Cat. No. | Product Name | Target | Signaling Pathways |
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TP1359L |
Amyloid β Peptide (42-1)(human) acetate
Amyloid β Peptide (42-1)(human) acetate(317366-82-8 free base) |
Beta Amyloid | Neuroscience |
Amyloid β Peptide (42-1)(human) acetate 是淀粉样蛋白 β 肽 (1-42) 的无活性形式。Amyloid β Peptide (42-1)(human) acetate 是由 42 个氨基酸组成的肽,其在阿尔茨海默病的发病机制中起关键作用。 | |||
TP1007L |
β-Amyloid (1-42), acetate (human)
β-Amyloid (1-42), human acetate (107761-42-2 Free base) |
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β-Amyloid (1-42), acetate (human) 是由 42 个氨基酸组成的肽,是 β-Amyloid 的一部分,常用于阿尔茨海默病造模。 | |||
TP1007 |
β-Amyloid (1-42), human
大豆肽,β-Amyloid (1-42), human,Amyloid β-Peptide (1-42) human |
Beta Amyloid | Neuroscience |
β-Amyloid (1-42), human 是一种由 42 个氨基酸组成的肽,在阿尔茨海默病的发病机制中起关键作用。 | |||
TP1359 |
β-Amyloid (42-1), human
Amyloid β Peptide (42-1)(human) |
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β-Amyloid (42-1), human is the inactive form of Amyloid β Peptide (1-42) which plays a key role in the pathogenesis of Alzheimer disease. | |||
T35499 |
β-Amyloid (1-42), (rat/mouse) (TFA)
Amyloid β-peptide (1-42) (human) TFA,166090-74-0 TFA |
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β-Amyloid (1-42), (rat/mouse) (TFA) 是由 42 个氨基酸组成的多肽片段,可用于研究阿尔茨海默症。 | |||
T37768 |
β-Amyloid (1-37) (human)
|
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β-Amyloid (1-37) (human) 与阿尔茨海默病的精神状态有潜在关联。 | |||
T38149 |
β-Amyloid (1-43)(human)
|
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The amyloid β-protein is a 39- to 43-amino acid polypeptide that is the primary constituent of senile plaques and cerebrovascular deposits in Alzheimer's disease and Down's syndrome. Additionally it acts as an inhibitor of the ubiquitin-dependent protein degradation in vitro. | |||
T80035 |
Biotin-β-Amyloid (1-42), human TFA
Biotin-amyloid β-peptide (1-42) (human) TFA |
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Biotin-β-Amyloid (1-42), human TFA(Biotin-Amyloid β-Peptide (1-42) (human) TFA)是一种标记有生物素的β-Amyloid (1-42)肽,由42个氨基酸构成,对阿尔茨海默病的发病机理有重要作用。 | |||
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.... | |||
T32106 |
Human beta-amyloid protein 42 (1-7)
Vanutide |
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Human beta-amyloid protein 42 (1-7) is a bioactive chemical. | |||
T1404 |
Stavudine
d4T,Sanilvudine,BMY-27857,NSC 163661,司他夫定 |
Apoptosis; Nucleoside Antimetabolite/Analog; HIV Protease; NOD-like Receptor (NLR); Reverse Transcriptase; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Stavudine (BMY-27857) 是一种口服活性核苷逆转录酶抑制剂,还抑制线粒体 DNA 的复制,具有抗HIV-1和HIV-2的活性。它降低 NLRP3 炎症小体激活,调节淀粉样 β 自噬,诱导细胞凋亡。 | |||
T80699 |
β Amyloid(28-35) human
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β Amyloid(28-35) human 是一种具有神经毒性的β-淀粉样肽,能够与神经元膜结合,影响其二级结构并加剧阿尔茨海默病的神经毒性。该肽段对酸性磷脂DPH表现出非均向性作用,从而增加脂质膜双层内部的流动性。该核心片段由脂质诱导形成。 | |||
T80700 |
β Amyloid(17-28) human
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β Amyloid(17-28) human 为β-淀粉样肽(Abeta)的一段核心片段,其结构受脂质诱导。本化合物能够促进β Amyloid40全长肽段的聚集,导致阿尔茨海默病(AD)中具毒性的聚集体形成。 | |||
T75930 |
β-Amyloid (1-43)(human) TFA
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β-Amyloid (1-43)(human) TFA 相较于 Aβ1-42 显示出更高的聚集倾向和毒性。它与 sAPPα 和 sAPPβ 有关联,且作为一种潜在的新型阿尔茨海默病(AD)生物标志物,具备与其他已知生物标志物相似的应用潜力。 | |||
T75926 |
β-Amyloid (42-1), human TFA
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β-Amyloid (42-1), human TFA 为淀粉样蛋白β肽(1-42)的无活性形式,包含42个氨基酸,对阿尔茨海默病发病机制扮演关键角色。 | |||
T80695 |
β-Amyloid precursor protein (96-110), cyclized (human)
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β-Amyloid precursor protein (96-110), cyclized (human) 为一种淀粉样前体蛋白衍生物,特别适用于阿尔茨海默病相关研究。 | |||
TP1140L |
Neuropeptide Y (29-64), amide, human acetate
