53
14
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T62899 |
Tau-aggregation and neuroinflammation-IN-1
|
Microtubule Associated; NO Synthase | Cytoskeletal Signaling; Immunology/Inflammation |
Tau-aggregation and neuroinflammation-IN-1 是一种有效的 Tau 蛋白聚集体抑制剂, 对 AcPHF6 和全长 tau 蛋白聚集体显示出显著的抑制活性。Tau-aggregation and neuroinflammation-IN-1具有抗炎活性且可减少 NO 释放。Tau-aggregation and neuroinflammation-IN-1 对 LSP 刺激的 BV2 细胞具有低细胞毒性。Tau-aggregation and neuroinflammation-IN-1 可逆转冈田酸诱导的大鼠记忆障碍。 | |||
T79590 |
Anti-neuroinflammation agent 1
|
NOD-like Receptor (NLR) | Immunology/Inflammation |
Anti-neuroinflammation agent 1 为一种效力显著的抗神经炎症药物,能有效调节BV2小胶质细胞从M1表型向M2表型极化。 | |||
T1814 |
ICILIN
AG-3-5 |
TRP/TRPV Channel | Membrane transporter/Ion channel |
ICILIN (AG-3-5) 是一种有效的的瞬时受体电位 M8 (TRPM8) 离子通道激动剂。 Icilin 激活 EGTA 中的 TRPM8,该激活作用具有剂量依赖性, EC50=1.4 μM。Icilin 通过调节 T 细胞反应减轻自身免疫性神经炎症。 | |||
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。 | |||
T23146 |
PHA 568487 free base
PHA 568487 |
AChR | Neuroscience |
PHA 568487 free base 是一种选择性的 α7 烟碱乙酰胆碱受体激动剂,可用于减缓神经炎症。 | |||
T21233 |
Dihydrolipoic acid
Reduced thioctic acid,Reduced lipoic acid,DHLA,USAF XR-12,6,8-Dihydrothioctic acid,二氢硫辛酸 |
Antioxidant | oxidation-reduction |
Dihydrolipoic acid (USAF XR-12) 是高效的抗氧化剂,对所有以氧为中心的自由基都有很强的清除能力。它在多种疾病中表现出抗炎特性。在 LPS 诱导的疾病行为大鼠中,它通过 ERK/Nrf2/HO-1/ROS/NLRP3 通路发挥预防作用。它还可以可用于抑郁症的研究。 | |||
T33519 |
MTOB
α-keto-γ-Methylthiobutyric acid,4-甲硫基-2-氧丁酸钠,KMBA,MTOB salt,4-methylthio 2-oxobutyric acid |
Others | Others |
MTOB (α-keto-γ-Methylthiobutyric acid) 是 c 末端结合蛋白 (CtBP) 的底物,可干扰 CtBP 在细胞培养物和小鼠中的致癌活性。它还积极调节 TCF-4 信号传导,导致癌症干细胞 (CSC) 生长和自我更新。 | |||
T1406 |
Amantadine hydrochloride
盐酸金刚烷胺,1-adamantanamine HCl,1-Adamantanamine hydrochloride,Symmetrel,CI-719,Amantadine HCl,1-Adamantylamine hydrochloride |
Dopamine Receptor; Influenza Virus | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Amantadine hydrochloride (CI-719) 是一种抗病毒药物,用于预防或对症治疗甲型流感和帕金森病。它阻断质子流通过 M2 离子通道,从而阻止病毒 RNA 释放到感染细胞的细胞质中。 | |||
T22378 |
Nilotinib hydrochloride
AMN-107 HCl |
Bcr-Abl; Autophagy | Angiogenesis; Autophagy; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Nilotinib hydrochloride(AMN-107 HCl) 是一种可口服的 Bcr-Abl 酪氨酸激酶抑制,具有抗肿瘤活性,可用于调节神经炎症和认知障碍,可用于研究慢性骨髓性白血病。 | |||
T4450 |
GIBH-130
|
IL Receptor; TNF; Interleukin | Apoptosis; Immunology/Inflammation |
GIBH130 是一种有效的神经炎症抑制剂,可作用于活化的小胶质细胞,明显抑制IL-1β的分泌(IC50:3.4 nM)。 | |||
TQ0057 |
AVE 0991
|
Others | Others |
AVE 0991 是血管紧张素-(1-7) [Ang-(1-7)] 的非肽类似物,是一种具有口服活性的 Mas 激动剂,对 [125I]-Ang-(1-7) 结合到牛主动脉内皮细胞膜有抑制作用,通过增强自噬来抑制星形胶质细胞介导的阿尔茨海默病神经炎症。 | |||
T11662L |
INT-777
S-EMCA |
GPCR19 | GPCR/G Protein |
