50
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14080 |
AA147
ATF6-activator-147 |
Others | Others |
AA147 (ATF6-activator-147) 是小分子内质网蛋白稳态调节剂,能够选择性激活未折叠蛋白反应的 ATF6臂。 | |||
T9999 |
Sirtuin modulator 2
N-(3-(imidazo[2,1-b]thiazol-6-yl)phenyl)-2-methoxybenzamide |
Others; Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair; Others |
Sirtuin modulator 2 (N-(3-(imidazo[2,1-b]thiazol-6-yl)phenyl)-2-methoxybenzamide) 具有抗糖尿病、抗炎和抗肿瘤活性。 | |||
T27462 |
GSK-239512
GSK239512,GSK 239512 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
GSK-239512 是 H3 受体拮抗剂,可用于治疗神经退行性疾病认知功能障碍的研究。 | |||
T28856 |
SSR180711 hydrochloride
SSR-180711A HCl,SSR-180711C HCl,SR-180711 HCl |
AChR | Neuroscience |
SSR180711 hydrochloride (SSR-180711A HCl) 是一种具有选择性的 Alpha7 尼古丁乙酰胆碱部分激动剂,可用于研究神经分裂和认知障碍。 | |||
T40542 |
Sinbaglustat
ACT-519276,Sinbaglustat,OGT2378 |
Transferase | Metabolism |
Sinbaglustat (OGT2378) (OGT2378) 是葡萄糖神经酰胺合成酶 (GCS) 和非溶酶体葡萄糖神经酰胺酶 (GBA2) 的双重抑制剂。Sinbaglustat 是一种可透过血脑屏障的的口服N-烷基亚氨基糖。Sinbaglustat 可用于治疗溶酶体贮积症和研究溶酶体功能障碍相关的中枢神经退行性疾病。 | |||
T5463 |
Verdiperstat
AZD3241,AZD 3241 |
Glutathione Peroxidase | Metabolism |
Verdiperstat (AZD 3241) 是一种不可逆的、选择性的、口服具有活力的髓过氧化物酶 (myeloperoxidase) 抑制剂,IC50=630 nM,可用于研究大脑神经退行性疾病。 | |||
T39566 |
ZT-1a
|
Others | Others |
ZT-1a 是一种有效的非 ATP 竞争性的选择性 SPAK 抑制剂。ZT-1a 对 SPAK 有抑制作用。ZT-1a 可用来预防和治疗神经退行性和神经认知障碍。 | |||
T61932 |
Nesuparib
JPI-547/OCN-201 |
PARP; Wnt/beta-catenin | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Stem Cells |
Nesuparib (JPI-547/OCN-201) 是一种有效的PARP抑制剂,对PARP 和TNKS1具有抑制作用。Nesuparib 具有抗肿瘤活性,可用于治疗肿瘤、内分泌与代谢疾病、泌尿生殖系统疾病,可用于研究神经性疼痛、神经退行性疾病和心血管疾病 。 | |||
T77565 |
Fluparoxan hydrochloride
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Fluparoxan hydrochloride 是一种高度选择性和有效的α2-肾上腺素受体拮抗剂,可用于预防、改善或治疗神经发育障碍和神经退行性疾病。 | |||
T77566 |
(3aR,9aR)-Fluparoxan
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
(3aR,9aR)-Fluparoxan 是一种高度选择性和有效的肾上腺素能受体α2B 拮抗剂,可用于预防、改善或治疗神经发育障碍和神经退行性疾病。 | |||
T67733 |
BT44
|
Others | Others |
BT44是一种新的、第二代神经胶质细胞系衍生的神经营养因子模拟物,具有改善的生物活性,是治疗神经退行性疾病的先导化合物。 | |||
T16782 |
Rolofylline
KW-3902,MK-7418,KF-15372 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Rolofylline (KW-3902) 是一种具有选择性腺苷 A1 受体拮抗剂,可用于研究急性充血性心力衰竭和肾功能障碍,可用与研究神经退行性疾病。 | |||
T10991 |
Dehydronitrosonisoldipine
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Dehydronitrosonisoldipine 是一种不育α和含TIR 图案1的抑制剂,可用于有关神经退行性疾病的研究。Dehydronitrosonisoldipine 抑制轴突退化和长春碱激活的神经元中cADPR 的产生。 | |||
T13287 |
VBIT-4
|
VDAC | Membrane transporter/Ion channel |
VBIT-4 是一种电压依赖性阴离子通道 1 (VDAC1) 寡聚化抑制剂(Kd:17 μM)。 VBIT-4 可用于治疗凋亡相关疾病(如神经退行性疾病和心血管疾病)。 | |||
T39252L |
Anticonvulsant agent 10 HCl
|
Others | Others |
