101
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9641 |
Aβ42-IN-2
|
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Aβ42-IN-2 是一种 γ-secretase 调节剂。Aβ42-IN-2 对 Αβ42 的 IC50 值为 6.5 nM 。Aβ42-IN-2 可用于阿尔茨海默症相关的研究。 | |||
T10211 |
Aβ42-IN-1
|
Others | Others |
Aβ42-IN-1,化合物 1v,是一种新型有效且具有口服活性的 γ 分泌酶调节剂 (GSM)。 Aβ42-IN-1 在不抑制 CYP3A4 的情况下,在培养细胞中有效降低Aβ42水平,IC50值为 0.091 μM。Aβ42-IN-1 显示出良好的药代动力学特征。 | |||
T10443 |
Aβ42-IN-1 free base
|
Others | Others |
Aβ42-IN-1 free base是一种口服活性的γ-secretase调节剂,具有高暴露度。该化合物能显著降低小鼠脑中Aβ42的水平,IC50为0.091 μM,显示出在阿尔茨海默病研究中的潜力。 | |||
T75174 |
Anti-inflammatory agent 42
|
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
Anti-inflammatory agent 42 具有抗炎活性,抑制 LPS 刺激的巨噬细胞 TNF-α 和 IL-6 的表达。 | |||
T6392 |
AR42
OSU-HDAC42,AR-42,(S)-(+)-N-羟基-4-(3-甲基-2-苯基丁酰氨基)苯甲酰胺,AR 42,HDAC-42 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
AR42 (OSU-HDAC42) 是一种 HDAC 抑制剂(IC50: 30 nM)。 | |||
T16321 |
NI-42
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
NI-42 是一种用于 BRPF 的结构正交化学探针,是有偏向性的BRPFs 溴结构域 (BRD)抑制剂,BRPF1、2和3的IC50为7.9、48和260 nM; BRPF1、2和3的Kd 值为40、210和940 nM,与非分类 IV BRD 蛋白相比具有很好的选择性。 | |||
T27029 |
cjoc42
cjoc 42,cjoc-42 |
||
Cjoc42 是gankyrin 的抑制剂, 以剂量依赖性方式抑制 gankyrin 活性。它可防止 p53 蛋白水平的降低。它恢复 p53 依赖性转录和对 DNA 损伤的敏感性。 | |||
T12268 |
NTP42
|
Prostaglandin Receptor; PPAR | DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism |
NTP42 是血栓素 A2 (TXA2) 受体的拮抗剂,IC50为 3.278 nM,可用于肺动脉高压的相关研究。 | |||
T32108 |
HXJ42
HXJ-42,HXJ 42 |
Others | Others |
HXJ42 是一种 PP1 类似物,可选择性地有效作用于野生型 ZAP-70 (AS)。 | |||
T20981 |
CES1-IN-42
2,2-Dimethoxy-1,2-diphenylethanone,2,2-Dimethoxy-2-phenylacetophenone |
Others | Others |
CES1-IN-42 (2,2-Dimethoxy-2-phenylacetophenone) 是一种光引发剂,可用于协助研究癌症。 | |||
TP1007L |
β-Amyloid (1-42), acetate (human)
β-Amyloid (1-42), human acetate (107761-42-2 Free base) |
||
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。 | |||
T22678 |
3,5-Bis(4-nitrophenoxy)benzoic acid
3,5-二(4-硝基苯氧基)苯甲酸,Compound W |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
3,5-Bis(4-nitrophenoxy)benzoic acid (Compound W) 是 γ-secretase 抑制剂。它导致 Aβ42 和 notch-1 Aβ-like peptide 25 (Nβ25) 的释放水平降低。它是母体血清中 3,3’-diiodothyronine sulfate (T2S) 的交叉反应物质,可作为胎儿甲状腺功能减退的标志物。 | |||
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。 | |||
T36536 |
SH-42
|
||
