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Volumn 56, Issue 7, 2012, Pages 3582-3586

Pharmacokinetic comparison of a single oral dose of polymorph form I versus form V capsules of the antiorthopoxvirus compound ST-246 in human volunteers

Author keywords

[No Author keywords available]

Indexed keywords

TECOVIRIMAT;

EID: 84862548012     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.06090-11     Document Type: Article
Times cited : (16)

References (13)
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    • Bailey TR, et al. 2007. N-(3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6- ethenocycloprop[f]isoindol-2-(1H)-yl)carboxamides: identification of novel orthopoxvirus egress inhibitors. J. Med. Chem. 50:1442-1444.
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    • Henderson DA, et al. 1999. Smallpox as a biological weapon: medical and public health management. JAMA 281:2127-2137.
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    • Single-dose safety and pharmacokinetics of ST-246, a novel orthopoxvirus egress inhibitor
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    • Jordan, R.1
  • 7
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    • Safety and pharmacokinetics of the antiorthopoxvirus compound ST-246 following repeat oral dosing in healthy adult subjects
    • Jordan R, et al. 2010. Safety and pharmacokinetics of the antiorthopoxvirus compound ST-246 following repeat oral dosing in healthy adult subjects. Antimicrob. Agents Chemother. 54:2560-2566.
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    • Efficacy of delayed treatment with ST-246 given orally against systemic orthopoxvirus infections in mice
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.