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Cat. No. | Product Name | Target | Signaling Pathways |
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T79444 |
HA-IN-1
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Influenza Virus | Microbiology/Virology |
HA-IN-1(compound 5g)是靶向血凝素(HA)胰蛋白酶切割位点的配体,表现出高亲和力。该化合物能够抑制HA介导的膜融合,并在体内有效降低肺部病毒滴度,展现其作为甲型流感病毒(IAV)抑制剂和抗流感药物的潜力。 | |||
T81037 |
Tat-HA-NR2B9c
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Tat-HA-NR2B9 是一种包括HIV-1 Tat细胞膜转导结构域片段、流感病毒血凝素(HA)表位标签以及NR2B(NR2B9c) C端9个氨基酸的化学复合物。该化合物能够降低大鼠缺血性脑损伤的梗塞面积,同时促进神经功能的恢复。 | |||
T62216 |
Influenza virus-IN-5
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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)。 | |||
T82229 |
HD-2a
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HA-2a通过降低RAW264.7细胞内circDcbld2的表达,从而抑制JAK2/STAT3信号传导途径。 | |||
T82150 |
Hyaluronan-IN-1
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Hyaluronan-IN-1是一种具有生物活性的12个氨基酸构成的肽类透明质酸(HA)抑制剂,HA为广泛存在于细胞外基质及细胞表面的高分子糖胺聚糖。该肽特异性地与可溶性、固定化及细胞相关的HA形态结合,能几乎完全抑制白细胞与HA底物的粘附。 | |||
T35433 |
α-hydroxy Farnesyl Phosphonic Acid
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α-hydroxy Farnesyl phosphonic acid is a nonhydrolyzable analog of farnesyl pyrophosphate which acts as a competitive inhibitor of farnesyl transferase (FTase). At concentrations greater than 1 μM, α-hydroxy farnesyl phosphonic acid inhibits the processing of Ras in Ha-ras-transformed NIH3T3 cells. | |||
T77158 | Diridavumab | ||
Diridavumab为一种针对HA茎的单克隆抗体。它能稳定HA的融合前结构,阻断细胞膜与病毒膜在核内体内因pH变化引起的融合。此抗体主要用于H2流感病毒研究。 | |||
T77095 | Nebacumab | ||
Nebacumab (HA-1A)为一种与内毒素的脂质A部分结合的单克隆抗体,适用于败血症研究。 | |||
T37466 | CAY10766 | ||
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. | |||
T74762 |
Influenza A virus-IN-8
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Influenza A virus-IN-8 (S5) 为一种大环肽,无细胞毒性,并作为甲型流感病毒 (IAV) 的有效抑制剂,显示出较好的蛋白酶稳定性。其对 H1 和 H5 变体的IC50值分别低至 6.7 nM 和 6.6 nM。此外,Influenza A virus-IN-8 能够与 HA 茎的一个保守区域结合,特别是对 H1 变体展现出 1.0 nM 的高亲和性Kd 值。 | |||
T37729 |
IMP-1700
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IMP-1700 is an inhibitor of bacterial DNA repair.1It potentiates the activity of the quinolone antibiotic ciprofloxacin against methicillin-resistantS. aureus(MRSA) with a combination index value of 0.7. IMP-1700 inhibits the ciprofloxacin-induced bacterial SOS response, a process that repairs DNA damage, in a reporter assay in a concentration-dependent manner. It is also active againstE. coli, as well as methicillin-resistant and -sensitive S. aureus, when used alone (EC50s = 0.5, 0.21, and 3.8... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T75743 | HA Peptide TFA | ||
HA Peptide (TFA) 为源自人类流感血凝素 (HA) 的九氨基酸多肽, 在细胞生物学与生物化学领域内广泛应用于目标蛋白的分离、纯化、检测及追踪。 | |||
T37272 |
9(S),12(S),13(S)-TriHOME
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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... |