김대기 명예교수

프로필 이미지 없음
김대기 교수는 약학과/약학대학 소속 교수로 재직 중이며, 신약개발의 권위자다. 미국 뉴욕주립대(Buffalo)에서 의약화학 전공으로 박사학위를 받았으며, 항암제, 섬유증 치료제 등의 신약을 개발하기 위한 연구를 진행하고 있다. 1999년 국내신약1호인 백금착체항암제 '선플라'를 상품화하였으며, 2007년 국내신약13호인 발기부전치료제 '엠빅스'를 상품화하였다. 2014년 항암제/섬유증 치료제 신약후보물질인 '백토서팁(EW-7197)'을 개발하여 미국 식품의약품안전국으로부터 임상시험을 승인받아, 현재 미국 및 한국에서 9건의 1b/2a 임상시험이 진행되고 있다. 현재까지 총 120편의 논문을 SCI급 국제학술지에 발표하였다.
연구실적
  • EW-7197, transforming growth factor β inhibitor, combined with irreversible electroporation for improving skin wound in a rat excisional model Scientific Reports, 2024, v.14 no.1, 12779
    SCIE Scopus dColl.
  • Beneficial Effects of a Curcumin Derivative and Transforming Growth Factor-β Receptor I Inhibitor Combination on Nonalcoholic Steatohepatitis DIABETES & METABOLISM JOURNAL, 2023, v.47 no.4, 500-513
    SCIE Scopus KCI dColl.
  • Different routes of administering EW-7197 versus EW-7197?HBr for preventing peritoneal adhesion in a rat model SURGERY, 2023, v.173 no.4, 1008-1014
    SCIE Scopus dColl.
  • Discovery of (E)-3-(3-((2-Cyano-4' -dimethylaminobiphenyl-4-ylmethyl)cyclohexanecarbonylamino)-5-fluorophenyl)acrylic Acid Methyl Ester, an Intestine-Specific, FXR Partial Agonist for the Treatment of Nonalcoholic Steatohepatitis JOURNAL OF MEDICINAL CHEMISTRY, 2022, v.65 no.14, 9974-10000
    SCIE Scopus dColl.
  • EW-7197 Attenuates the Progression of Diabetic Nephropathy in db/db Mice through Suppression of Fibrogenesis and Inflammation Endocrinology and Metabolism, 2022, v.37 no.1, 96-111
    SCIE Scopus KCI dColl.
  • Synthesis, biological evaluation and molecular modelling of 2,4-disubstituted-5-(6-alkylpyridin-2-yl)-1H-imidazoles as ALK5 inhibitors JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2020, v.35 no.1, 702-712
    SCIE Scopus dColl.
  • Vactosertib, a Novel, Orally Bioavailable Activin Receptor-Like Kinase 5 Inhibitor, Promotes Regression of Fibrotic Plaques in a Rat Model of Peyronie's Disease WORLD JOURNAL OF MENS HEALTH, 2020, v.38 no.4, 552-563
    SCIE KCI dColl.
  • EW-7197 eluting nano-fiber covered self-expandable metallic stent to prevent granulation tissue formation in a canine urethral model PLoS ONE, 2018, v.13 no.2, e0192430
    SCIE Scopus dColl.
  • EW-7197, an oral transforming growth factor beta type I receptor kinase inhibitor, for preventing peritoneal adhesion formation in a rat model SURGERY, 2018, v.164 no.5, 1100-1108
    SCIE Scopus dColl.
  • Cancer upregulated gene 2 induces epithelial-mesenchymal transition of human lung cancer cells via TGF-β signaling Oncotarget, 2017, v.8 no.3, 5092-5110
    SCIE Scopus dColl.
  • EW-7197, an activin-like kinase 5 inhibitor, suppresses granulation tissue after stent placement in rat esophagus GASTROINTESTINAL ENDOSCOPY, 2017, v.86 no.1, 219-228
    SCIE Scopus dColl.
  • Novel oral transforming growth factor-β signaling inhibitor EW-7197 eradicates CML-initiating cells Cancer Science, 2016, 26 JAN 2016
    SCIE Scopus dColl.
