Structure-Based Discovery of Novel Cyclophilin A Inhibitors for the Treatment of Hepatitis C Virus Infections
DC Field | Value | Language |
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dc.contributor.author | Yang, Suhui | - |
dc.contributor.author | Jyothi, K. R. | - |
dc.contributor.author | Lim, Sangbin | - |
dc.contributor.author | Choi, Tae Gyu | - |
dc.contributor.author | Kim, Jin-Hwan | - |
dc.contributor.author | Akter, Salima | - |
dc.contributor.author | Jang, Miran | - |
dc.contributor.author | Ahn, Hyun-Jong | - |
dc.contributor.author | Kim, Hee-Young | - |
dc.contributor.author | Windisch, Marc P. | - |
dc.contributor.author | Khadka, Daulat B. | - |
dc.contributor.author | Zhao, Chao | - |
dc.contributor.author | Jin, Yifeng | - |
dc.contributor.author | Kang, Insug | - |
dc.contributor.author | Ha, Joohun | - |
dc.contributor.author | Oh, Byung-Chul | - |
dc.contributor.author | Kim, Meehyein | - |
dc.contributor.author | Kim, Sung Soo | - |
dc.contributor.author | Cho, Won-Jea | - |
dc.date.available | 2020-02-28T06:44:57Z | - |
dc.date.created | 2020-02-06 | - |
dc.date.issued | 2015-12-24 | - |
dc.identifier.issn | 0022-2623 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/9803 | - |
dc.description.abstract | Hepatitis C virus (HCV) is a major cause of end-stage liver disease. Direct acting antivirals (DAAs), including inhibitors Of nonstructural proteins (NS3/4A protease, NS5A, and NS5B polymerase), represent key components of anti-HCV treatment, but these are associated with increased drug resistance and toxicity. Thus, the development of host-targeted antiviral agents, such as cyclophilin A inhibitors, is an alternative approach for more effective, selective, and safer treatment. Starting with the discovery of a bis-amide derivative 5 through virtual screening; the lead compound 25 was developed using molecular modeling-based design and systematic exploration of the structure-activity relationship. The lead 25 lacked cytotoxicity, had potent anti-HCV activity, and showed Selective and high binding affinity for CypA. Unlike cyclosporin A, 25 lacked immunosuppressive effects, successfully inhibited the HCV replication, restored host immune responses without acute toxicity in vitro and in vivo, and exhibited a high synergistic effect in combination with other drugs. These findings suggest that the bis-amides have significant potential to extend the arsenal of HCV therapeutics. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.relation.isPartOf | JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.subject | SOFOSBUVIR PLUS RIBAVIRIN | - |
dc.subject | HCV GENOTYPE 1 | - |
dc.subject | CYCLOSPORINE-A | - |
dc.subject | RNA REPLICATION | - |
dc.subject | ACTIVE-SITE | - |
dc.subject | INTERFERON | - |
dc.subject | NS5A | - |
dc.subject | THERAPIES | - |
dc.subject | RESISTANCE | - |
dc.subject | EMERGENCE | - |
dc.title | Structure-Based Discovery of Novel Cyclophilin A Inhibitors for the Treatment of Hepatitis C Virus Infections | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000367563100009 | - |
dc.identifier.doi | 10.1021/acs.jmedchem.5b01064 | - |
dc.identifier.bibliographicCitation | JOURNAL OF MEDICINAL CHEMISTRY, v.58, no.24, pp.9546 - 9561 | - |
dc.identifier.scopusid | 2-s2.0-84953268731 | - |
dc.citation.endPage | 9561 | - |
dc.citation.startPage | 9546 | - |
dc.citation.title | JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.volume | 58 | - |
dc.citation.number | 24 | - |
dc.contributor.affiliatedAuthor | Oh, Byung-Chul | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SOFOSBUVIR PLUS RIBAVIRIN | - |
dc.subject.keywordPlus | HCV GENOTYPE 1 | - |
dc.subject.keywordPlus | CYCLOSPORINE-A | - |
dc.subject.keywordPlus | RNA REPLICATION | - |
dc.subject.keywordPlus | ACTIVE-SITE | - |
dc.subject.keywordPlus | INTERFERON | - |
dc.subject.keywordPlus | NS5A | - |
dc.subject.keywordPlus | THERAPIES | - |
dc.subject.keywordPlus | RESISTANCE | - |
dc.subject.keywordPlus | EMERGENCE | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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