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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16980 |
Taminadenant
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Taminadenant 是一种腺苷受体拮抗剂。 | |||
T9522 |
Rimtuzalcap
CAD-1883 |
Potassium Channel | Membrane transporter/Ion channel |
Rimtuzalcap (CAD-1883) 是首创的,选择性的小电导钙激活钾通道 (SK 通道) 正变构调节剂。Rimtuzalcap 可用于运动障碍的研究,包括脊髓小脑性共济失调 (SCA)和特发性震颤 (ET)。 | |||
T12877L |
Seltorexant
JNJ-42847922 |
OX Receptor | GPCR/G Protein; Neuroscience |
Seltorexant (JNJ-42847922) 是一种可口服,高亲和性以及选择性的 orexin-2 受体(OX2R)拮抗剂,对人和大鼠中的 OX2R 的pKi 值分别为 8.0 和 8.1。它穿过血脑屏障,迅速占据大鼠大脑中的 OX2R 结合位点。 | |||
T7943 |
Fluphenazine decanoate
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Fluphenazine decanoate 是一种高度连续的多巴胺 D2受体阻滞剂,是一种长效吩噻嗪抗精神病药,用于精神分裂症的研究。 | |||
T0719 |
Tetrabenazine
Xenazine,丁苯那嗪,Ro 1-9569 |
Others; Dopamine Receptor; Monoamine Transporter | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience; Others |
Tetrabenazine (Ro 1-9569) 是 VMAT 抑制剂,用作抗精神病药和治疗各种运动障碍。 | |||
T67882 |
(2R,3S,11bS)-9,10-dimethoxy-3-(2-methylpropyl)-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-ol
|
Others | Others |
(2R,3S,11bS)-9,10-dimethoxy-3-(2-methylpropyl)-1H,2H,3H,4H,6H,7H,11bH-pyrido[2,1-a]isoquinolin-2-ol 是Tetrabenazine 的杂质,Tetrabenazine 是一种VMAT 抑制剂,用于治疗多动运动障碍。 | |||
T16811 |
RWJ-51204
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
RWJ-51204是选择性的腺苷 A2A 受体拮抗剂, 是 GABA(A) receptor 的部分激动剂(IC50: 0.2-2 nM)。其具有神经保护和改善运动的功效,可用于帕金森疾病的相关研究。 | |||
T71138L |
Binospirone
MDL 73005EF |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Binospirone (MDL 73005EF) 是一种 5-HT1A 受体激动剂,具有抗焦虑活性,可用于研究青光眼和与神经功能障碍相关的运动障碍。 | |||
T2162 |
Maribavir
BW1263W94,GW257406X,Benzimidavir,马立巴韦,1263W94 |
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Maribavir (GW257406X) 是一种可口服的苯并咪唑核苷化合物,具有抗巨细胞病毒的活性。 | |||
T72170 |
NaV1.2/1.6 channel blocker-1
|
Sodium Channel | Membrane transporter/Ion channel |
NaV1.2/1.6 channel blocker-1 是一种有效的 NaV1.2/1.6 channel 阻滞剂,对 rNaV1.6 和 hNaV1.2 有抑制作用。NaV1.2/1.6 channel blocker-1 可用于研究全身性癫痫和运动障碍。 | |||
T1751 |
Eliprodil
依利罗地,SL-820715 |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Eliprodil (SL-820715) 是NR2B-NMDA 受体高效选择性抑制剂,IC50值1uM。它对NR2A-和NR2C-NMDA 受体作用较弱,可用于研究帕金森病和运动障碍治疗的试验。 | |||
T1776L |
Plerixafor octahydrochloride
盐酸普乐沙福,JM3100 octahydrochloride,Plerixafor 8HCl (AMD3100 8HCl),Plerixafor 8HCl,SID791 octahydrochloride,AMD 3100 octahydrochloride,JM 3100 8HCl |
Virus Protease; HIV Protease; CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Plerixafor octahydrochloride (JM3100 octahydrochloride) 是一种选择性的CXCR4拮抗剂,IC50为 44 nM。Plerixafor 是一种具有造血干细胞动员活性的双环霉素。 | |||
T10826 |
CK-666
|
HIV Protease; Microtubule Associated | Cytoskeletal Signaling; Microbiology/Virology; Proteases/Proteasome |
CK-666 是一种肌动蛋白相关蛋白 Arp2/3 复合物的细胞渗透性抑制剂。 它与 Arp2/3 复合物结合,稳定复合物的非活性状态,阻止 Arp2 和 Arp3 亚基进入活化的丝状短节距构象。 | |||
T68216 | Sanguiin h 11 | ||
Sanguiin h 11 is a compound purified from the plant Sanguisorba officinalis and has proven to be a potent inhibitor of chemoattractant-dependent and independent neutrophil movement. | |||
T26342 |
YH16899
YH-16899,YH 16899,BC-K-YH16899 |
||
