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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5447 |
Anle138b
|
Beta Amyloid; Others | Neuroscience; Others |
Anle138b 是一种毒性低,口服生物利用度高,血脑屏障通透性好的低聚物聚集抑调节剂,可阻断朊病毒蛋白和 α-突触核蛋白病理性聚集的形成。它在体内强烈抑制低聚物积累、神经元变性和疾病进展。它阻断 Aβ 通道并挽救淀粉样变性小鼠模型的疾病表型。 | |||
T22012 |
7BIO
|
FLT; DYRK; Aurora Kinase | Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors |
7BIO 是靛玉红的衍生物,抑制细胞周期蛋白依赖性激酶5 和糖原合酶激酶-3β。它抑制 Aβ 寡聚体诱导的神经炎症、突触损伤、tau 过度磷酸化、星形胶质细胞和小胶质细胞的活化,并减轻 Aβ 寡聚体诱导的小鼠认知障碍。 | |||
T6909 |
NSC348884
N1,N1,N2,N2-四[(6-甲基-1H-苯并咪唑-2-基)甲基]-1,2-乙二胺 |
Apoptosis; p53 | Apoptosis |
NSC348884 是一种核磷蛋白抑制剂,可破坏寡聚体形成并诱导细胞凋亡,在不同的癌细胞系中以 IC50 为 1.7-4.0 μM 抑制细胞增殖。 | |||
T10789 |
Chitosan oligosaccharide
COS,壳聚糖低聚乳酸酯 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Chitosan oligosaccharide (COS) 是 β-(1→4)-连接的 D-氨基葡萄糖的寡聚体,Chitosan oligosaccharide可激活 AMPK ,抑制NF-κB 和 MAPK在内的炎症信号通路。 | |||
T12532 |
PQM130
|
Beta Amyloid | Neuroscience |
PQM130是一种魏罗酮-多奈哌齐杂化化合物,能透过大脑。PQM130是多靶点的候选药物,可用于Aβ1-42低聚物引起的神经毒性,还具有抗炎活性。它是具有神经保护作用的、有潜力的抗 AD 药物。 | |||
T14199 |
ALZ-801
Valiltramiprosate |
Beta Amyloid | Neuroscience |
ALZ-801 是一种可口服的小分子 β-淀粉样蛋白抗寡聚体和聚集抑制剂,是曲米酸的缬氨酸偶联前药,与母体化合物相比,具有显著改善的 PK 特性和胃肠道耐受性。它是治疗阿尔茨海默病的先进且显著改善的候选药物。 | |||
T38860 |
Golodirsen
Golodirsen,SRP-4053 |
||
Golodirsen (SRP-4053) is a phosphorodiamidate morpholino oligomer (PMO) designed to selectively bind and target exon 53 of dystrophin pre-mRNA, with applications in the investigation of Duchenne muscular dystrophy (DMD). | |||
T24779 | SEN-1269 | ||
SEN-1269 is an amyloid-β (AB) aggregation inhibitor that acts by blocking Aβ(1-42) aggregation and protecting neuronal cell lines exposed to Aβ(1-42), reducing Aβ oligomer-induced LTP and memory deficits in vivo. | |||
T34418 |
RS-0406
RS0406,Phenol |
||
RS-0406 is a new type of β-flakes blocker, which can reverse amyloid β-induced cytotoxicity and long-term enhanced damage in vitro, and inhibit amyloid-oligomer-induced behavior deterioration in vivo. | |||
T21097 |
Decamethyltetrasiloxane
Tetrasiloxane, decamethyl-,decamethyl-tetrasiloxan,D3780 |
||
Decamethyltetrasiloxane, a non-cyclic silicone oligomer, is used in the methylation of mercury(II) salts. It is transformed by a specific microflora. In the natural environment, it is degraded by mechanisms similar to other organic compounds. | |||
T38859 |
Casimersen
SRP-4045 |
||
Casimersen (SRP-4045) is an antisense oligonucleotide, specifically belonging to the phosphorodiamidate morpholino oligomer subclass. It binds to exon 45 of dystrophin pre-mRNA, effectively restoring the open-reading frame by skipping exon 45. This action ultimately leads to the production of a functional dystrophin protein, albeit internally truncated. Casimersen finds utility in Duchenne muscular dystrophy (DMD) research. | |||