INT-777(S-EMCA)是有效的 TGR5 激动剂,EC50 为 0.82 μM。 INT-777(S-EMCA)在大鼠蛛网膜下腔出血后通过 TGR3/cAMP/PKA 信号通路抑制 NLRP5-ASC 炎症小体介导的神经炎症。 | |||
T33514 |
MSC 2032964A
MSC-2032964A,MSC2032964A |
ASK | Apoptosis |
MSC 2032964A 是一种有效的选择性 ASK1 抑制剂 (IC50 = 93 nM),具有口服生物利用度和脑渗透性。它在小鼠 EAE 模型中抑制神经炎症,并在培养的小鼠星形胶质细胞中阻断 LPS 诱导的 ASK1 和 p38 磷酸化。 | |||
T73286 |
SRI-42127
|
HuR | Chromatin/Epigenetic |
SRI-42127 是一种新型 RNA 调节因子 HuR 的小分子抑制剂,抑制肿瘤生长,可减弱脂多糖诱导的神经炎症模型中的神经胶质活化,通过抑制神经炎症反应来减轻神经损伤后的神经性疼痛。 | |||
T33535 |
MW01-2-151SRM
MW 151,MW-151,MW012151SRM,MW151,MW01 2 151SRM |
Others | Others |
MW01-2-151SRM 是一种新型可穿过血脑屏障的小分子小胶质细胞活化抑制剂,具有抗神经炎作用,可减弱神经炎症模型中的神经胶质细胞因子上调,可用研究创伤性脑损伤、阿尔茨海默病和海藻氨酸毒性。 | |||
T15162 |
DPA-714
|
Others | Others |
DPA-714 是高亲和力的移位蛋白配体 (Ki=7 nM),它结构中有一个氟原子,能够被氟 -18 进行标记,并可通过正电子发射断层成像进行活体成像。它可在各种神经炎症模型及脑肿瘤模型中成功评估炎症的特异性成像。 | |||
T124358 |
Deferoxamine
Deferoxamine B,Desferrioxamine B |
Apoptosis; Antioxidant; HIF; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; oxidation-reduction |
Deferoxamine(Desferrioxamine B) 是一种铁螯合剂 (结合 Fe(III) 和许多其他金属阳离子),可抑制神经元病变,可用于改减少铁在组织中的积累和沉积,可通过抑制创伤性脑损伤后的铁死亡和神经炎症来改善神经功能障碍。Desferrioxamin-B 具有抗氧化、抗增殖、抗肿瘤活性,可诱导 HIF-1α 产生,诱导癌细胞凋亡和自噬。Desferrioxamin-B 可用于治疗急性铁中毒和与 COVID-19 相关疾病。 | |||
T61566 | P2X7 receptor antagonist-2 | ||
P2X7 receptor antagonist-2 is a highly potent antagonist of the P2X7 receptor, exhibiting a pIC50 value range of 6.5-7.5. Its efficacy in combating neuroinflammation has been demonstrated [1]. | |||
T1158L |
Phenoxybenzamine
NSC-37448,A688,NSC 37448,NSC37448,A-688 |
||
Phenoxybenzamine is an α-1 adrenergic receptor antagonist. Phenoxybenzamine may exert a neuroprotective effect by reducing neuroinflammation after traumatic brain injury. | |||
T25752 |
Lonchocarpic acid
AI3-01135,AI301135,AI3 01135 |
||
Lonchocarpic acid shows an anti-inflammatory mechanism of lonchocarpine in LPS- or poly(I:C)-induced neuroinflammation. | |||
T38787 | ER176 | ||
ER176 is a novel PET radioligand utilized for the visualization of 18 kDa translocator protein (TSPO), a neuroinflammation biomarker, marking the advancement in imaging technology. | |||
T78969 | PB131 | HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
PB131为选择性HDAC6抑制剂,能穿透血脑屏障且显示出高结合亲和性(IC50: 1.8 nM)。该化合物展现出显著的抗炎活性,适用于炎症特别是神经炎症的研究领域。 | |||
T38912 | Vicasinabin | ||
Vicasinabin, a potent agonist of cannabinoid receptor 2 (CB2), exhibits promising potential for researching chronic pain, atherosclerosis, regulation of bone mass, neuroinflammation, and related human diseases. | |||
T61620 | AChE/PDE4-IN-1 | ||
