HBV

Related Products

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 Related Products (33):

Cat. No.	Product Name	Effect	Purity

HY-100029

Bay 41-4109 Inhibitor 98.92%

BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV) with an IC₅₀ of 53 nM.
HY-13623A

Entecavir monohydrate Inhibitor 99.95%

Entecavir monohydrate (BMS200475 monohydrate) is a potent and selective inhibitor of HBV, with an EC₅₀ of 3.75 nM in HepG2 cell.
HY-13782

Tenofovir Disoproxil Fumarate Inhibitor 99.80%

Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used to treat HIV and chronic Hepatitis B.
HY-108917

Morphothiadin Inhibitor 99.59%

Morphothiadin is a potent inhibitor on the replication of both wild-type and adefovir-resistant HBV with an IC₅₀ of 12 nM.
HY-112142

AB-423 Inhibitor 99.60%

AB-423 is an inhibitor of HBV capsid assembly, and potent inhibits HBV replication with EC₅₀/EC₉₀ of 0.08-0.27 μM/0.33-1.32 μM in cells.

Bay 41-4109	Inhibitor	98.92%
BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV) with an IC₅₀ of 53 nM.

Entecavir monohydrate	Inhibitor	99.95%
Entecavir monohydrate (BMS200475 monohydrate) is a potent and selective inhibitor of HBV, with an EC₅₀ of 3.75 nM in HepG2 cell.

Tenofovir Disoproxil Fumarate	Inhibitor	99.80%
Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used to treat HIV and chronic Hepatitis B.

Morphothiadin	Inhibitor	99.59%
Morphothiadin is a potent inhibitor on the replication of both wild-type and adefovir-resistant HBV with an IC₅₀ of 12 nM.

AB-423	Inhibitor	99.60%
AB-423 is an inhibitor of HBV capsid assembly, and potent inhibits HBV replication with EC₅₀/EC₉₀ of 0.08-0.27 μM/0.33-1.32 μM in cells.

HY-19447

Besifovir	Inhibitor
Besifovir (LB80331), a parent drug converted by LB80380, further metabolizes to its active form, LB80317. LB80380 is potent antiviral agent against hepatitis B virus (HBV) .

HY-114314

BA-53038B	Inhibitor
BA-53038B is a HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner, with an EC₅₀ value of 3.32 μM.

HY-19447A

Besifovir Dipivoxil maleate	Inhibitor
Besifovir Dipivoxil maleate (LB80380 maleate) is an oral prodrug of LB80317. Besifovir Dipivoxil maleate (LB80380 maleate) is effective in hepatitis B virus (HBV) DNA suppression for both treatment-naive and lamivudine-resistant chronic hepatitis B (CHB) patients in preliminary studies^[2]

HY-16468

Squalamine Inhibitor >98.0%

Squalamine(MSI-1256) is an aminosterol compound with potent broad spectrum antiviral activity.
HY-101954

Inarigivir Inhibitor 99.20%

Inarigivir (ORI-9020;SB-9000) is a dinucleotide which can significantly reduce liver HBV DNA in transgenic mice expressing hepatitis B virus.
HY-13986

Merimepodib Inhibitor 98.37%

Merimepodib is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.
HY-B0255

Adefovir dipivoxil Inhibitor 98.50%

Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body.
HY-112564

JNJ-632 Inhibitor 99.36%

JNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator (CAM).

Squalamine	Inhibitor	>98.0%
Squalamine(MSI-1256) is an aminosterol compound with potent broad spectrum antiviral activity.

Inarigivir	Inhibitor	99.20%
Inarigivir (ORI-9020;SB-9000) is a dinucleotide which can significantly reduce liver HBV DNA in transgenic mice expressing hepatitis B virus.

Merimepodib	Inhibitor	98.37%
Merimepodib is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.

Adefovir dipivoxil	Inhibitor	98.50%
Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body.

JNJ-632	Inhibitor	99.36%
JNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator (CAM).

HY-117650A

RG7834	Inhibitor	99.29%
RG7834 (RO 7020322) is a highly selective and orally bioavailable HBV inhibitor, potently inhibits HBV antigens (both HBsAg and HBeAg) and HBV DNA, with IC₅₀s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells.

HY-107902

RIG-1 modulator 1	Inhibitor	98.81%
RIG-1 modulator 1 is an anti-viral compound which can be useful for the treatment of viral infections including influenza virus, HBV, HCV and HIV extracted from patent WO 2015172099 A1.

HY-B0955

Oxethazaine Inhibitor 99.86%

Oxethazaine is a topical anesthetic, in preventing acid-induced esophageal pain.
HY-B0017

Telbivudine Inhibitor 99.87%

Telbivudine, a specific inhibitor of hepatitis B virus (HBV) replication, is an antiviral drug used in the treatment of hepatitis B infection.
HY-B0766

Bicyclol Inhibitor 99.97%

Bicyclol(SY 801) is a anti-hepatitis drug.
HY-100029A

Bay 41-4109 racemate Inhibitor 98.02%

BAY 41-4109 racemate is the racemate of BAY 41-4109. BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV) with an IC₅₀ of 53 nM.
HY-13623

Entecavir Inhibitor 98.88%

Entecavir (SQ 34676; BMS 200475) is a potent and selective inhibitor of HBV, with an EC₅₀ of 3.75 nM in HepG2 cell.

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