Suvit Thaisrivongs - Concepedia

Author

Suvit Thaisrivongs

W.E. Upjohn Institute for Employment Research

Also Known As

S Thaisrivongs, S. THAISRIVONGS, S. Thaisrivongs, Suvit Thaisrivongs, Suvit. Thaisrivongs

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

W.E. Upjohn Institute for Employment Research

About

Suvit Thaisrivongs is an author at W.E. Upjohn Institute for Employment Research specializing in pharmacology, biochemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	23	27	1.9K
2	Biochemistry	23	27	1.9K
3	Medicine	20	26	1.8K
4	Biomolecular Engineering	10	11	835
5	Engineering	9	9	776

Suvit Thaisrivongs

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIV Protease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class Steve R. Turner, Joseph W. Strohbach, Rubén Tommasi, Journal of Medicinal Chemistry	1998	293
An inhibitor of the protease blocks maturation of human and simian immunodeficiency viruses and spread of infection. Per Ashorn, T. J. MCQUADE, Suvit Thaisrivongs, Proceedings of the National Academy of Sciences ImmunologyAntiviral DrugHuman Immunodeficiency VirusHuman RetrovirusAntiviral Drug Development	1990	185
The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A) Robert E. Ireland, Robert C. Anderson, R. Badoud, Journal of the American Chemical Society Pharmaceutical ScienceEngineeringOrganic ChemistryAntimicrobial ChemotherapyPharmaceutical Chemistry	1983	170
Enolate Claisen rearrangement of esters from furanoid and pyranoid glycals Robert E. Ireland, Suvit Thaisrivongs, Noel R. Vanier, The Journal of Organic Chemistry EngineeringEnolate Claisen RearrangementAltmetric Attention ScoreOrganic ChemistryChemistry	1980	155
Structure-Based Design of HIV Protease Inhibitors: 4-Hydroxycoumarins and 4-Hydroxy-2-pyrones as Non-peptidic Inhibitors Suvit Thaisrivongs, Paul K. Tomich, Keith David Watenpaugh, Journal of Medicinal Chemistry Hiv Protease InhibitorsAltmetric Attention ScorePharmacotherapyAntiviral DrugPharmaceutical Chemistry	1994	152
Design and synthesis of potent and specific renin inhibitors containing difluorostatine, difluorostatone, and related analogs Suvit Thaisrivongs, Donald T. Pals, Warren M. Kati, Journal of Medicinal Chemistry Tetrahedral IntermediateBioorganic ChemistryPharmacotherapyChemical BiologyPharmaceutical Chemistry	1986	134
Antiviral activity of the dihydropyrone PNU-140690, a new nonpeptidic human immunodeficiency virus protease inhibitor Susan M. Poppe, Dea Slade, K. T. Chong, Antimicrobial Agents and Chemotherapy Dihydropyrone Pnu-140690ImmunologyPharmacotherapyAntiviral DrugDrug Resistance	1997	121
Structure-Based Design of Novel HIV Protease Inhibitors: Carboxamide-Containing 4-Hydroxycoumarins and 4-Hydroxy-2-pyrones as Potent Nonpeptidic Inhibitors Suvit Thaisrivongs, Keith David Watenpaugh, W. Jeffrey Howe, Journal of Medicinal Chemistry	1995	121
(+)‐11,11′‐Di‐<i>O</i>‐methylelaiophylidene – preparation from elaiophylin and total synthesis from (<i>R</i>)‐3‐hydroxybutyrate and (<i>S</i>)‐malate Dieter Seebàch, Hak‐Fun Chow, Richard F. W. Jackson, Liebigs Annalen der Chemie Bioorganic ChemistryEngineeringOrganic ChemistryMedicinal ChemistryDiversity Oriented Synthesis	1986	100
Structure-Based Design of HIV Protease Inhibitors: Sulfonamide-Containing 5,6-Dihydro-4-hydroxy-2-pyrones as Non-Peptidic Inhibitors Suvit Thaisrivongs, Harvey I. Skulnick, Steve R. Turner, Journal of Medicinal Chemistry Hiv Protease InhibitorsPharmacotherapyAntiviral DrugChemical BiologyDrug Metabolism Research	1996	96

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