5-[(1S,2S)-2-[(Cyclopropylmethyl)amino]cyclopropyl]-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide hydrochloride 是一种环丙酶化合物,可作为赖氨酸特异性脱甲基酶-1抑制剂,可用于精神分裂症、发育障碍和神经退行性疾病。 | |||
T3320 |
Dizocilpine Maleate
(+)-Mk-801 Hydrogen Maleate,MK 801,地卓亚平马来酸盐,Dizocilpine hydrogen maleate,地佐环平马来酸盐,(+)-MK 801 maleate,(+)-MK 801 (Maleate) |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dizocilpine Maleate (MK 801) 是一种选择性和非竞争性的 NMDA 受体拮抗剂,Kd 值为 37.2 nM。它用于治疗 NMDA 受体可能发挥重要作用的多种神经退行性疾病或疾病。 | |||
T72073 |
AKOS037652256
|
||
AKOS037652256可作为 TRPML 调节剂,可用于治疗如溶酶体积存病、肌肉萎缩症、与年龄相关的常见神经退行性疾病、氧化应激或活性氧(ROS)相关疾病以及衰老等与 TRPML 活性相关的疾病。 | |||
T3637 |
Pifithrin-β hydrobromide
Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) |
Ferroptosis; p53 | Apoptosis |
Pifithrin-β hydrobromide (Cyclic PFT-α) 是一种 p53 的抑制剂,可逆地阻断 p53 依赖性转录激活和细胞凋亡。IC50值为23 μM。 | |||
T22043 |
BCATc Inhibitor 2
|
Others | Others |
BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂,可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM),hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1,存在于细胞质基质中的亚型。 | |||
T13853 |
Pyridazinediones-derivative-1
|
Others | Others |
Pyridazinediones-derivative-1 has potential in treating neurodegenerative disorders. | |||
T24621 |
PF-06648671
PF 6648671,PF 06648671,PF6648671,PF-6648671 |
||
PF-06648671 is a γ-secretase modulator for the treatment of neurodegenerative and/or neurological disorders. | |||
T61662 |
O-GlcNAcase-IN-4
|
||
O-GlcNAcase-IN-4 is an inhibitor of O-GlcNAcase. It holds potential for researching neurodegenerative diseases and disorders, including Alzheimer's disease [1]. | |||
T61578 |
BRD3731
|
||
BRD3731 is a selective inhibitor of GSK3β, demonstrating an IC50 value of 15 nM for GSK3β and 215 nM for GSK3α. Due to its inhibitory properties, BRD3731 holds promise for investigating various medical conditions, including post-traumatic stress disorder (PTSD), psychiatric disorders, diabetes, and neurodegenerative disorders [1]. | |||
T72439 |
Calpain Inhibitor XI
|
||
Calpain Inhibitor XI,一种可逆的calpain-1共价抑制剂,适用于神经退行性疾病的研究。 | |||
T78814 |
COH1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
COH1为核糖核苷酸还原酶(RR)抑制剂,主要应用于癌症、线粒体疾病和神经退行性疾病的研究领域。 | |||
T82068 |
Inonophenol C
|
||
Inonophenol C 作为一种神经营养剂,具有防治神经退行性疾病的保护作用。 | |||
T40354 |
IL-17A modulator-1
|
||
IL-17A modulator-1 is an effective inhibitor of IL-17A activity, exhibiting a pIC 50 value of 8.2. This compound holds great promise for studying diseases and disorders that involve the modulation of IL-17A, such as immune-related diseases, autoimmune pathologies, cancer, and neurodegenerative disorders. | |||
TP2069 |
BDNF (human)
|
||
Member of the neurotrophin growth factor family that binds and activates TrkB and p75 neurotrophin receptors. Enhances the survival, growth and differentiation of neurons. BDNF expression is altered in neurodegenerative disorders such as Parkinson's and A | |||