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Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Neuropeptide Y (29-64), amide, human acetate 参与阿尔茨海默病 (AD) 并保护大鼠皮质神经元免受 β-淀粉样蛋白毒性。 | |||
T77042 |
Aducanumab
BIIB037 |
Beta Amyloid | Neuroscience |
Aducanumab (BIIB037),一种选择性人免疫球蛋白γ-1(IgG1)单克隆抗体,靶向β淀粉样蛋白 (Aβ) 的聚集形式。Aducanumab 显示出脑渗透性,可用于治疗阿尔茨海默病 (AD) 。 | |||
T13253 |
Umibecestat
CNP520 |
BACE | Neuroscience |
Umibecestat 是一种β-位点淀粉样前体蛋白裂解酶-1 (BACE-1) 抑制剂,对人 BACE-1 和小鼠 BACE-1 的 IC50 分别为 11 nM 和 10 nM,可用于阿尔茨海默病的研究。 | |||
T6202 |
DAPT
LY-374973,GSI-IX |
Apoptosis; Beta Amyloid; Gamma-secretase; Autophagy | Apoptosis; Autophagy; Neuroscience; Proteases/Proteasome; Stem Cells |
DAPT (LY-374973) 是一种 γ 分泌酶抑制剂,抑制总 Aβ 和 Aβ42 (IC50=115/200 nM),具有口服活性。DAPT 也是一种 Notch 抑制剂。DAPT 可以诱导细胞分化、诱导细胞自噬和凋亡。 | |||
T36446 |
Neuropeptide Y (human) (TFA)
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Neuropeptide Y (human) TFA, a compound implicated in Alzheimer's disease (AD), exhibits protective effects against β-Amyloid toxicity in rat cortical neurons. | |||
T80701 |
β Amyloid (1-16) rat
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β-Amyloid (1-16) rat 是β-淀粉样肽 (Abeta) 金属结合域的片段,含有三个与人类相异的氨基酸替代,因此在大鼠和小鼠中降低了 AD 样神经退行性变的易感性。 | |||
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 | |||
T76683 | Gantenerumab | ||
Gantenerumab是一种完全人源化IgG1型抗Aβ (淀粉样蛋白β)单克隆抗体,具有持续的脑内Aβ结合能力,用于阿尔茨海默病的研究。 | |||
T75730 |
[D-Arg25]-Neuropeptide Y (human)
|
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[D-Arg25]-Neuropeptide Y (human) ([D-Arg25] NPY) 是Y1受体的选择性激动剂。与阿尔茨海默病相关,该化合物能够保护老鼠皮质神经元免受淀粉样蛋白毒性的损害。 | |||
T31828 |
AZD4694
Flutafuranol,AZD 4694,NAV-4694,AZD-4694,NAV 4694,NAV4694 |
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Flutafuranol, also known as AZD 4694 and NAV4694, is a bio-active chemical. AZD4694 shows high affinity for beta-amyloid fibrils in vitro (K(d) = 2.3 +/- 0.3 nM). The fluorine-18 labeled AZD4694 may have potential for PET-visualization of cerebral beta-am | |||
T39678 | Multitarget AD inhibitor-1 | ||
Multitarget AD inhibitor-1 is a reversible and selective inhibitor of butyrylcholinesterase (BuChE) with IC50 values of 7.22 μM and 1.55 μM for human BuChE (hBuChE) and equine serum BuChE (eqBuChE), respectively. Additionally, it exhibits inhibitory activity towards β-secretase (IC50 value of 41.60 μM), amyloid β aggregation (IC50 value of 3.09 μM), and tau aggregation. As a diphenylpropylamine derivative, Multitarget AD inhibitor-1 holds promise for research pertaining to the multifunctional, d... | |||
T36911 |
Pramlintide (acetate hydrate)
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Pramlintide is a non-amyloidogenic analog of the antidiabetic peptide hormone amylin that contains proline residues substituted at positions 25, 28, and 29. It stimulates cAMP production in HEK293 cells expressing human amylin receptor 1a (AMY1a), AMY2a, and AMY3a (EC50s = 0.35, 22.9, and 0.89 nM, respectively). Pramlintide inhibits human islet amyloid polypeptide fibrilization in a concentration-dependent manner. In vivo, pramlintide (200 pg/kg) reduces brain levels of amyloid-β (1-40) and incr... | |||
T72454 |
AChE/BChE/MAO-B-IN-4
|
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AChE/BChE/MAO-B-IN-4 是一种 1-茚满酮衍生物,是一种有效的MAO-B 抑制剂,对人MAO-B 的IC50为 0.0359 μM。AChE/BChE/MAO-B-IN-4 是一种有效的AChE 和BChE 酶抑制剂,对人AChE 和BChE 酶的IC50值分别为 0.0473 μM 和 0.0782 μM。AChE/BChE/MAO-B-IN-4 显示出显着的抗氧化活性,并防止β-淀粉样蛋白斑块聚集。AChE/BChE/MAO-B-IN-4 具有用于阿尔茨海默病 (AD) 研究的潜力。 | |||
T78739 |
PD07
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PD07是一种口服AChE抑制剂,对hAChE的IC50为0.29 μM。体外实验表明PD07也能抑制ChE、BACE1(IC50:13.42 μM)和Aβ1-42的聚集。作为抗氧化剂,PD07显示出DPPH抑制活性(IC50:26.46 μM),能改善因Scopolamine诱导而失忆的大鼠的记忆和认知功能。该化合物适用于阿尔茨海默病的研究。 |