SH-42 is an inhibitor of 24-dehydrocholesterol reductase (DHCR24; IC50= 4.2 nM).1It increases serum levels of desmosterol , the immediate precursor of cholesterol in the Bloch pathway, in mice when administered at a dose of 0.5 mg/animal per day. SH-42 increases levels of arachidonic acid and its metabolite prostaglandin E2, as well as docosahexaenoic acid and its metabolites 19,20-EpDPA and 19,20-DiHDPA, in the peritoneal lavage fluid in a mouse model of peritonitis induced by zymosan A .2 | |||
T38867 | Antibacterial agent 42 | ||
Antibacterial Agent 42 demonstrates potent antibacterial activity by effectively reducing the Minimum Inhibitory Concentration (MIC) of the broad-spectrum antibacterial agent Ceftazidime. | |||
T37589 |
GIP (3-42), human
Gastric Inhibitory Polypeptide (3-42) (human) |
IGF-1R | Tyrosine Kinase/Adaptors |
GIP (3-42), human (Gastric Inhibitory Polypeptide (3-42) (human)) 是一种多肽,可充当葡萄糖依赖性促胰岛素多肽 (GIP) 受体拮抗剂,在体内调节胰岛素分泌和 GIP 的代谢作用,可用于研究2型糖尿病。 | |||
T80370 |
Maximin 42
|
||
Maximin 42为一抗菌肽,针对S. aureus表现出抗菌活性(MIC: 37.5 μg/mL),同时对人红细胞具溶血活性。 | |||
T61630 | HDAC-IN-42 | ||
HDAC-IN-42 (compound 14f) is a highly potent and selective inhibitor of histone deacetylase (HDAC) enzymes, with IC50 values of 0.19 μM for HDAC1 and 4.98 μM for HDAC6. It exhibits remarkable anticancer properties and inhibits cell proliferation. Additionally, HDAC-IN-42 induces apoptosis and causes cell cycle arrest specifically at the G2/M phase [1]. | |||
T64029 | Antifungal agent 42 | ||
Antifungal agent 42 是一种抗真菌剂,对生物膜形成具有抑制作用。Antifungal agent 42 能够抑制 C.alb.的 lanosterol 14α-demethylase (CYP51)。 | |||
T61777 | Anticancer agent 42 | ||
Anticancer agent 42 (compound 10d) is an orally active, potent anticancer agent with demonstrated efficacy against MDA-MB-231 cells, exhibiting an IC50 of 0.07 μM. It exerts its anticancer activity through the activation of apoptotic pathways and p53 expression. Anticancer agent 42 is a valuable tool for investigating metastatic breast cancer [1]. | |||
T70469 |
AK-42
|
||
AK-42 is a novel potent and specific inhibitor of CLC-2, displaying unprecedented selectivity over CLC-1, the closest CLC-2 homolog, and exhibiting no off-target engagement against a panel of 61 common channels, receptors, and transporters expressed in brain tissue. | |||
T74457 | EGFR-IN-42 | ||
EGFR-IN-42 (Compound 17b) 是一种有效的 EGFR 抑制剂,具有单位数纳摩尔活性。EGFR-IN-42 通过共价键将他莫昔芬或安多昔芬与 EGFR 抑制剂吉非替尼连接起来。EGFR-IN-42 保留 ER 拮抗剂活性和 EGFR 抑制作用。EGFR-IN-42 具有优越的抗癌活性。 | |||