AChE/PDE4-IN-1 (compound 12c) is a highly effective and specific dual inhibitor of PDE4 and AChE, with IC50 values of 0.28 μM and 1.88 μM for AChE and PDE4D, respectively. This compound demonstrates notable potential in reducing neuroinflammation associated with Alzheimer's disease research [1]. | |||
T37815 |
PM226
PM 226 |
||
Potent and selective CB2 receptor agonist (Ki = 12.8 nM; EC50 = 38.67 nM). Exhibits negligible affinity for the CB1 receptor (Ki > 40,000 nM) and no activity at the GPR55. Suppresses neuroinflammation by reducing microglial activation in a multiple sclerosis mouse model. BBB permeable; anti-inflammatory and neuroprotective. | |||
T74409 | EVT-401 | ||
EVT-401 (P2X7 receptor antagonist-1),一种嘌呤能P2X7受体拮抗剂,具抗神经炎症作用。 | |||
TP1620 |
Cyclic MKEY
|
||
MKEY, a synthetic cyclic peptide inhibitor of CXCL4-CCL5 heterodimer formation, has been shown to protect against atherosclerosis and aortic aneurysm formation by mediating inflammation, but whether it modulates neuroinflammation and brain injury has not | |||
T61987 |
PHA 568487
|
||
PHA 568487 是选择性的、血脑屏障通透性的 α-7 烟碱乙酰胆碱受体 (α-7 nAchR) 激动剂。PHA 568487 可减少氧化应激和神经炎症。 | |||
T81075 |
SUCNR1-IN-2
|
||
SUCNR1-IN-2 (Statement 35) 作为succinate/succinate受体 1 抑制剂,专用于神经退行性疾病(例如神经炎症)的研究领域。 | |||
T79637 | CIAC001 | ||
CIAC001是一种丙酮酸激酶PKM2的抑制剂,它展现出了抗神经炎症活性。这种化合物能够抑制LPS诱导的一氧化氮(NO)产生(IC50=2.5 μM),并保护BV-2免疫活性细胞。在小鼠模型中,CIAC001减轻了慢性吗啡引起的成瘾和神经炎症症状。 | |||
T60868 | NF-κB-IN-4 | ||
NF-κB-IN-4 (化合物 17) 是有效的NF-κB 通路抑制剂,可透过血脑屏障(BBB)。NF-κB-IN-4 具有潜在的抗神经炎症活性,毒性低,可用于研究神经炎症相关疾病。NF-κB-IN-4 可阻断 IκBα 的活化及磷酸化,降低 NLRP3 的表达,从而抑制NF-κB 的激活。 | |||
T36851 |
Peptide5
|
||
Connexin43 mimetic peptide. Reduces swelling, astrogliosis, neuroinflammation and neuronal cell death following spinal cord injury ex vivo and in vivo. Exhibits analgesic effects in models of neuropathic pain. O'Carroll et al (2008) Connexin 43 mimetic peptides reduce swelling, astrogliosis and neuronal cell death after spinal cord injury. Cell.Commun.Adhes. 15 27 PMID:18649176 |Mao et al (2017) Characterisation of Peptide5 systemic administration for treating traumatic spinal cord injured rats.... | |||
T39677 |
MY33-3
MY33-3 |
||
MY33-3 is a powerful and specific inhibitor of receptor protein tyrosine phosphatase (RPTP)β/ζ, demonstrating an IC50 value of approximately 0.1 μM. Moreover, MY33-3 exhibits inhibitory activity against PTP-1B with an IC50 value of about 0.7 μM. Additionally, MY33-3 has been shown to effectively decrease ethanol consumption and alleviate neuroinflammation and cognitive dysfunction induced by Sevoflurane. | |||
T70595 |
Artemisinin B
|
||
