Inhibitors Of Zika Virus
More effective (IC50 at nanomolar range) than other small molecule inhibitors
Prophylactic, post-exposure prophylactic, and treatment option for Zika virus infections
Researchers at UCLA have identified small sulfonamide-based compounds that show potent anti-Zika activity in the low nanomolar range (IC50 = 2.3 nM). These small organic molecules can be synthesized inexpensively in large scale and administered orally as prophylactic, post-exposure prophylactic, and treatment option for Zika virus infections in general and in high-risk populations, including infected pregnant women.
Background Zika virus is an arthropod-borne flavivirus transmitted mainly by infected mosquitos, and it can also be transmitted via maternal to fetal vertical transmission, blood product transfusion, organ transplantation, as well as through sexual contact. Zika virus is linked to fetal developmental abnormalities such as microcephaly, eye defects, and impaired growth when infection occurs in pregnant women. Zika infection also leads to severe neurological complications and possibly male infertility in adults. Currently, there is an ongoing Zika virus outbreak in the Americas, the Caribbean, and the Pacific. However, there are no reliable treatment or vaccine options available to protect those infected by the virus. Bioactivity (IC50) reported to date for small molecules is in the micromolar range, and development of more effective treatment for Zika infection is needed. Additional Technologies by these Inventors Tech ID/UC Case 29055/2018-146-0 Related Cases 2018-146-0
美国
