1. Signaling Pathways
  2. Anti-infection
  3. HBV

HBV

HBV (Hepatitis B virus), abbreviated HBV, is a species of the genus Orthohepadnavirus, which is likewise a part of the Hepadnaviridae family of viruses. HBV causes the disease hepatitis B. The hepatitis B virus is classified as the type species of the Orthohepadnavirus, which contains three other species: the Ground squirrel hepatitis virus, Woodchuck hepatitis virus, and theWoolly monkey hepatitis B virus. The genus is classified as part of the Hepadnaviridae family. HBV is divided into four major serotypes (adr, adw, ayr, ayw) based on antigenic epitopes present on its envelope proteins, and into eight genotypes (A–H) according to overall nucleotide sequence variation of the genome. The genotypes have a distinct geographical distribution and are used in tracing the evolution and transmission of the virus. Differences between genotypes affect the disease severity, course and likelihood of complications, and response to treatment and possibly vaccination.

HBV 相关产品 (56):

Cat. No. Product Name Effect Purity
  • HY-15142
    Doxorubicin hydrochloride Activator 99.47%
    Doxorubicin hydrochloride (Hydroxydaunorubicin hydrochloride) 是一种有细胞毒性的蒽环类抗生素,常用作肿瘤化疗剂。Doxorubicin hydrochloride 抑制拓扑异构酶 II (topoisomerase-II),IC50 为 2.67 μM,从而抑制 DNA 复制。Doxorubicin hydrochloride 下调 AMPK 的基础磷酸化以及下游 acetyl-CoA 羧化酶。Doxorubicin hydrochloride 诱导凋亡 (apoptosis) 和自噬 (autophagy)。Doxorubicin hydrochloride 抑制人 DNA 拓扑异构酶 I (topoisomerase I),IC50 为 0.8 μM。
  • HY-107454
    OSS_128167 Inhibitor 98.22%
    OSS_128167 是一种有效的选择性沉默调节蛋白 6 (SIRT6) 抑制剂,对 SIRT6,SIRT1 和 SIRT2 的 IC50 分别为 89 μM,1578 μM 和 751 μM。OSS_128167 具有抗 HBV 活性,可抑制 HBV 的转录和复制。OSS_128167 具有抗癌,抗炎和抗病毒作用。
  • HY-13623A
    Entecavir monohydrate Inhibitor 99.95%
    Entecavir monohydrate (BMS200475 monohydrate; SQ34676 monohydrate) 是有选择且有效地HBV抑制剂。在HepG2细胞中的EC50值为3.75 nM。
  • HY-15601
    Vesatolimod Inhibitor 99.56%
    Vesatolimod (GS-9620) 是一种有效,选择性,可口服的 Toll 样受体7 (TLR7) 激动剂,EC50 值为291 nM。
  • HY-N0058
    4,5-Dicaffeoylquinic acid Inhibitor 99.98%
    异绿原酸 C (4,5-Dicaffeoylquinic acid) 是一种天然化合物,具有保护肝脏、抗乙肝的潜能。
  • HY-B1826
    Adefovir Inhibitor >98.0%
    Adefovir (GS-0393) 是一种单磷酸腺苷类似物抗病毒剂,在细胞内转化为 Adefovir diphosphate 后可抑制 HBV DNA 聚合酶。Adefovir 在 HepG2.2.15 细胞系中对 HBVIC50 为 0.7 μM。Adefovir 对多种病毒(包括 HBV 和疱疹病毒)具有良好的抗病毒活性。
  • HY-109137
    Selgantolimod Inhibitor
    Selgantolimod (GS-9688) 是一种口服活性,有效和选择性的 Toll 样受体 8 (TLR8) 激动剂,用于治疗乙型肝炎病毒 (HBV) 和 HIV 感染。
  • HY-N0063
    Punicalagin Inhibitor 99.80%
    Punicalagin 是一种从石榴 (Punica granatum L.) 或 Terminalia catappa L. 的叶子中分离的多酚成分。Punicalagin 是一种抗乙型肝炎病毒 (HBV) 药物,具有抗氧化,抗炎和抗癌作用。
  • HY-13782
    Tenofovir Disoproxil Fumarate Inhibitor 99.80%
    Tenofovir Disoproxil Fumarate是用于治疗 HIV 和慢性乙型肝炎核苷酸逆转录酶抑制剂。
  • HY-N0056
    Isochlorogenic acid A Inhibitor 99.22%
    Isochlorogenic acid A (3,5-Dicaffeoylquinic acid) 是一种具有抗氧化和抗炎活性的天然酚酸。
  • HY-100029
    Bay 41-4109 Inhibitor 98.39%
    BAY 41-4109是人乙型肝炎病毒 (HBV) 的有效抑制剂,IC50值为 53 nM。
  • HY-117650A
    RG7834 Inhibitor 99.29%
    RG7834 (RO 7020322) 是一种高度选择性、可口服的 HBV 抑制剂,在 dHepaRG 细胞中,能够有效抑制 HBV 抗原 HBsAg,HBeAg 和 HBV DNA,IC50 值分别为 2.8,2.6 和 3.2 nM。
  • HY-13986
    Merimepodib Inhibitor 98.91%
    Merimepodib (VX-497) 是非竞争型,有口服活性的肌苷一磷酸脱氢酶 (IMPDH) 抑制剂,具有广谱抗病毒活性。
  • HY-13910
    Tenofovir Inhibitor 99.81%
    Tenofovir (GS 1278) 是一种核苷酸逆转录酶 (nucleotide reverse transcriptase) 抑制剂,可用于治疗HIV和慢性乙型肝炎 (Hepatitis B; HBV)。
  • HY-108917
    Morphothiadin Inhibitor 99.59%
    Morphothiadin 是野生型和阿德福韦耐药 HBV 复制的有效抑制剂,其 IC50 值为 12 nM。
  • HY-112142
    AB-423 Inhibitor 99.60%
    AB-423 是一种 HBV 衣壳组装抑制剂,在细胞中,能够抑制 HBV 复制,EC50/EC90 值分别为 0.08-0.27 μM/0.33-1.32 μM。
  • HY-B0255
    Adefovir dipivoxil Inhibitor 99.87%
    Adefovir Dipivoxil可阻断HBV逆转录酶。
  • HY-N0054
    Osthole Inhibitor 99.90%
    Osthole 是一种天然抗组胺药替代试剂。Osthole 可有效抑制组胺 H1 受体 (histamine H1 receptor) 活性。Osthole 还可抑制细胞培养物中 HBV 的分泌。
  • HY-16468
    Squalamine Inhibitor >98.0%
    Squalamine(MSI-1256)是具有广谱抗病毒活性化的化合物。
  • HY-112564
    JNJ-632 Inhibitor 99.36%
    JNJ-632 是一种乙型肝炎病毒 (HBV) 衣壳组装调节剂 (CAM)。
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