Artemisinin B is a drug which may improve spatial memory in dementia patients and alter the levels of inflammatory cytokines in the hippocampus and the cortex. Artemisinin B may inhibit neuroinflammation and exert neuroprotective effects on cognitive functions by modulating the TLR4-MyD88-NF-κB signaling pathway. Artemisinin B has shown potential in the treatment of neuroinflammatory diseases. | |||
T72874 |
sEH/AChE-IN-2
|
||
sEH/AChE-IN-2 是可溶性环氧化物水解酶 (sEH) 和乙酰胆碱酯酶 (AChE) 的双重抑制剂。sEH/AChE-IN-2 提供对抗神经炎症和记忆障碍的累积效应。sEH/AChE-IN-2具有研究阿尔茨海默病 (AD) 的潜力。 | |||
T73302 |
FAAH-IN-7
|
||
FAAH-IN-7 是一种可逆且有效的FAAH 抑制剂,IC50为 8.29 nM。FAAH-IN-7 能够抑制 1321N1星形胶质细胞氧化应激,在离体神经炎症模型中表现出显著的神经保护作用。 | |||
T69664 | Umibecestat HCl | ||
Umibecestat, also known as CNP-520, is a beta-secretase inhibitor and is a drug candidate for prevention trials in Alzheimer's disease. CNP520 has a selectivity, pharmacodynamics, and distribution profile suitable for AD prevention studies. CNP520 reduced brain and cerebrospinal fluid (CSF) Aβ in rats and dogs, and Aβ plaque deposition in APP-transgenic mice. CNP520 reduces Aβ load and neuroinflammation in APP‐transgenic mice | |||
T79577 |
CB2 PET Radioligand 1
|
Cannabinoid Receptor | GPCR/G Protein |
CB2PET Radioligand 1 (compound [18F]9) 作为hCB2靶向的PET Radioligand (Ki=7.7 nM),采用Cu介导的18F-氟化方法制备,并在小鼠神经炎症模型中展现了高脑摄取率。 | |||
T73504 |
MR2938
|
||
MR2938 是一种有效的AChE 抑制剂,IC50为 5.04 μM。 MR2938 也明显抑制 NO 的产生 (IC50= 3.29 μM)。 MR2938 通过阻断MAPK/JNK 和NF-κB 信号通路抑制神经炎症。 MR2938 可用于阿尔茨海默病 (AD) 研究。 | |||
T64181 |
sEH/AChE-IN-1
|
||
sEH/AChE-IN-1 (Compound 12a) 是一种可溶性环氧化物水解酶 (sEH) 和乙酰胆碱酯酶 (AChE) 的双重抑制剂。sEH/AChE-IN-1 具有对抗神经炎症和记忆障碍的累积效应。sEH/AChE-IN-1 对阿尔茨海默病 (AD) 表现出研究潜力。 | |||
T62442 |
MY33-3 hydrochloride
|
||
MY33-3 hydrochloride 是一种有效的、选择性的蛋白酪氨酸磷酸酶 RPTPβ/ζ 抑制剂 (IC50~0.1 μM)。MY33-3 hydrochloride 对 PTP-1B 具有抑制作用 (IC50~0.7 μM)。MY33-3 hydrochloride 能够降低乙醇消耗,缓解 Sevoflurane 引起的神经炎症和认知功能障碍。 | |||
T35836 |
PMX-205 (trifluoroacetate salt)
|
||
PMX-205 is a cyclic hexapeptide that acts as a potent antagonist of C5a receptor (C5aR; IC50= 31 nM).1It is orally active and blocks inflammatory signaling and symptoms in animal models of colitis and allergic asthma.2,3PMX-205 is also brain penetrant and reduces neuroinflammation and neurodegeneration in an animal model of Alzheimer's disease.4 1.March, D.R., Proctor, L.M., Stoermer, M.J., et al.Potent cyclic antagonists of the complement C5a receptor on human polymorphonuclear leukocytes. Rela... | |||
T79484 |
Nrf2 activator-8
|
||
Nrf2 activator-8(化合物 10e)作为一种效能显著的Nrf2激活剂(EC50=37.9 nM),在BV-2微神经胶质细胞中展现出优异的抗氧化及抗炎效应。此外,Nrf2 activator-8可有效逆转脂多糖(LPS)诱导的小鼠神经炎症模型中的空间记忆缺失。 | |||
T13036 |
Sulfosuccinimidyl oleate
Sulfo-N-succinimidyl oleate |
Mitophagy | Autophagy |
