serotype

Ganciclovir sodium (Cytovene IV sodium) 是核苷类似物和口服抗病毒药物，具有抗病毒活性，尤其是针对巨细胞病毒和单纯疱疹病毒 1 型。

Ganciclovir (2'-Nor-2'-deoxyguanosine) 是核苷类似物和口服抗病毒药物，对CMV 具有抗病毒活性。它用于治疗与艾滋病相关的巨细胞病毒感染的并发症。

This is amino acids 427 to 441 fragment belongs to the FliC, serotype a of the S. FliC epitope recognized by a CD4+ T cell from naturally infected C57BL/6 mice is located in a region common to a number of distinct Salmonella serovars such as the S. paraty

A20FMDV2是一种由口蹄疫病毒（FMDV）血清型O的VP1衣壳蛋白上的α-螺旋RGD细胞相互作用域组成的肽，能够结合到αVβ6整合素上。该化合物在表达人αVβ6的H357舌鳞状细胞癌细胞中抑制αVβ6整合素依赖的细胞粘附（IC50 = 1.2 µM）。与111indium-DTPA耦合时，A20FMDV2（20 MBq）可结合于在乳腺癌小鼠异种移植模型中内源性表达的αVβ6整合素，用于放射成像分析。

Ganglioside GT1b is a trisialoganglioside that is characterized by having two sialic residues linked to the inner galactose unit. It binds to the neurotoxins botulinum toxin serotype A (BTxA), BTxA heavy chain, and tetanus toxin with IC50 values of 11, 0.74, and 7.2 μM, respectively.[1] Ganglioside GT1b-containing liposomes bind to the major coat protein VP1 from Merkel cell polyomavirus (MCPyV), which has been identified in Merkel cell carcinomas, identifying ganglioside GT1b as a putative MCPyV receptor. [2] Ganglioside GT1b decreases production of IL-6, IL-10, IgG, IgM, and IgA in human peripheral blood mononuclear cells (PBMCs) by 31.4, 30.5, 60, 59.5, and 58%, respectively, when used at a concentration of 10 μM [3] . Ganglioside GT1b mixture contains ganglioside GT1b molecular species with C18:1 and C20:1 sphingoid backbones.

UDP-N-acetyl-D-Glucosamine is a natural nucleotide sugar that is used by glycosyltransferases to transfer N-acetyl-D-glucosamine residues to substrates.1It is an important component of antibiotic biosynthesis pathways in fungi and lipopolysaccharide production in bacteria.2,3 1.Roseman, S.Reflections on glycobiologyJ. Biol. Chem.276(45)41527-41542(2001) 2.Kudo, F., and Eguchi, T.Biosynthetic genes for aminoglycoside antibioticsJ. Antibiot. (Tokyo)62(9)471-481(2009) 3.Mulrooney, E.F., Poon, K.K., McNally, D.J., et al.Biosynthesis of UDP-N-acetyl-L-fucosamine, a precursor to the biosynthesis of lipopolysaccharide in Pseudomonas aeruginosa serotype O11J. Biol. Chem.280(20)19535-19542(2005)

NITD-688 是一种具有口服活性的登革病毒 (dengue virus)NS4B 蛋白的泛血清型抑制剂。 NITD-688 可用于登革热病毒 (DENV) 的研究。

AAV-8 NSL epitope 是一种特定的 CD8+ T 细胞表位，从腺相关病毒血清型 8 的衣壳中分离得到。该表位与 MHC I 分子有着较高的亲和力，并能够激活 CD8+ T 细胞。它主要用于研究 T 细胞介导的免疫反应如何影响 AAV 介导的基因转移。

C562-1101 is a novel potent botulinum neurotoxin serotype E (BoNT/E) inhibitor.

Myelin Oligodendrocyte Glycoprotein (MOG) peptide 是 MOG 的一种内源性肽段截取，存在于髓鞘的细胞外表面。当与抗原血清型HLA-DR2结合时，MOG peptide 在通过中脑动脉阻塞（MCAO）诱导的缺血性中风模型中，能减少皮层和纹状体梗死体积，降低管-角转测试中的感觉运动障碍，增加对新奇气味的探索时间，以及增加雌性（但不是雄性）小鼠对笼伴侣发出的呼叫持续时间。

Panobacumab (KBPA101) 是一种完全人 IgM κ 单克隆抗体，由人类 B 淋巴细胞产生，对血清型 O11P. aeruginosa 的 LPS O 多糖具有抗性。

Mosnodenvir（JNJ-1802）是一种泛血清型登革热抗病毒药物，表现出较高的耐药性屏障，同时安全性和耐受性均优良。它通过阻断NS3-NS4B相互作用来抑制病毒复制复合体。在小鼠模型中，Mosnodenvir展示了从皮摩尔到低纳摩尔量级的体外抗病毒效能。

CBIP is a small-molecule inhibitors of botulinum neurotoxin serotype A light chain (BoNT/A LC). CBIP possesses low micromolar activity against BoNT/A.