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 (42):

Cat. No. Product Name Effect Purity
  • HY-15142
    Doxorubicin hydrochloride Inhibitor 99.47%
    Doxorubicin hydrochloride是一种有细胞毒性的蒽环类抗生素,用于治疗多种癌症。Doxorubicin 在癌细胞中起作用的可能机制是嵌入 DNA 和破坏 topoisomerase-II 介导的DNA修复。Doxorubicin hydrochloride 下调 AMPK 的基础磷酸化以及下游 acetyl-CoA 羧化酶。
  • 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-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-100029
    Bay 41-4109 Inhibitor 98.92%
    BAY 41-4109是人乙型肝炎病毒 (HBV) 的有效抑制剂,IC50值为 53 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-N6939
    Pseudolaric Acid B Inhibitor 99.47%
    Pseudolaric Acid B 是一种从 Pseudolarix kaempferi Gorden (pinaceae) 根部分离的二萜酸,具有抗癌、抗真菌、抗受精活性,并对 T 淋巴细胞也具有免疫抑制活性。Pseudolaric Acid B 通过凋亡和细胞周期阻滞抑制乙肝病毒 (HBV) 的分泌。Pseudolaric Acid B 诱导细胞自噬。
  • HY-19447
    Besifovir Inhibitor 98.00%
    Besifovir (LB8033) 是由 LB80380 转化而来的一种 LB80380 母体药物,进一步代谢为其活性形式 LB80317。Besifovir (LB8033) 是抗乙型肝炎病毒 (HBV) 的有效抗病毒药物。
  • 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 98.71%
    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-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-16468
    Squalamine Inhibitor >98.0%
    Squalamine(MSI-1256)是具有广谱抗病毒活性化的化合物。
  • HY-13910
    Tenofovir Inhibitor 99.77%
    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-B0255
    Adefovir dipivoxil Inhibitor 99.87%
    Adefovir Dipivoxil可阻断HBV逆转录酶。
  • 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-101954
    Inarigivir Inhibitor 99.20%
    Inarigivir (ORI-9020;SB-9000) 是一种二核苷酸,可显着减少表达乙型肝炎病毒转基因小鼠的 HBV DNA。
  • HY-N0664
    Aucubin Inhibitor >98.0%
    桃叶珊瑚苷 (Aucubin) 是一类环烯醚萜苷,具有广泛的生物活性,包括抗炎、抗菌、抑制疼痛及抗肿瘤等功效。
  • 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)。
  • HY-13986
    Merimepodib Inhibitor 98.37%
    Merimepodib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。
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