Sulfosuccinimidyl oleate (Sulfo-N-succinimidyl oleate) (Sulfo-N-succinimidyl oleate) 是一种长链脂肪酸,可抑制脂肪酸运输到细胞。Sulfosuccinimidyl oleate 是一种有效且不可逆的线粒体呼吸链抑制剂。Sulfosuccinimidyl oleate 与小胶质细胞表面上的CD36受体结合,具有抗炎效果。 | |||
T79670 | Anti-inflammatory agent 56 | COX | Immunology/Inflammation; Neuroscience |
Anti-inflammatory agent 56 (Compound 9) 是一种选择性COX-2抑制剂,IC50值为0.54 μM。该化合物展现出显著的抗氧化和抗炎效果,并能有效抑制氧化应激引起的细胞死亡。通过抑制Keap1、COX-2和iNOS,Anti-inflammatory agent 56减轻氧化应激及神经炎症。此外,其在小鼠中的急性毒性较低,LD50为1000 mg/kg。 | |||
T74860 | MAO-B-IN-21 | Monoamine Oxidase | Neuroscience |
MAO-B-IN-21是一种有效的MAO-B抑制剂,该化合物表现出抗氧化和抗Aβ聚集的活性。该化合物还可螯合金属离子,抗神经炎症(如NO、TNF-α),具有神经保护作用,并可穿透BBB。在Aβ1-42诱导的阿尔茨海默病小鼠模型中,MAO-B-IN-21显著改善了记忆与认知功能。 | |||
T73511 |
SZM679
|
RIP kinase | Apoptosis; NF-κB |
SZM679是一种口服有效的选择性RIPK1抑制剂,其对RIPK1的Kd值为8.6 nM,而对RIPK3的Kd值则大于5000 nM。该化合物能够逆转肿瘤坏死因子诱导的全身炎症反应,并在海马和皮质中降低Tau蛋白的过度磷酸化、神经炎症以及RIPK1磷酸化水平。SZM679可用于阿尔茨海默病(AD)的研究。 | |||
T36015 |
PDMP (hydrochloride)
|
||
PDMP is a ceramide analog first prepared in a search for inhibitors of glucosylceramide synthase. PDMP has two adjacent chiral centers (C1 and C2) allowing for the formation of four possible isomers. PDMP contains all four of these stereoisomers. PDMP inhibits glucosylceramide synthase by 90% when used at a concentration of 0.8 μM in MDCK cell homogenates, however, the ability to inhibit glucosylceramide synthase has been found to reside in the D-threo (1R,2R) enantiomer. The D-threo PDMP enanti... | |||
T83962 |
C 101248
|
||
C 101248是一种选择性且强效的小鼠和人类串联孔道卤素抑制K+通道1(THIK-1, IC50= 50 nM)抑制剂,对K2P家族成员TREK-1和TWIK-2以及Kv2.1无活性。C 101248能够阻断小鼠海马微胶质细胞中THIK-1 K+电流的整细胞膜片钳记录中的音调和ATP激发的电流。C 101248通过防止NLRP3依赖性IL-1β的释放,从而减少在分离的微胶质细胞中的神经炎症。 | |||
T78876 | DNL343 | ||
DNL343是一种可穿透血脑屏障的eIF2B激活剂,能够有效地抑制异常的整合应激反应(ISR)。该化合物能降低中枢神经系统(CNS)中的ISR活性,逆转神经退行性变化和神经炎症反应。DNL343还能预防带有eIF2B功能丧失(LOF)突变的小鼠模型出现运动障碍和过早死亡现象。此外,DNL343在治疗由eIF2B LOF和慢性ISR激活导致的白质消失病(VWMD)方面显示出明显的治疗潜力。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5575 |
Cycloastragenol
环黄芪醇,Cyclogalegenol,Astramembrangenin |
Epigenetic Reader Domain; Telomerase | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Cycloastragenol (Astramembrangenin) 是一种三萜皂苷类化合物,是黄芪主要活性成分的水解产物,具有抗氧化、抗炎、抗衰老、抗凋亡和心血管保护作用。它是端粒酶激活剂,可以延长端粒,还能缓解与年龄相关的骨丢失,改善骨微结构和生物力学特性。 | |||
TN6714 |
Geranylgeraniol
FT-0626663,Tetraprenol,CJ24095,CJ 24095,FT0626663,香叶基香叶醇,CJ-24095 |
Apoptosis | Apoptosis |
Geranylgeraniol (FT0626663) 是一种类异戊二烯,存在于水果、蔬菜和谷物中,包括大米。 Geranylgeraniol (FT0626663) 抑制生长并诱导各种肿瘤细胞的凋亡。 Geranylgeraniol (FT0626663) 保护单核细胞免受他汀类药物诱导的细胞毒性并抑制分枝杆菌的生长。 | |||
T7060 |
Amantadine
1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine |
Others | Others |
Amantadine (1-Aminoadamantane) 是抗病毒药物,也是是 NMDA 型谷氨酸受体的弱拮抗剂,能促进高多巴胺的释放,并阻断多巴胺的再摄取。 | |||
T3767 |
Polygalacic acid
