30
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3478 |
Ro 67-7476
|
GluR | Neuroscience |
Ro 67-7476 是mGluR1的正变位调节剂,能增强表达 rat mGluR1a 的 HEK293 细胞中谷氨酸诱导的钙释放,EC50为 60.1 nM。它是 P-ERK1/2 激动剂,可以在外源添加谷氨酸的情况下激活 ERK1/2 磷酸化 (EC50=163.3 nM)。 | |||
T2710 |
TCS 1102
|
OX Receptor | GPCR/G Protein; Neuroscience |
TCS 1102 是双食欲素受体拮抗剂,对 OX1和OX2受体的Ki 分别为3和 0.2 nM。 | |||
T22323 |
Enoxaparin sodium
|
Thrombin | Proteases/Proteasome |
Enoxaparin sodium 是一种低分子量肝素 (LMWH),已获得美国 FDA 批准,可用于医疗管理的 ST 段心肌梗死 (STEMI) 或 STEMI 及随后的经皮冠状动脉介入治疗 (PCI) 患者。它与抗凝血酶结合并增强其作用,并抑制凝血因子 XIa、IXa、Xa 和 IIa(凝血酶),从而防止血栓形成。 | |||
T1461 |
Candesartan
CV 11974,坎地沙坦 |
RAAS | Endocrinology/Hormones |
Candesartan (CV 11974) 是一种血管紧张素II 受体拮抗剂(IC50:0.26 nM)。 | |||
T2371 |
Emapunil
AC-5216,XBD-173 |
Others | Others |
Emapunil (XBD-173) 是一种选择性的、口服有效的TSPO(一种线粒体苯二氮受体) 的配体。在多种动物模型中,它显示出抗焦虑和抗抑郁特性。 | |||
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。 | |||
T0183 |
Pramiracetam
CI-879,普拉西坦 |
Others | Others |
Pramiracetam (CI-879) 来源于piracetam,能改善脑外伤引起的认知障碍。它是更有效的促智药物。 | |||
T60507 |
Utreloxastat
|
||
Utreloxastat 是一种用于 α-突触核蛋白病、tau 蛋白病、渐冻症、创伤性脑损伤和缺血再灌注相关损伤等疾病研究的化合物。 | |||
T10808 |
CHPG sodium salt
|
NF-κB; GluR | Neuroscience; NF-κB |
CHPG sodium salt 是 mGluR5 的选择性激动剂,可激活 ERK 和 Akt 信号通路。 CHPG 钠盐可用于创伤性脑损伤的研究。 | |||
T77691 |
Cyclopentyl phenyl ketone
Benzoylcyclopentane |
Others | Others |
Cyclopentyl phenyl ketone (Benzoylcyclopentane) 可用于预防和治疗创伤应激症。 | |||
T13329 |
Vofopitant
GR 205171 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Vofopitant (GR 205171) 是一种有效的 NK1 receptor 拮抗剂,具有抗焦虑和止吐活性,可用于研究创伤后应激障碍(PTSD)。 | |||
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。 | |||
T8807 |
Benzydamine
|
Others | Others |
Benzydamine 是一种苄基吲唑,具有镇痛、解热和抗炎作用。 Benzydamine 用于减少手术后和创伤后的疼痛和水肿,并促进愈合。 | |||
T22346 |
Indomethacin sodium hydrate
Indometacin sodium hydrate |
COX | Immunology/Inflammation; Neuroscience |
Indomethacin sodium hydrate (Indometacin sodium hydrate) 是一种口服活性、竞争性和可逆性的 COX1/2 抑制剂,具有潜在的抗炎活性,可诱发的偏头痛,诱导的胃肠道损伤,可用于研究成人继发于严重创伤性脑损伤的颅内压增高和类风湿性关节。 | |||
T34249 |
Rabeximod
ROB-803 |
TLR | Immunology/Inflammation |
Rabeximod 是一种有效的免疫调节剂,可降低鼠模型中自身免疫性疾病疾病严重程度。Rabeximod 通过刺激TLR2和TLR4下游阻断炎症细胞(可能是巨噬细胞)的激活,以时间依赖性的方式抑制关节炎。Rabeximod 能有效降低创伤性脑损伤抗炎治疗过程中小鼠的脑抗原呈递。 | |||
T1880 |
P7C3
|
Others | Others |
P7C3 是一种 aminopropyl carbazole 类化合物,具有口服活性,可透过血脑屏障,具有神经保护作用。它可用于神经退行性疾病,如帕金森病的研究。 | |||
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。 | |||
T33765 |
NVX-108
Dodecafluoropentane,DDFP,Perfluoropentane |
||
NVX-108 is an exceptional oxygen transporter which increases brain tissue oxygen tension (PbtO2) when administered soon after traumatic brain injury (TBI). | |||
T40775 |
SSR411298
SSR411298 |
||
SSR411298 is a reversible, orally active compound that selectively inhibits fatty acid amide hydrolase (FAAH). Its potential lies in the field of post-traumatic stress disorder (PTSD) research. | |||
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. | |||
T26627 |
Anatibant
LF16-0687,LF-16-0687,LF 160687,LF 16-0687,LF-160687 |
||
Anatibant 是一种有效的非肽缓激肽B2受体拮抗剂。Anatibant 降低实验性外伤性脑损伤后颅内高压和组织病理学损伤。 | |||
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]. | |||
