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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
UK-1
Category | Hepatitis C Virus (HCV) |
CAS | 151271-53-3 |
Description | UK-1, a benzoxazol derivative, has been found to be a Streptomyces metabolite that could exhibit anticancer activity and topoisomerase II restraination activity. |
Product Information
Synonyms | UK 1, UK-1, UK1; [2,4'-Bibenzoxazole]-4-carboxylicacid, 2'-(2-hydroxyphenyl)-, methyl ester; ACMC-20n661; CTK4C6968; ZINC598610 |
IUPAC Name | methyl 2-[2-(2-hydroxyphenyl)-1,3-benzoxazol-4-yl]-1,3-benzoxazole-4-carboxylate |
Molecular Weight | 386.36 |
Molecular Formula | C22H14N2O5 |
Canonical SMILES | COC(=O)C1=C2C(=CC=C1)OC(=N2)C3=C4C(=CC=C3)OC(=C5C=CC=CC5=O)N4 |
InChI | InChI=1S/C22H14N2O5/c1-27-22(26)14-8-5-11-17-19(14)24-21(29-17)13-7-4-10-16-18(13)23-20(28-16)12-6-2-3-9-15(12)25/h2-11,23H,1H3 |
InChIKey | KHQWPXPNDALATG-UHFFFAOYSA-N |
Boiling Point | 558.2°C at 760 mmHg |
Melting Point | 217-219°C |
Flash Point | 291.4°C |
Purity | 98% |
Density | 1.423g/cm3 |
Solubility | Soluble in DMF or DMSO. Limited solubility in ethanol and methanol. Poor water solubility. |
Appearance | White to off-white solid. |
Storage | Store in a cool and dry place and at 0 - 4 °C for short term (days to weeks) or -20 °C for long term (months to years). |
Complexity | 604 |
Exact Mass | 386.09027155 |
Index Of Refraction | 1.687 |
PSA | 98.59000 |
Target | HCV |
Vapor Pressure | 1.71E-12mmHg at 25°C |
XLogP3-AA | 4.4 |