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Profil bibliographique

Michael E. Richett

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

7Publications signalées
173Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Click Chemistry and ApplicationsMetal complexes synthesis and propertiesChemical Synthesis and AnalysisEnzyme function and inhibitionSynthesis and Characterization of Heterocyclic Compounds

Les publications récentes

Accès ouvert 2004 article OpenAlex

Acyl Sulfonamide Anti-Proliferatives: Benzene Substituent Structure−Activity Relationships for a Novel Class of Antitumor Agents

Karen L. Lobb, Philip A. Hipskind, James A. Aikins, Enrique L. Álvarez et autres

Two closely related diaryl acylsulfonamides were recently reported as potent antitumor agents against a broad spectrum of human tumor xenografts (colon, lung, breast, ovary, and prostate) in nude mice. Especially intriguing was their activity against colorectal cancer xenografts. In this paper, rapid …

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69 citations Journal of Medicinal Chemistry
2000 article OpenAlex

ChemInform Abstract: Diamino Benzo[b]thiophene Derivatives as a Novel Class of Active Site Directed Thrombin Inhibitors. Part 6. Further Focus on the Contracted C4′‐Side Chain Analogues.

Kumiko Takeuchi, Todd J. Kohn, Richard W. Harper, Ho‐Shen Lin et autres

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article …

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0 citations ChemInform
2000 article OpenAlex

Diamino Benzo[b]thiophene Derivatives as a Novel Class of Active Site Directed Thrombin Inhibitors. 5. Potency, Efficacy, and Pharmacokinetic Properties of Modified C-3 Side Chain Derivatives

Daniel J. Sall, Dianna L. Bailey, Jolie A. Bastian, John A. Buben et autres

A systematic investigation of the structure-activity relationships of the C-3 side chain of the screening hit 1a led to the identification of the potent thrombin inhibitors 23c, 28c, and 31c. Their activities (1240, 903, and 1271 x 10(6) L/mol, respectively) represent 2200- …

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31 citations Journal of Medicinal Chemistry

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