Discovery of Nonpungent Transient Receptor Potential Vanilloid 1 (TRPV1) Agonist as Strong Topical Analgesic
DC Field | Value | Language |
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dc.contributor.author | Ann, Jihyae | - |
dc.contributor.author | Kim, Ho Shin | - |
dc.contributor.author | Thorat, Shivaji A. | - |
dc.contributor.author | Kim, Hee | - |
dc.contributor.author | Ha, Hee-Jin | - |
dc.contributor.author | Choi, Kwanghyun | - |
dc.contributor.author | Kim, Young-Ho | - |
dc.contributor.author | Kim, Minseok | - |
dc.contributor.author | Hwang, Sun Wook | - |
dc.contributor.author | Pearce, Larry, V | - |
dc.contributor.author | Esch, Timothy E. | - |
dc.contributor.author | Turcios, Noe A. | - |
dc.contributor.author | Blumberg, Peter M. | - |
dc.contributor.author | Lee, Jeewoo | - |
dc.date.available | 2020-11-02T06:25:40Z | - |
dc.date.issued | 2020-01 | - |
dc.identifier.issn | 0022-2623 | - |
dc.identifier.issn | 1520-4804 | - |
dc.identifier.uri | https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/1103 | - |
dc.description.abstract | Paradoxically, some TRPV1 agonists are, at the organismal level, both nonpungent and clinically useful as topical analgesics. Here, we describe the scaled-up synthesis and characterization in mouse models of a novel, nonpungent vanilloid. Potent analgesic activity was observed in models of neuropathic pain, and the compound blocked capsaicin induced allodynia, showing dermal accumulation with little transdermal absorption. Finally, it displayed much weaker systemic toxicity compared to capsaicin and was negative in assays of genotoxicity. | - |
dc.format.extent | 7 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | American Chemical Society | - |
dc.title | Discovery of Nonpungent Transient Receptor Potential Vanilloid 1 (TRPV1) Agonist as Strong Topical Analgesic | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1021/acs.jmedchem.9b01046 | - |
dc.identifier.scopusid | 2-s2.0-85076391103 | - |
dc.identifier.wosid | 000507150400027 | - |
dc.identifier.bibliographicCitation | Journal of Medicinal Chemistry, v.63, no.1, pp 418 - 424 | - |
dc.citation.title | Journal of Medicinal Chemistry | - |
dc.citation.volume | 63 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 418 | - |
dc.citation.endPage | 424 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | CAPSAICIN | - |
dc.subject.keywordPlus | RESINIFERATOXIN | - |
dc.subject.keywordPlus | DESENSITIZATION | - |
dc.subject.keywordPlus | MUTAGENICITY | - |
dc.subject.keywordPlus | RATS | - |
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