T83173 | Activated T Subunit | ||
Activated T Subunit 用于合成可诱导外显子51跳跃的外显子跳跃寡聚物偶联物。该寡聚物偶联物与人类抗肌萎缩蛋白基因中选定靶位点互补,适用于肌肉萎缩症研究。 | |||
T83175 |
Activated DPG Subunit
|
||
Activated DPG Subunit 用于合成可诱导外显子 51 跳跃的外显子跳跃寡聚物偶联物。这些偶联物与人抗肌萎缩蛋白基因中选定的靶位点互补,有助于肌肉萎缩症的研究。 | |||
T81912 | LSP-GR3 | iGluR | Membrane transporter/Ion channel; Neuroscience |
LSP-GR3为一种新型化学修饰RNA寡核苷酸,亦即剪接调控寡聚体(SMOs),可特异性调控中枢神经系统内GluR的选择性剪接及GluR3-flip表达。 | |||
T81693 |
NCP2 Anchor
|
||
NCP2 Anchor用于合成外显子跳跃寡聚物偶联物。它的偶联物与人抗肌萎缩蛋白基因特定靶位点配对互补,从而诱导外显子52的跳跃。该偶联物常应用于肌肉萎缩症的科学研究。 | |||
T71855 |
Z640
|
||
Z640 an aPKC agonist. Z640 was further confirmed as a non‑selective aPKC agonist that can activate the kinase activity of both PKCι and PKCζ. In the cell‑based assay, Z640 was found to protect neuronal cell lines from amyloid‑β (Aβ) oligomer‑induced cell death by reducing reactive oxygen species production and restore mitochondrial function. In addition, Z640 could reduce Aβ40 generation in a dose‑dependent manner and shift amyloid precursor protein processing towards the non‑amyloid pathway | |||
T83176 | Activated C Subunit | ||
Activated C Subunit 用于合成可诱导外显子51跳跃的外显子跳跃寡聚物偶联物。所得寡聚物偶联物与人类抗肌萎缩蛋白基因特定靶位点互补,有助于研究肌肉萎缩症。 | |||
T76395 |
(Met(O)35)-Amyloid β-Protein (1-42)
|
||
'(Met(O)35)-Amyloid β-Protein (1-42),Aβ42的一种氧化形态,位于Met35。该化合物可形成与Aβ40具有相似大小和分布特征的寡聚体,适用于阿尔茨海默病(AD)研究。' | |||
T83177 | Activated A Subunit | ||
Activated A Subunit 适用于合成促进外显子跳跃的寡聚物偶联体。所合成的偶联体与人类抗肌萎缩蛋白基因内特定的序列配对互补,能够有效促进外显子51的跳跃,为肌萎缩疾病研究提供了一种工具。 | |||
T83174 | Activated EG3 Tail | ||
Activated EG3 Tail 适用于合成外显子跳跃寡聚物偶联物。该寡聚物偶联物能与人类抗肌萎缩蛋白基因特定的靶位点匹配,进而诱导外显子 51 的跳跃。此类偶联物对于肌肉萎缩症研究具有重要价值。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5650 |
2,2':5',2''-Terthiophene
alpha-三联噻吩,α-Terthienyl,Trithiophene |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
2,2':5',2''-Terthiophene (Trithiophene) 是杂环噻吩的低聚物,可用作有机合成的砌块 。 | |||
T2S0633 |
Raspberry ketone
Oxyphenalon,Rasketone,Aloenin,4-(4-Hydroxyphenyl)-2-butanone,p-Hydroxybenzyl acetone,Frambinone,覆盆子酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Raspberry ketone (p-Hydroxybenzyl acetone) 是覆盆子中主要的芳香族天然产物,主要用作化妆品的香料和食品增味剂,也可作 PPAR-α激动剂。 | |||
T38555 |
Chitotetraose tetrahydrochloride
|
||
Chitotetraose tetrahydrochloride is a short-chain chitin oligomer derived from arbuscular mycorrhizal (AM) fungi. This compound effectively activates the conserved symbiosis signaling pathway (CSSP) in actinorhizal plant species. | |||
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]. | |||
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]. | |||
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]. | |||
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]. | |||
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]. | |||
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。 |