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Cat. No.	Product Name	Target	Signaling Pathways
T9127	MYLS22	Others	Others
	MYLS22 是视神经萎缩 1 的选择性抑制剂。它通过影响 NFkB 活性和血管生成基因表达抑制血管生成，靶向作用于内皮细胞 OPA1 ，减少肿瘤的生长。
T63272	Edralbrutinib TG-1701	BTK	Angiogenesis; Tyrosine Kinase/Adaptors
	Edralbrutinib (TG-1701) 是有效的BTK抑制剂，具有抗癌活性，可用于治疗肿瘤、免疫系统疾病、血液及淋巴系统疾病。Edralbrutinib可用于研究膜性肾小球肾炎和视神经脊髓炎。
T77416	Opicinumab BIIB033	Others	Others
	Opicinumab (BIIB033) 是一种新型抗 LINGO-1 的单克隆抗体，可用于预防和延缓急性视神经炎和复发性多发性硬化。
T8644	Elamipretide Triacetate Elamipretide TriTFA	Others	Others
	Elamipretide Triacetate (Elamipretide TriTFA) 是一种芳香族阳离子四肽，可轻松穿透细胞膜并短暂定位于线粒体内膜，在此与心磷脂结合。它已用于研究 Leber 遗传性视神经病变治疗的试验。
T21509	CA 074	Cysteine Protease	Proteases/Proteasome
	CA 074 是一种高效的组织蛋白酶B (cathepsin B) 抑制剂， Ki 值为2 to 5 nM。CA 074 抑制灵长类动物缺血性海马神经元死亡，可减轻 SJL/J 小鼠诱导的实验性自身免疫性脑脊髓炎的视网膜病变和视神经炎。
T76713	Inebilizumab MEDI 551,MT-0551,16C4-aFuc,VIB-0551	Others	Others
	Inebilizumab 是一种人源化抗 CD19 单克隆抗体，对 B 细胞具有增强的抗体依赖细胞介导的细胞毒性。Inebilizumab 可用于治疗多发性硬化和视神经脊髓炎等一些与 CD19的B细胞相关的一系列自身免疫性疾病。
T73457	DN-1289	DNA Alkylation	DNA Damage/DNA Repair
	DN-1289 是一种可口服可通过血脑屏障且具有选择性高效性的抑制剂，对双亮氨酸拉链激酶 (DLK）的 IC50 值为17 nM，对亮氨酸拉链轴承激酶 (LZK）的 IC50 值为 40 nM。DN-1289 对小鼠模型中视神经挤压 (ONC) 诱导的 p-c-Jun 有显著的抑制作用。
T23985	Dextramycine Dextramycin,(+)-Chloramphenicol,Dextromycetin,L-threo-Chloramphenicol
	Dextramycine is an optic isomer of chloramphenicol.
T25107	Arginylphenylalaninamide Rfamide,Arg-phe-NH2
	Arginylphenylalaninamide, an FMRamide fragment, may be utilized as a neurotransmitter or neuromodulator by optic lobe neurons of different types.
T65489	Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride
	Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride is used as a probe for luminescent detection and quantitation of oxygen (absorption λmax=455 nm, luminescence λmax=613 nm). It is also used for fibre optic sensors. At the same time, Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride can be used in studies on oxygen in skin and skin tumors as well as measurement of oxygen flux through the skin.
T69600	Spermidine-d6
	Spermidine-d6 is intended for use as an internal standard for the quantification of spermidine by GC- or LC-MS. Spermidine is an endogenous polyamine. It is formed from putrescine by spermidine synthase. Spermidine (25 µM) inhibits the activity of the human inward-rectifying potassium channel Kir2.3 in a patch-clamp assay. It induces autophagy in HeLa cells when used at a concentration of 100 µM and increases the lifespan of D. melanogaster, yeast, and C. elegans. Spermidine (30 mM in the drinki...