T83186 | AChE-IN-42 | ||
AChE-IN-42(Compound 28)是一种有效的乙酰胆碱酯酶(AChE)抑制剂,其抑制常数(Ki)为0.44 μM。 | |||
T82203 |
Hexapeptide-42
|
||
Hexapeptide-42,一种具备生物活性的肽,常作为化妆品成分应用。 | |||
T80708 |
α-Glucosidase-IN-42
|
Glucosidase | Metabolism |
α-Glucosidase-IN-42(Compound 26)是一种9-O-小檗红素羧酸衍生物,展现出明显的α-葡萄糖苷酶抑制活性,其IC50值约为1.61 μM。此化合物适用于抗糖尿病研究领域。 | |||
T82100 |
ICMT-IN-42
|
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ICMT-IN-42 (化合物21)为一种有效的ICMT抑制剂,其IC50值为0.054 μM。 | |||
T83015 | Antiproliferative agent-42 | ||
Antiproliferative agent-42(compound 7m)为一种二氢双吡咯化合物,在Panc-1细胞系上显示出明显的抗增殖活性,其IC50值为12.54 μM。 | |||
T79268 | Tubulin polymerization-IN-42 | ||
Tubulin polymerization-IN-42(compound 10j)是一种具有抗癌活性的吲哚取代呋喃酮类微管蛋白聚合抑制剂。 | |||
T64071 | Antitumor agent-42 | ||
Antitumor agent-42 能够抑制微管多聚和 NO 释放,表现出抗血管生成、抑制集落形成和诱导凋亡作用。 | |||
T76393 |
Amyloid 17-42
|
||
Amyloid 17-42 (Aβ(17-42)),作为阿尔茨海默病中弥漫性斑块与唐氏综合症小脑前区的主要淀粉样蛋白成分,源于淀粉样蛋白前体蛋白(APP)经α与γ分泌酶的裂解作用。此外,Amyloid 17-42能通过Fas样/caspase-8途径促使神经细胞发生凋亡。 | |||
T78724 |
Acryl42-10
|
SARS-CoV | Microbiology/Virology |
Acryl42-10为针对SARS-CoV-2 Nsp14 N7-甲基转移酶的共价抑制剂,其半抑制浓度(IC50)为7 μM。 | |||
T37367 |
Amyloid-β (1-42) Peptide (trifluoroacetate salt)
|
||
Amyloid-β (1-42) (Aβ42) is a neurotoxic 42-amino acid protein fragment found in amyloid plaques in postmortem cerebral cortex from patients with Alzheimer's disease.1,2,3Aggregation of Aβ42 results in the formation of neurotoxic fibrils or globular oligomers.1Aβ42 accumulates in the brain of many transgenic mouse models of Alzheimer's disease and, in many models, the onset of amyloid deposition positively correlates with deficits in spatial learning and memory.4 1.Wolfe, M.S.Therapeutic strategi... | |||
T64238 | Aβ1–42 aggregation inhibitor 1 | ||
Aβ1-42 aggregation inhibitor 1 抑制乙酰胆碱酯酶 AChE 和丁酰胆碱酯酶 BuChE 的 IC50值分别为 2.64 μM 和 1.29 μM。Aβ1-42 aggregation inhibitor 1 是一种可以自身介导的Aβ1-42聚集抑制剂,在浓度为 25 μM 抑制 51.29%。Aβ1-42 aggregation inhibitor 1 可用于抗阿尔兹海默症的研究。 | |||
T78926 |
SARS-CoV-2-IN-42
|
SARS-CoV | Microbiology/Virology |
SARS-CoV-2-IN-42(Compound 8q)是一种有效的SARS-CoV-2复制抑制剂,具有较低的半抑制浓度(EC50: 0.4 μM),且对宿主细胞无明显毒性。 | |||
T60940 | ChE/Aβ1-42-IN-1 | ||
ChE/Aβ1-42-IN-1 (compound 28) 是一种有效的ChE 和Aβ1-42聚集抑制剂,具有良好的血脑屏障通透性。ChE/Aβ1-42-IN-1 对 AChE、BuChE 和 Aβ1-42聚集的IC50值分别为 0.062、0.767和1.227 μM。ChE/Aβ1-42-IN-1 是一种有效的多靶点抗阿尔茨海默病剂。 | |||
