• Title/Summary/Keyword: Kim Hye-jin

Search Result 6,261, Processing Time 0.046 seconds

Tissue Distribution of Novel Polymeric Micellar Paclitaxel in Mice

  • Kim, Hye-Jin;Kang, Min-Kyung;Kim, Kil-Soo
    • Proceedings of the PSK Conference
    • /
    • 2002.10a
    • /
    • pp.413.3-414
    • /
    • 2002
  • Paclitaxel is a diterpenoid isolated from Taxus brevifolia and is an active anticancer drug for the treatment of ovarian cancer, breast cancer and Kaposi's sarcoma. Due to its low solubility in water, it is dissolved in Cremophor EL(polyethoxylated castor oil) and ethanol, which cause serious side effects including hypersensitivity. BLK460 was developed as a novel polymeric micellar paclitaxel formulation containing Aceporol460 as solubilizer (omitted)

  • PDF

Automatic Registration of Quickbird Image and Digital Map (수치지도와 Quickbird 영상의 자동 기하보정)

  • Han, Dong-Yeob;Kim, Hye-Jin;Kim, Yong-Il
    • Proceedings of the KSRS Conference
    • /
    • 2007.03a
    • /
    • pp.109-112
    • /
    • 2007
  • 본 논문에서는 대축척 수치지도와 Quickbird 위성영상의 자동 보정을 영상공간에서 수행한다. 알고리즘은 보정변환식의 초기 계수값 결정과 정확한 변환계수 결정과정으로 나뉜다. 초기 계수값 결정은 보정변환식의 상수항을 결정하는 것으로 수치지형도의 지면개체와 영상에서 추출된 에지의 논리곱 연산을 적용하여 최적값을 추정하는 방식을 용한다. 보정 다항식의 정확한 변환계수를 결정하기 위하여 수치지형도의 지면 선형개체 점데이터와 영상의 에지개체 점데이터간 ICP 조정을 수행하였다. 제안된 방법의 정확도를 평가한 결과, 영상공간에서 1.72화소의 RMSE를 나타내었다.

  • PDF

Lead Informatics Using Protein 3D-Structures

  • Ro, Seong-Gu;Shin, Dong-Kyu;Han, Hui-Jong;Jeon, Young-Ho;Jeong, Eui-Jun;Hwang, Kwang-Yeon;Kim, Hye-Yeon;Heo, Yong-Seok;Lee, Tae-Gyu;Kim, Jin-Hwan
    • Proceedings of the PSK Conference
    • /
    • 2001.04a
    • /
    • pp.77-77
    • /
    • 2001
  • PDF

Facile One-Pot Synthesis of 1,3,5-Trisubstituted Pyrazoles from α,β-Enones

  • Yu, Jin;Kim, Ko Hoon;Moon, Hye Ran;Kim, Jae Nyoung
    • Bulletin of the Korean Chemical Society
    • /
    • v.35 no.6
    • /
    • pp.1692-1696
    • /
    • 2014
  • A practical and efficient one-pot synthesis of 1,3,5-trisubstituted pyrazoles from ${\alpha},{\beta}$-enones and arylhydrazine hydrochlorides has been developed. The pyrazoles were formed via a tandem formation of the corresponding pyrazolines and an acid-catalyzed aerobic oxidation process.