-2401) 是一种靶向可溶性聚集性 β 淀粉样蛋白 (Abeta)的 IgG1 单克隆抗体,对寡聚体、原纤维和不溶性原纤维具有活性,可用于研究阿尔茨海默病 (AD) 引起的轻度认知障碍和轻度 AD 痴呆。 | |||
T1132 |
Nicergoline
尼麦角林,Nicergolinum,Nimergoline |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Nicergoline (Nicergolinum) 是一种有效的,选择性的、具有口服活性的α1A-肾上腺素能受体拮抗剂,是一种溴烟碱酸的麦角林衍生物。它具有血管舒张作用,可以改善阿尔茨海默症小鼠的认知功能。 | |||
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。 | |||
T7003 |
Leucomethylene blue mesylate
N3,N3,N7,N7-四甲基-10H-吩噻嗪-3,7-二胺二甲磺酸盐,TRx0237 mesylate,TRx0237 (LMTX) mesylate,Methylene blue leuco base mesylate salt,Leucomethylene Blue Dimesylate |
Beta Amyloid; Microtubule Associated | Cytoskeletal Signaling; Neuroscience |
Leucomethylene blue mesylate (TRx0237 mesylate) 是一种 Methylene blue (亚甲基蓝)的还原形式, 亚甲基蓝是一种化学指示剂和生物染色剂。它是一种具有口服活性的二代 tau 蛋白聚集的抑制剂 (Ki=为0.12 μM),可用于阿尔兹海默症的研究。 | |||
T77053 |
Latozinemab
GSK-4527223,AL-001 |
Neurotensin Receptor | GPCR/G Protein |
Latozinemab (AL001) 是一种具有有效性和选择性的重组人源化针对 Sortilin 的单克隆抗体。Latozinemab 对 Sortilin具有很高的亲和力,可中断颗粒蛋白前体 (PGRN) 和 Sortilin 受体之间的相互作用。Latozinemab 可用于研究痴呆和阿尔兹海默症。 | |||
T67955 |
Ensaculin
Anseculin |
||
Ensaculin (Anseculin) 是一种用哌嗪部分取代的新型苯并吡喃酮,在正常和人工遗忘啮齿动物的被动和条件回避范式中显示出记忆增强作用。它在NMDA 毒性模型中表现出神经保护活性,在原代培养的大鼠脑细胞中表现出神经营养作用。Ensaculin 可用于治疗痴呆。 | |||
T11191 |
EN6
|
Proton pump; Autophagy | Autophagy; Membrane transporter/Ion channel |
EN6 是一种小分子体内自噬激活剂,其共价靶向溶酶体v-ATP 酶的 ATP6V1A 亚基中的半胱氨酸 277。它以溶酶体依赖性方式清除 TDP-43 聚集体,这是额颞叶痴呆的病原体。它介导的 ATP6V1A 修饰使 v-ATP 酶与 Rags 分离,从而抑制 mTORC1 信号传导、增加溶酶体酸化和激活自噬。 | |||
T11043 |
Dihydroergocristine mesylate
甲磺酸双氢麦角汀,DHEC (mesylate) |
Beta Amyloid | Neuroscience |
Dihydroergocristine mesylate (DHEC (mesylate)) 是一种 γ-secretase (GSI) 的抑制剂,能够阿尔茨海默氏病淀粉样蛋白 β 肽 (amyloid-β) 的产生,与 γ-secretase 和 Nicastrin 结合的平衡解离常数 (Kd) 值分别为 25.7 nM 和 9.8 μM。 | |||
T31057 |
CP-457920
CP-457,920,UNII-13BME2F602 |
||
CP-457920 is a selective α 5 GABAA receptor agonist for the treatment of dementia in Alzheimer's disease. | |||
T34751 |
Usmarapride free base
SUVN-D4010,SUVN-D 4010,SUVN-D-1208045,SUVN-1004028,SUVN D4010,SUVN-D1003019 |
||
SUVN-D4010 is an effective, selective, brain penetrant, and orally active agonist of 5-HT4 receptor partially used to treat Alzheimer's disease and other dementia-related cognitive dysfunction. | |||
T13107 | TDN345 | Others | Others |
TDN345 is a antagonist of Ca2+, for the treatment of vascular and senile dementia including Alzheimer's disease. | |||
T73769 | Isocitric acid | ||
Isocitric acid,一种存在于唾液和细胞细胞质中的内源代谢物,其研究应用范围包括阿尔茨海默氏症、路易体痴呆和缺氧。 | |||
T73785 | D-Fructose-6-phosphate | ||
D-Fructose 6-phosphate 是存在于唾液中的内源代谢物,可用于研究路易体痴呆。 | |||
T31177 |
Dabelotine, (S)-
UNII-494Y55877B |
||