YH16899 is a KRS-67LR interaction inhibitor by directly blocking the association between KRS and 67LR, suppressing the dynamic movement of the N-terminal extension of KRS and reducing membrane localization of KRS. | |||
T31264 |
Deanol acetamidobenzoate
Deanol p-acetamidobenzoate,Elevan,Diforene,Cervoxan,Deaner |
||
Deanol acetamidobenzoate is CNS stimulant. It can be caused elevated blood choline levels, can be used in Treatment of Choreiform Movement Disorders. | |||
T17047 |
Tetrabenazine-d6
Ro 1-9569 D6,丁苯那嗪 D6 |
Others | Others |
Tetrabenazine D6 is the deuterium-labeled Tetrabenazine. Tetrabenazine is a VMAT-inhibitor used for the treatment of hyperkinetic movement disorder. | |||
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. | |||
T26260 |
Tetrabenazine methanesulfonate
NSC169886,NSC 169886,NSC-169886 |
||
Tetrabenazine methanesulfonate is a medicine formerly utilized as an antipsychotic and therapy for various movement disorders. Tetrabenazine methanesulfonate blocks neurotransmitter uptake into adrenergic storage vesicles and has been used as a high-affin | |||
T36591 |
ABD459
|
||
ABD459 is a neutral antagonist of the central cannabinoid 1 (CB1) receptor (Ki = 8.6 nM). It inhibits food consumption in nonfasted mice without affecting motor activity. ABD459 reduces active food seeking for 5-6 hours after treatment, with no rebound after washout. ABD459 also diminishes rapid eye movement (REM) sleep, with no alterations of wakefulness or non-REM sleep. | |||
T81803 |
MFN2 agonist-1
|
||
MFN2 agonist-1 (B-A/l) 是一种有效促进缺陷细胞中MFN2表达的化合物,能够促进线粒体融合。在表达CMT2A突变型MFN2 T105M的小鼠培养神经元中,MFN2 agonist-1能够逆转线粒体的“聚集”现象(指静态线粒体聚集体的形成)并恢复其运动性。 | |||
T62380 | 20-HC-Me-Pyrrolidine | ||
20-HC-Me-Pyrrolidine 是一种有效的 Aster 蛋白抑制剂,对 Aster-A、Aster-B 和 Aster-C 具有抑制作用, IC50 分别为 0.11 μM、0.06 μM 和 0.71 μM。20-HC-Me-Pyrrolidine 阻止 Aster 蛋白结合和转移胆固醇,抑制低密度脂蛋白 (LDL) 胆固醇向内质网 (ER) 的移动。 | |||
T63590 |
c-Met-IN-10
|
||
c-Met-IN-10 是高效的 c-Met 激酶抑制剂 (IC50: 16 nM)。c-Met-IN-10 能够抑制癌细胞 A549、H460 和 HT-29 的活性,通过抑制 HT-29 细胞集落形成,进而诱导 HT-29 和 A549 细胞凋亡 apoptosis,抑制 A549 细胞移动。c-Met-IN-10 能够用于抗癌研究。 | |||
T78827 |
CVN417
|
||
CVN417,一种含 α6 亚基的口服nAChR拮抗剂,通过脉冲依赖的方式调控多巴胺能神经传递,并对nAChR亚基介导的Ca(2+)流出显示出抑制效应,其IC50s为0.086 μM (α6),2.56 μM (α3),以及0.657 μM (α4)。在啮齿类动物模型之研究中,CVN417减缓静息震颤,并展现对帕金森病等运动功能障碍改善的可能性。 | |||
T83851 |
Tat-QFNP12 TFA
|
||
Tat-QFNP12 是一种含有转录激活因子 (Tat) 跨膜结构域和抑制N-Myc下游调节基因2 (NDRG2) 与蛋白磷酸酶Mg2+/Mn2+依赖性1A (PPM1A) 蛋白-蛋白相互作用的肽。在以20 mg/kg剂量给药的内脑血管穿刺诱导的小鼠蛛网膜下腔出血模型中,它能减少由基质金属蛋白酶-9 (MMP-9) 浓度增高引起的血脑屏障内皮紧密连接的损失,减轻脑水肿,并且提高自发活动及肢体运动的对称性。 | |||
T83702 |
E70K TFA
|
||
E70K是一种抑制趋化因子(C-X-C)配体8 (CXCL8)与细胞膜外的糖胺聚糖(GAGs)之间相互作用的抑制剂。它对应于CXCL8 C末端GAG结合区的氨基酸序列,并在第70位上含有谷氨酸到赖氨酸的替换。在50 nM浓度下,E70K能够抑制初级人类中性粒细胞与人类脐静脉内皮细胞(HUVECs)的结合。当使用浓度范围为1至1,000 nM时,它能降低CXCL8诱导的初级人类中性粒细胞通过HMEC-1人类微血管内皮细胞层的跨内皮迁移。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5801 | 12-Hydroxyjasmonic acid | ||
12-Hydroxyjasmonic acid glucoside is a COI1-JAZ-independent activator of leaf-closing movement in samanea saman. | |||
TN5330 |
Lacinilene C
3,10-Dihydroxy-1,3,5,7-cadinatetraen-9-one |
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Lacinilene C, lacinilene C 7-methyl ether, scopoletin, 2-hydroxy-7-methoxycadalene and 2,7-dihydroxycadalene are 5 induced phytoalexins in cotton leaves. Lacinilene C methyl ether elicits contraction of TSM by enhancing the movement of calcium through pot |