T79056 |
Orexin receptor modulator-1
|
||
Orexin receptormodulator-1 是一款针对食欲素受体的调节剂,主要应用于物质成瘾、惊恐障碍、焦虑、创伤后应激障碍 (PTSD)、疼痛、抑郁、季节性情感障碍、进食障碍及高血压的科研领域。 | |||
T83963 |
Z-DEVD-FMK Caspase-3 Inhibitor
|
||
Z-DEVD-FMK Caspase-3 Inhibitor 是一种可渗透细胞膜的、不可逆的 caspase-3/CPP32 抑制剂,能够抑制肿瘤细胞的凋亡。在动物体内,它在大鼠发作后的海马区具有神经保护作用,且显著减少创伤后的细胞凋亡,并在诱发的大鼠创伤性脑损伤之前和之后改善神经学恢复情况。 | |||
T68579 | Fluvoxamine acid | ||
Fluvoxamine acid is a medication which functions as a selective serotonin reuptake inhibitor (SSRI) and σ1 receptor agonist. Fluvoxamine is used primarily for the treatment of obsessive-compulsive disorder (OCD), and is also used to treat major depressive disorder (MDD), and anxiety disorders such as panic disorder and post-traumatic stress disorder (PTSD). | |||
T73214 |
RX 801077
2 BFI free base |
||
RX 801077 (2 BFI free base) 为选择性咪唑啉 I2 受体 (I2R) 激动剂,其Ki值为70.1 nM,展现抗炎及神经保护效果,具备用于创伤性脑损伤 (TBI) 研究的潜力。 | |||
T82798 |
C3bot(154-182) TFA
|
||
C3bot(154-182) TFA 是C3 肽类化合物,能够通过促进脊髓损伤后下行纤维束的再生,增强其修复效能。此外,C3bot(154-182) TFA 或许能够促进中枢神经系统损伤后的轴突保护与修复,并有助于功能性恢复。 | |||
T79806 |
5-HT2A&5-HT2C agonist-1
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT2A&5-HT2C agonist-1 (Example 2) 是一种选择性的5-HT2A和5-HT2C受体激动剂,其IC50值分别为196 nM和0.9 nM。本化合物主要应用于研究抑郁症、酒精依赖、烟草和可卡因成瘾、炎症、丛集性头痛、PTSD、癫痫等中枢神经系统相关疾病。 | |||
T36903 |
Rasagiline-13C3 (mesylate)
Rasagiline-13C3 (mesylate) |
||
Rasagiline-13C3is intended for use as an internal standard for the quantification of rasagiline by GC- or LC-MS. Rasagiline is an inhibitor of monoamine oxidase B (MAO-B; IC50= 4.43 nM for the rat brain enzyme).1It is selective for MAO-B over MAO-A (IC50= 412 nM for the rat brain enzyme). It inhibits serum and NGF withdrawal-induced apoptosis of PC12 cells when used at concentrations ranging from 0.01 to 100 μM.2Rasagiline inhibits rat brain MAO-Bin vivo(ED50= 0.1 mg/kg).1It reduces cerebral ede... | |||
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.... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4454 |
Traumatic Acid
Dodec-2-Enedioic Acid,2E-Dodecenedioic Acid,愈伤酸,Trans-2-Dodecenedioic Acid |
Antioxidant | oxidation-reduction |
Traumatic Acid (Dodec-2-Enedioic Acid) 是一种单不饱和二元羧酸,从菜豆中分离得到。它可减少膜磷脂的过氧化,并表现出抗氧化和对胶原生物合成的刺激作用。它可用于许多与胶原蛋白生物合成障碍和氧化应激有关的皮肤疾病的研究。 | |||
T36857L |
Premarin
共轭雌激素,Estrone 3-sulfate,Estrone sulfate |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Premarin (Estrone 3-sulfate) 是一种硫酸雌激素,在创伤性脑损伤期间具有神经保护作用。 | |||
T2698 |
Asperosaponin VI
Akebia saponin D,Asperosaponin Ⅵ,川续断皂苷 VI |
Apoptosis; Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
Asperosaponin VI (Akebia saponin D) 是一种来自续断壁的皂苷组分。它通过增加 Bcl-2/Bax 比值,降低活性 caspase-3 表达,以及增强 p-Akt 和 p-CREB,从而抑制缺氧诱导的心肌细胞凋亡。它通过 BMP-2/p38 和 ERK1/2 信号途径诱导成骨细胞分化。 | |||
T4956 |
Tetrahydroxystilbene-2-O-β-D-glucoside
tetrahydroxyl diphenylethylene-2-o-gluco,何首乌苷,EH-201 |
Others | Others |
Tetrahydroxystilbene-2-O-β-D-glucoside (EH-201) 是一种低分子量的促红细胞生成素诱导剂。 | |||
T1208 |
Citicoline sodium
Citicoline sodium salt,CDP-choline,胞磷胆碱钠 |
Apoptosis; Others; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Citicoline sodium (CDP-choline) 是一种合成细胞膜组分磷脂酰胆碱的中间体,有神经保护作用。 |