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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7369L |
Gemigliptin Tartrate(911637-19-9 free base)
吉格列汀酒石酸盐,LC15-0444 tartrate |
Proteasome; DPP-4 | Proteases/Proteasome; Ubiquitination |
Gemigliptin Tartrate (LC15-0444 tartrate) 是一种选择性的,可逆的,竞争性的二肽基肽酶 4 (DPP-4) 抑制剂,对于人重组 DPP-4 的IC50=10.3 nM。Gemigliptin tartrate 具有很强的抗糖基化活性,能够用于晚期糖基化终产物相关的糖尿病并发症的研究。 | |||
T11877 |
LR-90
|
Others | Others |
LR-90, 作为一种高级糖基化终产品(AGE)抑制剂,在糖尿病动物模型研究中被广泛使用。LR-90 有效地抑制了人类单核细胞中的炎症反应。 | |||
T7143 |
Alagebrium chloride
4,5-二甲基-3-(2-氧代-2-苯基乙基)噻唑氯化物,ALT711,阿拉氯胺 |
Others; Endogenous Metabolite | Metabolism; Others |
Alagebrium chloride (ALT711) 是晚期糖基化终产物(AGE) 抑制剂。 | |||
T2507 |
Azeliragon
TTP488,阿齐瑞格 |
Beta Amyloid; advanced glycation end products | Neuroscience; Others |
Azeliragon (TTP488) 是一种生物可利用的、可穿过血脑屏障 (BBB)的晚期糖基化终产物 (RAGE) 受体抑制剂,可缓解轻度阿尔茨海默病 (AD) 的发展。 | |||
T8583 |
Tenilsetam
替尼西坦,3-(2-thienyl)- (9CI),Piperazinone |
Others | Others |
Tenilsetam (Piperazinone) 是一种核酸内切酶调节剂;一种促智剂和晚期糖基化终产物 (AGE) 抑制剂,具有治疗阿尔茨海默病 (AD) 的潜力。 | |||
T32098L |
Homocarnosine acetate
|
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Homocarnosine acetate 是大脑特有的二肽,由 γ-氨基丁酸 (GABA) 和组氨酸组成。它具有抗氧化和抗炎作用、预防 DNA 损伤和抑制晚期糖基化终产物形成 | |||
TP1935L1 |
RAGE antagonist peptide acetate
|
Beta Amyloid | Neuroscience |
RAGE antagonist peptide acetate 是一种高级的糖基化终产物 (RAGE) 拮抗剂。 它具有抗肿瘤和抗炎活性。 它可防止 RAGE 与其几个重要的配体结合,包括 HMGB-1、S100P 和 S100A4。 | |||
T39115 |
ABR-238901
|
TLR | Immunology/Inflammation |
ABR-238901是一种可口服的、有作用的 S100A8/A9阻滞剂,对 S100A8/A9与其受体 RAGE(晚期糖基化终产物受体)和TLR4 (toll 样受体4)的相互作用具有抑制作用。ABR-238901具有作为治疗心肌梗死(MI)化合物的潜力。 | |||
T9948 |
NecroX-7
LC-280126,LC28-0126,LC28 0126 |
NADPH-oxidase | Immunology/Inflammation |
NecroX-7 (LC-280126) 是一种有效的自由基清除剂和 HMGB1(高迁移率族蛋白 1) 抑制剂。NecroX-7 可以作为对乙酰氨基酚毒性的解毒剂。NecroX-7 通过抑制缺血/再灌注损伤中 HMGB1 的释放发挥保护作用。NecroX-7 抑制 HMGB1 诱导的 TNF 和 IL-6的释放,以及TLR-4和晚期糖基化终产物受体的表达,用于移植物抗宿主病 (GVHD) 研究。 | |||
T29819 |
Alagebrium bromide
ALT-711,ALT 711,ALT711 |
||
Alagebrium is a advanced glycation endproducts (AGE) cross-link breaker. | |||
T2507L2 |
Azeliragon HCl
TTP488 HCl,Azeliragon hydrochloride,TTP 488,Azeliragon dihydrochloride,TTP-488 |
||
Azeliragon is a potent and orally active inhibitor of RAGE (receptor for advanced glycation endproducts), a pattern recognition receptor, which affects the movement of amyloid, an Alzheimer's-associated protein, into the brain. | |||
T34066 |
Pimagedine
Monoaminoguanidine,Imino semicarbazide,Guanyl hydrazine,Aminate base,Aminoguanidine |
||
Pimagedine 是一种预防晚期糖基化终产物形成的原型治疗剂。Pimagedine 与α、β-二羰基化合物(如甲基乙二醛、乙二醛和3-脱氧葡糖酮)快速反应,防止晚期糖基化终产物(AGEs)的形成。 | |||
T70059 | ALT-946 HCl | ||
ALT-946 HCl is an inhibitor of advanced glycation that has been shown to improve severe nephropathy in the diabetic transgenic (mREN-2)27 rat. | |||
T68794 | ALT-946 free base | ||
ALT-946 free base is an inhibitor of advanced glycation that has been shown to improve severe nephropathy in the diabetic transgenic (mREN-2)27 rat. | |||
T35890 |
Pentosidine
|
||
