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TRPV1 길항제의 분자 설계 및 합성 : Fluvirucinine A₁과 fluvirucinine A₂의 입체선택적 전합성 : Design and syntheses of TRPV1 antagonists : Asymmetric total synthesis of fluvirucinine A₁and fluvirucinine A₂

DC Field Value Language
dc.contributor.advisor서영거-
dc.contributor.author이용실-
dc.date.accessioned2009-12-02T11:19:04Z-
dc.date.available2009-12-02T11:19:04Z-
dc.date.copyright2005.-
dc.date.issued2005-
dc.identifier.urihttp://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000052206-
dc.identifier.urihttps://hdl.handle.net/10371/18338-
dc.description학위논문(박사)--서울대학교 대학원 :제약학과 약품제조화학전공,2005.ko
dc.format.extentx, 168 장ko
dc.language.isoko-
dc.publisher서울대학교 대학원en
dc.subjectcapsaicinko
dc.subjectcapsaicinko
dc.subjectTRPV1ko
dc.subjectTRPV1ko
dc.subject바닐로이드 대체구조ko
dc.subjectvanilloid equivalentko
dc.subjectTRPV1 길항제ko
dc.subjectTRPV1 antagonistko
dc.titleTRPV1 길항제의 분자 설계 및 합성 : Fluvirucinine A₁과 fluvirucinine A₂의 입체선택적 전합성en
dc.title.alternativeDesign and syntheses of TRPV1 antagonists : Asymmetric total synthesis of fluvirucinine A₁and fluvirucinine A₂en
dc.typeThesisen
dc.contributor.department제약학과 약품제조화학전공-
dc.description.degreeDoctorko
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