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。 | |||
T13286 |
VBIT-3
|
Others | Others |
VBIT-3 is a voltage-dependent anion channel 1 (VDAC1) oligomerization inhibitor (Kd: 31.3 μM). VBIT-3 also is an apoptosis inhibitor, can be used for therapeutic purposes in apoptosis-associated disorders (such as neurodegenerative and cardiovascular diseases). | |||
T61128 |
c-ABL-IN-2
|
||
C-ABL-IN-2 is a highly effective inhibitor of the c-Abl protein, which plays a significant role in the development of several diseases, including cancer. This compound exhibits promise for investigating neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS) and Parkinson's disease (PD), as well as cancer. (Source: WO2020260871A1, compound 25) [1]. | |||
T74097 | THX-B | ||
THX-B为一高效非多肽类p75NTR(神经营养蛋白受体p75)拮抗剂,适用于糖尿病、肾病、神经退行性及炎症性疾病研究。 | |||
T78920 | HDAC-IN-58 | HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-58为HDAC抑制剂,特异性针对HDAC6,其IC50值达2.06 nM。适用于慢性疾病,如神经退行性和精神疾病的研究。 | |||
T60809 |
MIF-IN-1
|
||
MIF-IN-1 (compound 14) 是巨噬细胞迁移抑制因子(MIF)的抑制剂,pIC50为6.87。巨噬细胞迁移抑制因子 (MIF) 是一种与多种疾病相关的促炎细胞因子,包括神经退行性疾病。 | |||
T40355 | IL-17A modulator-2 | ||
IL-17A modulator-2, exhibits inhibitory properties towards IL-17A, with a pIC50 of 8.3. Its effectiveness lies in attenuating the biological effects associated with IL-17A activity. IL-17A modulator-2 finds utility in the study of diseases and disorders characterized by dysregulated IL-17A modulation, such as those involving immune dysfunction, autoimmune pathology, cancer, and neurodegenerative conditions. | |||
T81820 |
meso-Benzothiazole-BODIPY 505/515
|
||
meso-Benzothiazole-BODIPY 505/515 是一种BODIPY荧光探针,具备优异的粘度反应性及AIE特性,能够监测细胞内粘度变化与自噬过程。该探针适用于阿尔茨海默病、溶酶体贮积病以及其他神经退行性疾病的研究。 | |||
T81638 |
NSC363998 free base
|
||
NSC363998 (free base) 是一种具口服活性的化合物,能够抑制 rCGG90 诱导的神经毒性,并可应用于脆性 X 相关震颤/共济失调综合征 (FXTAS) 等神经退行性疾病的研究。 | |||
T79829 |
ASN90
|
||
ASN90为特异性O-GlcNAcase(OGA)酶抑制剂,口服活性,IC50为10.2 nM。用于tau蛋白病及α-突触核蛋白病等神经退行性疾病的研究。 | |||
T80104 |
Z-Phe-Ala-diazomethylketone
PADK |
||
Z-Phe-Ala-diazomethylketone 直接与 Aβ42 单体及其小型低聚物相结合,能抑制 Aβ42 在溶液中形成的十二聚体以及原纤维的生成,显示出在神经退行性疾病研究中的应用潜力。 | |||
T73455 | Ph-HTBA | ||
Ph-HTBA 是CaMKIIα的高亲和力、脑穿透调节剂。Ph-HTBA 对 CaMKIIα 具有结合亲和力,Kd 值为 757 nM。Ph-HTBA 可用于缺血和神经退行性疾病的研究。 | |||
T74963 | CypD-IN-3 | ||
CypD-IN-3是一种高效的CypD (亲环蛋白D) 选择性抑制剂,其对CypD的IC50值仅为0.01 μM。该化合物在氧化应激、神经退行性疾病、肝病、衰老、自噬及糖尿病等多种疾病的研究中有潜在应用。 | |||
T74964 | CypD-IN-4 | ||
CypD-IN-4是一种针对亲环蛋白D(CypD)的有效亚型选择性抑制剂,展现出0.057 μM的IC50,表明其对CypD具有高度亲和力。该化合物适用于氧化应激、神经退行性疾病、肝病、衰老、自噬及糖尿病等多种疾病的研究。 | |||
T72483 |
Sirtuin modulator 4
|
||
