K. Wang

发表

Novel lead generation through hypothetical pharmacophore three-dimensional database searching: discovery of isoflavonoids as nonsteroidal inhibitors of rat 5 alpha-reductase.

G. S. Chen, C. S. Chang, W. Kan, 2001, Journal of medicinal chemistry.

C-22 acid intermediates in the microbiological cleavage of the cholesterol side chain.

K. Wang, C. Sih, H. Tai, 1967, Journal of the American Chemical Society.

Mechanisms of steroid oxidation by microorganisms: V. Reduction of the δ6,7 double bond

K. Wang, C. Sih, Y. Tsong, 1964 .

Mechanisms of Steroid Oxidation by Microörganisms.1 II. Isolation and Characterization of 3aα-H-4α-[3″-Propionic acid]-7aβ-methylhexahydro-1,5-indanedione

K. Wang, C. Sih, 1963 .

Microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes - An alternative route to 6-methylsteroids

K. Wang, Shoei‐Sheng Lee, Jiann-Long Yan, 2000, Steroids.

Mechanisms of steroid oxidation by microorganisms. 13. C22 acid intermediates in the degradation of the cholesterol side chain.

K. Wang, C. Sih, H. Tai, 1968, Biochemistry.

Mechanisms of steroid oxidation by microorganisms. IX. On the mechanism of ring A cleavage in the degradation of 9,10-seco steroids by microorganisms.

K. Wang, D. Gibson, H. Whitlock, 1965, The Journal of biological chemistry.

An immunosuppressive factor interacts with membrane glycolipid asialo-GM1 structure.

K. Wang, C. Verret, R. Yu, 1987, Immunobiology.

Studies on quinazolines and 1,2,4-benzothiadiazine 1,1-dioxides. 8.1, 2 synthesis and pharmacological evaluation of tricyclic fused quinazolines and 1,2,4-benzothiadiazine 1,1-dioxides as potential alpha1-adrenoceptor antagonists.

K. Wang, J. Chern, M. Yen, 1998, Journal of medicinal chemistry.

Mechanisms of steroid oxidation by microorganisms. 8. 3,4-Dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione, an intermediate in the microbiological degradation of ring A of androst-4-ene-3,17-dione.

K. Wang, C. Sih, Y. Tsong, 1966, The Journal of biological chemistry.

3,4-Dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione. An Intermediate in the Microbiological Degradation of Ring A of Androst-4-ene-3,17-dione

K. Wang, C. Sih, Y. Tsong, 1965 .

ON THE MECHANISM OF RING A CLEAVAGE IN THE DEGRADATION OF 9,10-SECO STEROIDS BY MICROORGANISMS.

K. Wang, D. Gibson, H. Whitlock, 1965, Journal of the American Chemical Society.

Microbial transformation of dihydrosarsasapogenin with Mycobacterium sp.

K. Wang, S. S. Lee, G. Lin, 1998, Journal of natural products.

A NEW ROUTE TO ESTRONE FROM STEROLS.

K. Wang, C. Sih, 1965, Journal of the American Chemical Society.

Isoprenyl diphosphate synthases.

K. Wang, S. Ohnuma, S. Ohnuma, 2000, Biochimica et biophysica acta.

Microbial Transformation of Lanosterol Derivatives with Mycobacterium sp. (NRRL B-3805)

K. Wang, Shoei‐Sheng Lee, Jiann-Long Yan, 1995 .

AN EFFICIENT SYNTHESIS OF ESTRONE AND 19-NORSTEROIDS FROM CHOLESTEROL.

K. Wang, C. Sih, F. Chang, 1965, Journal of the American Chemical Society.

Chain-length determination mechanism of isoprenyl diphosphate synthases and implications for molecular evolution.

K. Wang, S. Ohnuma, S. Ohnuma, 1999, Trends in biochemical sciences.

Correlation between immunosuppressive activity and translation regulatory activity.

G. M. Iverson, K. Wang, R. Gershon, 1985, Immunology letters.

Transformation of Ginsenosides Rg1 and Rb1, and Crude Sanchi Saponins by Human Intestinal Microflora

K. Wang, Mei-Chih Lin, Shoei‐Sheng Lee, 2001 .

Microbial Transformation of Ceanothic Acid and Derivatives by Mycobacterium sp. (NRRL B-3805)

K. Wang, Shoei‐Sheng Lee, B. You, 1993 .

Microbial reduction of 2-(6-m-methoxyphenyl-3-oxohexyl)-2,4,4-trimethylcyclopenta-1,3-dione with Schizosaccharomyces pombe (NRRL Y-164)

K. Wang, Shoei‐Sheng Lee, Jiann-Long Yan, 1997 .

Synthesis of steroid intermediates via alkylation of dianion derived from acetoacetic ester.

K. Wang, S S Lee, K C Wang, 1994, Bioorganic & medicinal chemistry.

Derivatives of 10,11-dihydro-5H-dibenzo(a,d)cycloheptene and related compounds. 6. Aminoalkyl derivatives of the aza isosteres.

K. Wang, F. Villani, C. A. Ellis, 1972, Journal of medicinal chemistry.