교수소개

교수소개

교수소개
백두종
  • 학위: 박사
  • 연구실 : (K관)자연과학대학관 (K215)
  • 연락처 : 02-2287-5143
  • 세부전공 : 유기화학전공
이메일
학위
  • 박사, University of Illinois at Urbana - Champaign 화학과 (세부전공 : 유기화학), 198812
  • 석사, 서울대학교 화학과, 198002
  • 학사, 서울대학교 화학교육과 (세부전공 : 화학교육), 197802
경력
  • 기술고문, 중외제약, (1991.10~2001.12)
  • 박사후연구원, 컬럼비아 대학교, (1989.02~1991.07)
  • 이사, (사)한국창의인성교육연구원, ( . ~ )
논문
  • 광학 분할에 의한 (S)-(+)-Pranidipine의 제조방법, 대한화학회지, 201512
  • Garner’s Aldehyde의 대량 합성을 위한 합성법 개선, 대한화학회지, 201512
  • Discovery and biological evaluation of tetrahydrothieno[2,3-c]pyridine derivatives as selective metabotropic glutamate receptor 1 antagonists for the potential treatment of neuropathic pain, EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 201506
  • "Synthesis of Novel Dihydropyridothienopyrimidin-4,9-dione Derivatives", MOLECULES, 201505
  • Synthesis and Biological Evaluation of N-3-Alkyl-Thienopyrimidin-4-Ones as mGluR1 Antagonists, BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 201505
  • Synthesis and In vivo Evaluation of 5-Methoxy-2-(phenylethynyl) quinoline (MPEQ) and [11C]MPEQ Targeting Metabotropic Glutamate Receptor 5 (mGluR5), Bulletin of the Korean Chemical Society, 201408
  • Synthesis and Biological Evaluation of 2-Substituted Quinoline 6-Carboxamides as Potential mGluR1 Antagonists for the Treatment of Neuropathic Pain, CHEMICAL & PHARMACEUTICAL BULLETIN, 201406
  • Synthesis and biological evaluation of 2-(arylethynyl)quinoline derivatives as mGluR5 antagonists for the treatment of neuropathic pain, Bioorganic & Medicinal Chemistry Letters, 201303
  • 5-HT2C receptor selectivity and structure-activity relationship of N-methyl-N-(1-methylpiperidin-4-yl)benzenesulfonamide analogs, BIOORGANIC MEDICINAL CHEMISTRY LETTERS, 201201
  • Synthesis and Biological Evaluation of 1-Heteroarylmethyl 1,4-Diazepanes Derivatives as Potential T-type Calcium Channel Blockers, BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 201108
  • Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors, BIOORGANIC MEDICINAL CHEMISTRY LETTERS, 201105
  • Facile synthesis and biological evaluation of 3,3-diphenylpropanoyl piperazines as T-type calcium channel blockers, BIOORGANIC MEDICINAL CHEMISTRY LETTERS, 201101
  • In silico Analysis on hERG Channel Blocking Effect of a Series of T-type Calcium Channel Blockers, Bulletin of the Korean Chemical Society, 201101
  • Isolation and Identification of an Unauthorized Sildenafil Analogue in a Commercial Functional Food, 대한화학회지 (Journal of the Korean Chemical Society), 201008
  • 에피나스틴 항히스타민제의 합성법 개선, 대한화학회지 (Journal of the Korean Chemical Society), 201008
  • 시판 기능성식품으로부터의 타다라필 유도체 부정첨가물질의 분리 및 구조규명, 약학회지, 201008
지식재산
  • 2-벤질아닐린의 신규 제조방법 (출원번호:10-2016-0007948), 주식회사 엠씨켐, 20160122
  • N-[O-(P-피발로일옥시벤젠술포닐아미노)벤조일] 글리신의 신규 제조 방법 및 그 모노나트륨염 ・ 4 수화물의 동결 건조 제제의 제조 방법 (등록번호:10-1366706), 상명대학교서울산학협력단, 주식회사 엠씨켐, 20140218
  • 2-(2-아미노에틸)-1-메틸피롤리딘의 신규 제조방법 (등록번호:10-1330674), 상명대학교서울산학협력단, 주식회사 엠씨켐, 20131112
  • N-[O-(P-피발로일옥시벤젠술포닐아미노)벤조일] 글리신의 신규 제조 방법 및 그 모노나트륨염 ・ 4 수화물의 동결 건조 제제의 제조 방법 (등록번호:10-1247137), 주식회사 엠씨켐, 상명대학교 산학협력단, 투윈파마 주식회사, 20130319
  • 광학 분리에 의한 활성 피페리딘 화합물의 제조방법 (등록번호:10-1146009), 동인화학주식회사, 20120507
학술발표
  • Coordinative Amphiphilic siRNA Transporters, 대한화학회, 20170420
  • Synthesis and Biological Activity of α,β-unsaturated carbonyl conjugated carboxylic acid derivatives as S1P Receptor Agonist, 대한화학회, 20161013
  • Discovery of Novel S1P3-Sparing S1P1 & S1P5 Receptor Agonists for Treatment of Multiple Sclerosis, 대한화학회, 20161013
  • Discovery of Novel S1P1 & S1P5 Direct Agonist for Treatment of Multiple Sclerosis, 대한화학회, 20160422
  • Development of Novel S1P1 & S1P5 Receptor Agonist for Treatment of Multiple Sclerosis, Asian Federation for Medicinal Chemistry, 20151018
  • Synthesis and Biological Evaluation of Novel S1P1 Receptor Agonist for the Treatment of Multiple Sclerosis, 대한화학회 의약화학분과회, 20150205
  • Synthesis and biological evaluation of tetrahydrothieno[2,3-c]pyridine derivatives as mGluR1/5 negative allosteric modulators, 대한화학회, 20131016
  • Synthesis and biological evaluation of tetrahydrothieno[2,3-c]pyridine derivatives as mGluR5 negative allosteric modulators, 대한화학회, 20130417
  • mGluR1 Antagonists for Treatment of Neutopathic Pain, 대한화학회, 20130417
  • Synthesis and biological research of N-containing heteroaromatic compounds as mGluR5 negative allosteric modulators, 대한화학회, 20121017
  • Synthesis and Biological Evaluation of Quinoline Derivatives as Selective mGluR1/5 Modulators, Asian Federation for Medicinal Chemistry, 20111201
  • Synthesis and Biological Evaluation of Quinoline Derivatives as Selective mGluR1 Modulators, 대한화학회, 20110930
  • Synthesis and Biological Evaluation of Novel T-type Calcium Channel Blockers for Treating Neuropathic Pain, 대한화학회, 20110429
프로젝트
  • 초순수 항히스타민제 Epinastine HCl의 신규 공정 개발, 경기과학기술진흥원, (2016. ~ )
  • 광학분리에 의한 활성 피페리딘 화합물의 제조방법, 상명대학교, (2014. ~ )
  • 항히스타민제 개량신약 결정형 베포타스틴의 개발, 중소기업청, (2013. ~ )
  • Garner’s Aldehyde의 대량합성을 위한 합성법 개선, 상명대학교, (2013. ~ )
  • 폐손상 치료용 원료의약품인 Sivelestat Sodium Hydrate의 제조공정 개발(1/2), 중소기업청, (2011. ~2012. )
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