hemagglutinin

MBX2329 是一种流感病毒抑制剂，能特异性地抑制血凝素介导的病毒进入，HIV HA(H5) 的 IC90值为8.6 μM。它能够有效地抑制多种甲型流感病毒。

Influenza hemagglutinin is a type of hemagglutinin found on the surface of the influenza viruses. It is an antigenic glycoprotein. It is responsible for binding the virus to the cell that is being infected. Influenza hemagglutinin proteins bind to cells w

PROTACHemagglutinin Degrader-1 (Compound V3) 是一种有效的 PROTAC 流感病毒血凝素 (influenza hemagglutinin(HA)) 降解剂，降解中值浓度为 1.44 μM。PROTACHemagglutinin Degrader-1 具有广谱抗流感病毒活性。

Hemagglutinin (48-68) 为流感病毒血凝素的48至68片段，能够诱导肽特异性T细胞克隆增殖。

Anti-Influenza A H10 Hemagglutinin HA Antibody (8B805) 是一种靶向Influenza Influenza A H10 Hemagglutinin HA 的单克隆抗体，是一种 Mouse IgG1 抗体。

Partial antigenic glycoprotein

Phytohemagglutinin (PHA-M) 是一种普通豆菜豆的主要种子凝集素，聚集在子叶的薄壁细胞中。它是一种 T 细胞激活剂，能够刺激人单核白细胞，可诱导 ChAT mRNA 表达，增强 ACh 合成。

Phytohemagglutinin P（PHA-P，植物血凝素 P）是一种天然的凝集素(lectin)，是PHA的蛋白形式。PHA是选择性T细胞有丝分裂原，可以结合T细胞受体并增强HIV-1的复制。

BMY-27709 是一种流感病毒生长抑制剂，对 A WSN 33 病毒生长的 IC50 值为 3-8 μM，对流感病毒的部分亚型也展现出抑制活性。BMY-27709 对 H1 和 H2 病毒感染的早期起作用，通过抑制血凝素蛋白展现其抗病毒活性。然而，BMY-27709 对 H3 亚型病毒以及 B 型 Lee 40 流感病毒没有作用。

TBMP (butylated hydroxyanisole) 是病毒包膜蛋白血凝素 (HA) 介导的进入新型抑制剂。

Influenza HA 126-138 acetate 是一种流感病毒血凝素 (HA) 肽乙酸盐，包含氨基酸 126-138。 它诱导胸腺和外周 T 细胞凋亡。

Alimemazine (Trimeprazine) is generally used as an antipruritic agent and also a hemagglutinin (HA)-receptor antagonist. Alimemazine also acts as a partial agonist against the histamine H1 receptor (H1R) and other GPCRs.

JNJ4796 is an oral active fusion inhibitor of the influenza virus, by inhibiting hemagglutinin (HA)-mediated fusion to neutralizing the influenza A group 1 virus. JNJ4796 mimics the functionality of the broadly neutralizing antibodies (bnAbs).

N-butyl Lithocholic acid 是 lithocholic acid 的一个衍生物。研究显示，与载有胆固醇的脂质纳米粒子相比，小鼠中应用的包含 N-butyl Lithocholic acid 的脂质纳米粒子，这些粒子内封装有表达流感血凝素的 mRNA 疫苗，表现出在心脏、脾脏及肝脏的毒性显著降低。

6,6′-Trehalose dioleate（6,6′-TDO）是一种被广泛用于mRNA体内外递送的糖脂化合物。它能高效包裹流感A病毒血凝素A（HA）编码的mRNA，在脂质纳米粒子（LNPs）中使用，用于增强隔离小鼠脾细胞分泌Ifn-γ, Il-2和Tnf-α。在肌肉注射进入小鼠体内后，包含6,6′-TDO的LNPs主要在肝脏与脾脏中集中。区别于未含6,6′-TDO的LNP配方，这种LNPs不会引起血清中血尿素氮（BUN）、乳酸脱氢酶（LDH）、肌钙蛋白I、丙氨酸氨基转移酶（ALT）、及天门冬氨酸氨基转移酶（AST）水平的改变。此外，该LNPs还能提升小鼠血清中IgG1与IgG2a抗体的滴度。

Ingavirin, a novel inhibitor of the influenza virus reproduction, inhubits the formation of the virus specific hemagglutinin.

9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME (1 g animal) enhances the antiviral IgA and IgG antibody responses induced by a nasal influenza hemagglutinin (HA) vaccine by 5.2- and 2-fold, respectively, in mice.4 1.Hamberg, M., and Hamberg, G.Peroxygenase-catalyzed fatty acid epoxidation in cereal seeds: Sequential oxidation of linoleic acid into 9(S),12(S),13(S)-trihydroxy-10(E)-octadecenoic acidPlant Physiol.110(3)807-815(1996) 2.Hong, S.S., and Oh, J.S.Inhibitors of antigen-induced degranulation of RBL-2H3 cells isolated from wheat branJ. Korean Soc. Appl. Biol. Chem.5569-74(2012) 3.Kim, C.S., Kwon, O.W., Kim, S.Y., et al.Five new oxylipins from Chaenomeles sinensisLipids49(11)1151-1159(2014) 4.Shirahata, T., Sunazuka, T., Yoshida, K., et al.Total synthesis, elucidation of absolute stereochemistry, and adjuvant activity of trihydroxy fatty acidsTetrahedron62(40)9483-9496(2006) 5.Fuchs, D., Tang, X., Johnsson, A.-K., et al.Eosinophils synthesize trihydroxyoctadecenoic acids (TriHOMEs) via a 15-lipoxygenase dependent processBiochim. Biophys. Acta Mol. Cell Biol. Lipids1865(4)158611(2020)

CAY10766 is an antiviral compound.1It inhibits entry of influenza virus-like particles pseudotyped with hemagglutinin A (HA) from H5N1 influenza A virus into A549 cells (EC50= 0.24 μM). CAY10766 (1 μM) reduces H1N1 and H5N1 influenza A viral titers in infected MDCK cells. It also exhibits synergy with oseltamivir carboxylate in MDCK cells infected with the influenza A reporter PR8-NS1-Gluc virus.

Influenza HA (110-119) refers to a specific fragment (110-119) derived from the hemagglutinin protein of the influenza virus. This fragment has the ability to induce the proliferation of Treg cells.

Influenza HA (110-119) acetate 是流感病毒血凝素的 110-119 片段，可刺激 Treg 细胞增殖。

Influenza virus-IN-5 (Compound 5f) 是一种流感病毒血球凝集素 (hemagglutinin (HA)) 抑制剂，能够作用于 A H3N2 病毒 (EC50: 1 nM)。

CBS1194 is a novel antiviral agent against influenza A virus (IAV), and is more specifically, a group 2 IAV fusion inhibitor. CBS1194 prevents membrane fusion of the virus through the inhibition of the conformational change of hemagglutinin (HA). CBS1194 causes steric hinderance that prevents the rearrangement of the HA that would normally be induced by low-pH, by fitting into the pocket by the fusion peptide.

IAV inhibitor 4l is an IAV inhibitor targeting hemagglutinin and mediates viral entry by preventing HA-membrane fusion.

Nylidrin (Buphenine) 是一种结构相关的非哌啶，具有抗高血压活性，通过靶向甲型流感病毒的血凝素 2 介导的膜融合显示出抗病毒活性。