Dabelotine, (S)- 是 Dabelotine 的 S 型异构体。Dabelotine 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T31176 |
Dabelotine, (R)-
UNII-3NZJ1HNE7Y |
||
Dabelotine, (R)- 是 Dabelotine 的 R 型异构体。Dabelotine 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T69954 | Fasoracetam monohydrate | ||
Fasoracetam monohydrate is a small synthetic molecule and a metabotropic glutamate receptor activator, which has previously undergone extensive Phase I-III clinical trials in humans for vascular dementia. | |||
T8443L |
MCI-225 hydrochloride hydrate
AA-10021,AA10021,MCI225,DDP-225,AA-10025,AA-10026 |
||
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 | |||
T34752 |
Samelisant dihydrochloride
SUVN-G3031,SUVN-G 3031,SUVN G3031,SUVN-G3031 HCl |
||
Samelisant dihydrochloride (SUVN-G3031) is a antagonist of histamine H3 receptor with potential for the treatment of cognitive impairment, dementia, attention deficit hyperactivity disorder, epilepsy, sleep disorders, obesity, schizophrenia, eating disorders, and pain. | |||
T11448 | GOAT-IN-1 | Others | Others |
GOAT-IN-1 is an inhibitor of ghrelin O-acyltransferase (GOAT), which could be useful for the prophylaxis or treatment of diabetes, hyperlipidemia, non-alcoholic fatty liver, Alzheimer’s disease, Parkinson’s disease, cerebrovascular dementia, cerebral infa | |||
T68257 |
Hydromethylthionine HBr
|
||
Hydromethylthionine, also known as LMTM and Leucomethylene Blue, is a apotent tau aggregation inhibitor for the treatment of Alzheimer's disease (AD) and frontotemporal dementia. Hydromethylthionine showed pharmacological activity on brain structure and function as both monotherapy and as an add-on to symptomatic treatment in certain patients with Alzheimer’s disease. | |||
T79038 | Tau protein aggregation-IN-1 | ||
Tau protein aggregation-IN-1(化合物 0c)是一种针对Tau protein聚集的抑制剂。该化合物主要应用于研究蛋白质折叠障碍类疾病,包括阿尔茨海默病、痴呆、帕金森病、亨廷顿舞蹈病及基于朊病毒引起的海绵状脑病。 | |||
T60042 | NPT200-11 | Others | Others |
NPT200-11 是一种口服生物利用度和脑穿透性 ASYN 错误折叠和聚集抑制剂。 NPT200-11 可用于突触核蛋白病的潜在病理学研究,包括帕金森病 (PD)、路易体痴呆 (DLB) 和多系统萎缩 (MSA)。 | |||
T19628 |
GSK 189254 HCl
GSK-189254A,GSK 189254A,GSK 189254 hydrochloride,GSK189254A |
||
GSK 189254A is a histamine H3 receptor antagonist for the treatment of narcolepsy. Histamine H3 receptor antagonists have been shown to increase the release of neurotransmitters in the brain and to enhance cognition in vivo. The compound may also be usefu | |||
T70595 |
Artemisinin B
|
||
Artemisinin B is a drug which may improve spatial memory in dementia patients and alter the levels of inflammatory cytokines in the hippocampus and the cortex. Artemisinin B may inhibit neuroinflammation and exert neuroprotective effects on cognitive functions by modulating the TLR4-MyD88-NF-κB signaling pathway. Artemisinin B has shown potential in the treatment of neuroinflammatory diseases. | |||
