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Cat. No.	Product Name	Target	Signaling Pathways
T40114	RSV-IN-2
	RSV-IN-2 is a powerful compound that acts as a dual inhibitor of both wild-type and mutant respiratory syncytial virus (RSV) fusion proteins. It efficiently inhibits the activity of these proteins, with an EC50 value of 0.27 nM for the wild-type and 0.70 nM for the D486N-mutant protein.
T61291	RSV/IAV-IN-2
	RSV/IAV-IN-2 (compound 14c) 是一种有效的 RSV/IAV 双重抑制剂。RSV/IAV-IN-2 的细胞毒性低于临床药物利巴韦林。RSV/IAV-IN-2 具有研究 RSV 和/或 IAV 感染的潜力。
T79217	RSV L-protein-IN-2	RSV	Microbiology/Virology
	RSVL-protein-IN-2 (Compound A)为一种RSV聚合酶的非竞争性抑制剂，其IC50值为4.5 μM。此化合物对长RSV株表现出抗病毒活性，EC50值达1.3 μM。
T73253	EIDD-2749 4'-Fluorouridine,4'-FlU ; 4'-Fluorouridine,4'-FlU
	EIDD-2749 (4'-Fluorouridine) 是一种口服有效的RdRp 抑制剂。EIDD-2749 能有效抑制RSV 和SARS-CoV-2的复制。EIDD-2749 还表现出抗HCV 和淋巴细胞性脉络丛脑膜炎病毒 (LCMV) 的活性。EIDD-2749 是一种很有潜力的COVID-19口服治疗候选剂，也适用于其他 RNA 病毒的研究。
T79219	RSV L-protein-IN-3	RSV	Microbiology/Virology
	RSVL-protein-IN-3为一野生型RSV聚合酶抑制剂，具IC50值10.4 μM及EC50值2.1 μM(RSV)。相较之下，RSV/IAV-IN-2之细胞毒性显著低于临床活性分子Ribavirin。
T60910	RSV-IN-4
	RSV-IN-4 (Compound 2) 具有抗 RSV 活性，EC50值为11.76 μM。RSV-IN-4 是呼吸道合胞病毒 (RSV) 和甲流病毒 A (IAV) 的双重抑制剂。
T79221	RSV L-protein-IN-5	RSV	Microbiology/Virology
	RSVL-protein-IN-5（compound E）是一种高效针对呼吸道合胞病毒（RSV）的抑制剂，拥有EC50值为0.1 μM。该化合物在IC50为0.66 μM的条件下能够抑制聚合酶（Polymerase），并通过阻断病毒转录物的鸟苷酸化过程来抑止RSVmRNA的合成。RSVL-protein-IN-5具有中等细胞毒性（CC50为10.7 μM，HEp-2细胞），同时，在每日4.1 mg/kg剂量下，能减少RSV感染小鼠模型中的病毒滴度。
T36440	GS-441524 tris-isobutyryl ester
	GS-441524tris-isobutyryl ester is a prodrug form of the antiviral nucleoside analog and remdesivir metabolite GS-441524 .1It reduces the cytopathic effect of respiratory syncytial virus (RSV) in infected HEp-2 cells with an EC50value of 0.26 μM. 1.Mackman, R.L., Hui, H.C., Perron, M., et al.Prodrugs of a 1’-CN-4-aza-7,9-dideazaadenosine C-nucleoside leading to the discovery of remdesivir (GS-5734) as a potent inhibitor of respiratory syncytial virus with efficacy in the african green monkey mode...
T37295	Ganglioside GM1 Asialo Mixture
	Ganglioside GM1 asialo is a component of cellular lipid rafts and can be formed by the cleavage of the sialic acid residue from ganglioside GM1 by neuraminidase. Ganglioside GM1 asialo is a glycolipid receptor for P. aeruginosa flagellin and stimulates defensive responses in host cells, including extracellular ATP release, calcium mobilization, and ERK1/2 phosphorylation when stimulated by flagellin and an anti-ganglioside GM1 asialo antibody. The percentage of ganglioside GM1 asialo-positive na...
T38297	Ribavirin-13C5 Ribavirin-13C5
	Ribavirin-13C5is intended for use as an internal standard for the quantification of ribavirin by GC- or LC-MS. Ribavirin is an antiviral guanosine nucleoside analog.1,2Upon entry into cells, ribavirin is metabolized to an active triphosphate form that induces viral RNA chain termination and inhibits viral polymerases. It reduces replication in a panel of seven RNA and four DNA viruses in Vero cells (EC50s = 2-95 μg/ml).3Ribavirin also reduces replication of severe acute respiratory syndrome coro...