Theodros Asberom - Concepedia

Author

Theodros Asberom

Merck & Co., Inc., Rahway, NJ, USA (United States)

Also Known As

Asberom, T., T Asberom, T. ASBEROM, Theodros Asberom

Publications

881

Citations

H-Index

Concepts

All Affiliations

Merck & Co., Inc., Rahway, NJ, USA (United States)LabCorp (United States)Duke University

About

Theodros Asberom is an author at Merck & Co., Inc., Rahway, NJ, USA (United States) specializing in drug discovery, natural sciences, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	14	491
2	Natural Sciences	11	12	513
3	Biochemistry	11	12	488
4	Engineering	2	2	160
5	Biomolecular Engineering	1	1	75

Theodros Asberom

Publications

795

Citations

H-Index

Page 1

	Year	Citations
Discovery of Potent Orally Active Thrombin Receptor (Protease Activated Receptor 1) Antagonists as Novel Antithrombotic Agents Samuel Chackalamannil, Yan Xia, William J. Greenlee, Journal of Medicinal Chemistry ImmunologyPharmacotherapyNovel Thrombin ReceptorNovel Antithrombotic AgentsNatural Product Himbacine	2005	123
A Highly Efficient Total Synthesis of (+)-Himbacine Samuel Chackalamannil, Robert J. Davies, Theodros Asberom, Journal of the American Chemical Society Chemical EngineeringBiosynthesisBioorganic ChemistryEngineeringBiochemistry	1996	85
The chemistry of cyclic vinyl ethers. 6. Total synthesis of polyether ionophore antibiotics of the calcimycin (A-23187) class Robert K. Boeckman, André B. Charette, Theodros Asberom, Journal of the American Chemical Society HeterocyclicCyclic Vinyl EthersAntibioticsMedicineTotal Synthesis	1991	81
A convergent general synthetic protocol for construction of spirocyclic ketal ionophores: an application to the total synthesis of (-)-A-23187 (calcimycin) Robert K. Boeckman, André B. Charette, Theodros Asberom, Journal of the American Chemical Society Combinatorial ChemistryDiversity Oriented SynthesisMolecular SciencesEngineeringBiochemistry	1987	75
Total Synthesis of (+)-Himbacine and (+)-Himbeline Samuel Chackalamannil, Robert J. Davies, Yuguang Wang, The Journal of Organic Chemistry	1999	58
Cyclic Hydroxyamidines as Amide Isosteres: Discovery of Oxadiazolines and Oxadiazines as Potent and Highly Efficacious γ-Secretase Modulators in Vivo Z. J. Sun, Theodros Asberom, Thomas Bara, Journal of Medicinal Chemistry	2011	52
2,6-Disubstituted N-arylsulfonyl piperidines as γ-secretase inhibitors Dmitri Pissarnitski, Theodros Asberom, Thomas Bara, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyMedicinal ChemistryBiochemistryMedicineNatural Sciences	2006	39
Tetrahydroquinoline sulfonamides as γ-secretase inhibitors Theodros Asberom, Thomas Bara, John W. Clader, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyMedicinal ChemistryBiochemistryMedicineNatural Sciences	2006	37
Design and synthesis of xanthine analogues as potent and selective PDE5 inhibitors Yuguang Wang, Samuel Chackalamannil, Zhiyong Hu, Bioorganic & Medicinal Chemistry Letters Combinatorial ChemistryMedicinal ChemistryPharmaceutical ChemistrySelective Pde5 InhibitorsMedicine	2002	36
Identification of Presenilin 1-Selective γ-Secretase Inhibitors with Reconstituted γ-Secretase Complexes Julie Lee, Lixin Song, Giuseppe Terracina, Biochemistry	2011	34

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