אפשרויות חיפוש:
eun ju » eun jung (הרחבת חיפוש)
eur j » eus j (הרחבת חיפוש)
kuo j » guo j (הרחבת חיפוש), kuo c (הרחבת חיפוש), kuo i (הרחבת חיפוש)
kuo _ » guo _ (הרחבת חיפוש), kuo c (הרחבת חיפוש), luo _ (הרחבת חיפוש)
luo j » guo j (הרחבת חיפוש)
eun j » eun ji (הרחבת חיפוש), sun j (הרחבת חיפוש), jun j (הרחבת חיפוש)
chem » chen (הרחבת חיפוש)
A mostrar 1 - 20 resultados de 894 para a pesquisa '((((eur j) OR (((((kuo j) OR (kuo _))) OR (luo j))))) OR (((eun j) OR (eun ju)))) med chem', זמן שאילתה: 0.86seg Refinar resultados
Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries
Editorial – IChemE Special Issue on Climate Change

Preparation of polyoxometalate-doped aminosilane-modified silicate hybrid as a new barrier of chem-bio toxicant
Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles

Effect of cinnamamides on atopic dermatitis through regulation of IL-4 in CD4(+) cells
Anti-AIDS Agents 81. Design, Synthesis and Structure-Activity Relationship Study of Betulinic Acid and Moronic Acid Derivatives as Potent HIV Maturation Inhibitors

Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria
Design and synthesis of 6,7-methylenedioxy-4-substituted phenylquinolin-2(1H)-one derivatives as novel anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase

Synthesis and antitumor activity of bis(hydroxymethyl)propionate analogs of pterostilbene in cisplatin-resistant human oral cancer cells
Effect of structural modification in the amine portion of substituted aminobutyl-benzamides as ligands for binding σ(1) and σ(2) receptors

Antitumor Agents 286. Design, Synthesis and Structure-Activity Relationships of 3′R,4′R-Disubstituted-2′,2′-dimethyldihydropyrano[2,3-f]chromone (DSP) Analogs as Potent Chemosensitizers to Overcome Multidrug Resistance
Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogs as Potent Antitumor Agents that Inhibit Tubulin Assembly

Design, synthesis, and mechanism of action of 2-(3-hydroxy-5-methoxyphenyl)-6-pyrrolidinylquinolin-4-one as a potent anticancer lead
Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells

Design, synthesis, and structure activity relationship analysis of new betulinic acid derivatives as potent HIV inhibitors
Novel Curcumin Analogs to Overcome EGFR-TKI Lung Adenocarcinoma Drug Resistance and Reduce EGFR-TKI-induced GI Adverse Effects

Synthesis and β-amyloid binding properties of rhenium 2-phenylbenzothiazoles
Cancer Preventive Agents 9. Betulinic Acid Derivatives as Potent Cancer Chemopreventive Agents (†)

Anti-AIDS agents 89. Identification of DCX derivatives as anti-HIV and chemosensitizing dual function agents to overcome P-gp-mediated drug resistance for AIDS therapy
Structural and bioactive studies of terpenes and cyclopeptides from the Genus Rubia

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