Virgaureagenin G,毛果一枝黄花皂苷元G,远志酸 |
MMP; AChR; AChE | Neuroscience; Proteases/Proteasome |
Polygalacic acid (Virgaureagenin G) 是一种从远志 Polygala tenuifolia Willd 根中分离出来的三萜,可抑制 MMP 表达。它对认知障碍有显著的神经保护作用,PA 通过抑制乙酰胆碱酯酶活性,增加胆碱乙酰转移酶活性,提高海马和额皮质中的乙酰胆碱水平来提高胆碱能系统反应性。 它可以用于骨关节炎相关研究。 | |||
TN2003 |
Obtucarbamate A
4-甲基苯-1,3-二氨基甲酸二甲酯,钝叶扁柏氨基甲酸酯 A,钝叶扁柏氨基甲酸酯A |
NO Synthase | Immunology/Inflammation |
Obtucarbamate A 分离自Disporum cantoniense 中,具有镇咳作用。 | |||
T3824 |
Jaceosidin
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Apoptosis; BCL; COX; UGT | Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience |
Jaceosidin 是从毛莲蒿中得到的一种黄酮类天然产物,可激活Bax,下调 Mcl-1 和 c-FLIP 的表达,诱导癌细胞凋亡。它能够降低炎性因子水平,激活 NF-κB,抑制COX-2的表达,具有抗癌和抗炎作用。 | |||
TJS1779 |
Protosappanin A
原苏木素A,PTA |
NADPH-oxidase; IL Receptor; IκB/IKK; TNF; NF-κB; TLR; ROS; COX; HIV Protease; JAK; NO Synthase; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells |
Protosappanin A (PTA) 是从苏木中分离得到的免疫抑制成分和主要联苯化合物,通过下调 JAK2和 STAT3的磷酸化,抑制 JAK2/STAT3依赖的炎症通路。 | |||
T5S1172 |
Tiliroside
银椴甙,Tribuloside,银椴苷;椴树苷 |
Antioxidant | oxidation-reduction |
Tiliroside (Tribuloside) 是糖苷类黄酮,是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收,具有抗糖尿病作用。 | |||
T4S0969 |
Obtusifolin
决明蒽醌,决明蒽醌;美决明子素 |
Antioxidant; NF-κB | NF-κB; oxidation-reduction |
Obtusifolin 是分离自决明子的种子中,能够抑制NF-kB 通路,调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。 | |||
TN4315 |
Isonardosinone
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NF-κB; MAPK | MAPK; NF-κB |
Isonardosinone shows potential role in the treatment of neuroinflammation conditions, it inhibits NF-κB- and MAPK-mediated inflammatory pathways. | |||
T80904 |
Ulmoidol
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Ulmoidol通过干扰PU.1转录信号通路,抑制神经炎症。 | |||
TN2193 |
Scutebarbatine W
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Others | Others |
Scutebarbatine W can inhibit nitric oxide production efficiently with IC50 values of lower than 50 μM, it may have potential effects on the reduction of neuroinflammation. | |||
TN2194 |
Scutebarbatine X
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Others | Others |
Scutebarbatine X can inhibit nitric oxide production efficiently with IC50 values of lower than 50 μM, it may have potential effects on the reduction of neuroinflammation. | |||
TN5901 |
Cudratricusxanthone A
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Cudratricusxanthone A has potent anti-proliferative, antioxidative, and monoamine oxidase inhibitory effects, it also possesses anti-cancer activities and provide a basis for developing effective therapeutic agents to inhibit growth and metastasis of brea |