A strategy for finding new medicines against the novel coronavirus disease (COVID-19) derived from base pairing with DNA damages
<p>The spread of the novel coronavirus disease (COVID-19) has caused a global pandemic. Exiting agents that act on proteins including 3-chymotrypsin-like protease (3CLpro), papain-like protease (PLpro), helicase, RNA-dependent RNA polymerase (RdRp), spike glycoprotein (S protein), and others i...
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| Format: | Book |
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Global Journal of Infectious Diseases and Clinical Research - Peertechz Publications,
2020-12-22.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | peertech__10_17352_2455-5363_000038 | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Katsuhito Kino |e author |
| 700 | 1 | 0 | |a Takayuki Ohshima |e author |
| 700 | 1 | 0 | |a Taishu Kawada |e author |
| 700 | 1 | 0 | |a Takanobu Kobayashi |e author |
| 700 | 1 | 0 | |a Hiroshi Miyazawa |e author |
| 245 | 0 | 0 | |a A strategy for finding new medicines against the novel coronavirus disease (COVID-19) derived from base pairing with DNA damages |
| 260 | |b Global Journal of Infectious Diseases and Clinical Research - Peertechz Publications, |c 2020-12-22. | ||
| 520 | |a <p>The spread of the novel coronavirus disease (COVID-19) has caused a global pandemic. Exiting agents that act on proteins including 3-chymotrypsin-like protease (3CLpro), papain-like protease (PLpro), helicase, RNA-dependent RNA polymerase (RdRp), spike glycoprotein (S protein), and others in similar viruses [1,2] are likely used as antiviral drugs against the novel coronavirus (SARS-CoV-2). Data on Chemical Abstract Service show that the potential drug candidates against 3CLpro and RdRp are more than those against other targets [2].</p><p><br></p> | ||
| 540 | |a Copyright © Katsuhito Kino et al. | ||
| 546 | |a en | ||
| 655 | 7 | |a Opinion |2 local | |
| 856 | 4 | 1 | |u https://doi.org/10.17352/2455-5363.000038 |z Connect to this object online. |