T70326 |
Mevidalen HBA
|
||
Mevidalen, also known as LY3154207, is a novel, potent, and subtype selective human D1 positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50 = 3 nM). In contrast to orthosteric agonists, LY3154207 showed a distinct pharmacological profile without a bell-shaped dose-response relationship or tachyphylaxis in preclinical models. Identification of a crystalline form of free LY3154207 from the discovery lots was not successful. Instead, a novel cocrystal form with superi... | |||
T60412 |
BPN-15477
|
||
BPN-15477 是一种剪接调节剂化合物 (SMC),可恢复 ELP1 外显子 20 的正确剪接。它可用作于额颞叶痴呆研究。 BPN-15477 纠正了 ELP1 转录本的剪接,显着提高了体内所有组织(包括大脑)中功能蛋白的水平。 | |||
T72804 |
Isograndifoliol
|
||
Isograndifoliol 是一种选择性丁酰胆碱酯酶 (BChE) 抑制剂,IC50值为 0.9 μM。Isograndifoliol 对乙酰胆碱酯酶 (AChE) 有一定的抑制作用,IC50值为 342.9 μM。Isograndifoliol 还具有血管松弛作用和抗肿瘤作用。Isograndifoliol 可用于研究神经退行性疾病引起的痴呆。 | |||
T72227 |
PI3K/Akt/CREB activator 1
|
||
PI3K/Akt/CREB activator 1 是一种口服有效的PI3K/Akt/CREB 的激活剂。PI3K/Akt/CREB activator 1 通过 PI3K/Akt/CREB 通路上调脑源性神经营养因子,促进神经元增殖,诱导 Neuro-2a 细胞分化成神经元样形态,加速海马原代神经元轴突-树突极化的建立。PI3K/Akt/CREB activator 1 可用于血管性痴呆 (VaD) 的研究。 | |||
T72714 |
JNK3 inhibitor-3
|
JNK | MAPK |
JNK3inhibitor-3(compound 15g)是一种选择性的c-Jun N-terminal kinase3(JNK3)抑制剂,具有良好的血脑屏障穿透性和口服生物利用度。其对JNK1、JNK2和JNK3的IC50分别为147.8 nM、44.0 nM和4.1 nM。在小鼠痴呆模型中,JNK3inhibitor-3能显著改善记忆功能,因此有望作为阿尔茨海默病研究的工具化合物。 | |||
T35498 |
β-Amyloid (1-14),mouse,rat
|
||
β-Amyloid (1-14),mouse,rat is a 1 to 14 fragment of Amyloid-β peptide. β-Amyloid (1-14),mouse,rat is produced through the proteolytic processing of a transmembrane protein, amyloid precursor protein (APP), by β- and γ-secretases. β-Amyloid (1-14),mouse,rat accumulation in the brain is proposed to be an early toxic event in the pathogenesis of Alzheimer’s disease, which is the most common form of dementia associated with plaques and tangles in the brain[1]. [1]. Chen GF, et al. Amyloid beta: stru... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4954 |
SMILAGENIN ACETATE
Nsc15488,乙酰知母皂苷元 |
Others | Others |
Smilagenin acetate 是 sapogenin 衍生物,在细胞实验中能上调乙酰胆碱 m2 受体的表达,可用于痴呆的研究。 | |||
T3394 |
Timosaponin BII
知母皂苷BII,Prototimosaponin A III |
Beta Amyloid; Others; BACE | Neuroscience; Others |
Timosaponin BII (Prototimosaponin A III) 是一种甾体皂苷,发现于知母根茎中,具有神经保护、抗炎和抗氧化作用。 | |||
T3885 |
ROSIRIDIN
6'-O-Deacetylrosiridoside C,络塞定,(-)-Rosiridin |
Others; Monoamine Oxidase | Neuroscience; Others |
Rosiridin (6'-O-Deacetylrosiridoside C) 能够抑制 MAO A 和 MAO B,有潜在的抑郁症和老年性痴呆作用。它在 10 μM 时对 MAO B 的抑制率为 83.8% (pIC50=5.38)。 | |||
