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Pharmacological Characterization and Investigation of NTerminal Loop Amino Acids of Adrenomedullin 2 That Are Important for Receptor Activation

English

Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2-C-Methylcytidine

English

Transition-Metal-Free Cyclization of Propargylic Alcohols With Aryne: Synthesis of 3Benzofuranyl-2-Oxindole and 3Spirooxindole Benzofuran Derivatives

English

Design and Synthesis of 1-Indol-1-Yl-Propan-2-Ones as Inhibitors of Human Cytosolic Phospholipase A2a

English

Combination Treatment of Ligustrazine Piperazine Derivate DLJ14 and Adriamycin Inhibits Progression of Resistant Breast Cancer Through Inhibition of the EGFR/PI3K/Akt Survival Pathway and Induction of Apoptosis

Drug discoveries & therapeutics

English

Synthesis, Spectral Characterization, DFT and in Vitro Antibacterial Activity of Zn(II), Cd(II) and Hg(II) Complexes Derived From a New Thiosemicarbazide

Letters in Applied NanoBioScience

2019

English

Figure 2: Average AgNPs UV–vis Spectra at Different Synthesis Temperature.

English

A Convenient Synthesis of Four Stereoisomers of 6-Acetoxy-5-Hexadecanolide, the Major Component of the Mosquito Oviposition Attractant Pheromone.

Agricultural and Biological Chemistry

1985

English

A Carboxy-Terminally Truncated Human CPSF6 Lacking Residues Encoded by Exon 6 Inhibits HIV-1 cDNA Synthesis and Promotes Capsid Disassembly

English

Microbial Growth on C1compounds. 2. Synthesis of Cell Constituents by Methanol- And Formate-grownPseudomonasAM 1, and Methanol-grownHyphomicrobium Vulgare

Biochemical Journal

1961

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Pharmacological Characterization and Investigation of NTerminal Loop Amino Acids of Adrenomedullin 2 That Are Important for Receptor Activation

Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2-C-Methylcytidine

Transition-Metal-Free Cyclization of Propargylic Alcohols With Aryne: Synthesis of 3Benzofuranyl-2-Oxindole and 3Spirooxindole Benzofuran Derivatives

Design and Synthesis of 1-Indol-1-Yl-Propan-2-Ones as Inhibitors of Human Cytosolic Phospholipase A2a

Combination Treatment of Ligustrazine Piperazine Derivate DLJ14 and Adriamycin Inhibits Progression of Resistant Breast Cancer Through Inhibition of the EGFR/PI3K/Akt Survival Pathway and Induction of Apoptosis

Synthesis, Spectral Characterization, DFT and in Vitro Antibacterial Activity of Zn(II), Cd(II) and Hg(II) Complexes Derived From a New Thiosemicarbazide

Figure 2: Average AgNPs UV–vis Spectra at Different Synthesis Temperature.

A Convenient Synthesis of Four Stereoisomers of 6-Acetoxy-5-Hexadecanolide, the Major Component of the Mosquito Oviposition Attractant Pheromone.

A Carboxy-Terminally Truncated Human CPSF6 Lacking Residues Encoded by Exon 6 Inhibits HIV-1 cDNA Synthesis and Promotes Capsid Disassembly

Microbial Growth on C1compounds. 2. Synthesis of Cell Constituents by Methanol- And Formate-grownPseudomonasAM 1, and Methanol-grownHyphomicrobium Vulgare