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Antiviral API
- Arenavirus
- Cytomegalovirus (CMV)
- Dengue virus
- Endogenous Metabolite
- Enterovirus (EV)
- Epstein-Barr virus (EBV)
- Filovirus
- Flavivirus
- HCV Protease
- Hepatitis B Virus (HBV)
- Hepatitis C Virus (HCV)
- Herpes simplex Virus (HSV)
- HIF/HIF Prolyl-Hydroxylase
- HIV Integrase
- HIV Protease
- Human immunodeficiency Virus (HIV)
- Human papillomavirus (HPV)
- Influenza Virus
- Nipah virus
- Orthopoxvirus
- Others
- Rabies virus (RABV)
- Respiratory syncytial Virus (RSV)
- Reverse Transcriptases (RTs)
- SARS-CoV
- Tobacco mosaic virus (TMV)
- Vesicular stomatitis virus (VSV)
- Virus Protease
- West Nile virus
- Antiviral intermediates
Telbivudine
Category | Hepatitis B Virus (HBV) |
CAS | 3424-98-4 |
Description | Telbivudine is an antiviral drug used in the treatment of hepatitis B infection. It is marketed by Swiss pharmaceutical company Novartis under the trade names Sebivo (Europe) and Tyzeka (United States). Clinical trials have shown it to be significantly more effective than lamivudine or adefovir, and less likely to cause resistance. |
Product Information
Synonyms | LDT 600; LD-T600; LDT600; Telbivudine; Tyzeka; Epavudine |
IUPAC Name | 1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione |
Molecular Weight | 242.23 |
Molecular Formula | C10H14N2O5 |
Canonical SMILES | CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O |
InChI | InChI=1S/C10H14N2O5/c1-5-3-12(10(16)11-9(5)15)8-2-6(14)7(4-13)17-8/h3,6-8,13-14H,2,4H2,1H3,(H,11,15,16)/t6-,7+,8-/m1/s1 |
InChIKey | IQFYYKKMVGJFEH-GJMOJQLCSA-N |
Melting Point | 185-186 °C |
Purity | 98% |
Density | 1.452 g/cm3 |
Solubility | Soluble in Water (10 mg/mL) |
Appearance | White to Off-White Solid |
Application | Antiviral Agents |
Storage | Store at -20°C |
Complexity | 381 |
Exact Mass | 242.09027155 |
Index Of Refraction | 1.584 |
In Vitro | Telbivudine reverses B19V-induced dysregulation of BIRC3, thus, intervening in the Apoptosis pathway and protecting susceptible cells from cell death. |
PSA | 104.55000 |
Target | HBV |
XLogP3-AA | -1.2 |