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The compounds were evaluated for activity and selectivity with regard to 17β-HSD2, ERα and ERβ.
Ni/Al2O3 catalysts doped with cerium oxide were evaluated for activity and metal dispersion to investigate the promoter effects.
Variously substituted indolin-2-ones were synthesized and evaluated for activity against KDR, Flt-1, FGFR-1 and PDGFR.
Selected compounds were also evaluated for activity against reverse transcriptase, and had lower IC50 values than that of nevirapine.
cis- and trans-isoxazolidine phosphonates obtained herein were evaluated for activity against a broad range of DNA and RNA viruses.
A series of monopyrrolinone-based HIV-1 protease inhibitors possessing rationally designed P2′ side chains have been synthesized and evaluated for activity against wild-type HIV-1 protease.
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Two vanillin derivatives have been designed and synthesized and their biological activities were also evaluated for antimicrobial activity.
These compounds were further biologically evaluated for analgesic activity, and few of them showed activity.
SLE patients were evaluated for disease activity by using the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) [ 21].
Lignocellulose degrading fungal spp. were isolated and evaluated for the activity of lignocellulolytic enzymes.
The isolates were evaluated for biodegradation activity against PAHs, phenol and sodium sulfate.
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