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Cat. No. | Product Name | Target | Signaling Pathways |
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T14284 |
β-Amyloid (25-35)
β-Amyloid peptide(25-35),Aβ25-35,BETA-淀粉样蛋白片断25-35,Amyloid beta-peptide(25-35) |
Beta Amyloid | Neuroscience |
β-Amyloid (25-35) (Aβ25-35) 是一种阿尔茨海默氏淀粉样蛋白β肽的Aβ(25-35) 片段,在培养细胞中显示出神经毒性作用。 | |||
T7680 |
GSNKGAIIGLM(131602-53-4(free base))
Amyloid beta-peptide(25-35),BETA-淀粉样蛋白片断25-35 |
Beta Amyloid | Neuroscience |
GSNKGAIIGLM(131602-53-4(free base)) (Amyloid beta-peptide(25-35)) 是阿尔茨海默病淀粉样蛋白 β-肽的片段 Aβ(25-35)。 | |||
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。 | |||
T80539 |
[Ala28]-β Amyloid(25-35)
β(25-35)KA |
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"[Ala28]-β Amyloid(25-35) (β(25-35)KA)为Aβ(25-35)的一种电中性变体,能够促进萤火虫荧光素酶聚集。" | |||
T37370 |
Amyloid-β (25-35) Peptide (human) (trifluoroacetate salt)
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Amyloid-β (25-35) (Aβ (25-35)) is an 11-residue fragment of the Aβ protein that retains the physical and biological characteristics of the full length peptide. It forms fibrils that react to thioflavin T and Congo red and are organized in a cross-β arrangement of β-strands similar to Aβ (1-40) and Aβ (1-42) fibrils. Aggregated Aβ (25-35) decreases the viability of rat adrenal PC12 cells. It also decreases the viability of primary rat cortical neurons at concentrations ranging from 1 nM to 30 μM.... | |||
T82395 |
FITC-β-Ala-β-Amyloid (25-35)
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FITC-β-Ala-β-Amyloid (25-35) 是一种FITC标记的荧光产物,适用于阿尔茨海默病研究。 | |||
TP1338 |
Neuropeptide Y (29-64), amide, human TFA
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Neuropeptide Y (29-64), amide, human (TFA) is involved in Alzheimer's disease (AD) and protects rat cortical neurons against β-Amyloid toxicity.It is showed that Neuropeptide Y (29-64), amide, human (TFA) is able to protect cortical neurons from Aβ25-35 t | |||
T72824 |
RAGE/SERT-IN-1
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RAGE/SERT-IN-1 是一种 RAGE 和 SERT 抑制剂,口服活性良好,IC50 分别为 8.26 μM 和 31.09 nM。它对 Aβ25-35 诱发的神经元损伤具有显著神经保护效果,并可缓解小鼠抑郁症状。RAGE/SERT-IN-1 适用于阿尔茨海默病与抑郁症并发症的研究。 | |||
T35560 |
SAR502250
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SAR502250 is a potent, selective, ATP competitive, orally active and brain-penetrant inhibitor of GSK3, with an IC50 of 12 nM for human GSK-3β. SAR502250 displays antidepressant-like activity. SAR502250 can be used for the research of Alzheimer’s disease (AD)[1][2]. SAR502250 (0.01-1 μM; 36 h) attenuates the Aβ25-35-induced cell death in rat embryonic hippocampal neurons[2]. SAR502250 (1-100 mg/kg; a single p.o,) attenuates tau hyperphosphorylation in the cortex and spinal cord of transgenic mic... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T32614 |
L-Clausenamide
(-)-Clausenamide |
Microtubule Associated | Cytoskeletal Signaling |
L-Clausenamide 是从黄皮 (Clausena lansium (Lour) skeels) 的树叶中提取出来的生物碱,可用于提高认知功能。L-Clausenamide 对β-淀粉样蛋白 (Aβ) 毒性有抑制作用,通过抑制 tau 蛋白磷酸化阻止神经纤维缠结的形成。L-Clausenamide 具有神经保护活性,可用于调节 Aβ25-35 引发的刺激。L-Clausenamide 可用于研究阿尔兹海默症类的神经系统疾病。 | |||
T3385 |
Gypenoside XVII
GP-17,Gynosaponin S,七叶胆苷XVII |
Estrogen Receptor/ERR; GSK-3; Endogenous Metabolite | Endocrinology/Hormones; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells |
Gypenoside XVII (Gynosaponin S) 是一种绞股蓝皂甙类的新型植物雌激素,能够激活雌激素受体。 |