Advanced glycation end products (AGEs) are compounds formed by non-enzymatic chemical reactions following the bonding of sugars to proteins or lipids during diabetes, uremia, aging, rheumatic arthritis, and other conditions. A receptor for the AGEs (RAGE) binds certain members of this class to initiate cell signaling.[1][2] Pentosidine is a well-characterized natural AGE that is often used as a biomarker for the production of all AGEs. While pentosidine can be measured in urine, the majority of ... | |||
TP1935 |
RAGE antagonist peptide
|
||
Receptor for advanced glycation end products (RAGE) antagonist. Blocks S100P, S100A4 and HMGB-1 mediated RAGE activation in vitro and in vivo. Inhibits growth and metastasis of rat glioma tumors. Reduces cell growth and RAGE-mediated NF-κB activity in hum | |||
T73818 | Homocarnosine TFA | ||
Homocarnosine TFA, 作为一种大脑特定的γ-氨基丁酸(GABA)与组氨酸的二肽, 具备抑制性神经调节功能。它在神经元内由GABA合成,既显示出抗惊厥效应,也表现抗氧化、抗炎作用,能防止DNA损伤并抑制晚期糖基化终产物的形成。 | |||
T72824 |
RAGE/SERT-IN-1
|
||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S2384 |
Poliumoside
|
Reductase | Endocrinology/Hormones; Metabolism |
Poliumoside 是从 Brandisia hancei 的茎和叶中分离出来的咖啡酰化的苯丙烷糖苷。Poliumoside 能够抑制晚期糖基化终产物的形成和大鼠晶状体醛糖还原酶,IC50分别为 19.69 和 8.47 μM。Poliumoside 具有抗炎和抗氧化特性。 | |||
TN1471 |
Cassiaside C
决明子苷C,Toralactone 9-O-β-D-gentiobioside |
Others; Endogenous Metabolite | Metabolism; Others |
Cassiaside C (Toralactone 9-O-β-D-gentiobioside) 是一种萘酚类化合物,从决明子种子中分离得到,对晚期糖基化终产物 (AGE) 的形成具有抑制作用。 | |||
T10183 |
6-Methoxytricin
|
Others | Others |
6-Methoxytricin is a flavonoid isolated from Artemisia iwayomogi. It is an inhibitor on aldose reductase (AR) and advanced glycation endproduct (AGE) formation activities (IC50s: 30.29 μM and 134.88 μM). 6-Methoxytricin has potential as an anti-diabetic c | |||
T12588 |
Pyridoxylamine
pyridoxamine,吡多胺 |
Endogenous Metabolite | Metabolism |
Pyridoxylamine (pyridoxamine) 是脂质化终产物和糖基化终产物抑制剂,能够防止糖尿病引起的视网膜血管病变。 | |||
TN2165 |
Rubrofusarin gentiobioside
Rubrofusarin-6-O-beta-D-gentiobioside,红链霉素-龙胆二糖苷,芸苔红素龙胆苷 |
ERK; NF-κB; TGF-beta/Smad | MAPK; NF-κB; Stem Cells |
Rubrofusarin gentiobioside (Rubrofusarin-6-O-beta-D-gentiobioside) 一种分离自决明子的、具有清除自由基作用的化合物。 | |||
T10619 |
Bromelain
|
Apoptosis; Others | Apoptosis; Others |
Bromelain 是来源于菠萝茎的一种抗炎药,可诱导细胞凋亡,具有纤维蛋白溶解、抗癌、抗水肿和抗血栓形成活性。它通过下调血浆激肽原,抑制前列腺素 E2 表达,降解晚期糖基化终产物受体,在COX 途径上游发生抗氧化作用以及调节血管生成生物标志物而发挥作用。 | |||
TN1042 |
Chebulic acid
|
Others | Others |
Chebulic acid 是一种分离自Terminalia chebula 中的酚羧酸化合物,具有显著的抗氧化作用,它能够打破由晚期糖基化终产物 (AGEs) 诱导的蛋白质交联,阻碍 AGEs 的形成。它能够有效控制代谢参数升高、氧化应激和肾损害,支持其在糖尿病肾病中的有益作用。 | |||
TN3972 |
Epimedokoreanin B
|
Apoptosis; Others; Antibacterial | Apoptosis; Microbiology/Virology; Others |
Epimedokoreanin B (EKB) 是一种从韩国淫羊藿中分离出的异戊烯化类黄酮,在人非小细胞肺癌(NSCLC)A549和NCI-H292细胞中展现出抗癌活性。Epimedokoreanin B 还具有抗炎和抗菌活性,可有清除 DPPH 自由基的活性,能以剂量依赖的方式抑制 MCF-7 和 HepG2 的增殖。Epimedokoreanin B 能显著抑制 N (δ) -(羧甲基)赖氨酸(CML)和 N (Ï) -(羧甲基)精氨酸(CMA)的形成,可通过抑制高级糖化终产物(AGEs)预防糖尿病的临床并发症。 | |||
TN2894 |
3,5-Di-O-caffeoylquinic acid methyl ester
金银花 |
HSV | Microbiology/Virology |
3,5-Di-O-caffeoylquinic acid methyl ester exhibits potent inhibitory activities against the formation of advanced glycation end products (AGEs); it exhibits cytotoxicity actions against human cervix carcinoma HeLa cells. 3,5-Di-O-caffeoylquinic acid methyl ester shows high efficiency and low toxicity with antivirus activity against RSV. | |||
T81905 |
Lucidin-ω-Me ether
|
||
Lucidin-ω-Me ether(化合物2),一种自Knoxia valerianoides的根中分离得到的化合物,具有抑制体外晚期糖基化终末产物(AGE)形成的活性,其IC50为62.79 μM。 |