T61388 |
hAChE/Aβ1-42-IN-1
|
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hAChE/Aβ1-42-IN-1 (Compound 16) 是一种有效的 hAChE 和 Aβ1-42聚集抑制剂。hAChE/Aβ1-42-IN-1 对 hepG2 细胞系显示出可接受的相对安全性,并具有良好的 BBB 渗透性和较宽的安全范围。hAChE/Aβ1-42-IN-1具有研究阿尔茨海默病 (AD) 的潜力。 | |||
T83123 |
Amyloid β-Protein (3-42)
|
||
Amyloid β-Protein (3-42) 为Pyr肽前体, 其焦谷氨酸修饰的形式 Aβ (pEAβ) (3-42) 构成阿尔茨海默病淀粉样斑块的关键。pEAβ (3-42) 能促进 Aβ(1-42) 聚集,并且 Aβ(1-42) 显著延缓pEAβ(3-42) 的初级及次级成核过程。 | |||
T62287 | HIV-1 inhibitor-42 | ||
HIV-1 inhibitor-42 (compound 5b) 是一种 HIV-1 的有效抑制剂 (IC50: 0.06 μM)。HIV-1 inhibitor-42 能够抑制 HIV-1 RT RNA 依赖性 DNA 聚合酶 (IC50: 0.518 μM) 和 DNA 依赖性 DNA 聚合酶 (IC50: 0.072 μM) 。 | |||
T76401 |
Amyloid β-Protein (33-42) (TFA)
|
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Amyloid β-Protein (33-42) TFA,β-淀粉样蛋白残基的33-42段,能够抑制Aβ42诱导的毒性。 | |||
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。 | |||
T37589L |
GIP (3-42), human acetate
GIP (3-42), human acetate(1802086-25-4 Free base) |
IGF-1R | Tyrosine Kinase/Adaptors |
GIP (3-42), human acetate 是葡萄糖依赖性促胰岛素多肽 (GIP) 受体的拮抗剂,可调节体内胰岛素分泌和 GIP 代谢。 | |||
T37472 |
TAMRA-Amyloid-β (1-42) Peptide (trifluoroacetate salt)
|
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TAMRA-Amyloid-β (1-42) peptide is a fluorescently labeled peptide. Amyloid-β (1-42) (Aβ42) is a neurotoxic 42-residue protein fragment found in amyloid plaques in postmortem cerebral cortex from patients with Alzheimer's disease. Aggregation of Aβ42 results in the formation of neurotoxic fibrils or globular oligomers. TAMRA-Amyloid-β (1-42) peptide is a labeled form of Aβ42 containing carboxytetramethyl rhodamine (TAMRA), which displays excitation/emission maxima of 543/572 nm, respectively. | |||
T37200 |
Biotin-Amyloid-β (1-42) Peptide (trifluoroacetate salt)
|
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Biotin-amyloid-β (1-42) peptide is an affinity probe that allows amyloid-β (1-42) (Aβ42) to be detected or immobilized through interaction with the biotin ligand. It has been used to identify Aβ42 interaction partners in rat hippocampal synaptosomal membranes. | |||
T64095 |
KRAS G12C inhibitor 42
|
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KRAS G12C inhibitor 42 是 KRAS G12C 的有效抑制剂。其中 Ras 蛋白家族是一种重要的细胞内信号分子,在生长发育中发挥着重要作用。KRAS G12C inhibitor 42 对 KRAS G12C 介导的癌症表现出研究潜力。 | |||
T76425 |
(Glu20)-Amyloid β-Protein (1-42)
|
