Pharmacological activities trang 1 tải miễn phí từ TAILIEUCHUNG

"Pharmacological activities" trang 1 - tải miễn phí từ Tailieuchung

A review of traditional pharmacological uses, phytochemistry, and pharmacological activities of Tribulus terrestris

A review of traditional pharmacological uses, phytochemistry, and pharmacological activities of Tribulus terrestris

16 102 0

A brief review on bitter apple - Pharmacological activities

A brief review on bitter apple - Pharmacological activities

7 38 1

Functionalized formazans: A review on recent progress in their pharmacological activities

Functionalized formazans: A review on recent progress in their pharmacological activities

14 63 0

Review on pharmacological properties of glory lily (Gloriosa superba Linn.): An endangered medicinal plant

Review on pharmacological properties of glory lily (Gloriosa superba Linn.): An endangered medicinal plant

6 66 0

A review on ethnobotany and promising pharmacological aspects of an endangered medicinal plant, Curcuma caesia Roxb.

A review on ethnobotany and promising pharmacological aspects of an endangered medicinal plant, Curcuma caesia Roxb.

9 44 1

Synthesis and antibacterial and antifungal activities of N-(tetra-O-acet yl-β-d-glucopyranosyl)thiosemicarbazones of substituted 4-formylsydnones

Synthesis and antibacterial and antifungal activities of N-(tetra-O-acet yl-β-d-glucopyranosyl)thiosemicarbazones of substituted 4-formylsydnones

14 72 0

Genus mallotus (Euphorbiaceae): A review on traditional medicinal use, phytochemistry, and biological activities

Genus mallotus (Euphorbiaceae): A review on traditional medicinal use, phytochemistry, and biological activities

35 2 1

Pharmacological prospection and structural characterization of two purified sulfated and pyruvylated homogalactans from green algae Codium isthmocladum

Pharmacological prospection and structural characterization of two purified sulfated and pyruvylated homogalactans from green algae Codium isthmocladum

9 8 1

Palladium(0) catalyzed Suzuki cross-coupling reaction of 2,5-dibromo-3-methylthiophene: Selectivity, characterization, DFT studies and their biological evaluations

Palladium(0) catalyzed Suzuki cross-coupling reaction of 2,5-dibromo-3-methylthiophene: Selectivity, characterization, DFT studies and their biological evaluations

12 59 0

4-aroylpiperidines and 4-(α-hydroxyphenyl)piperidines as selective sigma-1 receptor ligands: Synthesis, preliminary pharmacological evaluation and computational studies

4-aroylpiperidines and 4-(α-hydroxyphenyl)piperidines as selective sigma-1 receptor ligands: Synthesis, preliminary pharmacological evaluation and computational studies

15 77 0

Synthesis and biological evaluation of quinoline-triazole and quinolone-triazole conjugates

Synthesis and biological evaluation of quinoline-triazole and quinolone-triazole conjugates

14 44 1

Synthesis and anti-nociceptive potential of isoxazole carboxamide derivatives

Synthesis and anti-nociceptive potential of isoxazole carboxamide derivatives

13 120 0

Synthesis and anticancer activity of novel quinazolinone‑based rhodanines

Synthesis and anticancer activity of novel quinazolinone‑based rhodanines

10 59 0

A facile access and evaluation of some novel thiazole and 1,3,4-thiadiazole derivatives incorporating thiazole moiety as potent anticancer agents

A facile access and evaluation of some novel thiazole and 1,3,4-thiadiazole derivatives incorporating thiazole moiety as potent anticancer agents

8 81 0

Molecular docking, synthesis and biological significance of pyrimidine analogues as prospective antimicrobial and antiproliferative agents

Molecular docking, synthesis and biological significance of pyrimidine analogues as prospective antimicrobial and antiproliferative agents

17 88 0

Pharmacokinetic and metabolomic analyses of Mangiferin calcium salt in rat models of type 2 diabetes and non-alcoholic fatty liver disease

Pharmacokinetic and metabolomic analyses of Mangiferin calcium salt in rat models of type 2 diabetes and non-alcoholic fatty liver disease

12 73 1

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