T7792 |
Hispidin
6-[(1E)-2-(3,4-二羟基苯基)乙烯基]-4-羟基-2H-吡喃-2-酮 |
Endogenous Metabolite; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism |
Hispidin 是来自裂蹄木层孔菌的酚类天然产物,是一种 PKC 抑制剂,具有很强的抗氧化、抗癌、抗糖尿病和抗痴呆作用。 | |||
T3S1816 |
Parishin B
|
Others | Others |
Parishin B 是一种分离自天麻中的 Parishin 衍生物,可能具有抗氧化活性。 | |||
T6S1294 |
Nicotiflorin
Nictoflorin,Kaempferol-3-O-Rutinoside,山奈酚-3-O-芸香糖苷,Nicotifloroside |
Others | Others |
Nicotiflorin (Kaempferol-3-O-Rutinoside) 是一种黄酮苷,从传统中药Flos Carthami 中提取得到。它有抗糖化活性和神经保护作用。 | |||
T4439 |
sn-Glycero-3-phosphocholine
Choline Alfoscerate,甘磷酸胆碱,Glycerophosphocholine,Glycerophosphorylcholine,Alpha-GPC,Choline glycerophosphate,L-α-GPC |
Endogenous Metabolite; AChE | Metabolism; Neuroscience |
sn-Glycero-3-phosphocholine (Choline glycerophosphate) 是脑磷脂生物合成的前体,能够提高胆碱在神经组织中的生物利用度。它对认知功能有显著影响,同时具有良好的耐受性和安全性,因此能够用于阿尔茨海默病和痴呆症的研究。 | |||
T40967 |
D-Octamannuronic acid
|
||
D-Octamannuronic acid, an alginate oligomer, is derived from marine brown algae and a restricted group of Gram-negative bacteria. It is research-oriented for the study of pain and vascular dementia [4]. | |||
T38981 |
D-Tetramannuronic acid
|
||
D-Tetramannuronic acid, an alginate oligomer, is derived from marine brown algae and certain Gram negative bacteria. It serves as a valuable compound for pain and vascular dementia research[4]. | |||
T39276 |
D-Pentamannuronic acid
|
||
D-Pentamannuronic acid is an alginate oligomer, synthesized by marine brown algae and a select group of Gram-negative bacteria. This chemical compound is valuable for research related to pain and vascular dementia[4]. | |||
T66362 | Galantamine Hydrobromide | ||
Galantamine hydrobromid is used for treatment of mild to moderate dementia of the Alzheimer type. | |||
T35614 |
D-Trimannuronic acid
|
||
D-Trimannuronic acid is an alginate oligomer that originates from seaweed. It can induce TNF-α secretion by mouse macrophage cell lines, making it valuable in pain and vascular dementia research [1][2][3]. | |||
T39277 | D-Hexamannuronic acid | ||
D-Hexamannuronic acid, an alginate oligomer, is derived from marine brown algae and a restricted group of Gram negative bacteria. This compound serves as a valuable tool for investigating pain and vascular dementia[4]. | |||
T40966 |
D-Heptamannuronic acid
|
||
D-Heptamannuronic acid, an alginate oligomer, is derived from marine brown algae and a select group of Gram-negative bacteria. This compound serves as a valuable research tool in the study of pain and vascular dementia[4]. | |||
T82535 |
D-Nonamannuronic acid
|
||
D-Nonamannuronic acid 是海洋褐藻及部分革兰氏阴性细菌产生的藻酸盐低聚物。该化合物用于疼痛与血管性痴呆的研究应用。 |