  • TGF-β Type I Receptor Kinase Inhibitor EW-7197 Suppresses Cholestatic Liver Fibrosis by Inhibiting HIF1α-Induced Epithelial Mesenchymal Transition Cellular Physiology and Biochemistry, 2016, v.38 no.2, 571-588
    SCIE Scopus dColl.
  • Antitubercular activities of the novel synthesized 1,2,4-triazole derivatives Bulletin of the Korean Chemical Society, 2015, v.36 no.1, 43-51
    SCIE KCI Scopus dColl.
  • Combinatorial TGF-β attenuation with paclitaxel inhibits the epithelial-to-mesenchymal transition and breast cancer stem-like cells Oncotarget, 2015, v.6 no.35, 37526-37543
    SCIE Scopus dColl.
  • EW-7197 inhibits hepatic, renal, and pulmonary fibrosis by blocking TGF-β/Smad and ROS signaling Cellular and molecular life sciences : CMLS, 2015, v.72 no.10, 2023-2039
    Scopus SCIE dColl.
  • Phosphorylation status determines the opposing functions of Smad2/Smad3 as STAT3 cofactors in TH17 differentiation Nature Communications, 2015, v.6
    SCIE Scopus dColl.
  • Synthesis and biological evaluation of 5-(fluoro-substituted-6-methylpyridin-2-yl)-4-([1,2,4]triazolo[1,5-a]pyridin-6-yl)imidazoles as inhibitors of transforming growth factor-β type i receptor kinase Bioorganic and Medicinal Chemistry Letters, 2015, v.25 no.22, 5228-5231
    SCIE Scopus dColl.
  • 4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5(3)-(6-methylpyridin-2-yl)imidazole and -pyrazole derivatives as potent and selective inhibitors of transforming growth factor-beta type I receptor kinase BIOORGANIC & MEDICINAL CHEMISTRY, 2014, v.22 no.9, 2724-2732
    SCIE Scopus dColl.
  • An novel inhibitor of TGF-β type I receptor, IN-1130, blocks breast cancer lung metastasis through inhibition of epithelial-mesenchymal transition Cancer Letters, 2014, v.351 no.1, 72-80
    SCIE Scopus dColl.
  • Discovery of N-((4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5-(6-methylpyridin-2-yl)-1H-imidazol-2-yl)methyl)-2-fluoroaniline (EW-7197) : A Highly Potent, Selective, and Orally Bioavailable Inhibitor of TGF-beta Type I Receptor Kinase as Cancer Immunotherapeutic/Antifibrotic Agent JOURNAL OF MEDICINAL CHEMISTRY, 2014, v.57 no.10, 4213-4238
    SCIE Scopus dColl.
  • EW-7197, a novel ALK-5 kinase inhibitor, potently inhibits breast to lung metastasis Molecular Cancer Therapeutics, 2014, v.13 no.7, 1704-1716
    SCIE Scopus dColl.
  • [학술지논문] Synthesis, biological evaluation and molecular modelling of 2,4-disubstituted-5-(6-alkylpyridin-2-yl)-1H-imidazoles as ALK5 inhibitors JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2020, v.35 no.1 , 702-712
    SCI
강의
학력

State University of New York at Buffalo Ph.D.(Medicinal Chemistry)

서울대학교 약학석사(약학과)

서울대학교 약학사(약학과)

경력

인투젠 대표이사 2000-07-13 ~ 2002-08-31

SK 케미칼 대우이사/상무보/상무대우 1997-01-01 ~ 2001-02-10

선경인더스트리 선임연구원/책임연구원 1989-01-21 ~ 1996-12-31

한국화학연구소 선임연구원 1987-09-22 ~ 1988-12-04

ICN-Nucleic Acid Research Institute (Postdoc) 1986-10-01 ~ 1987-09-30