Sirtuinmodulator 4 是 sirtuin 调节剂。Sirtuinmodulator 4 对 SIRTl 具有抑制效应,EC50值为 51-100 μM。Sirtuinmodulator 4 可用于延长细胞寿命以及预防各种疾病和紊乱的研究,例如:糖尿病、肥胖、神经退行性疾病、心血管疾病、炎症和癌症 。 | |||
T79074 | Lp-PLA2-IN-14 | Phospholipase | Metabolism |
Lp-PLA2-IN-14(Compound 19)是一种选择性的Lp-PLA2抑制剂,其对rhLp-PLA2表现出较高亲和力,pIC50值达到8.4。该化合物主要适用于对抗与神经退行性疾病相关的研究,包括阿尔茨海默病(AD)、青光眼、年龄相关性黄斑变性(AMD),以及心血管疾病如动脉粥样硬化等。 | |||
T38027 |
Ganglioside GM2 Asialo Mixture
Ganglioside GM2 Asialo Mixture |
||
Ganglioside GM2 asialo (asialo- GM2) is a glycosphingolipid containing three monosaccharide residues and a fatty acid of variable chain length but lacking the sialic acid residue present on ganglioside M2. Asialo-GM2 levels are low-to-undetectable in normal human brain, but it accumulates in the brain of patients with Tay-Sachs and Sandhoff disease, which are neurodegenerative disorders characterized by deficiency of lysosomal β-hexosaminidase A and B, respectively. It also binds to various bact... | |||
T74965 | CypE-IN-1 | ||
CypD-IN-1 是一种有效的亚型选择性亲环蛋白 E (CypE) 抑制剂。CypD-IN-1 具有 CypE 亲和力,IC50和 Ki 值分别为 0.013 μM 和 0.072 μM。CypD-IN-1 可用于多种疾病的研究,如氧化应激、神经退行性疾病、肝病、衰老、自噬和糖尿病。 | |||
T80258 |
WRW4-OH
|
||
WRW4-OH 是一种抑制 WKYMVm(一种 FPRL1 激动剂)与其受体结合的生物活性肽。FPRL1,作为典型的趋化受体,在外周血液和大脑的吞噬细胞中有表达,其激活过程与宿主的防御机制及神经退行性疾病相关炎症反应紧密相连。 | |||
T60824 |
Dyrk1A-IN-3
|
||
Dyrk1A-IN-3 (Compound 8b) 是双特异性酪氨酸调节激酶 1A (DYRK1A) 的高选择性抑制剂。Dyrk1A-IN-3与 DYRK1A 结合具有高结合亲和力,IC50值为76 nM。Dyrk1A-IN-3可用于研究神经退行性疾病,例如,阿尔茨海默病、亨廷顿病和帕金森病等。 | |||
T74672 |
Sirtuin modulator 5
|
||
Sirtuinmodulator 5 是一种sirtuin 调节剂。Sirtuinmodulator 5 可以激活SIRTl,DC50值 <50 μM。Sirtuinmodulator 5 可用于增加细胞的寿命并用于研究多种疾病,包括例如与衰老或压力、糖尿病、肥胖症、神经退行性疾病、心血管疾病、凝血障碍、 炎症、癌症和/或潮红以及将受益于线粒体活性增加的疾病或病症。 | |||
T37791 |
A-971432
|
||
A-971432 is a sphingosine-1-phosphate receptor 5 (S1P5) agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.006, 0.362, and >10 µM, respectively). It inhibits forskolin-induced cAMP production in CHO cells expressing S1P5 (EC50 = 4.1 nM). A-971432 (1 µM) increases electrical resistance of hCMEC/D3 cells in an in vitro blood-brain barrier model, indicating enhanced barrier integrity, and attenuates blood-brain barrier leakage in an R6/2 transgenic mouse model of Huntington’s ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TC0039 |
Vasicinone
|
Others | Others |
Vasicinone 是一种喹唑啉类生物碱,分离自凡士林植物中。它是具有研究帕金森病和其他氧化应激相关神经退行性疾病的潜力。 | |||
T3787 |
Didymin
Isosakuranetin-7-O-rutinoside,Neoponcirin,香风草甙 |
Apoptosis; Others | Apoptosis; Others |
Didymin (Neoponcirin) 从柑橘类水果中提取的一种膳食类黄酮苷,具有抗氧化特性。它通过抑制 N-Myc 和上调 RKIP 诱导凋亡。 | |||
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。 | |||
T4S0797 |
Berberine
小檗碱,Berberin,Umbellatine,黄连素 |
Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Berberine (Umbellatine) 是从中草药黄连中分离出来的一种生物碱抗生素。它诱导活性氧生成并抑制 DNA 拓扑异构酶,具有抗肿瘤特性。 |