Authors:
Suzuki, T
Nagasaki, A
Okumura, K
Shin, CG
Citation: T. Suzuki et al., Convenient syntheses of fragment B and linear main skeleton [Fragment A-B-C '] derivatives of an antibiotic, GE 2270 A, HETEROCYCLE, 55(5), 2001, pp. 835-840
Citation: R. Ushiyama et al., Convenient synthesis of (3S,5S)-5-Hydroxy- and (3R,5S)-5-chloropiperazic acids of a peptide antibiotic, monamycin G(3), CHEM LETT, (11), 2001, pp. 1172-1173
Citation: Rs. Appa et al., Role of the nonspecific DNA-binding region and alpha helices within the core domain of retroviral integrase in selecting target DNA sites for integration, J BIOL CHEM, 276(49), 2001, pp. 45848-45855
Authors:
Yonezawa, Y
Hirosaki, T
Hayashi, T
Shin, CG
Citation: Y. Yonezawa et al., Convenient synthesis and conversion of a (Z)-alpha,beta-didehydroornithinederivative to alpha,beta-didehydrokyotorphin, SYNTHESIS-S, (1), 2000, pp. 144-148
Authors:
Kwon, HC
Jung, CM
Shin, CG
Lee, JK
Choi, SU
Kim, SY
Lee, KR
Citation: Hc. Kwon et al., A new caffeoyl quinic acid from Aster scaber and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase, CHEM PHARM, 48(11), 2000, pp. 1796-1798
Citation: Yt. Oh et Cg. Shin, Comparison of enzymatic activities of the HIV-1 and HFV integrases to their U5 LTR substrates, BIOC MOL B, 47(4), 1999, pp. 621-629