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(Glu20)-Amyloid β-Protein (1-42) 是一种具有 Glu20 突变的淀粉样蛋白β (Aβ) 变体,该变体的原纤维化速度较慢。此突变能够减少 Aβ 的聚集倾向,进而阻止缓慢原纤化肽的累积。它是阿尔茨海默病中血管及脑内淀粉样沉积物的关键组成部分。 | |||
T83694 |
Gastric Inhibitory Peptide (1-42) (porcine) TFA
GIP (1-42),Glucose-dependent Insulinotropic Polypeptide (1-42) |
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胃抑制肽(GIP) (1-42)是一种内源性的42氨基酸肽类肠促素激素,能诱导胰岛素分泌。该激素在肠道神经内分泌K细胞和颌下腺中表达,并在餐后释放到循环中。GIP (1-42)抑制由组胺、五肽和胰岛素引起的胃酸和胃蛋白酶分泌,增加葡萄糖诱导的胰岛素释放,并在大鼠中刺激胃排空。 | |||
T76625 |
(Lys22)-Amyloid β-Protein (1-42)
|
||
(Lys22)-Amyloid β-Protein (1-42) 是 WT Amyloid β-Protein (1-42) 肽的突变。 | |||
T76424 |
(Gly22)-Amyloid β-Protein (1-42)
|
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(Gly22)-Amyloid β-Protein (1-42) 为淀粉样蛋白β-蛋白(Aβ)的一种肽段,主要在阿尔茨海默病患者的血管和脑组织中形成淀粉样沉积。Aβ中Glu22至Gly22的突变显著促进了该蛋白的聚集。 | |||
T76588 |
(Asp37)-Amyloid β-Protein (1-42)
|
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(Asp37)-Amyloid β-Protein (1-42) 是野生型 Amyloid-beta (1-42) 肽的 G37D 突变体。 | |||
T76434 |
Biotinyl-Amyloid β-Protein (1-42) (ammonium)
|
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Biotinyl-Amyloid β-Protein (1-42) ammonium 是一种生物素化的 Amyloid β-Protein (1-42). Amyloid β-Protein (1-42) ammonium 可用于 Aβ1-42 在大脑中转化为 Aβ1-40 的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0883 |
Tramiprosate
Homotaurine,3-Amino-1-propanesulfonic acid,Alzhemed,高牛黄酸 |
Beta Amyloid; GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Tramiprosate (Alzhemed) 是一种具有口服活性的、可透过血脑屏障的天然氨基酸,存在于各种红色海藻中,能够可溶性 Aβ 结合并以非原纤维形式维持 Aβ。它是一种 GABA 类似物,具有神经保护,抗惊厥和抗高血压的活性。 | |||
T1686 |
Hematoxylin
苏木精,Hydroxybrazilin,Natural Black 1,Haematoxylin |
Beta Amyloid; Others | Neuroscience; Others |
Hematoxylin (Natural Black 1) 是一种天然存在的类黄酮化合物,衍生自木柴树Haematoxylon campechianum。它是一种组织学上的核染色剂,也是一种有效的Aβ42原纤维形成的抑制剂,IC50=1.6 µM。 | |||
TN7246 |
3-Sulfopropanoic acid
3-SPA |
Drug Metabolite | Metabolism |
3-Sulfopropanoic acid 是曲吡罗酯及其前药ALZ-801的主要代谢产物,是存在于AD患者的脑脊液(CSF)中的内源性分子,可抑制 Aβ42 寡聚体的形成。 | |||
T4S0350 |
Licochalcone B
甘草查尔酮 B,甘草查尔酮B |
Beta Amyloid; Others | Neuroscience; Others |
Licochalcone B 是从Glycyrrhiza inflate 根中提取的。它能够抑制淀粉样蛋白 β 自聚集作用 (IC50=2.16 μM) ,分解预先形成的 Aβ42原纤维,并通过螯合金属离子抑制金属诱导的 Aβ42聚集。 | |||
T83407 | 2',3'-Dihydroxy-4',6'-dimethoxychalcone | ||
2',3'-Dihydroxy-4',6'-dimethoxychalcone 能够抑制β淀粉样蛋白(Aβ42)的纤维化与聚集,并具有口服活性,在大脑中可进行检测。 |