Alpha 2.0
Login Register
» Authors » A N Pae

A N Pae

Explore the profile of A N Pae including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 10
Citations 3
Followers 0
Related Specialties
Pharmacology
Infectious Diseases
Biochemistry
Top 10 Co-Authors
Y S Cho
K I Choi
H Y Koh
J H Cha
M H Chang
H Y Kang
J Y Kong
D Jeong
J H Choi
H Y Kim
Published In
J Antibiot (Tokyo)
Bioorg Med Chem Lett
Arch Pharm (Weinheim)
Affiliations
Soon will be listed here.
Recent Articles
1.
Synthesis and In vitro binding affinities of 1-azabicyclic compounds as muscarinic ligands
Cha J, Cho Y, Pae A, Koh H, Jeong D, Kong J, et al.
Bioorg Med Chem Lett . 2001 Oct; 11(21):2855-7. PMID: 11597415
Two series of compounds, 2 and 3, were synthesized and their binding affinities were evaluated for the human recombinant muscarinic M(1) receptor subtype expressed in CHO cells. Comparing their binding...
2.
Binding affinities of 3-(3-phenylisoxazol-5-yl)methylidene-1-azabicycles to acetylcholine receptors
Choi K, Cha J, Cho Y, Pae A, Jin C, Yook J, et al.
Bioorg Med Chem Lett . 1999 Oct; 9(19):2795-800. PMID: 10522693
A series of 3-(3-phenylisoxazol-5-yl)methylidene-1-azabicycles synthesized showed different binding characteristics to acetylcholine receptors depending on the substituents on the phenyl ring. Small polar substituents gave preferential binding affinity to nicotinic receptors,...
3.
3D QSAR studies on new oxazolidinone antibacterial agents by comparative molecular field analysis
Pae A, Kim S, Kim H, Joo H, Cho Y, Choi K, et al.
Bioorg Med Chem Lett . 1999 Oct; 9(18):2685-90. PMID: 10509916
Three-dimensional QSAR studies for two series of new oxazolidinone antibacterial agents were conducted using the comparative molecular field analysis (CoMFA). In vitro activities (MICs) of the compounds against methicillin-resistant Staphylococcus...
4.
Synthesis and in vitro activity of new oxazolidinone antibacterial agents having substituted isoxazoles
Pae A, Kim H, Joo H, Kim B, Cho Y, Choi K, et al.
Bioorg Med Chem Lett . 1999 Oct; 9(18):2679-84. PMID: 10509915
Two series of oxazolidinone derivatives having substituted isoxazoles were synthesized and tested for antibacterial activities against several Gram-positive strains including the resistant strains of Staphylococcus and Enterococcus, such as MRSA,...
5.
Synthesis and evaluation of 2 beta-oxyimino and alkenylpenicillanic acid sulfone derivatives as beta-lactamase inhibitors
Cho Y, Ha Y, Kwon J, Pae A, Choi K, Koh H, et al.
Arch Pharm (Weinheim) . 1999 Mar; 332(1):7-12. PMID: 10073138
The synthesis and in vitro synergies of 2 beta-alkenyl and oxyiminopenam sulfone derivatives are described. Most of the compounds synthesized exhibited good inhibitory activities and synergistic antibacterial activities with piperacillin...
6.
Studies on novel 3-isoxazolylvinyl-cephalosporins: II. Synthesis and biological activity of 7-[2-(2-aminothiazol-4-yl)-2-hydroxy-iminoacetamido] derivatives
Choi K, Cha J, Pae A, Cho Y, Kim Y, Chang M, et al.
J Antibiot (Tokyo) . 1999 Feb; 51(12):1122-5. PMID: 10048574
No abstract available.
7.
Studies on novel 3-isoxazolylvinyl-cephalosporins: I. Synthesis and biological activity of 7-[2-(2-aminothiazol-4-yl)-2-(alkoxy)-iminoacetamido] derivatives
Choi K, Cha J, Pae A, Cho Y, Chang M, Koh H
J Antibiot (Tokyo) . 1999 Feb; 51(12):1117-21. PMID: 10048573
No abstract available.
8.
Studies on new catechol containing cephalosporins. III. Synthesis and structure-activity relationships of cephalosporins having a pyridone moiety at the C-7 position
Choi K, Cha J, Pae A, Cho Y, Koh H, Chang M, et al.
J Antibiot (Tokyo) . 1997 Mar; 50(3):279-82. PMID: 9127205
No abstract available.
9.
Studies on new catechol containing cephalosporins. II. Synthesis and structure-activity relationships of cephalosporins having a catechol moiety at the C-7 position
Choi K, Cha J, Pae A, Cho Y, Kang H, Koh H, et al.
J Antibiot (Tokyo) . 1995 Nov; 48(11):1375-7. PMID: 8557588
No abstract available.
10.
Studies on new catechol containing cephalosporins. I. Synthesis and structure-activity relationships of cephalosporins having a catechol moiety at the C-3 position
Choi K, Cha J, Pae A, Cho Y, Kang H, Koh H, et al.
J Antibiot (Tokyo) . 1995 Nov; 48(11):1371-4. PMID: 8557587
No abstract available.