C. T.‐C. CHANG - Concepedia

Author

C. T.‐C. CHANG

KU Leuven

Also Known As

C. T.‐C. CHANG, C.T.-C. Chang, Charles T. C. Chang, Charles T.-C. Chang

Publications

384

Citations

H-Index

Concepts

All Affiliations

KU Leuven United States Military Academy Rega Institute for Medical Research

About

C. T.‐C. CHANG is an author at KU Leuven specializing in biochemistry, natural sciences, and medicinal chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	4	4	131
2	Biochemistry	4	4	131
3	Medicine	3	3	116
4	Biomolecular Engineering	1	1	65
5	Chemical Biology	1	1	30

C. T.‐C. CHANG

Publications

354

Citations

H-Index

Page 1

	Year	Citations
Non-Peptide Fibrinogen Receptor Antagonists. 2. Optimization of a Tyrosine Template as a Mimic for Arg-Gly-Asp Melissa S. Egbertson, C. T.‐C. CHANG, Mark E. Duggan, Journal of Medicinal Chemistry	1994	178
Non-Peptide Fibrinogen Receptor Antagonists. 7. Design and Synthesis of a Potent, Orally Active Fibrinogen Receptor Antagonist Mark E. Duggan, Adel M. Naylor-Olsen, James J. Perkins, Journal of Medicinal Chemistry Chimpanzee PlateletsThrombosisMedicinal ChemistryThrombopoiesisLow-molecular Weight	1995	65
Oxime and dithiolane derivatives of 5-formyl-2'-deoxyuridine and their 5'-phosphates: antivirial effects and thymidylate synthetase inhibition Joon Sup Park, C. T.‐C. CHANG, Charles L. Schmidt, Journal of Medicinal Chemistry Host Cell DnaBioorganic ChemistrySynthetic VirologyAntiviral DrugChemical Biology	1980	30
Antiviral, antitumor, and thymidylate synthetase inhibition studies of 5-substituted styryl derivatives of 2′-deoxyuridine and their 5′-phosphates Erik De Clercq, Jan Balzarini, J Descamps, Biochemical Pharmacology Medicinal ChemistryDerivative (Chemistry)DerivativesBiochemistryNatural Sciences	1981	21
5-(.alpha.-Bromoacetyl)-2'-deoxyuridine 5'-phosphate: an affinity label for thymidylate synthetase Christie B. Brouillette, C. T.‐C. CHANG, Mathias P. Mertes Journal of Medicinal Chemistry	1979	19
5-Nitro-2′-deoxyuridine 5′-monophosphate is a potent irreversible inhibitor of Lactobacillus caesi thymidylate synthetase Mathias P. Mertes, C. T.‐C. CHANG, Erik De Clercq, Biochemical and Biophysical Research Communications Biochemistry5-Nitro-2′-deoxyuridine 5′-MonophosphatePotent Irreversible InhibitorBiocatalysisNatural Sciences	1978	15
Synthesis of 5-[(methylthio)methyl]-2'-deoxyuridine, the corresponding sulfoxide and sulfone, and their 5'-phosphates: antiviral effects and thymidylate synthetase inhibition Charles L. Schmidt, C. T.‐C. CHANG, Erik De Clercq, Journal of Medicinal Chemistry	1980	15
5-[(4-Methyl-1,2,3,4-tetrahydroquinoxalyl)methyl]-2'-deoxyuridine 5'-phosphate: an analogue of a proposed intermediate in thymidylate synthetase catalysis Joon Sup Park, C. T.‐C. CHANG, Mathias P. Mertes Journal of Medicinal Chemistry	1979	11

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