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Postion:Product Catalog >Vonafexor
Vonafexor
  • Vonafexor

Vonafexor NEW

Price $54 $89 $185
Package 5mg 10mg 25mg
Min. Order:
Supply Ability: 10g
Update Time: 2024-11-19

Product Details

Product Name: Vonafexor CAS No.: 1192171-69-9
Purity: 98.74% Supply Ability: 10g
Release date: 2024/11/19

Product Introduction

Bioactivity

NameVonafexor
DescriptionVonafexor (EYP001) is a farnesoid X receptor (FXR, NR1H4) agonist, with anti-HBV effects
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 22.5 mg/mL (45.94 mM)
KeywordsNR1H4 | HBV | FXR | Inhibitor | EYP-001 | inhibit | PLX-007 | Vonafexor | PLX 007 | Hepatitis B virus | EYP 001
Inhibitors RelatedDoxorubicin hydrochloride | Forskolin | Osthole | Cetylpyridinium Chloride | Tenofovir Disoproxil Fumarate | Obeticholic Acid | Lithocholic acid | Sevelamer hydrochloride | 4-Hydroxyacetophenone | Telbivudine | Tenofovir | Bifendate
Related Compound LibrariesNuclear Receptor Compound Library | Bioactive Compound Library | Drug Repurposing Compound Library | Anti-Viral Compound Library | NO PAINS Compound Library | Lipid Metabolism Compound Library | Metabolism Compound Library | Clinical Compound Library | Bioactive Compounds Library Max | Anti-Infection Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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